] |
negatively . | bestimmtes Beuteschema kann Partnersuche . | ||||||
? | Tool Terminfindung ? |
While New Mexico State University’s Clayton Livestock Research Center usually showcases research during its annual field day event, this year’s event will feature a number of new amenities, as well as an opportunity for the public to meet the center’s new research director.
This year’s field day will take place from 9 a.m. to 1 p.m. Sept. 16 at the center, located at 15 NMSU Lane in Clayton, New Mexico.
Mozart Fonseca began his role as Clayton’s research director in 2024 and is also an associate professor of animal and range sciences at NMSU. Coinciding with Fonseca’s arrival at the center are a number of upgrades that have taken place through funding from the New Mexico Legislature.
The center now features new signage and a renovated workroom and sample prep area, as well as a foyer. There is also a feed mill augmented with upgraded electrical and computer-controlled operations for state-of-the-art ration blending and delivery. The center also has a new pivot irrigation system, digital individual animal feeders and waterers, greenhouse gas emissions monitoring equipment, and soil carbon measuring instrumentation that will provide opportunities for additional funding and research to help meet the needs of the livestock industry.
Research presentations at this year’s field day include:
• Impact of bovine respiratory disease on finishing heifers: DART scores, performance and carcass quality.
• Evaluation of perennial versus annual forage production as a sustainable grazing strategy for the southwestern United States.
• The relationship between fiber, starch and isoacids: unlocking gut health dynamics.
• Water use, smoke and sustainable grazing systems for New Mexico and beyond.
The field day is free and open to the public. Individuals with a disability who are in need of an auxiliary aid or service to participate may contact Luiza Cardone at 575-646-3586 or [email protected] . To register to attend, visit https://rsvp.nmsu.edu/rsvp/clayton .
PHOTO CAPTION: The Clayton Livestock Research Center in Clayton, New Mexico, will host its annual field day Sept. 16. The field day will highlight research presentations, along with a number of facility upgrades to the center. (NMSU photo by Josh Bachman)
IMAGE DESCRIPTION: Aerial photo
Implementation Science Communications volume 2 , Article number: 120 ( 2021 ) Cite this article
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Implementation frameworks may support local implementation strategies with a sound theoretical foundation. The Consolidated Framework for Implementation Research (CFIR) facilitates identification of contextual barriers and facilitators, and the Expert Recommendations for Implementing Change (ERIC) allows identifying adequate implementation strategies. Both instruments are already used in German-speaking countries; however, no standardised and validated translation is available thus far. The aim of this study was to translate the CFIR and ERIC framework into German, in order to increase the use of these frameworks and the adherence to evidence-based implementation efforts in German-speaking countries.
The translation of the original versions of the CFIR and ERIC framework was guided by the World Health Organisation’s recommendations for the process of translating and adapting both conceptual frameworks. Accordingly, a four-step process was employed: first, forward translation from English into German was conducted by a research team of German native speakers with fluent knowledge of the English language. Second, a bilingual expert panel comprising one researcher with German as his mother tongue and expert command of the English language and one English language expert and university teacher reviewed the translation and discussed inconsistencies with the initial translators. Third, back-translation into English was conducted by an English native speaking researcher. The final version was pre-tested with 12 German researchers and clinicians who were involved in implementation projects using cognitive interviews.
The translation and review process revealed some inconsistencies between the original version and the German translations. All issues could be solved by discussion. Central aspects of the items were confirmed in 60 to 70% of the items, and modifications were proposed in 30% of the items. Finally, we revised one CFIR-item heading after pre-testing. The final version was given consent by all involved parties.
Now, two validated and tested implementation frameworks to guide implementation efforts are available in the German language and can be used to increase the application of agreed-on implementation strategies into practice.
Peer Review reports
To increase the application of CFIR and ERIC implementation frameworks in German-speaking countries, these concepts are now available in German
The conceptual frameworks can be used by clinicians, researchers, managers and organisations to increase adherence to evidence-based implementation activities, and to improve the transferability of this experience into local practice
The frameworks were translated into German using a standardised WHO approach, including pre-testing with German health care professionals, researchers, and clinicians
Many interventions in health care are considered to be effective, but efficacy in terms of achieving desired changes in patient-relevant health outcomes is critically dependent on successful implementation [ 1 , 2 ]. Lack of information about a study’s local context and poor reporting of implementation strategies employed may be accountable for the critical gap between implementation research and clinical practice [ 2 , 3 ]. The use of implementation frameworks may help to increase adherence to evidence-based implementation strategies and to establish a consensus terminology for German-speaking implementation experts [ 4 ].
The Consolidated Framework for Implementation Research (CFIR) [ 1 ] provides a tool box of different constructs arranged across five domains that should be used in a range of settings. It can help to identify potential barriers and help facilitators to change, and can be used as theory-based constructs for developing effective implementation strategies [ 1 ].The Expert Recommendations for Implementing Change (ERIC) systematically catalogued implementation strategies via input from a wide range of stakeholders and structured them into different categories and definitions [ 5 , 6 ].
Identifying barriers and facilitators at different dimensions and tailoring interventions appear crucial to successful implementation of interventions into practice. Moreover, a Cochrane review [ 7 ] concluded that tailored interventions addressing implementation barriers are more likely to improve professional practice than untailored interventions, e.g., clinical practice guidelines alone, while more research is needed on the causal mechanisms for successful implementation and how to address these determinants. As a first step for implementation researchers, the CFIR provides a systematic framework to categorise potential barriers and facilitators. As a second step and to tailor the implementation, ERIC catalogues potential implementation strategies. To connect those, a tool was built that linked the context assessment using CFIR and implementation strategies to be considered using ERIC, the CFIR–ERIC–matching tool (available under www.cfirguide.org ) [ 8 ].
Both taxonomies are already used in various studies with a wide range of objectives, methods, and settings [ 9 ] including German-speaking countries [ 10 ]. However, no standardised and validated translation into German was available thus far.
The aim of this study was to develop a German translation of both CFIR and ERIC in order to increase adherence to evidence-based implementation activities in German-speaking countries.
We followed the translation process suggested by the World Health Organisation (WHO) [ 11 ] that comprises forward translation, expert panel discussion, back-translation, and pre-testing (see Fig. 1 ).
Flowchart describing the WHO translation and pre-testing process [ 11 ]. Legend: R = Randomisation
The research team, all familiar with the content of CFIR and ERIC and German native speakers with fluent knowledge of the English language, translated the original English version of CFIR [ 1 ] and ERIC [ 6 ] into German. The aim was to find conceptually equivalent wordings and phrases.
First, a small (unilingual) expert panel with a German-speaking researcher, who already had translated and used a German version of CFIR, and members of the research team was established. Differences between the result of the forward translation of CFIR and the older version were discussed and led to the revision of some items.
Second, a bilingual expert panel discussed both the translation of CFIR and ERIC. The expert panel, which consisted of a collaborating Canadian researcher (TR) with German as his mother tongue and expert command of the English language and one English language expert and university teacher (CC), revised the German translation. They recommended changes of distinct phrases. Inconsistencies were discussed among the research team and the bilingual experts.
The work of the expert panels led to a first German version of CFIR and ERIC.
Back-translation
Back-translation of the instruments into English was conducted by an independent English native-speaking researcher (AP) living and working in Germany for several years. As recommended by the WHO method, the back-translator had no specific knowledge of the instruments. Inconsistencies between the back-translation and the original versions were discussed among the research team using dictionaries and several online translators. This resulted in the second version of the German translation that went into pre-testing with potential users of the tools.
Research team.
VR and ES conducted the individual, semi-structured interviews with experts working in implementation and/or health care research and who could potentially use the translated instruments. The interviewers knew some of the participants personally. No bias or assumptions are to be reported from the interviewers.
We conducted individual semi-structured interviews. Potential participants, in particular health care researchers were recruited from universities and research institutes in German-speaking countries and were approached via e-mail. To limit the burden for the participants, we decided to present only a subset of the items to each participant. Considering a total number of 112 items and an estimated interview time of about 2 min for each item, we predefined a sample size of 12 participants to discuss 10 items per 20-min interview. Items of each instrument were randomised to the number of participants using a computer-generated sequence number (Random Sequence Generator, available at https://www.random.org/sequences/ ). All participants gave written informed consent and filled in a short sociodemographic questionnaire prior to the interview.
Since there was no established strategy for pre-testing or validating of these instruments, we had to develop our own strategy. This contains cognitive interviews that involve a “think-aloud-probing” procedure, in which interviewers instruct participants to verbalise thoughts while answering the posed questions [ 12 ]. In parts, we relied on the key stages of cognitive interviewing according to Willis et al. [ 13 ]. This full strategy comprised five steps.
Step 1: To warm up with the item during the interview, the interviewees were asked to describe the given definition in their own words.
Step 2: Interviewees were asked to formulate a heading that describes the content best after reading the detailed definitions. The aim of this step was to generate information about the perceived central focus of those items.
Step 3: Then, the translated heading in German was compared with the interviewee-suggested heading and discussed afterwards.
Step 4: To rate this comparison, a traffic light system was used to rate whether our translated heading was perceived as appropriate. In this rating system, “green” means “approved”, “yellow” “partially approved”, and “red” “rejected”. Additionally, text notes were made about why the participants rate “yellow” or “red”.
Step 5: Items rated “green” were immediately considered to be accepted. In the case of “yellow”, the proposed modifications were recorded and discussed within the research team and adapted if the considered modifications were rated to be meaningful. In the case of ”red”, the item was re-tested in a second interview. When the item was then rated as “green”, it was considered approved. In any other case, we revised the item as recommended by the two interviews and amended the heading with our initial translation in brackets.
Interviews were conducted by phone. Researchers had a short interview guide, and questions were allocated by the randomised items per interviewee. The interview guide was pilot tested with two persons and adapted prior to the interviews. Our initial pilot-tests revealed that rating CFIR barriers together with ERIC strategies was too complex and confusing due to the different foci. Thus, we decided to present items of only one respective framework per interview. In our interviews, we provided the example of implementing an electronic assessment system in a general practice or physiotherapy practice to support participants contextualising implementation items.
No repeated interviews were carried out. All interviews were guided and audio-recorded by one of the two experienced research associate (VR or ES). Field notes were made during the interviews. Audio-records were neither transcribed nor coded. Interviews were recorded to be available as backup for the field notes. Field notes were used to categorise items, and percentages of ratings per interview were calculated. Total percentages were calculated using mean values of percentages for each tool.
We translated the short instructions of the tool into German and contacted the authors. We inserted the final versions of CFIR and ERIC into the matching tool and checked its function.
Our initial forward translation of each instrument (see Additional file 1 ) was revised by the expert panel. Recommendations for changes and our decisions for or against changes are described in Additional file 2 . The recommendations included correctness and style like using linguistic synonyms, keeping the ideas of “and/or”, using correct grammar and punctuation marks. For example: CFIR; Item no. 2.3: Peer pressure . Initial translation: Druck durch Kollegen . Recommendation by the expert panel: Change “Druck durch Kollegen” into “Gruppenzwang” because this word is more usual . All issues could be solved by discussion. Then, these first versions were translated back into the original language (see Additional file 3 ). Then we compared the original English version to the back-translated version, and synonyms were identified. For example: CFIR; Item no. 1.5: Trialability . Backtranslation into original language: Testability . ERIC; Item no. 61. Original: Stage implementation scale up ; Backtranslation into original language: Proceed step by step with the implementation .
Characteristics of participants.
We contacted 12 individuals, all of whom agreed to participate. Mean age of the participants was 36 years, and most of the participants were female ( n = 10; 83%). All participants had at least a master’s degree, and most were working as research associates ( n = 10; 83%) and had experience in implementation of health care interventions (see Table 1 ). The interviews lasted between 9 and 36 min.
In brief, the similar central focus of our German translations of CFIR and ERIC compared to the English original was confirmed in most items.
Among the CFIR items (see Table 2 ), two items (5%) were rejected in the first round and presented in a second interview. Of these, one item was again rejected, and one was partially approved. In total, 27 items (69%) were approved in the first round. Modifications were proposed for 11 (28%) items. Only one item (3%) had to be revised after pre-testing. Recommendations for modifications can be seen in Additional file 4 .
Among the ERIC items (see Table 3 ), two items were rejected in the first round and accepted in the second round. In summary, 47 items (64%) were approved. No item had to be revised. Modifications were proposed for 26 items (36%). Recommendations for modifications can be seen in Additional file 4 .
Final version
After pre-testing, we revised the rejected item, but kept our pre-tested translation in brackets (see Additional file 5 ). The final versions were agreed upon by all parties involved in the translation process. A German version of CFIR-ERIC-Matching tool is available upon request.
A German version of two conceptual frameworks for shaping implementation activities in health care, CFIR and ERIC, as well as the corresponding matching tool, are now available.
A rigorous translation and pre-testing process guided us through the WHO translation process to a final version of each framework. The pre-testing process proved to be feasible.
In our initial forward translation, we aimed to keep the original linguistic structure as far as possible. In the expert panel, we discussed alternative translations to items which appeared to be in “Denglish” jargon (a variety of German containing a high proportion of English words), but accepted English words which are common in German (e.g., CFIR, headings 2 and 3, “Äußeres/Inneres Setting”; ERIC, item 35, “Champions identifizieren und vorbereiten”). Beside this, we also tried to keep a coherent structure of the Original and our German translation as possible. Since we referred to Powell et al. [ 6 ] in carrying out our forward translation of ERIC, we did not additionally translate the nine categories outlined in Waltz et al. [ 5 ]. When using the CFIR-ERIC-matching tool, the categories above the implementation strategies appear not crucial to know, but we would recommend its translation when using ERIC itself in a conceptual context.
Faced with the high number of items, the bilingual expert panels were quite time-consuming. Both ERIC and CFIR documents were very detailed, including health care-specific vocabulary, and nuances that required careful translation, all of which led to taking a lot of time. We recommended a considerable number of changes to the early translation.
Regarding back-translation of the instruments, we predominantly found synonyms to the English original. Close attention was given to the health care-specific vocabulary. This remained a difficult task for the back-translator:
We were not able to identify and use an established strategy for pre-testing or validating these frameworks. A developed checklist in form of a traffic light system to test the usefulness of the translated heading was successful.
The translation and pre-testing process also revealed that even headings in the original version did not comprise the whole content of the detailed definition. For example, CFIR 4.1; Original heading: Knowledge and Beliefs about the Intervention ; Original description: Stakeholders have negative attitudes toward the innovation, they place low value on implementing the innovation, and/or they are not familiar with facts, truths, and principles about the innovation . Pre-tested description: Beteiligte haben negative Einstellungen gegenüber der Innovation, sie schreiben ihr geringen Wert zu und/oder sind mit den Fakten, Wahrheiten und Prinzipien der Innovation nicht vertraut ; Pre-tested heading: Wissen und Überzeugungen über die Innovation ; Selected heading by the interviewee: Ablehnung der Innovation; Recommendation of the interviewee: The negative perception is missing in the original heading .
During the translation, expert panel and back-translation process, several issues were discussed and kept in the original English language to provide a clear and correct message.
In total, 4 of 112 items were discussed in a second interview. This might indicate selection bias in terms of our interview participants (e.g., allocating an item to “yellow” (partly approved) rather than to “red” (rejected) because participants wanted to be perceived as nice). Since we predominantly tested one item per interviewee, a different sample of participants might have rejected more items. Our sample comprised different researchers and academics experienced in specific terms like “evidence” or “validity”. A pre-test with a different sample of non-academic individuals might have led to different results.
Transferring theoretical frameworks from one language to another is challenging beyond the linguistic perspective but also from the perspective of validity since the contained constructs and relationships between them largely depend on context, such as different health care systems. However, since both frameworks are already being used in German health care, we believe that a standardised and agreed on translated version may increase understanding, uptake, transparency, and reproducibility of implementation research in German speaking countries. Moreover, the standard of English may differ widely between healthcare professionals in Germany.
Future applications of the translated German version of CFIR and ERIC should monitor and report problems and limitations and may lead to further revisions.
Both translated frameworks can now be used within implementation research in German-speaking countries. This might improve adherence to evidence-based implementation into practice in German-speaking countries. We recommend a patient version of the translated implementation frameworks, which use a lay language (not exceeding German 6th class middle school writing).
Expert Recommendations for Implementation Change
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Verena Regauer & Eva Seckler
Institute for Medical Information Processing, Biometry and Epidemiology, Ludwig-Maximilians-Universität München, Marchioninistraße 17, 81377, Munich, Germany
Verena Regauer, Eva Seckler & Amanda Phillips
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Craig Campbell
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Correspondence to Verena Regauer .
Ethics approval and consent to participate.
Ethics approval and consent: both implementation frameworks (CFIR and ERIC) have been published in the literature, and are publicly available. The Ethical Committee of the Ludwig Maximilian University of Munich has approved the study protocol under the number 20-801. Moreover, all interviewed participants are close collaborators of the senior author and gave their written informed consent to participate in the interviews.
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Additional file 1..
Initial forward version
Summary of recommendations by the expert panel
Additional file 4..
Summary of problems found during the pre-testing of the instrument and the modifications proposed
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Regauer, V., Seckler, E., Campbell, C. et al. German translation and pre-testing of Consolidated Framework for Implementation Research (CFIR) and Expert Recommendations for Implementing Change (ERIC). Implement Sci Commun 2 , 120 (2021). https://doi.org/10.1186/s43058-021-00222-w
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Home » Research Findings – Types Examples and Writing Guide
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Definition:
Research findings refer to the results obtained from a study or investigation conducted through a systematic and scientific approach. These findings are the outcomes of the data analysis, interpretation, and evaluation carried out during the research process.
There are two main types of research findings:
Qualitative research is an exploratory research method used to understand the complexities of human behavior and experiences. Qualitative findings are non-numerical and descriptive data that describe the meaning and interpretation of the data collected. Examples of qualitative findings include quotes from participants, themes that emerge from the data, and descriptions of experiences and phenomena.
Quantitative research is a research method that uses numerical data and statistical analysis to measure and quantify a phenomenon or behavior. Quantitative findings include numerical data such as mean, median, and mode, as well as statistical analyses such as t-tests, ANOVA, and regression analysis. These findings are often presented in tables, graphs, or charts.
Both qualitative and quantitative findings are important in research and can provide different insights into a research question or problem. Combining both types of findings can provide a more comprehensive understanding of a phenomenon and improve the validity and reliability of research results.
Research findings typically consist of several parts, including:
Writing research findings requires careful planning and attention to detail. Here are some general steps to follow when writing research findings:
Following is a Research Findings Example sample for students:
Title: The Effects of Exercise on Mental Health
Sample : 500 participants, both men and women, between the ages of 18-45.
Methodology : Participants were divided into two groups. The first group engaged in 30 minutes of moderate intensity exercise five times a week for eight weeks. The second group did not exercise during the study period. Participants in both groups completed a questionnaire that assessed their mental health before and after the study period.
Findings : The group that engaged in regular exercise reported a significant improvement in mental health compared to the control group. Specifically, they reported lower levels of anxiety and depression, improved mood, and increased self-esteem.
Conclusion : Regular exercise can have a positive impact on mental health and may be an effective intervention for individuals experiencing symptoms of anxiety or depression.
Research findings can be applied in various fields to improve processes, products, services, and outcomes. Here are some examples:
Research findings can be used in a variety of situations, depending on the context and the purpose. Here are some examples of when research findings may be useful:
The purpose of research findings is to contribute to the knowledge and understanding of a particular topic or issue. Research findings are the result of a systematic and rigorous investigation of a research question or hypothesis, using appropriate research methods and techniques.
The main purposes of research findings are:
Research findings have several key characteristics that distinguish them from other types of information or knowledge. Here are some of the main characteristics of research findings:
Research findings have many advantages, which make them valuable sources of knowledge and information. Here are some of the main advantages of research findings:
While research findings have many advantages, they also have some limitations. Here are some of the main limitations of research findings:
Researcher, Academic Writer, Web developer
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Research noun —, forschung f (über) (often used), recherche f, research ( sth. ) verb ( researched , researched ) —, erforschen v, etw. akk recherchieren v, research associate n —, legal research n —, future research n —, survey research n —, research framework n —, quantitative research n —, user research n —, comparative research n —, research environment n —, fields of research pl —, joint research activities pl —, bibliographic research n —, branch of research n —, pre-competitive research n —, maritime research n —, telephone research n —, genetics research n —, complementary research n —, permanent research n —, genealogy research n —, federal waterways engineering and research institute n —, research marketing n —, cooperative industrial research n —, total research n —, medieval research n —, special research field n —, applied social research n —, research-oriented specialisation be n —, security research n —, comparing research n —, research procedures pl —, ▸ wikipedia, ▾ external sources (not reviewed).
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development expenses: the appropriate allocations of direct personnel and material costs and related overheads for internal or external application technology, engineering and other departments that provide the respective services; costs for experimental and pilot facilities (including the depreciation and write-downs on buildings or parts of buildings used evelopment purposes); costs for clin ular costs for the utilization of third parties' patents development purposes; plant taxes relate lities; and fees for the filing and registration of self-generated [...] [...] | [...] her zäh cklungskosten insbesondere die Einzel- und Gemeinkostenanteile von Personal- und Sachkosten für eigene oder fremde anwendungstechnische, ingenieurtechnische und sonstige Abteilungen, sofern von diesen entsprechende Dienste erbracht werden, die Kosten für Versuchsanlagen und Technika (einschließlich der planmäßigen und außerplanmäßigen Abschreibungen von Gebäuden oder Gebäudeteilen, die für de cklung genutzt werden), die Kosten der klin die laufenden Kosten für die Nutzung fremder Paten ntwicklungszwecke und Betriebsteuern, soweit n; darüber [...] [...] |
[...] [...] financing, high share of b t on the other hand they raise issues as to the quality of the scientific output, the growing internationalizatio the growing number of cooperations [...] [...] | [...] [...] Basisfinanzierung; h aber zum anderen auf die Qualität des wissenschaftlichen Outputs, die wachsende International uch noch [...] [...] |
[...] [...] Boltzmann Institute the Consequences [...] [...] | [...] [...] Boltzmann-Insti Dokumentationsarchives [...] [...] |
[...] [...] universitie itutes); cooperating with other networks and "clusters"; launching, developing and suppor ects of OEC partners, for example supported by the "Energie-Technologie-Programm ETP" (the Upper Austrian Energy Technology R & D Programme); representing the OEC internationally; supporting export activities of the cluster partners in co-operation with the Chamber of Commerce; networking with energy agencies and institutions from other countries; compiling information material on green energy topics, promoting the OEC in Austria and abroad; and implementing PR, ma market development [...] | [...] nd Betreuung von Kooperationsprojekten [...] zwischen OEC-Partner-Unternehmen und Technologietransfer-Einrichtungen (z. B. Unive ation mit anderen Netzwerken und Clustern; Initiierung und Bet rtner, u. a. mit Unterstützung durch das Energie-Technologie-Programm ETP; Internationale Repräsentation des OEC, Unterstützung von Unternehmen beim Export in Zusammenarbeit mit der Wirtschaftskammer; Vernetzung mit ausländischen Energieagenturen und -Institutionen; Erstellung von Ökoenergie-Informationsmaterialien, Positionierung des OEC im In- und Ausland und PR-Ar icklung. |
[...] [...] solid progress in duct development, [...] [...] | [...] [...] Fortschrit twicklung [...] [...] |
[...] [...] used to fu abroad The personal knowledge gained and contacts made as a result of these visits form a basis for future coopera ning Groups also collaborate with institutions in neighbouring European countries as well as with countries overseas Similarly, Priority Programmes and Collabora res are becoming increasingly international This creates synergetic effects and, at the same time, serves to enhance the competitivenes ermany | [...] [...] für einen Auslandsaufenthalt genutzt Die persönlichen Kenntnisse und Verbindungen, die dadurch entstehen, sind die Basis künftiger Zusammenarbe e Graduiertenkollegs pflegen Kooperationen mit Einrichtungen in europäischen Nachbarländern, teils auch in Übersee Ebenso werden jetzt Schwerpunktprogramme und Sonderforschungsbereiche zunehmend grenzüberschreitend oder international organisiert All dies schafft Synergien und dient zugleich der Wettbewerb d |
[...] [...] and completion of elopment and clinical [...] [...] | [...] [...] Fertig lungsprojekten [...] [...] |
[...] [...] number of issues for further poss . | [...] [...] für wei . |
[...] [...] take account of the relationship [...] [...] | [...] [...] berücksichtigt iehung [...] [...] |
[...] [...] strategie astructures, to develop long-term plans for the investments and to coordinate their future activities among themselves, taking account of the orientation proposed by ESFRI, thereby generating economies of scale and enabling a more efficient development and us cities within the Euro . | [...] [...] und St n bzw. auszubauen, langfristige Investitionspläne auszuarbeiten und ihre künftigen Maßnahmen untereinander zu koordinieren und auf diese Weise Größenvorteile zu erzielen und eine effizientere Entwicklung und Nutzung uro lichen. |
[...] [...] taken on the guidelines of the future Coal and S despite the fact that its administrative expenditure would have to be met from the general budget; wonders how the Parliament as one arm of the budgetary authority could approve this additional expenditure and give discharge to the Fund if it does not have any influence on the implementation of its activities; stresses that it cannot accept such a passive role, which is contradictory to present-day requirements of transparency and accountability; considers that the legislative acts laying down the multiannual financial and technical guidelines of the Coal and S should be brought under the co-decision procedure, [...] [...] | [...] [...] des kü le pracherecht überlassen würden, obwohl dessen Verwaltungsausgaben aus dem Gesamthaushaltsplan bestritten werden müssten; fragt sich, wie es als ein Teil der Haushaltsbehörde diese zusätzlichen Ausgaben billigen und dem Fonds die Entlastung erteilen kann, wenn es keinen Einfluss auf die Durchführung seiner Tätigkeiten hat; betont, dass es eine solche passive Rolle, die im Widerspruch zu den heutigen Erfordernissen der Transparenz und Rechenschaftspflicht steht, nicht akzeptieren kann; vertritt die Auffassung, dass die Rechtsakte zur Festlegung der mehrjährigen technischen Leit und Sta hmen des Mitentscheidungsverfahrens [...] |
[...] [...] transit countries, en diversification [...] | [...] [...] Transitländern, en zierung [...] |
[...] [...] the Euro em more efficient and effective, and the possible contribution of the Framework Programme to the efforts towards, inter alia, finding solutions to climate change and sustainability, the health of Europe's population and the reinvigoration of the Lisbon strategy, there is a need for Commu vities. | [...] [...] Erhöhung der Effizienz de hen Beitrags des Rahmenprogramms zu den Bemühungen beispielsweise um Lösung der Probleme der Klimaänderung und der Nachhaltigkeit, zur Gesundheit der europäischen Bevölkerung und zur Neubelebung der Strategie von Lis . |
[...] [...] following factors: trend development, cyclical [...] [...] | [...] [...] Entwicklung ng, Konjunktureinflüsse [...] [...] |
vities of the two companies were combined directly after acquisition to form a new unit based in Iselin, New Jersey (USA). | |
[...] [...] subject of int as important [...] [...] | [...] [...] Gegenstand in tiges [...] nd raumfüllende Inszenierungen; [...] |
[...] [...] Photovol us: Solar he University [...] [...] | [...] [...] für Ph r Universität [...] [...] |
[...] [...] of scient technological development; - looks forward with interest to future actions to be undertaken in view of an efficient and concrete follow-up to the decisions adopted in Barcelona in November 1995 in the field of scient xpects that [...] [...] | [...] [...] Europäischen Union im Bereich wis sche Entwicklung; - sieht mit Interesse den künftigen Aktionen zur wirkungsvollen und konkreten Umsetzung der Beschlüsse zur wisse im November 1995 in Barcelona gefaßt [...] [...] |
[...] creating incentives for private industry to invest more in AIDS vac development for example through the incentives proposed in the orphan drug regulation presently discussed in the Parliament; creating a more credible market in developing countries by ensuring provision for existing vaccines in the national budgets and in the Community aid budgets; creating (together with our main partners) a potential market for the future by pledging financial support for countries to purchase the new vaccine once it becomes available; and increasing support from public sector finance for the development of an AIDS vaccine appropriate for developing countries. | [...] [...] Investitionen icklung von Impfstoffen, etwa die, die in der zur Zeit im Parlament erörterten Verordnung über "Orphan drugs" vorgeschlagen werden; ferner gehören dazu die Schaffung eines glaubwürdigen Markts in den Entwicklungsländern durch Bereitstellung von Mitteln für verfügbare Impfstoffe in den Staatshaushalten und in den Budgets der Gemeinschaftshilfe, die Schaffung (in Zusammenarbeit mit unseren wichtigsten Partnern) eines potentiellen Marktes für die Zukunft durch Zusagung einer Unterstützung der Länder beim Kauf eines neuen Impfstoffs, sobald er verfügbar ist, und schließlich die verstärkte Förderung Entwicklung [...] [...] |
[...] evidence for the exis ity according to international standard in the diffe s, especially in the areas defining the university's profile, and for the quality and structure of the promotion of young researchers, such as: centers established in competitive procedures; established funding of collabora l. other than DFG funding); Graduate Schools and Clusters of Excellence approved for first programme phase of the Excellence Initiative (please also include Graduate Schools and Clusters of Excellence planned for the second phase); projects supported in the context of state initiatives; results of evaluations or comparative assessments; if available a bibliometric evaluation of ormance, patents, [...] [...] | [...] Sie die tionalem Niveau in den verschied insbesondere in den Profilbereichen der Universität, sowie die Qualität und Struktur der Nachwuchsförderung nach: z. B. durch in Wettbewerben entstandene Zentren, etablierte als der DFG), in der ersten Programmphase der Exzellenzinitiative bewilligte Graduiertenschulen und Exzellenzcluster (bitte nennen Sie hier auch die für die zweiten Programmphase geplanten Graduiertenschulen und Exzellenzcluster), durch im Rahmen von Länderinitiativen geförderte Projekte, Ergebnisse von Evaluationen oder vergleichenden Bewertungsverfahren, durch eine bibliometrische Au eise und [...] |
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Published on August 30, 2022 by Tegan George . Revised on July 18, 2023.
A results section is where you report the main findings of the data collection and analysis you conducted for your thesis or dissertation . You should report all relevant results concisely and objectively, in a logical order. Don’t include subjective interpretations of why you found these results or what they mean—any evaluation should be saved for the discussion section .
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How to write a results section, reporting quantitative research results, reporting qualitative research results, results vs. discussion vs. conclusion, checklist: research results, other interesting articles, frequently asked questions about results sections.
When conducting research, it’s important to report the results of your study prior to discussing your interpretations of it. This gives your reader a clear idea of exactly what you found and keeps the data itself separate from your subjective analysis.
Here are a few best practices:
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If you conducted quantitative research , you’ll likely be working with the results of some sort of statistical analysis .
Your results section should report the results of any statistical tests you used to compare groups or assess relationships between variables . It should also state whether or not each hypothesis was supported.
The most logical way to structure quantitative results is to frame them around your research questions or hypotheses. For each question or hypothesis, share:
In quantitative research, it’s often helpful to include visual elements such as graphs, charts, and tables , but only if they are directly relevant to your results. Give these elements clear, descriptive titles and labels so that your reader can easily understand what is being shown. If you want to include any other visual elements that are more tangential in nature, consider adding a figure and table list .
As a rule of thumb:
Don’t forget to also mention any tables and figures you used within the text of your results section. Summarize or elaborate on specific aspects you think your reader should know about rather than merely restating the same numbers already shown.
A two-sample t test was used to test the hypothesis that higher social distance from environmental problems would reduce the intent to donate to environmental organizations, with donation intention (recorded as a score from 1 to 10) as the outcome variable and social distance (categorized as either a low or high level of social distance) as the predictor variable.Social distance was found to be positively correlated with donation intention, t (98) = 12.19, p < .001, with the donation intention of the high social distance group 0.28 points higher, on average, than the low social distance group (see figure 1). This contradicts the initial hypothesis that social distance would decrease donation intention, and in fact suggests a small effect in the opposite direction.
Figure 1: Intention to donate to environmental organizations based on social distance from impact of environmental damage.
In qualitative research , your results might not all be directly related to specific hypotheses. In this case, you can structure your results section around key themes or topics that emerged from your analysis of the data.
For each theme, start with general observations about what the data showed. You can mention:
Next, clarify and support these points with direct quotations. Be sure to report any relevant demographic information about participants. Further information (such as full transcripts , if appropriate) can be included in an appendix .
When asked about video games as a form of art, the respondents tended to believe that video games themselves are not an art form, but agreed that creativity is involved in their production. The criteria used to identify artistic video games included design, story, music, and creative teams.One respondent (male, 24) noted a difference in creativity between popular video game genres:
“I think that in role-playing games, there’s more attention to character design, to world design, because the whole story is important and more attention is paid to certain game elements […] so that perhaps you do need bigger teams of creative experts than in an average shooter or something.”
Responses suggest that video game consumers consider some types of games to have more artistic potential than others.
Your results section should objectively report your findings, presenting only brief observations in relation to each question, hypothesis, or theme.
It should not speculate about the meaning of the results or attempt to answer your main research question . Detailed interpretation of your results is more suitable for your discussion section , while synthesis of your results into an overall answer to your main research question is best left for your conclusion .
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I have completed my data collection and analyzed the results.
I have included all results that are relevant to my research questions.
I have concisely and objectively reported each result, including relevant descriptive statistics and inferential statistics .
I have stated whether each hypothesis was supported or refuted.
I have used tables and figures to illustrate my results where appropriate.
All tables and figures are correctly labelled and referred to in the text.
There is no subjective interpretation or speculation on the meaning of the results.
You've finished writing up your results! Use the other checklists to further improve your thesis.
If you want to know more about AI for academic writing, AI tools, or research bias, make sure to check out some of our other articles with explanations and examples or go directly to our tools!
Research bias
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The results chapter of a thesis or dissertation presents your research results concisely and objectively.
In quantitative research , for each question or hypothesis , state:
In qualitative research , for each question or theme, describe:
Don’t interpret or speculate in the results chapter.
Results are usually written in the past tense , because they are describing the outcome of completed actions.
The results chapter or section simply and objectively reports what you found, without speculating on why you found these results. The discussion interprets the meaning of the results, puts them in context, and explains why they matter.
In qualitative research , results and discussion are sometimes combined. But in quantitative research , it’s considered important to separate the objective results from your interpretation of them.
If you want to cite this source, you can copy and paste the citation or click the “Cite this Scribbr article” button to automatically add the citation to our free Citation Generator.
George, T. (2023, July 18). How to Write a Results Section | Tips & Examples. Scribbr. Retrieved September 9, 2024, from https://www.scribbr.com/dissertation/results/
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"research" in german, research {v.i.}.
Research [ researched|researched ] {intransitive verb}, research [ researched|researched ] {verb}.
Research {adjective}.
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English how to use "research" in a sentence, english how to use "forschen" in a sentence, english how to use "forscherisch" in a sentence, collocations, "genealogical research" in german.
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Nature Aging ( 2024 ) Cite this article
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Reproductive aging is a major cause of fertility decline, attributed to decreased oocyte quantity and developmental potential. A possible cause is aging of the surrounding follicular somatic cells that support oocyte growth and development by providing nutrients and regulatory factors. Here, by creating chimeric follicles, whereby an oocyte from one follicle was transplanted into and cultured within another follicle whose native oocyte was removed, we show that young oocytes cultured in aged follicles exhibited impeded meiotic maturation and developmental potential, whereas aged oocytes cultured within young follicles were significantly improved in rates of maturation, blastocyst formation and live birth after in vitro fertilization and embryo implantation. This rejuvenation of aged oocytes was associated with enhanced interaction with somatic cells, transcriptomic and metabolomic remodeling, improved mitochondrial function and higher fidelity of meiotic chromosome segregation. These findings provide the basis for a future follicular somatic cell-based therapy to treat female infertility.
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Data availability.
All raw RNA-seq data, as well as processed datasets, can be found in the Gene Expression Omnibus database under accession number GSE270016 . Metabolomics data are available in Supplementary Table 5 . The rest of the data generated or analyzed during this study are all included in the published article and its Supplementary Information files. Source data are provided with this paper. All other data are available from the corresponding authors upon reasonable request.
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We thank S. Xiao (Rutgers University) for the helpful discussion on mouse follicle in vitro culture method. We thank M.l Lampson (University of Pennsylvania) for providing Rec8 antibody. We thank T. S. Kitajima (RIKEN Center for Developmental Biology) for providing pGEMHE–2mEGFP–CENP-C plasmid. Graphics from Figs. 2a,f , 3a , 4a,e and 8g and Extended Data Figs. 3b , 6a and 7a were created with BioRender. This work was supported by a grant from the National University of Singapore Bia-Echo Asia Centre for Reproductive Longevity and Equality and by the National Research Foundation, Singapore, under its mid-sized grant (NRF-MSG-2023-0001) to R.L. The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.
Authors and affiliations.
Mechanobiology Institute, National University of Singapore, Singapore, Singapore
HaiYang Wang, Xingyu Shen, Yaelim Lee, XinJie Song, Chang Shu, Jin Zhu & Rong Li
NUS Bia Echo Asia Centre for Reproductive Longevity and Equality, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore
Zhongwei Huang
Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore
Department of Obstetrics and Gynaecology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore
Cardiovascular Research Institute, National University Health System, Singapore, Singapore
Lik Hang Wu, Leroy Sivappiragasam Pakkiri, Poh Leong Lim & Chester Lee Drum
Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore
Department of Pharmacy, Faculty of Science, National University of Singapore, Singapore, Singapore
Lik Hang Wu
Center for Cell Dynamics and Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD, USA
Xi Zhang & Rong Li
Department of Biological Sciences, National University of Singapore, Singapore, Singapore
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H.W. and R.L. conceived the study. H.W. and R.L. designed the experiments and methods for data analysis. H.W. performed experiments and analyzed the data with assistance from Z.H., X.J.S., X.S. and C.S., with the following exceptions: L.H.W., P.L.L. and L.S.P. performed the MS experiments and data analysis; C.S. measured the distance between sister kinetochores; X.Z. generated MTS–mCherry–GFP 1–10 mice strain; J.Z. supervised the RNA-seq experiments and analyzed the data with Y.L.; and C.L.D. and L.S.P. supervised the MS analysis. H.W. and R.L. wrote the paper and prepared the figures with input from all authors. R.L. supervised the study.
Correspondence to HaiYang Wang or Rong Li .
Competing interests.
We disclose that we have filed a patent for this study. The applicants and inventors for this patent are R.L. and H.W. The patent application, titled ‘Somatic Cell-Based Therapy to Treat Female Infertility’, was filed under number PCT/SG2023/050339 and has been published with the publication number WO 2023/224556 A1. The other authors declare no competing interests.
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Nature Aging thanks the anonymous reviewers for their contribution to the peer review of this work.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Extended data fig. 1 follicles accumulate age-related abnormalities..
a,b , Representative images of Ki-67 staining in ovarian sections ( a ). F-actin was stained with phalloidin. Scale bar, 50 μm. Quantitative analysis of the percentage of Ki-67-positive cells per follicle is shown in ( b) . n = 31 (young), 25 (aged) follicles. c , Quantification of γH2AX foci in GCs from follicles in ovarian sections. n = 37 (young), 38 (aged) follicles. d-f , CM-H2DCFDA staining in isolated oocyte-GC complexes ( d ). Scale bar, 30 μm. Scatter plots ( e ) show the correlation between ROS levels in GCs and oocytes (simple linear regression and two-tailed analysis). Gray areas around fit lines indicate 95% confidence intervals, with Pearson’s correlation coefficient (r). Comparison of ROS intensity in young and aged oocytes or GCs is shown in ( f ). n = 76 (young), 43 (aged). 2-month-old (young) and 14-month-old (aged) mice were used in ( b, c, e, f ). Box plots in (b, c, f) show mean (black square), median (center line), quartiles (box limits), and 1.5× interquartile range (whiskers). Box plots inside the violins in ( f ) show mean (black circle), quartiles (box limits), and 1.5× interquartile range (whiskers). Two-tailed unpaired t-tests for ( b, c, f ). P value: **** P < 0.0001, *** P < 0.001. Exact P values are in the Source Data. Data are from at least three independent experiments.
Extended data fig. 2 comparison of in vivo and in vitro grown oocytes..
a , Diameter of oocytes grown in vivo or in vitro . n = 109 ( in vivo ), 90 ( in vitro ). b , Quantification of oocyte maturation rate. Sample sizes: n = 126 ( in vivo ) and n = 98 ( in vitro ) oocytes, with 4 biological replicates in each group. Data are shown as mean ± SD. c , Analysis of embryo development potential. n = 83 ( in vivo ) and 75 ( in vitro ). d-f , Transcriptome analysis of oocytes grown in vitro and in vivo . Volcano plot ( d) of DEGs (p.adjust < 0.05 and log 2 fold change > 0.5 or < −0.5) between in vitro and in vivo oocytes. Two-sided Wald-test adjusted with Benjamini-Hochberg method. Correlation heatmap ( e) with hierarchical clustering to show the sample-to-sample distances. PCA analysis (f) of the normalized gene expression data. Ellipses fit a multivariate t-distribution at confidence level of 0.8. n = 8 in vivo and 8 in vitro . g , Dot plots illustrating follicle size changes over time during 3D ex vivo culture. Color bar and circle size represent follicle size. 2-month-old (young, n = 18) and 14-month-old (aged, n = 18) mice were used. h,i , Representative images ( h ) of 3D ex vivo cultured young and aged follicles. Follicles were considered atretic if there was disruption of contact between the oocyte (red asterisk) and GCs, leading to the release of oocytes from the follicles (bottom left), or if the follicles contained apoptotic or dead oocytes (bottom right). Antrum is indicated by the white arrowhead. Scale bar, 100 μm. Atresia rate was quantified (i) in young (2-3 months) and aged (14-15 months) follicles after 3D ex vivo culture. The median is represented by the center line, with individual dots representing biological replicates for each group. Sample sizes: n = 166 (young), 199 (aged) follicles, with 5 biological replicates in each group. 2-3 month-old mice were used in ( a - f ). Box plots inside the violins in ( a ) show mean (black circle), quartiles (box limits), and 1.5× interquartile range (whiskers). Two-tailed unpaired t-tests for ( a, b, i ). Two-tailed Fisher’s exact test for (c) . P value: ** P < 0.01, ns, not significant ( P > 0.05). Exact P values are in the Source Data. All data are from at least three independent experiments.
a , Procedure for generating reconstituted chimeric follicles. Red arrow points to the oocyte used for transplantation. Red asterisk indicates the oocyte within the r-follicle that will be replaced. Refer to Supplementary Video 1 and Methods for further details. b , To distinguish between the donor oocyte and the r-follicle, we employed oocytes from mTmG transgenic mice exhibiting membrane-localized tdTomato (pseudo-colored yellow). In contrast, the r-follicles were sourced from non-fluorescent wild-type mice. The mTmG oocytes served as donors as referenced in Fig. 2g and Extended Data Fig. 3c–e . c , RCF size increased during 3D ex vivo culture. Oocytes from transgenic mTmG mice and follicular somatic cells from wild-type mice, as shown in ( b ). Scale bars, 50 μm. d , Cumulus-oocyte complexes (COCs) isolated from antral RCFs were induced for oocyte maturation with hCG for 16 hours in vitro . Note that cumulus cells surrounding the oocytes (from mTmG mice) expanded, and oocytes resumed meiosis, extruded the PB1 as shown in ( e ). Scale bars, 200 μm. e , Representative image of mature eggs derived from RCFs as shown in ( c and d ). The cumulus cells were removed after maturation to visualize mature eggs with the first polar body (PB1, arrows). Scale bars, 40 μm. All images are representative of at least three independent experiments.
a . Representative confocal images of cellular ROS stained with CM-H2DCFDA in oocytes from YY and YA RCFs. Scale bar, 100 μm. b . Quantification of CM-H2DCFDA fluorescence intensity in oocytes from YY and YA RCFs, as well as Y. n = 104 (Y), 122 (YY), 97 (YA). 2-month-old (young) and 14-month-old (aged) wide-type ICR mice were used. c . Fluorescence images of oocyte stained with MitoTracker Green (MTG, cyan) and mitochondrial membrane potential-sensitive dye TMRM (red). Scale bar, 100 μm. d . Quantification of the fluorescence intensity ratio of TMRM to MTG in oocytes from YY and YA RCFs, as well as Y. n = 110 (Y), 94 (YY), 72 (YA). 2-month-old (young) and 14-month-old (aged) wide-type ICR mice were used. Box plots in (b, d) show mean (black square), median (center line), quartiles (box limits), and 1.5× interquartile range (whiskers). One-way ANOVA, Tukey’s multiple comparisons test for ( b , d ). P value: **** P < 0.0001, ns, not significant ( P > 0.05). The exact P values are presented in the Source Data. All data are from at least three independent experiments.
a , Quantification of oocyte death rates. Data are presented as mean ± SD. Sample sizes: n = 77 (YY), 65 (AA), 142 (AY) oocytes. Individual dots represent biological replicates for each group. Young: 2-3 months old, aged: 14-15 months old. b-e , Representative live-cell images ( b ) showing spindle and chromosomes in MII oocytes. Scale bar, 10 µm. Quantification of the percentage of chromosomal misalignment ( c ) and spindle abnormalities ( d ). Panel ( e ) presents a separate quantitative analysis of various classes of spindle abnormalities. Young: 2-3 months old, aged: 14-17 months old. f,g , Representative image of DAPI-stained blastocysts ( f ). Scale bars, 20 μm. Cell numbers per blastocyst were quantified in (g) . n = 57 (YY), 43 (AY), 26 (AA). h-m , Comparison of various parameters between AA and AY RCFs and A: ( h ) cellular ROS levels, ( i ) oocyte maturation rates, ( j ) chromosomal misalignment, ( k ) spindle abnormalities, ( l ) blastocyst formation rate, and ( m ) blastocyst size. For ( h ), n = 72 (A), 72 (AA), 72 (AY); for ( m ), n = 25 (A), 28 (AA), 31 (AY). In ( c, d, i, j, k, l ), the oocyte numbers are specified in brackets. 2-month-old (young) and 14-month-old (aged) mice were used in ( g-m ). Box plots in ( g, m ) show mean (black square), median (center line), quartiles (box limits), and 1.5× interquartile range (whiskers). Box plots inside the violins in ( h ) show mean (black circle), quartiles (box limits), and 1.5× interquartile range (whiskers). One-way ANOVA with Tukey’s multiple comparisons test was used for ( a, g, h, m ). Two-tailed Fisher’s exact test for ( c, d, i-l ). P value: **** P < 0.0001, *** P < 0.001, ** P < 0.01, * P < 0.05, ns, not significant ( P > 0.05). Exact P values are in the Source Data. All data are from at least three independent experiments.
a , Schematic demonstrating TZPs from GCs that pass through the zona pellucida, forming either adherens junctions or gap junctions on the oocyte surface. b , TZP regenerated within 3 hours of RCF culturing. RCF containing follicular somatic cells from mTmG mouse and wild-type oocytes were cultured within Alginate-rBM beads for 3 h. Somatic cells were then removed to visualize TZP regeneration. Scale bars, 20 μm. c , Histogram displays the number of up-regulated or down-regulated DEGs between oocytes from YY and AA, AY and AA, or YY and AY RCFs. d,e , Representative GO terms associated with the genes that were downregulated ( d ) and upregulated ( e ) in aged oocytes from AA RCFs when compared to young oocytes from YY RCFs. One-sided hypergeometric test with FDR adjustment for multiple comparisons.
a . Experimental design to study mitochondrial transport within RCFs. RCFs were created using somatic cells from transgenic MTS-mCherry-GFP 1-11 mice, which express mitochondria-targeted mCherry, and unlabelled oocytes from wild-type mice. b . Confocal microscopy images of mCherry-labelled mitochondria in oocytes. Top panel: Positive control, an RCF formed by transplanting an MTS-mCherry-GFP 1-11 oocyte into an MTS-mCherry-GFP 1-10 r-follicle. Middle panel: RCF generated by transplanting a wild-type oocyte into an MTS-mCherry-GFP 1-10 r-follicle. Bottom panel: Negative control, an RCF generated by transplanting a wild-type oocyte into a wild-type r-follicle. Rightmost panel of each row: overexposed images corresponding to the second column (mCherry). Somatic cells were partially removed before imaging to better observe oocyte fluorescence. Scale bar, 20 µm. All images are representative of at least three independent experiments.
This analysis examines various parameters of oocyte quality and developmental potential across four different RCF groups (YY, YA, AY, AA): ( a ) oocyte maturation rates (n = 12 YY, 4 YA, 10 AY, 9 AA), ( b ) chromosome misalignment (n = 9 YY, 4 YA, 5 AY, 5 AA), ( c ) spindle abnormalities (n = 9 YY, 4 YA, 5 AY, 5 AA), ( d ) blastocyst formation rates (n = 9 YY, 5 YA, 7 AY, 7 AA), ( e ) cellular ROS accumulation (n = 150 YY, 97 YA, 38 AY, 26 AA), ( f ) mitochondrial membrane potential (n = 153 YY, 72 YA, 57 AY, 53 AA). All metrics were normalized to those of the YY group in the same experiments using the non-normalized data as in Figs. 2h, j, k, l , 3b, d , 6f, j , Extended Data Fig. 4 b, d, and 5c, d . The data were analyzed by one-way ANOVA, Tukey’s multiple comparisons test. P value: **** P < 0.0001, *** P < 0.001, ** P < 0.01, * P < 0.05, ns, not significant ( P > 0.05). The exact P values are presented in the Source Data. All results are presented as mean ± SD. All data are from at least three independent experiments.
Reporting summary, supplementary video 1.
Chimeric follicle generation process. This video demonstrates a step-by-step example of creating a RCF, highlighting the process of transplanting an oocyte into an r-follicle.
An example of sister kinetochore pair distance measurement. This video demonstrates the measurement of sister kinetochore pair distances in oocytes expressing 2mEGFP–CENP-C (green) and H2B–mCherry (red) to label kinetochores and chromosomes, respectively. See Methods for a detailed description of the measurement protocol.
Supplementary Table 1. Differential gene expression analysis in vitro oocytes versus in vivo oocytes. Two-sided Wald test adjusted with the Benjamini–Hochberg method. Supplementary Table 2. Differential gene expression analysis in oocytes from AA RCFs versus YY RCFs. Two-sided Wald test adjusted with the Benjamini–Hochberg method. Supplementary Table 3. Differential gene expression analysis in oocytes from AA RCFs versus AY RCFs. Two-sided Wald test adjusted with the Benjamini–Hochberg method. Supplementary Table 4. Differential gene expression analysis in oocytes from AY RCFs versus AA RCFs. Two-sided Wald test adjusted with the Benjamini–Hochberg method. Supplementary Table 5. Metabolomic profiling of oocytes from YY, AA, and AY RCFs. Two-sided Wald test.
Statistical source data.
Source data fig. 3, source data fig. 4, source data fig. 6, source data fig. 7, source data fig. 8, source data extended data fig. 1, source data extended data fig. 2, source data extended data fig. 4, source data extended data fig. 5, source data extended data fig. 6, source data extended data fig. 8, rights and permissions.
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Wang, H., Huang, Z., Shen, X. et al. Rejuvenation of aged oocyte through exposure to young follicular microenvironment. Nat Aging (2024). https://doi.org/10.1038/s43587-024-00697-x
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