Evidence map›Paper›PMID 39829852›Full record

ArticlebioRxiv : the preprint server for biology2025

Transcriptional Integration of Meiotic Prophase I Progression and Early Oocyte Differentiation.

Kimberly M Abt, Myles A Bartholomew, Anna Nixon, Hanna E Richman, Megan A Gura, Kimberly A Seymour, Richard N Freiman

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Kimberly M AbtMCB Graduate Program, Cell Biology, and Biochemistry, Brown University, 70 Ship St., Box G-E4, Providence, RI 02903, USA.
Myles A BartholomewMCB Graduate Program, Cell Biology, and Biochemistry, Brown University, 70 Ship St., Box G-E4, Providence, RI 02903, USA.
Anna NixonMCB Graduate Program, Cell Biology, and Biochemistry, Brown University, 70 Ship St., Box G-E4, Providence, RI 02903, USA.
Hanna E RichmanDepartment of Molecular Biology, Cell Biology, and Biochemistry, Brown University, 70 Ship St., Box G-E4, Providence, RI 02903, USA.
Megan A GuraMCB Graduate Program, Cell Biology, and Biochemistry, Brown University, 70 Ship St., Box G-E4, Providence, RI 02903, USA.
Kimberly A SeymourDepartment of Molecular Biology, Cell Biology, and Biochemistry, Brown University, 70 Ship St., Box G-E4, Providence, RI 02903, USA.
Richard N FreimanMCB Graduate Program, Cell Biology, and Biochemistry, Brown University, 70 Ship St., Box G-E4, Providence, RI 02903, USA.ORCID 0000-0002-7269-3630

Funding

Dynamic Regulation of the Ovarian ReserveR01HD091848 · NICHD · BROWN UNIVERSITY · PI FREIMAN, RICHARD NEIL · 2018 to 2021
$1.7M
Regulating Establishment of the Mammalian Ovarian ReserveR01HD113567 · NICHD · BROWN UNIVERSITY · PI Richard Neil Freiman · 2024 to 2026
$1.4M
BD FACSAria Flow CytometerS10RR021051 · NCRR · BROWN UNIVERSITY · PI BROSSAY, LAURENT · 2007 to 2007
$403k
Fertility and TAF4b: Transcriptional Regulation of Murine Ovarian Reserve EstablishmentF31HD105340 · NICHD · BROWN UNIVERSITY · PI ABT, KIMBERLY M · 2021 to 2023
$140k
Unscrambling Eggs: TAF4B and Transcriptional Regulation of Meiosis I in Mouse OocytesF31HD097933 · NICHD · BROWN UNIVERSITY · PI GURA, MEGAN A · 2018 to 2021
$136k
NCRR NIH HHS S10 RR021051NICHD NIH HHS F31 HD097933NICHD NIH HHS F31 HD105340NICHD NIH HHS R01 HD091848NICHD NIH HHS R01 HD113567
6 · The paper itself

Abstract

Female reproductive senescence results from the regulated depletion of a finite pool of oocytes called the ovarian reserve. This pool of oocytes is initially established during fetal development, but the oocytes that comprise it must remain quiescent for decades until they are activated during maturation in adulthood. In order for developmentally competent oocytes to populate the ovarian reserve they must successfully initiate both meiosis and oogenesis. As the factors that regulate the timing and fidelity of these early events remain elusive, we assessed the precise function and timing of the transcriptional regulator TAF4b during meiotic prophase I progression in mouse fetal oocytes. Compared to matched controls, E14.5

Identifiers

PMID39829852
PMCPMC11741336

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.