Evidence map›Paper›PMID 17660231›Full record

ArticleReproduction (Cambridge, England)2007

Actions of anti-Mullerian hormone on the ovarian transcriptome to inhibit primordial to primary follicle transition.

Eric Nilsson, Natalie Rogers, Michael K Skinner

Open access · bronzeAbstract read
In one paragraph

Article in Reproduction (Cambridge, England), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
10.4field-weighted citation impact, top 2% of its field
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

72 citing papers in PubMed, 197 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. The Effect of AMH on Folliculogenesis.Reproductive sciences (Thousand Oaks, Calif.) · 2025
    Review
  6. Article
  7. The elusive function of AMH signaling in folliculogenesis.Journal of assisted reproduction and genetics · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Loss of ERβ Disrupts Gene Regulation in Primordial and Primary Follicles.International journal of molecular sciences · 2024
    Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Therapeutic options for premature ovarian insufficiency: an updated review.Reproductive biology and endocrinology : RB&E · 2022
    Review
  19. Article
  20. Ovarian Reserve Biomarkers and Menstrual Cycle Length in a Prospective Cohort Study.The Journal of clinical endocrinology and metabolism · 2021
    Article

12 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Eric NilssonCenter for Reproductive Biology, School of Molecular Biosciences, Washington State University, Pullman, Washington 99164-4231, USA.
Natalie Rogers
Michael K Skinner
Washington State University · US

Funding

Ovarian Primordial Follicle DevelopmentR01HD048898 · NICHD · WASHINGTON STATE UNIVERSITY · PI SKINNER, MICHAEL K · 2006 to 2010
$1.2M
NICHD NIH HHS R01 HD048898
6 · The paper itself

Abstract

The oocytes found within the primordial follicles of mammalian ovaries remain quiescent for months to years until they receive the appropriate signals to undergo the primordial to primary follicle transition and initiate folliculogenesis. The molecular mechanisms and extracellular signaling factors that regulate this process remain to be fully elucidated. The current study investigates the mechanisms utilized by anti-Müllerian hormone (AMH; i.e. Müllerian inhibitory substance) to inhibit the primordial to primary follicle transition. Ovaries from 4-day-old rats were placed into organ culture and incubated in the absence or presence of AMH, either alone or in combination with known stimulators of follicle transition, including basic fibroblast growth factor (bFGF), kit ligand (KITL), or keratinocyte growth factor (KGF). Following 10 days of culture, the ovaries were sectioned, stained, and morphologically evaluated to determine the percentage of primordial versus developing follicles. As previously demonstrated, AMH treatment decreased primordial to primary follicle transition. Interestingly, AMH inhibited the stimulatory actions of KITL, bFGF, and KGF. Therefore, AMH can inhibit the basal and stimulated development of primordial follicles. To investigate the mechanism of AMH actions, the influence AMH has on the ovarian transcriptome was analyzed. AMH treatment when compared with controls was found to alter the expression of 707 genes. The overall effect of AMH exposure is to decrease the expression of stimulatory factors, increase the expression of inhibitory factors, and regulate cellular pathways (e.g. transforming growth factor beta signaling pathway) that result in the inhibition of primordial follicle development. Analysis of the regulatory factors and cellular pathways altered by AMH provides a better understanding of the molecular control of primordial follicle development.

Indexed as

AnimalsAnimals, NewbornAnti-Mullerian HormoneFemaleFibroblast Growth Factor 2Fibroblast Growth Factor 7Gene ExpressionGene Expression ProfilingGene Expression Regulation, DevelopmentalHumansMAP Kinase Signaling SystemOligonucleotide Array Sequence AnalysisOocytesOrgan Culture TechniquesOvarian FollicleOvaryAnti-Mullerian HormoneFibroblast Growth Factor 2Fibroblast Growth Factor 7Recombinant ProteinsStem Cell FactorTransforming Growth Factor beta

Identifiers

PMID17660231
PMCPMC8260025
OpenAlexW2006835285

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.