Evidence map›Paper›PMID 31883000›Full record

ArticleEndocrinology2020

Oviductal Retention of Embryos in Female Mice Lacking Estrogen Receptor α in the Isthmus and the Uterus.

Gerardo G B Herrera, Sydney L Lierz, Emily A Harris, Lauren J Donoghue, Sylvia C Hewitt, Karina F Rodriguez, Wendy N Jefferson, John P Lydon, Francesco J DeMayo, Carmen J Williams and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  7. Review
  8. METTL3 is essential for normal progesterone signaling during embryo implantation via mProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
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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

12 authors at 3 institutions in 1 country.

Gerardo G B HerreraSchool of Molecular Biosciences, Center for Reproductive Biology, College of Veterinary Medicine, Washington State University, Pullman, Washington, US.
Sydney L LierzReproductive and Developmental Biology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health (NIH/NIEHS), Department of Health and Human Services, Research Triangle Park, North Carolina, US.
Emily A HarrisSchool of Molecular Biosciences, Center for Reproductive Biology, College of Veterinary Medicine, Washington State University, Pullman, Washington, US.
Lauren J DonoghueReproductive and Developmental Biology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health (NIH/NIEHS), Department of Health and Human Services, Research Triangle Park, North Carolina, US.
Sylvia C HewittReproductive and Developmental Biology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health (NIH/NIEHS), Department of Health and Human Services, Research Triangle Park, North Carolina, US.
Karina F RodriguezReproductive and Developmental Biology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health (NIH/NIEHS), Department of Health and Human Services, Research Triangle Park, North Carolina, US.
Wendy N JeffersonReproductive and Developmental Biology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health (NIH/NIEHS), Department of Health and Human Services, Research Triangle Park, North Carolina, US.
John P LydonDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, US.
Francesco J DeMayoReproductive and Developmental Biology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health (NIH/NIEHS), Department of Health and Human Services, Research Triangle Park, North Carolina, US.
Carmen J WilliamsReproductive and Developmental Biology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health (NIH/NIEHS), Department of Health and Human Services, Research Triangle Park, North Carolina, US.
Kenneth S KorachReproductive and Developmental Biology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health (NIH/NIEHS), Department of Health and Human Services, Research Triangle Park, North Carolina, US.
Wipawee WinuthayanonSchool of Molecular Biosciences, Center for Reproductive Biology, College of Veterinary Medicine, Washington State University, Pullman, Washington, US.
National Institutes of Health · USWashington State University · USBaylor College of Medicine · US

Funding

Environmental influence on reproductive tract functionZIAES102405 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI WILLIAMS, CARMEN · 2009 to 2025
$20.6M
Molecular Analysis of Uterine ReceptivityR01HD042311 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI LYDON, JOHN P · 2009 to 2023
$4.8M
The actions of steroid hormones on oviduct functionR01HD097087 · NICHD · WASHINGTON STATE UNIVERSITY · PI WINUTHAYANON, WIPAWEE · 2019 to 2023
$1.7M
NICHD NIH HHS R01 HD042311NICHD NIH HHS R01 HD097087
6 · The paper itself

Abstract

Estrogen receptor α (ESR1; encoded by Esr1) is a crucial nuclear transcription factor for female reproduction and is expressed throughout the female reproductive tract. To assess the function of ESR1 in reproductive tissues without confounding effects from a potential developmental defect arising from global deletion of ESR1, we generated a mouse model in which Esr1 was specifically ablated during postnatal development. To accomplish this, a progesterone receptor Cre line (PgrCre) was bred with Esr1f/f mice to create conditional knockout of Esr1 in reproductive tissues (called PgrCreEsr1KO mice) beginning around 6 days after birth. In the PgrCreEsr1KO oviduct, ESR1 was most efficiently ablated in the isthmic region. We found that at 3.5 days post coitus (dpc), embryos were retrieved from the uterus in control littermates while all embryos were retained in the PgrCreEsr1KO oviduct. Additionally, serum progesterone (P4) levels were significantly lower in PgrCreEsr1KO compared to controls at 3.5 dpc. This finding suggests that expression of ESR1 in the isthmus and normal P4 levels allow for successful embryo transport from the oviduct to the uterus. Therefore, alterations in oviductal isthmus ESR1 signaling and circulating P4 levels could be related to female infertility conditions such as tubal pregnancy.

Indexed as

Embryonic DevelopmentAnimalsEstradiolEstrogen Receptor alphaFallopian TubesFemaleFertilityLuteinizing HormoneMiceMice, KnockoutPituitary GlandPregnancyPregnancy, TubalProgesteroneUterusEstradiolEstrogen Receptor alphaLuteinizing HormoneProgesteroneembryo transportestrogen receptor αoviductpituitary glanduterus

Identifiers

PMID31883000
PMCPMC7295936
OpenAlexW2997169958

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.