Evidence map›Paper›PMID 28646221›Full record

ArticleScientific reports2017

Aberrant activation of the human sex-determining gene in early embryonic development results in postnatal growth retardation and lethality in mice.

Tatsuo Kido, Zhaoyu Sun, Yun-Fai Chris Lau

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Y chromosome in health and diseases.Cell & bioscience · 2020
    Review
  6. Putative contributions of the sex chromosome proteins SOX3 and SRY to neurodevelopmental disorders.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2019
    Article
  7. Article
  8. Article
  9. Review
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.

Tatsuo KidoDepartment of Medicine, VA Medical Center, and Institute for Human Genetics, University of California, San Francisco, San Francisco, California, USA.
Zhaoyu SunDepartment of Medicine, VA Medical Center, and Institute for Human Genetics, University of California, San Francisco, San Francisco, California, USA.
Yun-Fai Chris LauDepartment of Medicine, VA Medical Center, and Institute for Human Genetics, University of California, San Francisco, San Francisco, California, USA. chris.lau@ucsf.edu.
San Francisco VA Medical Center · US

Funding

FUNCTIONS OF SRY AND SRY INTERACTIVE PROTEIN GENESR01HD038117 · NICHD · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI LAU, YUN-FAI CHRIS · 2000 to 2004
$1.3M
Role of the Y-Located TSPY Gene in Human OncogenesisI01BX000865 · VA · VETERANS AFFAIRS MED CTR SAN FRANCISCO · PI LAU, YUN-FAI CHRIS · 2011 to 2014
–
BLRD Research Career Scientist Award ApplicationIK6BX004854 · VA · VETERANS AFFAIRS MED CTR SAN FRANCISCO · PI LAU, YUN-FAI CHRIS · 2020 to 2025
–
BLRD VA I01 BX000865BLRD VA I01 BX004446BLRD VA IK6 BX004854NICHD NIH HHS R01 HD038117
6 · The paper itself

Abstract

Sexual dimorphisms are prevalent in development, physiology and diseases in humans. Currently, the contributions of the genes on the male-specific region of the Y chromosome (MSY) in these processes are uncertain. Using a transgene activation system, the human sex-determining gene hSRY is activated in the single-cell embryos of the mouse. Pups with hSRY activated (hSRY

Indexed as

Genes, LethalAnimalsBiomarkersEctopic Gene ExpressionEmbryonic DevelopmentGene ExpressionGene Expression Regulation, DevelopmentalGene TargetingGrowth DisordersHumansMiceMice, TransgenicOrgan SpecificityPhenotypeSex Determination ProcessesSex-Determining Region Y ProteinBiomarkersSex-Determining Region Y Protein

Identifiers

PMID28646221
PMCPMC5482865
OpenAlexW2633485401

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.