Evidence map›Paper›PMID 15755804›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2005

Analysis of mouse embryonic patterning and morphogenesis by forward genetics.

María J García-García, Jonathan T Eggenschwiler, Tamara Caspary, Heather L Alcorn, Michael R Wyler, Danwei Huangfu, Andrew S Rakeman, Jeffrey D Lee, Evan H Feinberg, John R Timmer and 1 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing 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

77 citing papers in PubMed.

  1. Article
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  11. Shape shifting: The multiple conformational substates of the PTEN N-terminal PIPProtein science : a publication of the Protein Society · 2022
    Article
  12. Article
  13. Article
  14. p120-catenin regulates WNT signaling and EMT in the mouse embryo.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  15. Article
  16. STRIP1, a core component of STRIPAK complexes, is essential for normal mesoderm migration in the mouse embryo.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  17. Review
  18. Article
  19. Review
  20. CK1 in Developmental Signaling: Hedgehog and Wnt.Current topics in developmental biology · 2017
    Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

María J García-GarcíaDevelopmental Biology Program, Sloan-Kettering Institute, 1275 York Avenue, New York, NY 10021, USA.
Jonathan T Eggenschwiler
Tamara Caspary
Heather L Alcorn
Michael R Wyler
Danwei Huangfu
Andrew S Rakeman
Jeffrey D Lee
Evan H Feinberg
John R Timmer
Kathryn V Anderson

Funding

ISOLATION OF NOVEL MUTATIONS AFFECTING THE MOUSE EMBRYOR01HD035455 · NICHD · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI HADJANTONAKIS, ANNA-KATERINA, HUANGFU, DANWEI · 1998 to 2022
$7.1M
Isolation of Novel Mutations Affecting the Mouse EmbryoR37HD035455 · NICHD · SLOAN-KETTERING INST CAN RESEARCH · PI ANDERSON, KATHRYN V · 2008 to 2017
$6.9M
Recessive Mutations that Disrupt Develop of Mouse EmbryoU01HD043478 · NICHD · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI ANDERSON, KATHRYN V · 2002 to 2006
$4.6M
ISOLATION OF NOVEL MUTATIONS AFFECTING THE MOUSE EMBRYOR55HD035455 · NICHD · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI ANDERSON, KATHRYN V · 1996 to 1996
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NICHD NIH HHS HD043478NICHD NIH HHS HD35455NICHD NIH HHS R01 HD035455NICHD NIH HHS R37 HD035455NICHD NIH HHS U01 HD043478
6 · The paper itself

Abstract

Many aspects of the genetic control of mammalian embryogenesis cannot be extrapolated from other animals. Taking a forward genetic approach, we have induced recessive mutations by treatment of mice with ethylnitrosourea and have identified 43 mutations that affect early morphogenesis and patterning, including 38 genes that have not been studied previously. The molecular lesions responsible for 14 mutations were identified, including mutations in nine genes that had not been characterized previously. Some mutations affect vertebrate-specific components of conserved signaling pathways; for example, at least five mutations affect previously uncharacterized regulators of the Sonic hedgehog (Shh) pathway. Approximately half of all of the mutations affect the initial establishment of the body plan, and several of these produce phenotypes that have not been described previously. A large fraction of the genes identified affect cell migration, cellular organization, and cell structure. The findings indicate that phenotype-based genetic screens provide a direct and unbiased method to identify essential regulators of mammalian development.

Indexed as

AnimalsBody PatterningChromosome MappingGenes, RecessiveMammalsMiceMorphogenesisMutationNervous SystemSpecies Specificity

Identifiers

PMID15755804
PMCPMC1087930

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.