Evidence map›Paper›PMID 32071086›Full record

ArticleThe Journal of biological chemistry2020

The two splice variant forms of Cdc42 exert distinct and essential functions in neurogenesis.

Makoto Endo, Joseph E Druso, Richard A Cerione

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-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

17 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  10. Disorders of ubiquitylation: unchained inflammation.Nature reviews. Rheumatology · 2022
    Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Molecular subversion of Cdc42 signalling in cancer.Biochemical Society transactions · 2021
    Review
  17. 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.

Makoto EndoDepartment of Molecular Medicine, College of Veterinary Medicine, Cornell University, Ithaca, New York 14853.
Joseph E DrusoDepartment of Molecular Medicine, College of Veterinary Medicine, Cornell University, Ithaca, New York 14853.
Richard A CerioneDepartment of Molecular Medicine, College of Veterinary Medicine, Cornell University, Ithaca, New York 14853 rac1@cornell.edu.ORCID 0000-0003-4512-5897
Cornell University · US

Funding

Training and OutreachP30GM124166 · NIGMS · CORNELL UNIVERSITY · PI RICHARD A. CERIONE · 2019 to 2026
$28.3M
The unique roles of the GTP-binding/protein crosslinking enzyme transglutaminase-2 and signaling partners in aggressive cancersR01CA201402 · NCI · CORNELL UNIVERSITY · PI CERIONE, RICHARD A. · 2016 to 2024
$4.3M
New frontiers in extracellular signalingR35GM122575 · NIGMS · CORNELL UNIVERSITY · PI CERIONE, RICHARD A. · 2017 to 2021
$3.0M
NCI NIH HHS R01 CA201402NIGMS NIH HHS P30 GM124166NIGMS NIH HHS R35 GM122575
6 · The paper itself

Abstract

The small GTPase cell division cycle 42 (CDC42) plays essential roles in neurogenesis and brain development. Previously, using murine embryonic P19 cells as a model system, we showed that CDC42 stimulates mTOR complex 1 (mTORC1) activity and thereby up-regulates transcription factors required for the formation of neural progenitor cells. However, paradoxically, although endogenous CDC42 is required for both the initial transition of undifferentiated P19 cells to neural progenitors and their ultimate terminal differentiation into neurons, ectopic CDC42 overexpression promotes only the first stage of neurogenesis (

Indexed as

Amino Acid SequenceAnimalsBraincdc42 GTP-Binding ProteinCell DifferentiationMechanistic Target of Rapamycin Complex 1MiceMouse Embryonic Stem CellsNestinNeural Stem CellsNeurogenesisNeuronsProtein IsoformsProtein-Tyrosine KinasesRNA InterferenceRNA, Small Interferingcdc42 GTP-Binding ProteinCdc42 protein, mouseMechanistic Target of Rapamycin Complex 1NestinProtein IsoformsProtein-Tyrosine KinasesRNA, Small InterferingTnk2 protein, mouseACKCDC42CDC42bCDC42udifferentiationmTOR complex (mTORC)neurogenesissmall GTPasesplice variantstem cells

Identifiers

PMID32071086
PMCPMC7136000
OpenAlexW3007169104

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.