Evidence map›Paper›PMID 31050647›Full record

ArticleeLife2019

GIPC proteins negatively modulate Plexind1 signaling during vascular development.

Jorge Carretero-Ortega, Zinal Chhangawala, Shane Hunt, Carlos Narvaez, Javier Menéndez-González, Carl M Gay, Tomasz Zygmunt, Xiaochun Li, Jesús Torres-Vázquez

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 30% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  4. Loss ofLife (Basel, Switzerland) · 2025
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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

9 authors at 2 institutions in 1 country.

Jorge Carretero-OrtegaDepartment of Cell Biology, Skirball Institute of Biomolecular Medicine, New York University Langone Medical Center, New York, United States.
Zinal ChhangawalaDepartment of Cell Biology, Skirball Institute of Biomolecular Medicine, New York University Langone Medical Center, New York, United States.
Shane HuntDepartment of Cell Biology, Skirball Institute of Biomolecular Medicine, New York University Langone Medical Center, New York, United States.
Carlos NarvaezDepartment of Cell Biology, Skirball Institute of Biomolecular Medicine, New York University Langone Medical Center, New York, United States.
Javier Menéndez-GonzálezDepartment of Cell Biology, Skirball Institute of Biomolecular Medicine, New York University Langone Medical Center, New York, United States.
Carl M GayDepartment of Cell Biology, Skirball Institute of Biomolecular Medicine, New York University Langone Medical Center, New York, United States.
Tomasz ZygmuntDepartment of Cell Biology, Skirball Institute of Biomolecular Medicine, New York University Langone Medical Center, New York, United States.
Xiaochun LiDepartment of Population Health, New York University School of Medicine, New York, United States.
Jesús Torres-VázquezDepartment of Cell Biology, Skirball Institute of Biomolecular Medicine, New York University Langone Medical Center, New York, United States.ORCID 0000-0002-3808-3978
NYU Langone Health · USNew York University · US

Funding

Molecular Regulation of Vascular Sprout FormationR01HL133687 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI TORRES-VÁZQUEZ, JESÚS · 2016 to 2019
$2.4M
Zeiss LSM 710 confocal microscopeS10RR024708 · NCRR · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NANCE, JEREMY · 2009 to 2009
$438k
NCRR NIH HHS S10 RR024708NHLBI NIH HHS R01 HL133687NIH HHS 1R01HL133687-01
6 · The paper itself

Abstract

Semaphorins (SEMAs) and their Plexin (PLXN) receptors are central regulators of metazoan cellular communication. SEMA-PLXND1 signaling plays important roles in cardiovascular, nervous, and immune system development, and cancer biology. However, little is known about the molecular mechanisms that modulate SEMA-PLXND1 signaling. As PLXND1 associates with GIPC family endocytic adaptors, we evaluated the requirement for the molecular determinants of their association and PLXND1's vascular role. Zebrafish that endogenously express a Plxnd1 receptor with a predicted impairment in GIPC binding exhibit low penetrance angiogenesis deficits and antiangiogenic drug hypersensitivity. Moreover,

Indexed as

Neovascularization, PhysiologicSignal TransductionAnimalsCarrier ProteinsEndothelial CellsProtein BindingReceptors, Cell SurfaceSemaphorinsZebrafishZebrafish ProteinsCarrier ProteinsGIPC1 protein, zebrafishplxnd1 protein, zebrafishReceptors, Cell SurfaceSemaphorinsZebrafish Proteinsangiogenesiscell signalingdevelopmental biologyGIPCPlexinD1zebrafishZebrafish

Identifiers

PMID31050647
PMCPMC6499541
OpenAlexW2942839002

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.