Evidence map›Paper›PMID 35606055›Full record

ArticleCurrent topics in developmental biology2022

Pulling back the curtain: The hidden functions of receptor tyrosine kinases in development.

James F Clark, Philippe M Soriano

Open access · greenAbstract read
In one paragraph

Article in Current topics in developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. DiverseGenes & development · 2024
    Article
  4. DiversebioRxiv : the preprint server for biology · 2024
    Article
  5. Article
  6. Article
  7. Article
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

2 authors at 1 institution in 1 country.

James F ClarkDepartment of Cell, Developmental, and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Philippe M SorianoDepartment of Cell, Developmental, and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY, United States. Electronic address: philippe.soriano@mssm.edu.
Icahn School of Medicine at Mount Sinai · US

Funding

FGF Signaling Pathways and Craniofacial DevelopmentR01DE022778 · NIDCR · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SORIANO, PHILIPPE M · 2012 to 2022
$6.6M
Growth Factor Signaling and Craniofacial DevelopmentR01DE022363 · NIDCR · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SORIANO, PHILIPPE M · 2012 to 2022
$6.4M
Novel Effectors of FGF Signaling in Craniofacial DevelopmentF32DE029387 · NIDCR · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CLARK, JAMES · 2020 to 2022
$208k
NIDCR NIH HHS F32 DE029387NIDCR NIH HHS R01 DE022363NIDCR NIH HHS R01 DE022778
6 · The paper itself

Abstract

Receptor tyrosine kinases (RTKs) are a conserved superfamily of transmembrane growth factor receptors that drive numerous cellular processes during development and in the adult. Upon activation, multiple adaptors and signaling effector proteins are recruited to binding site motifs located within the intracellular domain of the RTK. These RTK-effector interactions drive subsequent intracellular signaling cascades involved in canonical RTK signaling. Genetic dissection has revealed that alleles of Fibroblast Growth Factor receptors (FGFRs) that lack all canonical RTK signaling still retain some kinase-dependent biological activity. Here we examine how genetic analysis can be used to understand the mechanism by which RTKs drive multiple developmental processes via canonical signaling while revealing noncanonical activities. Recent data from both FGFRs and other RTKs highlight potential noncanonical roles in cell adhesion and nuclear signaling. The data supporting such functions are discussed as are recent technologies that have the potential to provide valuable insight into the developmental significance of these noncanonical activities.

Indexed as

Receptor Protein-Tyrosine KinasesSignal TransductionPhosphorylationReceptors, Fibroblast Growth FactorTyrosineReceptor Protein-Tyrosine KinasesReceptors, Fibroblast Growth FactorTyrosineCell adhesionFibroblast growth factor signalingNuclear signalingReceptor tyrosine kinases

Identifiers

PMID35606055
PMCPMC9127239
OpenAlexW4214661069

What OpenQuestion holds

Textmetadata
LicenceTDM
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.