Evidence map›Paper›PMID 25662260›Full record

ReviewCurrent topics in developmental biology2015

Receptor tyrosine kinase signaling: regulating neural crest development one phosphate at a time.

Katherine A Fantauzzo, Philippe Soriano

Open access · greenAbstract readReview
In one paragraph

Review in Current topics in developmental biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
4.9field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 2 syntheses or guidelines pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Downstream branches of receptor tyrosine kinase signaling act interdependently to shape the face.Developmental dynamics : an official publication of the American Association of Anatomists · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Pathogenicity of p.Phe147del in RET in familial Hirschsprung's disease.American journal of translational research · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Pten regulates neural crest proliferation and differentiation during mouse craniofacial development.Developmental dynamics : an official publication of the American Association of Anatomists · 2018
    Article
  20. 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

2 authors at 1 institution in 1 country.

Katherine A FantauzzoDepartment of Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, USA. Electronic address: katherine.fantauzzo@mssm.edu.
Philippe SorianoDepartment of Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, USA.
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
PI3K/Akt-mediated PDGFRalpha signaling in craniofacial developmentF32DE022719 · NIDCR · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI FANTAUZZO, KATHERINE ANN · 2012 to 2013
$108k
NIDCR NIH HHS F32 DE022719NIDCR NIH HHS F32DE022719NIDCR NIH HHS R01 DE022363NIDCR NIH HHS R01DE022363NIDCR NIH HHS R01 DE022778NIDCR NIH HHS R01DE022778
6 · The paper itself

Abstract

Receptor tyrosine kinases (RTKs) bind to a subset of growth factors on the surface of cells and elicit responses with broad roles in developmental and postnatal cellular processes. Receptors in this subclass consist of an extracellular ligand-binding domain, a single transmembrane domain, and an intracellular domain harboring a catalytic tyrosine kinase and regulatory sequences that are phosphorylated either by the receptor itself or by various interacting proteins. Once activated, RTKs bind signaling molecules and recruit effector proteins to mediate downstream cellular responses through various intracellular signaling pathways. In this chapter, we highlight the role of a subset of RTK families in regulating the activity of neural crest cells (NCCs) and the development of their derivatives in mammalian systems. NCCs are migratory, multipotent cells that can be subdivided into four axial populations, cranial, cardiac, vagal, and trunk. These cells migrate throughout the vertebrate embryo along defined pathways and give rise to unique cell types and structures. Interestingly, individual RTK families often have specific functions in a subpopulation of NCCs that contribute to the diversity of these cells and their derivatives in the mammalian embryo. We additionally discuss current methods used to investigate RTK signaling, including genetic, biochemical, large-scale proteomic, and biosensor approaches, which can be applied to study intracellular signaling pathways active downstream of this receptor subclass during NCC development.

Indexed as

AnimalsHumansIntercellular Signaling Peptides and ProteinsMammalsMiceMultigene FamilyNeural CrestPhosphatesReceptor Protein-Tyrosine KinasesSignal TransductionIntercellular Signaling Peptides and ProteinsPhosphatesReceptor Protein-Tyrosine KinasesAllelic seriesBiosensorsGrowth factorMass spectrometryMouseNeural crestPhospho-antibodiesProteomicsReceptor tyrosine kinase

Identifiers

PMID25662260
PMCPMC4363133
OpenAlexW2395949328

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.