Leucine-rich repeat, immunoglobulin-like and transmembrane domain 3 (LRIT3) is a modulator of FGFR1 (Q24337453)

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English	Leucine-rich repeat, immunoglobulin-like and transmembrane domain 3 (LRIT3) is a modulator of FGFR1	scientific article

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instance of

scholarly article

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title

Leucine-rich repeat, immunoglobulin-like and transmembrane domain 3 (LRIT3) is a modulator of FGFR1 (English)

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main subject

biophysics

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cell biology

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structural biology

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transmembrane protein

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Leucine rich repeat, Ig-like and transmembrane domains 3

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stated in

GOA release 2020-03-11

regulation of fibroblast growth factor receptor signaling pathway

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stated in

GOA release 2020-03-11

author name string

Sun-Don Kim

series ordinal

1

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Jia Lie Liu

series ordinal

2

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Tony Roscioli

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3

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Michael F Buckley

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4

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Garima Yagnik

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5

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Simeon A Boyadjiev

series ordinal

6

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Jinoh Kim

series ordinal

7

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language of work or name

English

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publication date

21 May 2012

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published in

FEBS Letters

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volume

586

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issue

10

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page(s)

1516-21

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cites work

Cellular signaling by fibroblast growth factor receptors

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stated in

PubMed Central

reference URL

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19 March 2017

Promotion and attenuation of FGF signaling through the Ras-MAPK pathway

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PubMed Central

reference URL

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19 March 2017

A lipid-anchored Grb2-binding protein that links FGF-receptor activation to the Ras/MAPK signaling pathway

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PubMed Central

reference URL

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19 March 2017

Regulation of phosphoinositide-specific phospholipase C isozymes

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PubMed Central

reference URL

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19 March 2017

High-throughput tissue microarray analysis of 3p25 (RAF1) and 8p12 (FGFR1) copy number alterations in urinary bladder cancer

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PubMed Central

reference URL

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19 March 2017

Activating mutations in the extracellular domain of the fibroblast growth factor receptor 2 function by disruption of the disulfide bond in the third immunoglobulin-like domain

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PubMed Central

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19 March 2017

Fibroblast growth factors and their receptors in cancer

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PubMed Central

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27 September 2017

Impaired fibroblast growth factor receptor 1 signaling as a cause of normosmic idiopathic hypogonadotropic hypogonadism

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PubMed Central

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27 September 2017

A cell surface interaction network of neural leucine-rich repeat receptors

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PubMed Central

reference URL

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27 September 2017

Genetics of craniosynostosis: genes, syndromes, mutations and genotype-phenotype correlations

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PubMed Central

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27 September 2017

Genetic analysis of non-syndromic craniosynostosis

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PubMed Central

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27 September 2017

A role for fibronectin-leucine-rich transmembrane cell-surface proteins in homotypic cell adhesion

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PubMed Central

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27 September 2017

Functions and regulations of fibroblast growth factor signaling during embryonic development

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PubMed Central

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27 September 2017

Regulation of signal transduction and signal diversity by receptor oligomerization

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PubMed Central

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27 September 2017

Signal peptides: exquisitely designed transport promoters

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PubMed Central

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27 September 2017

The signal peptide

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PubMed Central

reference URL

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27 September 2017

Role of N-cadherin and protein kinase C in osteoblast gene activation induced by the S252W fibroblast growth factor receptor 2 mutation in Apert craniosynostosis

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PubMed Central

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30 May 2018

Heparin-induced oligomerization of FGF molecules is responsible for FGF receptor dimerization, activation, and cell proliferation

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21 January 2018

The transmembrane protein XFLRT3 forms a complex with FGF receptors and promotes FGF signalling

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Crossref

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21 January 2018

Constitutive Activation of Fibroblast Growth Factor Receptor-2 by a Point Mutation Associated with Crouzon Syndrome

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21 January 2018

Sustained platelet-derived growth factor receptor alpha signaling in osteoblasts results in craniosynostosis by overactivating the phospholipase C-gamma pathway

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Crossref

reference URL

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retrieved

21 January 2018

Epidemiology and genetics of craniosynostosis

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PubMed Central

reference URL

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retrieved

29 November 2018

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22673519

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Toward understanding the pathogenesis of craniosynostosis through clinical and molecular correlates

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3372856

retrieved

29 November 2018

Identifiers

DOI

10.1016/J.FEBSLET.2012.04.010

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PMC publication ID

3372856

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PubMed publication ID

22673519

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ResearchGate publication ID

225278698

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