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Constitutive receptor activation by Crouzon syndrome mutations in fibroblast growth factor receptor (FGFR)2 and FGFR2/Neu chimeras
scientific journal article
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scholarly article
1 reference
stated in
PubMed
PubMed ID
8755573
retrieved
3 February 2017
title
Constitutive receptor activation by Crouzon syndrome mutations in fibroblast growth factor receptor (FGFR)2 and FGFR2/Neu chimeras
(English)
1 reference
stated in
PubMed
PubMed ID
8755573
retrieved
3 February 2017
author name string
B. D. Galvin
series ordinal
1
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stated in
PubMed
PubMed ID
8755573
retrieved
3 February 2017
K. C. Hart
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
8755573
retrieved
3 February 2017
A. N. Meyer
series ordinal
3
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stated in
PubMed
PubMed ID
8755573
retrieved
3 February 2017
M. K. Webster
series ordinal
4
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stated in
PubMed
PubMed ID
8755573
retrieved
3 February 2017
D. J. Donoghue
series ordinal
5
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PubMed
PubMed ID
8755573
retrieved
3 February 2017
language of work or name
English
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publication date
23 July 1996
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PubMed
PubMed ID
8755573
retrieved
3 February 2017
published in
Proceedings of the National Academy of Sciences of the United States of America
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stated in
PubMed
PubMed ID
8755573
retrieved
3 February 2017
volume
93
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stated in
PubMed
PubMed ID
8755573
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3 February 2017
page(s)
7894–7899
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PubMed
PubMed ID
8755573
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3 February 2017
issue
15
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PubMed
PubMed ID
8755573
retrieved
3 February 2017
cites work
Constitutive activation of fibroblast growth factor receptor 3 by the transmembrane domain point mutation found in achondroplasia
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PubMed Central
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Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability
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PubMed Central
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17 March 2017
Structural and functional diversity in the FGF receptor multigene family
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PubMed Central
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Developmental localization of the splicing alternatives of fibroblast growth factor receptor-2 (FGFR2)
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PubMed Central
reference URL
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17 March 2017
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
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=38845
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17 March 2017
Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2
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PubMed Central
reference URL
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17 March 2017
A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome
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PubMed Central
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17 March 2017
Activation of RET as a dominant transforming gene by germline mutations of MEN2A and MEN2B
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PubMed Central
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Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome
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PubMed Central
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17 March 2017
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes
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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=38845
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17 March 2017
Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndrome
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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=38845
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17 March 2017
Related fibroblast growth factor receptor genes exist in the human genome
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PubMed Central
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17 March 2017
Cloning and expression of two distinct high-affinity receptors cross-reacting with acidic and basic fibroblast growth factors
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17 March 2017
A novel form of fibroblast growth factor receptor 2. Alternative splicing of the third immunoglobulin-like domain confers ligand binding specificity
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17 March 2017
Determination of ligand-binding specificity by alternative splicing: two distinct growth factor receptors encoded by a single gene
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17 March 2017
Fibroblast-growth-factor receptor mutations in human skeletal disorders
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Stabilization of an active dimeric form of the epidermal growth factor receptor by introduction of an inter-receptor disulfide bond
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Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
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PubMed Central
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29 September 2017
Achondroplasia is defined by recurrent G380R mutations of FGFR3
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PubMed Central
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29 September 2017
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
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PubMed Central
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Analysis of phenotypic features and FGFR2 mutations in Apert syndrome.
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Increased tyrosine kinase activity associated with the protein encoded by the activated neu oncogene
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29 September 2017
Intracellular retention of membrane-anchored v-sis protein abrogates autocrine signal transduction
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Homodimerization and constitutive activation of the erythropoietin receptor
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PubMed Central
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A soluble form of K-sam/FGFR2 protein in the culture medium of human gastric cancer cells
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3 June 2018
Stop codon FGFR3 mutations in thanatophoric dwarfism type 1.
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3 June 2018
Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson-Weiss syndrome
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=38845
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3 June 2018
The neu oncogene encodes an epidermal growth factor receptor-related protein
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=38845
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3 June 2018
Multiple independent activations of the neu oncogene by a point mutation altering the transmembrane domain of p185.
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=38845
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3 June 2018
Point mutation in the exoplasmic domain of the erythropoietin receptor resulting in hormone-independent activation and tumorigenicity
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3 June 2018
Multiple mRNAs code for proteins related to the BEK fibroblast growth factor receptor.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=38845
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3 June 2018
Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=38845
retrieved
27 November 2018
Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3.
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=38845
retrieved
27 November 2018
Effect on splicing of a silent FGFR2 mutation in Crouzon syndrome
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=38845
retrieved
27 November 2018
FGFR2 mutations in Pfeiffer syndrome
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=38845
retrieved
27 November 2018
A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
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=38845
retrieved
27 November 2018
A glycine 375-to-cysteine substitution in the transmembrane domain of the fibroblast growth factor receptor-3 in a newborn with achondroplasia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8755573
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Predisposition for cysteine substitutions in the immunoglobulin-like chain of FGFR2 in Crouzon syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8755573
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Crouzon Syndrome. A clinical and roentgencephalometric study
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8755573
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Oligomerization is essential for transport of vesicular stomatitis viral glycoprotein to the cell surface
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8755573
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Isolation of chicken-bek and a related gene; identification of structural variation in the ligand-binding domains of the FGF-receptor family
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8755573
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A Crouzon syndrome synonymous mutation activates a 5' splice site within the IIIc exon of the FGFR2 gene
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8755573
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1073/PNAS.93.15.7894
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3850998
ADS bibcode
1996PNAS...93.7894G
0 references
OpenCitations bibliographic resource ID
3850998
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3850998
PMCID
38845
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3850998
PubMed ID
8755573
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3850998
ResearchGate publication ID
14446242
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