(Q24672101)

5

object named as

Lynn B Jorde

0 references

author name string

Anna E Brassington

2

0 references

Pinar Bayrak-Toydemir

3

0 references

Patrycja A Krakowiak

4

0 references

Frank G Whitby

6

0 references

Nicola Longo

7

0 references

David H Viskochil

8

0 references

John C Carey

9

0 references

Michael J Bamshad

American Journal of Human Genetics

10

0 references

language of work or name

English

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publication date

November 2006

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published in

0 references

volume

79

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issue

5

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page(s)

935-41

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cites work

Fibroblast growth factor receptor 3 is a negative regulator of bone growth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698566

Structure of the FGF receptor tyrosine kinase domain reveals a novel autoinhibitory mechanism

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698566

A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698566

Mutations in different components of FGF signaling in LADD syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698566

FGFs, their receptors, and human limb malformations: clinical and molecular correlations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698566

Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698566

A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698566

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698566

The site of action of neuronal acidic fibroblast growth factor is the organ of Corti of the rat cochlea

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698566

Multiple activation loop conformations and their regulatory properties in the insulin receptor's kinase domain

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698566

Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698566

A single-base change in the tyrosine kinase II domain of ovine FGFR3 causes hereditary chondrodysplasia in sheep

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698566

Naturally occurring amino acid substitutions at Arg1174 in the human insulin receptor result in differential effects on receptor biosynthesis and hybrid formation, leading to discordant clinical phenotypes

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698566

Chemical rescue of a mutant protein-tyrosine kinase

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17033969

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Radiographic diagnosis of hereditary chondrodysplasia in newborn lambs

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17033969

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Expression of a dominant-negative mutant human insulin receptor in the muscle of transgenic mice

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17033969

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/508433

1 reference

1 reference

1 reference

PubMed publication ID

17033969

1 reference