(Q34177207)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21479780%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

title

A missense mutation in Fgfr1 causes ear and skull defects in hush puppy mice (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21479780%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21479780%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

6

Karen P Steel

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21479780%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

author name string

Jennifer A Calvert

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21479780%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Skarlatos G Dedos

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21479780%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Kelvin Hawker

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21479780%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Michelle Fleming

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21479780%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

publication date

10 April 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21479780%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

number of pages

16

1 reference

inferred from page(s)

published in

Mammalian Genome

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21479780%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

volume

22

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21479780%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

issue

5-6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21479780%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

page(s)

290-305

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21479780%20AND%20SRC:MED&resulttype=core&format=json

describes a project that uses

28 January 2020

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3099004/fullTextXML

inferred from PubMed Central ID database lookup

exact match

https://scigraph.springernature.com/pub.10.1007/s00335-011-9324-8

0 references

cites work

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Extracellular point mutations in FGFR2 elicit unexpected changes in intracellular signalling

5 July 2018

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Wnt11/Fgfr1b cross-talk modulates the fate of cells in palate development

5 July 2018

1 reference

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SOX3 activity during pharyngeal segmentation is required for craniofacial morphogenesis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Impaired FGF signaling contributes to cleft lip and palate

5 July 2018

1 reference

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Dusp6 (Mkp3) is a negative feedback regulator of FGF-stimulated ERK signaling during mouse development

5 July 2018

1 reference

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Differential signal transduction of alternatively spliced FGFR2 variants expressed in human mammary epithelial cells

5 July 2018

1 reference

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A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome

5 July 2018

1 reference

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Intracellular retention, degradation, and signaling of glycosylation-deficient FGFR2 and craniosynostosis syndrome-associated FGFR2C278F

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Receptor specificity of the fibroblast growth factor family. The complete mammalian FGF family

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Fibroblast growth factor receptor 1 (Fgfr1) is not essential for lens fiber differentiation in mice

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Cellular signaling by fibroblast growth factor receptors

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Hush puppy: a new mouse mutant with pinna, ossicle, and inner ear defects

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Mutations that cause osteoglophonic dysplasia define novel roles for FGFR1 in bone elongation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

FRS2-dependent SRC activation is required for fibroblast growth factor receptor-induced phosphorylation of Sprouty and suppression of ERK activity

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Fgf9 signaling regulates inner ear morphogenesis through epithelial-mesenchymal interactions

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

A natural allele of Nxf1 suppresses retrovirus insertional mutations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Parathyroid hormone increases the sensitivity of inositol trisphosphate receptors by a mechanism that is independent of cyclic AMP.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Fgfr1 regulates patterning of the pharyngeal region

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

FGFR1 is required for the development of the auditory sensory epithelium

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Microtubule-associated protein 1A is a modifier of tubby hearing (moth1).

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Critical role for the docking-protein FRS2 alpha in FGF receptor-mediated signal transduction pathways

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Primer3 on the WWW for general users and for biologist programmers

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Opposite phenotypes of hypomorphic and Y766 phosphorylation site mutations reveal a function for Fgfr1 in anteroposterior patterning of mouse embryos

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Binding of Shp2 tyrosine phosphatase to FRS2 is essential for fibroblast growth factor-induced PC12 cell differentiation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Embryological and genetic aspects of middle ear development.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

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

5 July 2018

1 reference

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A new DNA sequence assembly program

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Crystal structure of the tyrosine kinase domain of the human insulin receptor

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Cloning and expression of fibroblast growth factor receptor-1 isoforms in the mouse heart: evidence for isoform switching during heart development.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

A new generation of Ca2+ indicators with greatly improved fluorescence properties

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Characterization of binding and phosphorylation defects of erythrocyte insulin receptors in the type A syndrome of insulin resistance

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

The protein kinase family: conserved features and deduced phylogeny of the catalytic domains

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Detection of an alteration in the insulin-receptor gene in a patient with insulin resistance, acanthosis nigricans, and the polycystic ovary syndrome (type A insulin resistance).

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Functional properties of a naturally occurring Trp1200----Ser1200 mutation of the insulin receptor

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

FGFR-4, a novel acidic fibroblast growth factor receptor with a distinct expression pattern

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Requirement of heparan sulfate for bFGF-mediated fibroblast growth and myoblast differentiation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Complexity of FGF receptors: genetic basis for structural diversity and functional specificity

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3099004

Expression of members of the Fgf family and their receptors during midfacial development.

5 July 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9324-8

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9324-8

Skeletal development is regulated by fibroblast growth factor receptor 1 signalling dynamics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9324-8

FGF signaling through FGFR1 is required for olfactory bulb morphogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9324-8

Context-specific requirements for Fgfr1 signaling through Frs2 and Frs3 during mouse development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9324-8

Genome-wide, large-scale production of mutant mice by ENU mutagenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9324-8

21 January 2018

The genetics of deafness

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9324-8

Reversible kallmann syndrome, delayed puberty, and isolated anosmia occurring in a single family with a mutation in the fibroblast growth factor receptor 1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9324-8

Fgfr mRNA isoforms in craniofacial bone development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9324-8

Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9324-8

FGF signaling acts upstream of the NOTCH and WNT signaling pathways to control segmentation clock oscillations in mouse somitogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9324-8

An essential heparin-binding domain in the fibroblast growth factor receptor kinase

21 January 2018

1 reference

12 December 2020

fgfr-1 is required for embryonic growth and mesodermal patterning during mouse gastrulation

1 reference

12 December 2020

Murine FGFR-1 is required for early postimplantation growth and axial organization

1 reference

12 December 2020

Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2)

1 reference

12 December 2020

Different abilities of the four FGFRs to mediate FGF-1 translocation are linked to differences in the receptor C-terminal tail

1 reference

12 December 2020

10.1007/S00335-011-9324-8

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21479780%20AND%20SRC:MED&resulttype=core&format=json

release_yo3myvfzhncgzjhnmr3lbhod3u

28 January 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/yo3myvfzhncgzjhnmr3lbhod3u

24 November 2022

mapped directly with Wikidata item

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21479780%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

1 reference