(Q28294004)

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Pleiotropic features of syndromic craniosynostoses correlate with differential expression of fibroblast growth factor receptors 1 and 2 during human craniofacial development

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Pleiotropic features of syndromic craniosynostoses correlate with differential expression of fibroblast growth factor receptors 1 and 2 during human craniofacial development (English)

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C T Chan

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P Thorogood

2

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publication date

January 1999

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Pediatric Research

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45

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1

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46-53

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A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Perinatal lethality and multiple craniofacial malformations in MSX2 transgenic mice.

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Fibroblast-growth-factor receptor mutations in human skeletal disorders

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

The molecular pathology of syndromic craniosynostosis

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Promiscuity of fibroblast growth factor receptors

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Determination of ligand-binding specificity by alternative splicing: two distinct growth factor receptors encoded by a single gene

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasia

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Profound ligand-independent kinase activation of fibroblast growth factor receptor 3 by the activation loop mutation responsible for a lethal skeletal dysplasia, thanatophoric dysplasia type II

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Activation of Stat1 by mutant fibroblast growth-factor receptor in thanatophoric dysplasia type II dwarfism

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Constitutive receptor activation by Crouzon syndrome mutations in fibroblast growth factor receptor (FGFR)2 and FGFR2/Neu chimeras

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Ligand-independent activation of fibroblast growth factor receptors by point mutations in the extracellular, transmembrane, and kinase domains

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

FGFR activation in skeletal disorders: too much of a good thing

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Developmental localization of the splicing alternatives of fibroblast growth factor receptor-2 (FGFR2)

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Magnetic resonance imaging in the assessment of craniosynostosis

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

The central nervous system in the Apert syndrome

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Subdural intracranial pressure monitoring in craniosynostosis: its role in surgical management.

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Intracranial pressure in craniostenosis

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Differential expression patterns of mRNAs for members of the fibroblast growth factor receptor family, FGFR-1-FGFR-4, in rat brain

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Fibroblast growth factor stimulates the proliferation and differentiation of neural precursor cells in vitro

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Activation of the FGF receptor underlies neurite outgrowth stimulated by L1, N-CAM, and N-cadherin

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

Cutaneous manifestations of Apert syndrome

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199901000-00008

21 January 2018

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10.1203/00006450-199901000-00008

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