(Q44589915)

4 December 2017

title

A Ser252Trp [corrected] substitution in mouse fibroblast growth factor receptor 2 (Fgfr2) results in craniosynostosis (English)

1 reference

4 December 2017

A Ser250Trp substitution in mouse fibroblast growth factor receptor 2 (Fgfr2) results in craniosynostosis (English)

1 reference

https://api.crossref.org/works/10.1016/S8756-3282(03)00222-9

11 March 2024

0 references

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14499350

11 March 2024

1 reference

https://api.crossref.org/works/10.1016/S8756-3282(03)00222-9

11 March 2024

Lin Chen

1 reference

4 December 2017

Dan Li

1 reference

4 December 2017

Cuiling Li

1 reference

4 December 2017

April Engel

1 reference

4 December 2017

Chu-Xia Deng

1 reference

4 December 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14499350

11 March 2024

publication date

1 August 2003

1 reference

full work available at URL

4 December 2017

https://api.elsevier.com/content/article/PII:S8756328203002229?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S8756-3282(03)00222-9

https://api.elsevier.com/content/article/PII:S8756328203002229?httpAccept=text/plain

11 March 2024

1 reference

https://api.crossref.org/works/10.1016/S8756-3282(03)00222-9

11 March 2024

1 reference

4 December 2017

1 reference

4 December 2017

1 reference

4 December 2017

page(s)

169-178

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Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand

4 December 2017

cites work

1 reference

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7 January 2021

Gly369Cys mutation in mouse FGFR3 causes achondroplasia by affecting both chondrogenesis and osteogenesis

1 reference

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7 January 2021

A Ser(365)-->Cys mutation of fibroblast growth factor receptor 3 in mouse downregulates Ihh/PTHrP signals and causes severe achondroplasia

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7 January 2021

Craniosynostosis update 1987.

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7 January 2021

Sutural biology and the correlates of craniosynostosis

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7 January 2021

Growth pattern in the Apert syndrome

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7 January 2021

Birth prevalence study of the Apert syndrome

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7 January 2021

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

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7 January 2021

Fibroblast growth factor receptor-1 (FGFR-1) is essential for normal neural tube and limb development.

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7 January 2021

Location of crossovers during gene targeting with insertion and replacement vectors

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Osf2/Cbfa1: a transcriptional activator of osteoblast differentiation

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7 January 2021

Respiratory complications during anaesthesia in Apert syndrome

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7 January 2021

Functions of fibroblast growth factors in vertebrate development

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7 January 2021

A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes

1 reference

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7 January 2021

A neonatal lethal mutation in FGFR3 uncouples proliferation and differentiation of growth plate chondrocytes in embryos.

1 reference

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7 January 2021

Highly activated Fgfr3 with the K644M mutation causes prolonged survival in severe dwarf mice

1 reference

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7 January 2021

Syndromes involving craniosynostosis and midface hypoplasia

1 reference

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7 January 2021

Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts

1 reference

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7 January 2021

Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndromes

1 reference

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7 January 2021

Efficient in vivo manipulation of mouse genomic sequences at the zygote stage

1 reference

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7 January 2021

The Ser252Trp fibroblast growth factor receptor-2 (FGFR-2) mutation induces PKC-independent downregulation of FGFR-2 associated with premature calvaria osteoblast differentiation

1 reference

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7 January 2021

Increased osteoblast apoptosis in apert craniosynostosis: role of protein kinase C and interleukin-1.

1 reference

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7 January 2021

A Lys644Glu substitution in fibroblast growth factor receptor 3 (FGFR3) causes dwarfism in mice by activation of STATs and ink4 cell cycle inhibitors

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2803%2900222-9

7 January 2021

Signaling by fibroblast growth factors (FGF) and fibroblast growth factor receptor 2 (FGFR2)-activating mutations blocks mineralization and induces apoptosis in osteoblasts

1 reference

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7 January 2021

The roles of FGFs in the early development of vertebrate limbs

1 reference

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7 January 2021

The pleiotropic effects of fibroblast growth factor receptors in mammalian development.

1 reference

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7 January 2021

Genetic control of the cell proliferation-differentiation balance in the developing skull vault: roles of fibroblast growth factor receptor signalling pathways.

1 reference

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7 January 2021

Fibroblast-growth-factor receptor mutations in human skeletal disorders

1 reference

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7 January 2021

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

1 reference

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7 January 2021

FGF signaling in skeletal development.

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2803%2900222-9

7 January 2021

Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2803%2900222-9

7 January 2021

Crystal structures of two FGF-FGFR complexes reveal the determinants of ligand-receptor specificity

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2803%2900222-9

7 January 2021

Management of craniosynostoses

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2803%2900222-9

7 January 2021

Crystal structure of a ternary FGF-FGFR-heparin complex reveals a dual role for heparin in FGFR binding and dimerization

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2803%2900222-9

7 January 2021

Fibroblast growth factors as multifunctional signaling factors

1 reference

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7 January 2021

A mouse model for achondroplasia produced by targeting fibroblast growth factor receptor 3.

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2803%2900222-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2803%2900222-9

7 January 2021

Murine fibroblast growth factor receptor 1alpha isoforms mediate node regression and are essential for posterior mesoderm development

1 reference

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7 January 2021

Fibroblast growth factor receptors (FGFRs) and their roles in limb development

1 reference

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7 January 2021

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

1 reference

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7 January 2021

The tumor suppressor SMAD4/DPC4 is essential for epiblast proliferation and mesoderm induction in mice

1 reference

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7 January 2021

Loss of fibroblast growth factor receptor 2 ligand-binding specificity in Apert syndrome.

1 reference

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7 January 2021

A Pro250Arg substitution in mouse Fgfr1 causes increased expression of Cbfa1 and premature fusion of calvarial sutures

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2803%2900222-9

7 January 2021

The FGF family of growth factors and oncogenes

1 reference

https://api.crossref.org/works/10.1016/S8756-3282(03)00222-9

Cephalometric study of the Apert syndrome in adolescence and adulthood

11 March 2024

1 reference

https://api.crossref.org/works/10.1016/S8756-3282(03)00222-9

Increased calvaria cell differentiation and bone matrix formation induced by fibroblast growth factor receptor 2 mutations in Apert syndrome

11 March 2024

1 reference

https://api.crossref.org/works/10.1016/S8756-3282(03)00222-9

Craniosynostosis syndromes

11 March 2024

1 reference

https://api.crossref.org/works/10.1016/S8756-3282(03)00222-9

11 March 2024

Identifiers

1 reference

4 December 2017

1 reference