FGFR2c-mediated ERK-MAPK activity regulates coronal suture development (Q41586944)

4 October 2017

FGFR2c-mediated ERK-MAPK activity regulates coronal suture development (English)

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4 October 2017

Miles J Pfaff

1

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4 October 2017

Ke Xue

2

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4 October 2017

Li Li

3

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4 October 2017

Mark C Horowitz

4

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4 October 2017

Derek M Steinbacher

5

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4 October 2017

Jacob V P Eswarakumar

6

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4 October 2017

language of work or name

English

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publication date

28 March 2016

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4 October 2017

Developmental Biology

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4 October 2017

415

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4 October 2017

2

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4 October 2017

242-250

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describes a project that uses

4 October 2017

ImageJ

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC5580088/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

Further analysis of the Crouzon mouse: effects of the FGFR2(C342Y) mutation are cranial bone-dependent

1 reference

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Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2(+P253R) mice

6 June 2018

1 reference

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Noonan syndrome is associated with enhanced pERK activity, the repression of which can prevent craniofacial malformations

6 June 2018

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Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology

6 June 2018

1 reference

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Syndromic craniosynostosis: from history to hydrogen bonds

6 June 2018

1 reference

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Cellular signaling by fibroblast growth factor receptors

6 June 2018

1 reference

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A gain-of-function mutation of Fgfr2c demonstrates the roles of this receptor variant in osteogenesis.

6 June 2018

1 reference

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Cranial sutures as intramembranous bone growth sites

6 June 2018

1 reference

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Identification of a novel inhibitor of mitogen-activated protein kinase kinase

6 June 2018

1 reference

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Craniosynostosis: genes and mechanisms

6 June 2018

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Fibroblast-growth-factor receptor mutations in human skeletal disorders

6 June 2018

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Structural and functional diversity in the FGF receptor multigene family

6 June 2018

1 reference

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

6 June 2018

1 reference

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HistoChoice as an alternative to formalin fixation of undecalcified bone specimens

6 June 2018

1 reference

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The IIIc alternative of Fgfr2 is a positive regulator of bone formation.

19 August 2018

1 reference

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Tissue origins and interactions in the mammalian skull vault

19 August 2018

1 reference

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Birth prevalence studies of the Crouzon syndrome: comparison of direct and indirect methods

19 August 2018

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RNA interference and inhibition of MEK-ERK signaling prevent abnormal skeletal phenotypes in a mouse model of craniosynostosis

19 August 2018

1 reference

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Fgfr1 and Fgfr2 have distinct differentiation- and proliferation-related roles in the developing mouse skull vault

19 August 2018

1 reference

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10.1016/J.YDBIO.2016.03.026

19 August 2018

Identifiers

DOI

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4 October 2017

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4 October 2017

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