p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice (Q36005424)

11 August 2017

p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice (English)

1 reference

11 August 2017

Michael Rendl

14

0 references

Christopher J Percival

object named as

Christopher J Percival

9

0 references

Pavel Krejčí

object named as

Pavel Krejci

11

0 references

Ethylin Wang Jabs

object named as

Ethylin Wang Jabs

15

0 references

author name string

Yingli Wang

1

1 reference

11 August 2017

Xueyan Zhou

2

1 reference

11 August 2017

Kurun Oberoi

3

1 reference

11 August 2017

Robert Phelps

4

1 reference

11 August 2017

Ross Couwenhoven

5

1 reference

11 August 2017

Miao Sun

6

1 reference

11 August 2017

Amélie Rezza

7

1 reference

11 August 2017

Greg Holmes

8

1 reference

11 August 2017

Jenna Friedenthal

10

1 reference

11 August 2017

Joan T Richtsmeier

12

1 reference

11 August 2017

David L Huso

13

1 reference

11 August 2017

language of work or name

English

0 references

publication date

15 May 2012

1 reference

Journal of Clinical Investigation

11 August 2017

1 reference

11 August 2017

122

1 reference

11 August 2017

6

1 reference

11 August 2017

2153-2164

1 reference

describes a project that uses

11 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3366414/fullTextXML

inferred from PubMed Central ID database lookup

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Insights into the molecular basis for fibroblast growth factor receptor autoinhibition and ligand-binding promiscuity

2 October 2017

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Fibroblast growth factors: key players in epithelial morphogenesis, repair and cytoprotection

2 October 2017

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A crucial role for Fgfr2-IIIb signalling in epidermal development and hair follicle patterning

2 October 2017

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Conditional inactivation of FGF receptor 2 reveals an essential role for FGF signaling in the regulation of osteoblast function and bone growth

2 October 2017

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FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease

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Getting under the skin of epidermal morphogenesis

2 October 2017

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2 October 2017

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2 October 2017

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

2 October 2017

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2 October 2017

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A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans

2 October 2017

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

2 October 2017

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Receptor specificity of the fibroblast growth factor family

2 October 2017

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

2 October 2017

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The function of KGF in morphogenesis of epithelium and reepithelialization of wounds

2 October 2017

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Specific receptor detection by a functional keratinocyte growth factor-immunoglobulin chimera

2 October 2017

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

2 October 2017

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

2 October 2017

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Acanthosis nigricans: a study of 90 cases

2 October 2017

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Diverse forms of a receptor for acidic and basic fibroblast growth factors

2 October 2017

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Beare-Stevenson cutis gyrata syndrome

2 October 2017

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

2 October 2017

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Role of p38 MAPK in burn-induced intestinal barrier breakdown

2 October 2017

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Keratinocyte but not endothelial cell-specific overexpression of Tie2 leads to the development of psoriasis

11 July 2018

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A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis

11 July 2018

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Activating mutations of the tyrosine kinase receptor FGFR3 are associated with benign skin tumors in mice and humans

11 July 2018

1 reference

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Mutation in the FGFR2 gene in a Taiwanese patient with Beare-Stevenson cutis gyrata syndrome

11 July 2018

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Prevalence of acanthosis nigricans in an unselected population

11 July 2018

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Acanthosis Nigricans, insulin action, and hyperandrogenism: clinical, histological, and biochemical findings.

11 July 2018

1 reference

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The A391E mutation enhances FGFR3 activation in the absence of ligand

11 July 2018

1 reference

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Genetic basis of potential therapeutic strategies for craniosynostosis

23 September 2018

1 reference

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FGFs in endochondral skeletal development.

23 September 2018

1 reference

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A population-based study of craniosynostosis in metropolitan Atlanta, 1989-2003.

23 September 2018

1 reference

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Second case of Beare-Stevenson syndrome with an FGFR2 Ser372Cys mutation

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366414

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

23 September 2018

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The new bone biology: pathologic, molecular, and clinical correlates

23 September 2018

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Speech, cognitive, and behavioral outcomes in nonsyndromic craniosynostosis

23 September 2018

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Abnormalities in cartilage and bone development in the Apert syndrome FGFR2(+/S252W) mouse

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366414

Beare-Stevenson syndrome: Two South American patients with FGFR2 analysis

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366414

A case of Beare-Stevenson cutis gyrata syndrome confirmed by mutation analysis of the fibroblast growth factor receptor 2 gene

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366414

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

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366414

Prenatal sonographic appearance of Beare-Stevenson cutis gyrata syndrome: two- and three-dimensional ultrasonographic findings

23 September 2018

1 reference

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

23 September 2018

1 reference

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Cutis gyratum, acanthosis nigricans and other congenital anomalies. A new syndrome

23 September 2018

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Topical anti-inflammatory effect of hypocholesterolaemic drugs

21 October 2018

1 reference

12 December 2020

1 reference

12 December 2020

p38 mitogen-activated protein kinase regulates osteoblast differentiation through osterix

1 reference

12 December 2020

Therapeutic potential of inhaled p38 mitogen-activated protein kinase inhibitors for inflammatory pulmonary diseases

1 reference

12 December 2020

Activation of epidermal growth factor receptor/ERK signaling correlates with suppressed differentiation in malignant acanthosis nigricans

1 reference

12 December 2020

Cutis gyratum and acanthosis nigricans associated with other anomalies: a distinctive syndrome

1 reference

12 December 2020

1 reference

12 December 2020

Precision, Repeatability, and Validation of the Localization of Cranial Landmarks Using Computed Tomography Scans

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12 December 2020

Identifiers

DOI

10.1172/JCI62644

1 reference

11 August 2017

1 reference

11 August 2017

PubMed publication ID

22585574

1 reference