Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice - Wikidata - awgldk - TriplyDB

Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice

Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice

http://www.wikidata.org/entity/Q30583934

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Fibroblast growth factor signaling in skeletal development and disease Developmental and Evolutionary Significance of the Zygomatic Bone A computational analysis of bone formation in the cranial vault in the mouse Integration of comprehensive 3D microCT and signaling analysis reveals differential regulatory mechanisms of craniofacial bone development.Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses.Mice lacking the conserved transcription factor Grainyhead-like 3 (Grhl3) display increased apposition of the frontal and parietal bones during embryonic development.Understanding craniosynostosis as a growth disorder Morphometrics, 3D Imaging, and Craniofacial Development.Integration of Brain and Skull in Prenatal Mouse Models of Apert and Crouzon Syndromes.Effects of thyroxine exposure on the Twist 1 +/- phenotype: A test of gene-environment interaction modeling for craniosynostosis

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P2860

Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice

http://www.wikidata.org/entity/Q30583934

description

2014 nî lūn-bûn

@nan

2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice

@ast

Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice

@en

type

label

Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice

@ast

Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice

@en

prefLabel

Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice

@ast

Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice

@en

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BMC Developmental Biology

P1476

Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice

@en

P2093

Joan T Richtsmeier

http://www.w3.org/2001/XMLSchema#string

Susan M Motch Perrine

http://www.w3.org/2001/XMLSchema#string

Theodore M Cole

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P2860

Fibroblast growth factors

Simplification as a trend in synapsid cranial evolution

Evolution and tinkering

Analysis of phenotypic features and FGFR2 mutations in Apert syndrome.

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

Quantification of facial skeletal shape variation in fibroblast growth factor receptor-related craniosynostosis syndromes.

Cranial sutures as intramembranous bone growth sites.

Beyond the closed suture in apert syndrome mouse models: evidence of primary effects of FGFR2 signaling on facial shape at birth.

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

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

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8

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scholarly article

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10.1186/1471-213X-14-8

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1

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14

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Kristina Aldridge

Ethylin Wang Jabs

Neus Martínez-Abadías

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2014-02-28T00:00:00Z

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1000017691

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24580805

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4101838

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