Facial suture synostosis of newborn Fgfr1(P250R/+) and Fgfr2(S252W/+) mouse models of Pfeiffer and Apert syndromes (Q56329626)

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30 January 2020

title

Facial suture synostosis of newborn Fgfr1(P250R/+) and Fgfr2(S252W/+) mouse models of Pfeiffer and Apert syndromes (English)

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30 January 2020

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3

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30 January 2020

author name string

Roopa Purushothaman

series ordinal

1

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30 January 2020

Timothy C Cox

series ordinal

2

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30 January 2020

Michael L Cunningham

series ordinal

4

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30 January 2020

language of work or name

English

0 references

publication date

28 April 2011

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21538817%20AND%20SRC:MED&resulttype=core&format=json

Birth Defects Research Part A: Clinical and Molecular Teratology

30 January 2020

published in

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30 January 2020

volume

91

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30 January 2020

issue

7

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30 January 2020

page(s)

603-609

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Expression of members of the Fgf family and their receptors during midfacial development.

30 January 2020

cites work

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The emergence of ectomesenchyme

21 January 2018

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Rare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamily

21 January 2018

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From genotype to phenotype: the differential expression of FGF, FGFR, and TGFbeta genes characterizes human cranioskeletal development and reflects clinical presentation in FGFR syndromes

21 January 2018

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Toward pathogenesis of Apert cleft palate: FGF, FGFR, and TGF beta genes are differentially expressed in sequential stages of human palatal shelf fusion

21 January 2018

1 reference

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

21 January 2018

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Patterning the neural crest derivatives during development of the vertebrate head: insights from avian studies

21 January 2018

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Cellular signaling by fibroblast growth factor receptors

21 January 2018

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Skeletal development is regulated by fibroblast growth factor receptor 1 signalling dynamics.

21 January 2018

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Evidence that Fgf10 contributes to the skeletal and visceral defects of an Apert syndrome mouse model

21 January 2018

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Functional evolutionary history of the mouse Fgf gene family

21 January 2018

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Tissue origins and interactions in the mammalian skull vault

21 January 2018

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Genetics of craniosynostosis

21 January 2018

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An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly

21 January 2018

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Role of the neural crest in face and brain development

21 January 2018

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

21 January 2018

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Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S.

21 January 2018

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

21 January 2018

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Cranial base in craniofacial development: developmental features, influence on facial growth, anomaly, and molecular basis

21 January 2018

1 reference

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De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome

21 January 2018

1 reference

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Receptor specificity of the fibroblast growth factor family

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.20811

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

21 January 2018

1 reference

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Clinical findings in a patient with FGFR1 P252R mutation and comparison with the literature.

21 January 2018

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

21 January 2018

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

21 January 2018

1 reference

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