(Q33600186)

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Morphological comparison of the craniofacial phenotypes of mouse models expressing the Apert FGFR2 S252W mutation in neural crest- or mesoderm-derived tissues.

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10 March 2020

Morphological comparison of the craniofacial phenotypes of mouse models expressing the Apert FGFR2 S252W mutation in neural crest- or mesoderm-derived tissues (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24632501%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

1

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10 March 2020

Ethylin Wang Jabs

4

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10 March 2020

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Nandini Singh

2

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10 March 2020

Claudio Basilico

3

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10 March 2020

Greg Holmes

5

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10 March 2020

Joan T Richtsmeier

6

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10 March 2020

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13 March 2014

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10 March 2020

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10 March 2020

63

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10 March 2020

101-109

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10 March 2020

The widely used Wnt1-Cre transgene causes developmental phenotypes by ectopic activation of Wnt signaling

1 reference

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21 June 2018

Hand in glove: brain and skull in development and dysmorphogenesis

1 reference

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21 June 2018

From shape to cells: mouse models reveal mechanisms altering palate development in Apert syndrome

1 reference

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21 June 2018

Augmentation of Smad-dependent BMP signaling in neural crest cells causes craniosynostosis in mice

1 reference

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21 June 2018

Tissue-specific responses to aberrant FGF signaling in complex head phenotypes

1 reference

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21 June 2018

A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9

1 reference

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21 June 2018

The effect of a Beare-Stevenson syndrome Fgfr2 Y394C mutation on early craniofacial bone volume and relative bone mineral density in mice

1 reference

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21 June 2018

Mesodermal expression of Fgfr2S252W is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018479

21 June 2018

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

1 reference

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21 June 2018

Brain phenotypes in two FGFR2 mouse models for Apert syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018479

21 June 2018

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

1 reference

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21 June 2018

Development and tissue origins of the mammalian cranial base.

1 reference

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21 June 2018

Syndromic craniosynostosis: from history to hydrogen bonds

1 reference

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21 June 2018

A functional approach to craniology

1 reference

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21 June 2018

Canalization, developmental stability, and morphological integration in primate limbs

1 reference

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21 June 2018

Cranial sutures as intramembranous bone growth sites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018479

21 June 2018

MesP1 is expressed in the heart precursor cells and required for the formation of a single heart tube

1 reference

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21 June 2018

Generalized lacZ expression with the ROSA26 Cre reporter strain

1 reference

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21 June 2018

Modification of gene activity in mouse embryos in utero by a tamoxifen-inducible form of Cre recombinase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018479

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018479

21 June 2018

Use of a recombinant retrovirus to study post-implantation cell lineage in mouse embryos

1 reference

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21 June 2018

Birth prevalence study of the Apert syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018479

21 June 2018

Differential closure of the spheno-occipital synchondrosis in syndromic craniosynostosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018479

30 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018479

30 October 2018

Craniosynostosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018479

30 October 2018

Elements of morphology: standard terminology for the head and face.

1 reference

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30 October 2018

Cell lineage in mammalian craniofacial mesenchyme.

1 reference

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30 October 2018

Phenotypic variability and craniofacial dysmorphology: increased shape variance in a mouse model for cleft lip.

1 reference

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30 October 2018

Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis

1 reference

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30 October 2018

Canalization and developmental stability in the Brachyrrhine mouse

1 reference

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30 October 2018

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

1 reference

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30 October 2018

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

1 reference

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30 October 2018

Tissue origins and interactions in the mammalian skull vault

1 reference

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30 October 2018

Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice.

1 reference

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30 October 2018

Identifiers

10.1016/J.BONE.2014.03.003

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Europe PubMed Central

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10 March 2020

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10 March 2020

PubMed publication ID

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Europe PubMed Central

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10 March 2020

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