Postnatal brain and skull growth in an Apert syndrome mouse model. (Q54444041)

29 May 2018

title

Postnatal brain and skull growth in an Apert syndrome mouse model. (English)

1 reference

29 May 2018

1 reference

Neus Martínez-Abadías

2

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29 May 2018

Ethylin Wang Jabs

6

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29 May 2018

Kristina Aldridge

object named as

Kristina Aldridge

8

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author name string

Cheryl A Hill

1

1 reference

29 May 2018

Susan M Motch

3

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29 May 2018

Jordan R Austin

4

1 reference

29 May 2018

Yingli Wang

5

1 reference

29 May 2018

Joan T Richtsmeier

7

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29 May 2018

language of work or name

English

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publication date

12 March 2013

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29 May 2018

American Journal of Medical Genetics

published in

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29 May 2018

volume

161A

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29 May 2018

issue

4

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29 May 2018

page(s)

745-757

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29 May 2018

FGF/FGFR signaling coordinates skull development by modulating magnitude of morphological integration: evidence from Apert syndrome mouse models

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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

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

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Brain phenotypes in two FGFR2 mouse models for Apert syndrome

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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

4 June 2018

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4 June 2018

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4 June 2018

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Structural basis for fibroblast growth factor receptor 2 activation in Apert syndrome

4 June 2018

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Uncoupling fibroblast growth factor receptor 2 ligand binding specificity leads to Apert syndrome-like phenotypes

4 June 2018

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Management of craniosynostoses

4 June 2018

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Loss of fibroblast growth factor receptor 2 ligand-binding specificity in Apert syndrome.

4 June 2018

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Cranial sutures as intramembranous bone growth sites

4 June 2018

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Decreased proliferation and altered differentiation in osteoblasts from genetically and clinically distinct craniosynostotic disorders

4 June 2018

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Preoperative morphology and development in sagittal synostosis.

4 June 2018

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Increased calvaria cell differentiation and bone matrix formation induced by fibroblast growth factor receptor 2 mutations in Apert syndrome

4 June 2018

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Skull base and calvarial deformities: association with intracranial changes in craniofacial syndromes.

4 June 2018

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An updated pediatric perspective on the Apert syndrome.

4 June 2018

1 reference

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A coordinate-free approach to the analysis of growth patterns: models and theoretical considerations

4 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

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

4 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Analysis of phenotypic features and FGFR2 mutations in Apert syndrome.

4 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Agenesis of the corpus callosum and limbic malformation in Apert syndrome (type I acrocephalosyndactyly).

4 June 2018

1 reference

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The central nervous system in the Apert syndrome

4 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Characteristics of the infant Apert skull and its subsequent development

4 June 2018

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The craniofacial anatomy of Apert syndrome.

4 June 2018

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Agenesis of the corpus callosum. Its associated anomalies and syndromes with special reference to the Apert syndrome.

4 June 2018

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Birth prevalence study of the Apert syndrome

4 June 2018

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Modularity in the skull and cranial vasculature of laboratory mice: implications for the evolution of complex phenotypes.

4 June 2018

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Dynamic morphological changes in the skulls of mice mimicking human Apert syndrome resulting from gain-of-function mutation of FGFR2 (P253R).

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Fibroblast growth factor receptor 2 plays an essential role in telencephalic progenitors.

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Effects of aneuploidy on skull growth in a mouse model of Down syndrome.

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

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

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

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

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Craniofacial variability and modularity in macaques and mice.

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

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

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Brain-to-body ratios and time of maturation of the mouse brain

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Expression of FGF receptors 1, 2, 3 in the embryonic and postnatal mouse brain compared with Pdgfralpha, Olig2 and Plp/dm20: implications for oligodendrocyte development.

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

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

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Fetal craniofacial structure and intracranial morphology in a case of Apert syndrome.

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Expression of fibroblast growth factor receptors (FGFR1, FGFR2, FGFR3) in the developing head and face.

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Cranial size and configuration in the Apert syndrome.

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Analysis of intracranial volume in apert syndrome genotypes

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Genotype-phenotype analysis in Apert syndrome suggests opposite effects of the two recurrent mutations on syndactyly and outcome of craniofacial surgery

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Suture formation, premature sutural fusion, and suture default zones in Apert syndrome

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Growth pattern in the Apert syndrome

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

A study of intracranial volume in Apert syndrome

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Crouzon and Apert syndromes: intracranial volume measurements before and after cranio-orbital reshaping in childhood

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Craniofacial growth in apert syndrome as measured by finite-element scaling analysis

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3606655

Central nervous system phenotypes in craniosynostosis

13 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FAJMG.A.35805

Strain induced osteogenesis of the craniofacial suture upon controlled delivery of low-frequency cyclic forces

21 January 2018

1 reference

12 December 2020

Differential effects of trisomy on brain shape and volume in related aneuploid mouse models

1 reference

12 December 2020

A COMPARATIVE ANALYSIS OF MORPHOLOGICAL VARIATION PATTERNS IN THE PAPIONINS.

1 reference

12 December 2020

PHENOTYPIC, GENETIC, AND ENVIRONMENTAL MORPHOLOGICAL INTEGRATION IN THE CRANIUM.

1 reference

12 December 2020

Precision, repeatability, and validation of the localization of cranial landmarks using computed tomography scans

1 reference

12 December 2020

Identifiers

DOI

10.1002/AJMG.A.35805

1 reference

29 May 2018

PMCID

3606655

1 reference

29 May 2018

PubMed ID

23495236

1 reference

29 May 2018