Further analysis of the Crouzon mouse: effects of the FGFR2(C342Y) mutation are cranial bone-dependent (Q36780832)

16 August 2017

Further analysis of the Crouzon mouse: effects of the FGFR2(C342Y) mutation are cranial bone-dependent (English)

1 reference

16 August 2017

Jin Liu

1

1 reference

16 August 2017

Hwa Kyung Nam

series ordinal

2

1 reference

16 August 2017

Estee Wang

series ordinal

3

1 reference

16 August 2017

Nan E Hatch

series ordinal

4

1 reference

16 August 2017

language of work or name

English

0 references

publication date

29 January 2013

1 reference

Calcified Tissue International

16 August 2017

1 reference

16 August 2017

92

1 reference

16 August 2017

5

1 reference

16 August 2017

451-466

1 reference

https://scigraph.springernature.com/pub.10.1007/s00223-013-9701-2

16 August 2017

0 references

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Craniofacial reconstruction as a treatment for elevated intracranial pressure

29 September 2017

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

29 September 2017

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Activation of FGF signaling mediates proliferative and osteogenic differences between neural crest derived frontal and mesoderm parietal derived bone

29 September 2017

1 reference

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Prevalence and complications of single-gene and chromosomal disorders in craniosynostosis.

29 September 2017

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Guidelines for assessment of bone microstructure in rodents using micro-computed tomography

29 September 2017

1 reference

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

29 September 2017

1 reference

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Intellectual outcomes following protocol management in Crouzon, Pfeiffer, and Muenke syndromes

29 September 2017

1 reference

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

29 September 2017

1 reference

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Differential FGF ligands and FGF receptors expression pattern in frontal and parietal calvarial bones

29 September 2017

1 reference

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FGF2 stimulation of the pyrophosphate-generating enzyme, PC-1, in pre-osteoblast cells is mediated by RUNX2.

29 September 2017

1 reference

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Priorities for public health research on craniosynostosis: summary and recommendations from a Centers for Disease Control and Prevention-sponsored meeting

29 September 2017

1 reference

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Genetic analysis of non-syndromic craniosynostosis

29 September 2017

1 reference

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Syndromic craniosynostosis: from history to hydrogen bonds

29 September 2017

1 reference

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Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies

29 September 2017

1 reference

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A gain-of-function mutation of Fgfr2c demonstrates the roles of this receptor variant in osteogenesis.

29 September 2017

1 reference

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Management of craniosynostoses

29 September 2017

1 reference

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Signaling by fibroblast growth factors (FGF) and fibroblast growth factor receptor 2 (FGFR2)-activating mutations blocks mineralization and induces apoptosis in osteoblasts

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Sutural biology and the correlates of craniosynostosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Two distinct osteoblast-specific cis-acting elements control expression of a mouse osteocalcin gene

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Functional prognosis of surgical treatment of craniosynostosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Upper and lower airway compromise in the Apert syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Expression of bone morphogenetic protein messenger RNA in prolonged cultures of fetal rat calvarial cells

27 June 2018

1 reference

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Treatment for delayed presentation of sagittal synostosis: challenges pertaining to occult intracranial hypertension.

27 June 2018

1 reference

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Different endogenous threshold levels of Fibroblast Growth Factor-ligands determine the healing potential of frontal and parietal bones.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Skeletal analysis of the Fgfr3(P244R) mouse, a genetic model for the Muenke craniosynostosis syndrome.

5 September 2018

1 reference

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The craniofacial phenotype of the Crouzon mouse: analysis of a model for syndromic craniosynostosis using three-dimensional MicroCT.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Sudden infant death in a patient with FGFR3 P250R mutation

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Proline to arginine mutations in FGF receptors 1 and 3 result in Pfeiffer and Muenke craniosynostosis syndromes through enhancement of FGF binding affinity

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

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

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Increased osteoblast apoptosis in apert craniosynostosis: role of protein kinase C and interleukin-1.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Fgfr1 and Fgfr2 have distinct differentiation- and proliferation-related roles in the developing mouse skull vault

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Fgfr2 and osteopontin domains in the developing skull vault are mutually exclusive and can be altered by locally applied FGF2.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Birth prevalence studies of the Crouzon syndrome: comparison of direct and indirect methods

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

A Pro250Arg substitution in mouse Fgfr1 causes increased expression of Cbfa1 and premature fusion of calvarial sutures

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Ocular anterior chamber dysgenesis in craniosynostosis syndromes with a fibroblast growth factor receptor 2 mutation

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Visual failure caused by raised intracranial pressure in craniosynostosis

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Craniofacial growth in plagiocephaly and Crouzon syndrome

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3631296

Drug export activity of the human canalicular multispecific organic anion transporter in polarized kidney MDCK cells expressing cMOAT (MRP2) cDNA

5 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00223-013-9701-2

Further biochemical and molecular characterization of primary rat parietal bone cell cultures

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23358860

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Cranio-facial dysostosis of Crouzon; report of a case in which the malformation occurred in four generations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23358860

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00223-013-9701-2

1 reference

16 August 2017

1 reference

16 August 2017

1 reference