(Q43145663)

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Molecular analysis of coronal perisutural tissues in a craniosynostotic rabbit model using polymerase chain reaction suppression subtractive hybridization

scientific article published in July 2011

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Molecular analysis of coronal perisutural tissues in a craniosynostotic rabbit model using polymerase chain reaction suppression subtractive hybridization (English)

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

author name string

James J Cray

1

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Phillip H Gallo

2

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Emily L Durham

3

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Joseph E Losee

4

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Mark P Mooney

5

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Sandeep Kathju

6

1 reference

Europe PubMed Central

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14 November 2017

Gregory M Cooper

7

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Europe PubMed Central

PMC publication ID

14 November 2017

language of work or name

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publication date

1 July 2011

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Europe PubMed Central

PMC publication ID

14 November 2017

Plastic and Reconstructive Surgery

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

128

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Europe PubMed Central

PMC publication ID

14 November 2017

1

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

95-103

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

describes a project that uses

polymerase chain reaction

1 reference

based on heuristic

inferred from title

Genetics of craniosynostosis: review of the literature.

1 reference

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1 reference

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Future therapeutic targets in osteoporosis

1 reference

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Pharmacological inhibitors to identify roles of cathepsin K in cell-based studies: a comparison of available tools

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1 reference

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25 May 2018

Genetics of craniosynostosis

1 reference

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Twist1 dimer selection regulates cranial suture patterning and fusion

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FGF signalling in craniofacial development and developmental disorders

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

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Apert and Crouzon syndromes: clinical findings, genes and extracellular matrix.

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Structural basis for fibroblast growth factor receptor activation

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Understanding the molecular basis of Apert syndrome

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High-dose retinoic acid modulates rat calvarial osteoblast biology

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A soluble form of fibroblast growth factor receptor 2 (FGFR2) with S252W mutation acts as an efficient inhibitor for the enhanced osteoblastic differentiation caused by FGFR2 activation in Apert syndrome

1 reference

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Molecular and cellular bases of syndromic craniosynostoses

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

1 reference

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Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome

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Suppression subtractive hybridization: a versatile method for identifying differentially expressed genes

1 reference

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A rabbit model of human familial, nonsyndromic unicoronal suture synostosis. II. Intracranial contents, intracranial volume, and intracranial pressure

1 reference

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Craniosynostosis: genes and mechanisms

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Coronal suture pathology and synostotic progression in rabbits with congenital craniosynostosis.

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Genetic study of scaphocephaly

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Craniosynostosis with autosomal dominant transmission in New Zealand white rabbits.

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Suppression subtractive hybridization: a method for generating differentially regulated or tissue-specific cDNA probes and libraries

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Evolution of the face in Loeys-Dietz syndrome type II: longitudinal observations from infancy in seven cases.

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Referral pattern and surgical outcome of sagittal synostosis

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Identification of genes differentially expressed by prematurely fused human sutures using a novel in vivo - in vitro approach

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A rabbit model of human familial, nonsyndromic unicoronal suture synostosis. I. Synostotic onset, pathology, and sutural growth patterns

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Development of a strain of rabbits with congenital simple nonsyndromic coronal suture synostosis. Part I: Breeding demographics, inheritance pattern, and craniofacial anomalies

1 reference

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1 reference

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1 reference

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12 December 2020

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10.1097/PRS.0B013E31821740E8

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

release_roczlahkezdqxhyk3iuicwcde4

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https://api.fatcat.wiki/v0/release/roczlahkezdqxhyk3iuicwcde4

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

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