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

Author

Andrew Oliver Mungo Wilkie

1959 -

Published in: Journal of Anatomy

Date of publication: November 2005

Language: English

Main subject: cell biology, histology, craniosynostosis

Bibliographic databases:

Cites articles 90

Date

Title

Authors

June 1, 1975

Migration of cranial neural crest cells in a cell-free hyaluronate-rich matrix
January 1, 1979

Craniofrontonasal dysplasia
September 1, 1982

Intracranial pressure in craniostenosis
June 3, 1983

Neural crest cells contribute to normal aorticopulmonary septation
November 1, 1986

The effects of Streptomyces hyaluronidase on tissue organization and cell cycle time in rat embryos
November 1, 1986

Analysis of cranial neural crest cell migration and early fates in postimplantation rat chimaeras
April 1, 1987

The twist gene: isolation of a Drosophila zygotic gene necessary for the establishment of dorsoventral pattern
February 1, 1988

A morphological and experimental study of the mesencephalic neural crest cells in the mouse embryo using wheat germ agglutinin-gold conjugate as the cell marker
January 1, 1992

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

,
January 1, 1992

Clonal analysis of cell fate during gastrulation and early neurulation in the mouse
April 1, 1992

Migration of cranial neural crest cells to the pharyngeal arches and heart in rat embryos
October 1, 1992

Vital dye analysis of cranial neural crest cell migration in the mouse embryo
January 1, 1993

Structural and functional diversity in the FGF receptor multigene family
November 1, 1993

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
April 1, 1993

Hox genes and pattern formation in the branchial region of the vertebrate head
February 1, 1993

Two FGF-receptor homologues of Drosophila: one is expressed in mesodermal primordium in early embryos
September 1994

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
November 1994

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome
August 1, 1994

The contribution of both forebrain and midbrain crest cells to the mesenchyme in the frontonasal mass of mouse embryos
December 1, 1994

fgfr-1 is required for embryonic growth and mesodermal patterning during mouse gastrulation
February 1995

Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes
March 15, 1995

twist is required in head mesenchyme for cranial neural tube morphogenesis
February 1, 1995

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
November 1, 1995

Constitutive Activation of Fibroblast Growth Factor Receptor-2 by a Point Mutation Associated with Crouzon Syndrome
December 1996

The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences
June 21, 1996

Receptor specificity of the fibroblast growth factor family
March 22, 1996

Fibroblast growth factor receptor 3 is a negative regulator of bone growth
December 1, 1996

Heartless, a Drosophila FGF receptor homolog, is essential for cell migration and establishment of several mesodermal lineages
April 1, 1996

Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3.
October 1, 1996

Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes

,
November 1, 1996

Studies in cranial suture biology: IV. Temporal sequence of posterior frontal cranial suture fusion in the mouse
January 1997

Mutations of the TWIST gene in the Saethre-Chotzen syndrome

,

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