Inventaire - your friends and communities are your best library

Genetics of craniofacial development and malformation

Author

Andrew Oliver Mungo Wilkie

1959 -

Published in: Nature Reviews Genetics

Date of publication: June 1, 2001

Language: English

Bibliographic databases:

Cites articles 111

Date

Title

Authors

March 1, 1973

The pathogenesis of the first and second branchial arch syndrome
April 15, 1983

Neural Crest and the Origin of Vertebrates: A New Head
December 1, 1992

Epithelial-mesenchymal interactions in the outgrowth of limb buds and facial primordia in chick embryos
December 31, 1993

Sonic hedgehog, a member of a family of putative signaling molecules, is implicated in the regulation of CNS polarity
November 1, 1993

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
December 31, 1993

Hoxa-2 mutant mice exhibit homeotic transformation of skeletal elements derived from cranial neural crest
December 31, 1993

A homeotic transformation is generated in the rostral branchial region of the head by disruption of Hoxa-2, which acts as a selector gene
April 1994

The origin and early diversification of tetrapods
November 1994

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

Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity
October 1, 1994

Transgenic mouse model of hemifacial microsomia: cloning and characterization of insertional mutation region on chromosome 10.
April 1, 1994

Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
September 23, 1994

The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping
September 1994

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
February 1, 1995

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

Cloning, expression, and chromosomal location of SHH and IHH: two human homologues of the Drosophila segment polarity gene hedgehog
November 1, 1995

Mouse Otx2 functions in the formation and patterning of rostral head.
February 10, 1995

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus
November 1, 1995

Constitutive Activation of Fibroblast Growth Factor Receptor-2 by a Point Mutation Associated with Crouzon Syndrome
December 1995

Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction
December 1, 1995

Transforming growth factor-beta 3 is required for secondary palate fusion
February 1, 1995

A fibrillar collagen gene, Col11a1, is essential for skeletal morphogenesis
October 3, 1996

Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function
November 1, 1996

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

,
November 1, 1996

Sek4 and Nuk receptors cooperate in guidance of commissural axons and in palate formation
November 1, 1996

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly
October 11, 1996

Cholesterol modification of hedgehog signaling proteins in animal development
February 1996

Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome. The Treacher Collins Syndrome Collaborative Group
October 1, 1996

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

,
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
February 1, 1996

What's in a face?
September 1996

A family with Stickler syndrome type 2 has a mutation in the COL11A1 gene resulting in the substitution of glycine 97 by valine in alpha 1 (XI) collagen

Article -

Welcome to inventaire

The library of your friends and communities

Learn more