Inventaire - your friends and communities are your best library

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

Published in: Nature Genetics

Date of publication: September 1994

Language: English

Main subject: fibroblast growth factor receptor 2, embryonic cranial skeleton morphogenesis

Bibliographic databases:

Cites articles 29

Date

Title

Authors

June 1984

Strategies for multilocus linkage analysis in humans

,
September 11, 1987

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression
January 1, 1987

Thanatophoric dysplasia and cloverleaf skull

,
December 1, 1988

Novel tyrosine kinase identified by phosphotyrosine antibody screening of cDNA libraries
February 11, 1988

A simple salting out procedure for extracting DNA from human nucleated cells
July 1, 1989

Purification and complementary DNA cloning of a receptor for basic fibroblast growth factor
November 1, 1989

Receptor for acidic fibroblast growth factor is related to the tyrosine kinase encoded by the fms-like gene (FLG).
April 1, 1989

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms
February 1, 1990

Two forms of the basic fibroblast growth factor receptor-like mRNA are expressed in the developing mouse brain
June 1, 1990

A murine fibroblast growth factor (FGF) receptor expressed in CHO cells is activated by basic FGF and Kaposi FGF
October 1990

Related fibroblast growth factor receptor genes exist in the human genome
August 1, 1990

A distinctive family of embryonic protein-tyrosine kinase receptors
September 1991

The human fibroblast growth factor receptor genes: a common structural arrangement underlies the mechanisms for generating receptor forms that differ in their third immunoglobulin domain
February 15, 1991

Isolation of an additional member of the fibroblast growth factor receptor family, FGFR-3
May 1, 1991

Assignment by in situ hybridization of a fibroblast growth factor receptor gene to human chromosome band 10q26
October 1992

The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7p
January 1, 1992

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

,
January 1, 1992

BEK, a receptor for multiple members of the fibroblast growth factor (FGF) family, maps to human chromosome 10q25.3----q26
November 1, 1993

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

Developmental localization of the splicing alternatives of fibroblast growth factor receptor-2 (FGFR2)
September 1, 1993

Control of BEK and K-SAM splice sites in alternative splicing of the fibroblast growth factor receptor 2 pre-mRNA.
June 1, 1993

Newly recognized autosomal dominant disorder with craniosynostosis
February 1, 1993

Assignment of a gene locus involved in craniosynostosis to chromosome 5qter
October 1, 1993

Cytogenetic evidence that the Saethre-Chotzen gene maps to 7p21.2.
October 1, 1993

Saethre-Chotzen syndrome with familial translocation at chromosome 7p22
January 1, 1994

Genetic heterogeneity among craniosynostosis syndromes: mapping the Saethre-Chotzen syndrome locus between D7S513 and D7S516 and exclusion of Jackson-Weiss and Crouzon syndrome loci from 7p,Genetic Heterogeneity among Craniosynostosis Syndromes: Mapping the Saethre-Chotzen Syndrome Locus between D7S513 and D7S516 and Exclusion of Jackson-Weiss and Crouzon Syndrome Loci from 7p
June 1, 1994

A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10.

,
July 1, 1994

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
March 1, 1994

Crouzon syndrome is not linked to craniosynostosis loci at 7p and 5qter

Article -

Welcome to inventaire

The library of your friends and communities

You are offline