Literature DB >> 10830010

Fibroblast growth factor receptor mutations and craniosynostosis: three receptors, five syndromes.

A O Wilkie1.   

Abstract

The post eighteen months have been exciting time for craniosynostosis research. In a rapid flurry of publications, mutations of fibroblast growth factor receptors (FGFRs) have been identified in three of the best known craniosynostosis syndromes, namely Apert, Crouzon and Pfeiffer syndromes, as well as in Jackson-Weiss syndrome and thanatophoric dysplasia. These findings open many new avenues for craniosynostosis research including studies of diagnosis, pathogenesis, and mutagenesis. Here the major findings and their implications have been briefly reviewed.

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Year:  1996        PMID: 10830010     DOI: 10.1007/bf02751527

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  34 in total

1.  Stop codon FGFR3 mutations in thanatophoric dwarfism type 1.

Authors:  F Rousseau; P Saugier; M Le Merrer; A Munnich; A L Delezoide; P Maroteaux; J Bonaventure; F Narcy; M Sanak
Journal:  Nat Genet       Date:  1995-05       Impact factor: 38.330

Review 2.  Functions of fibroblast growth factors and their receptors.

Authors:  A O Wilkie; G M Morriss-Kay; E Y Jones; J K Heath
Journal:  Curr Biol       Date:  1995-05-01       Impact factor: 10.834

3.  Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2.

Authors:  E W Jabs; X Li; A F Scott; G Meyers; W Chen; M Eccles; J I Mao; L R Charnas; C E Jackson; M Jaye
Journal:  Nat Genet       Date:  1994-11       Impact factor: 38.330

4.  Two craniosynostotic syndrome loci, Crouzon and Jackson-Weiss, map to chromosome 10q23-q26.

Authors:  X Li; A F Lewanda; F Eluma; H Jerald; H Choi; I Alozie; C Proukakis; C C Talbot; C Vander Kolk; L M Bird
Journal:  Genomics       Date:  1994-07-15       Impact factor: 5.736

5.  Developmental localization of the splicing alternatives of fibroblast growth factor receptor-2 (FGFR2).

Authors:  A Orr-Urtreger; M T Bedford; T Burakova; E Arman; Y Zimmer; A Yayon; D Givol; P Lonai
Journal:  Dev Biol       Date:  1993-08       Impact factor: 3.582

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

Authors:  A O Wilkie; S F Slaney; M Oldridge; M D Poole; G J Ashworth; A D Hockley; R D Hayward; D J David; L J Pulleyn; P Rutland
Journal:  Nat Genet       Date:  1995-02       Impact factor: 38.330

7.  Genetic study of nonsyndromic coronal craniosynostosis.

Authors:  E Lajeunie; M Le Merrer; C Bonaïti-Pellie; D Marchac; D Renier
Journal:  Am J Med Genet       Date:  1995-02-13

8.  Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson-Weiss syndrome.

Authors:  M C Gorry; R A Preston; G J White; Y Zhang; V K Singhal; H W Losken; M G Parker; N A Nwokoro; J C Post; G D Ehrlich
Journal:  Hum Mol Genet       Date:  1995-08       Impact factor: 6.150

9.  Analysis of phenotypic features and FGFR2 mutations in Apert syndrome.

Authors:  W J Park; C Theda; N E Maestri; G A Meyers; J S Fryburg; C Dufresne; M M Cohen; E W Jabs
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

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

Authors:  W Reardon; R M Winter; P Rutland; L J Pulleyn; B M Jones; S Malcolm
Journal:  Nat Genet       Date:  1994-09       Impact factor: 38.330

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