Functional analysis of Ectodysplasin-A mutations causing selective tooth agenesis-Reference-Cited by-同舟云学术

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Functional analysis of Ectodysplasin-A mutations causing selective tooth agenesis

Published:2009-07-22 Issue:1 Volume:18 Page:19-25
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Mues Gabriele,Tardivel Aubry,Willen Laure,Kapadia Hitesh,Seaman Robyn,Frazier-Bowers Sylvia,Schneider Pascal,D'Souza Rena N

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2009127.pdf

Reference34 articles.

1. Thesleff I : Epithelial-mesenchymal signaling regulating tooth morphogenesis. J Cell Sci 2003; 116: 1647–1648.

2. Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman C : A human MSX1 homeodomain missense mutation causes selective tooth agenesis. Nat Genet 1996; 13: 417–421.

3. Stockton DW, Das P, Goldenberg M, D’Souza RN, Patel PI : Mutation of PAX9 is associated with oligodontia. Nat Genet 2000; 24: 18–19.

4. Lammi L, Arte S, Somer M et al: Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer. Am J Hum Genet 2004; 74: 1043–1050.

5. Van den Boogaar M-JH, Dorland M, Beemer FA, Ploos van Amstel HK : MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans. Nat Genet 2000; 24: 342–343. Erratum: Nat Genet 2000; 25: 125.

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3. Oligodontia in the Clinical Spectrum of Syndromes: A Systematic Review;Dentistry Journal;2023-12-04

4. Molecular basis and genetics of hypohidrotic ectodermal dysplasias;Vavilov Journal of Genetics and Breeding;2023-11-02

5. A novel deletion of exon 4 in the Ectodysplasin A gene associated with X-linked hypohidrotic ectodermal dysplasia;Archives of Oral Biology;2023-06

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