A meckelin–filamin A interaction mediates ciliogenesis-Reference-Cited by-同舟云学术

A meckelin–filamin A interaction mediates ciliogenesis

Published:2011-11-25 Issue:6 Volume:21 Page:1272-1286
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Adams Matthew,Simms Roslyn J.,Abdelhamed Zakia,Dawe Helen R.,Szymanska Katarzyna,Logan Clare V.,Wheway Gabrielle,Pitt Eva,Gull Keith,Knowles Margaret A.,Blair Edward,Cross Sally H.,Sayer John A.,Johnson Colin A.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/21/6/1272/17258134/ddr557.pdf

Reference42 articles.

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2. MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome;Kyttala;Nat. Genet.,2006

3. The transmembrane protein meckelin (MKS3) is mutated in Meckel–Gruber syndrome and the wpk rat;Smith;Nat. Genet.,2006

4. Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes;Valente;Nat. Genet.,2010

5. A gene for Meckel syndrome maps to chromosome 11q13;Roume;Am. J. Hum. Genet.,1998

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