Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies-Reference-Cited by-同舟云学术

Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies

Published:2012-01-06 Issue:8 Volume:21 Page:1808-1823
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Ashe Alyson,Butterfield Natalie C.,Town Liam,Courtney Andrew D.,Cooper Ashley N.,Ferguson Charles,Barry Rachael,Olsson Fredrik,Liem Karel F.,Parton Robert G.,Wainwright Brandon J.,Anderson Kathryn V.,Whitelaw Emma,Wicking Carol

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/21/8/1808/17258982/ddr613.pdf

Reference69 articles.

1. The primary cilium: a signalling centre during vertebrate development;Goetz;Nat. Rev. Genet.,2010

2. Ciliopathies: an expanding disease spectrum;Waters;Pediatr. Nephrol.,2011

3. Modeling human disease in humans: the ciliopathies;Novarino;Cell,2011

4. IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy;Beales;Nat. Genet.,2007

5. Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis;Mill;Am. J. Hum. Genet.,2011

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