Bardet-Biedl syndrome 3 regulates the development of cranial base midline structures-Reference-Cited by-同舟云学术

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Bardet-Biedl syndrome 3 regulates the development of cranial base midline structures

Published:2017-08 Issue: Volume:101 Page:179-190
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Kawasaki Makiri,Izu Yayoi,Hayata Tadayoshi,Ideno Hisashi,Nifuji Akira,Sheffield Val C.,Ezura Yoichi,Noda Masaki

Funder

Grant-in-Aid for JSPS Fellows

Grant-in-Aid for Scientific Research

TBRF

Abnormal Metabolism Research Foundation

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference30 articles.

1. Mechanistic insights into Bardet-Biedl syndrome, a model ciliopathy;Zaghloul;J. Clin. Invest.,2009

2. Planar cell polarity acts through septins to control collective cell movement and ciliogenesis;Kim;Science,2010

3. Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy;Otto;Nat. Genet.,2010

4. Exome sequencing identifies mutations in LZTFL1, a BBSome and smoothened trafficking regulator, in a family with Bardet–Biedl syndrome with situs inversus and insertional polydactyly;Marion;J. Med. Genet.,2012

5. Exome sequencing of Bardet-Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18);Scheidecker;J. Med. Genet.,2014

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