Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates-Reference-Cited by-同舟云学术

Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates

Published:2005-09-18 Issue:10 Volume:37 Page:1135-1140
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Ross Alison J,May-Simera Helen,Eichers Erica R,Kai Masatake,Hill Josephine,Jagger Daniel J,Leitch Carmen C,Chapple J Paul,Munro Peter M,Fisher Shannon,Tan Perciliz L,Phillips Helen M,Leroux Michel R,Henderson Deborah J,Murdoch Jennifer N,Copp Andrew J,Eliot Marie-Madeleine,Lupski James R,Kemp David T,Dollfus Hélène,Tada Masazumi,Katsanis Nicholas,Forge Andrew,Beales Philip L

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1644.pdf

Reference30 articles.

1. Torban, E., Kor, C. & Gros, P. Van Gogh-like2 (Strabismus) and its role in planar cell polarity and convergent extension in vertebrates. Trends Genet. 20, 570–577 (2004).

2. Keller, R. Shaping the vertebrate body plan by polarized embryonic cell movements. Science 298, 1950–1954 (2002).

3. Ansley, S.J. et al. Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome. Nature 425, 628–633 (2003).

4. Li, J.B. et al. Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene. Cell 117, 541–552 (2004).

5. Lu, X. et al. PTK7/CCK-4 is a novel regulator of planar cell polarity in vertebrates. Nature 430, 93–98 (2004).

Cited by 519 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Centriole Translational Planar Polarity in Monociliated Epithelia;Cells;2024-08-23

2. Structure, function, and research progress of primary cilia in reproductive physiology and reproductive diseases;Frontiers in Cell and Developmental Biology;2024-06-03

3. Emx2 is an essential regulator of ciliated cell development across embryonic tissues;2024-01-04

4. Functions of cilia in cardiac development and disease;Annals of Human Genetics;2023-10-23

5. Heterozygous FOXJ1 Mutations Cause Incomplete Ependymal Cell Differentiation and Communicating Hydrocephalus;Cellular and Molecular Neurobiology;2023-08-24