DYX1C1 is required for axonemal dynein assembly and ciliary motility
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Published:2013-07-21
Issue:9
Volume:45
Page:995-1003
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ISSN:1061-4036
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Container-title:Nature Genetics
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language:en
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Short-container-title:Nat Genet
Author:
Tarkar Aarti, , Loges Niki T, Slagle Christopher E, Francis Richard, Dougherty Gerard W, Tamayo Joel V, Shook Brett, Cantino Marie, Schwartz Daniel, Jahnke Charlotte, Olbrich Heike, Werner Claudius, Raidt Johanna, Pennekamp Petra, Abouhamed Marouan, Hjeij Rim, Köhler Gabriele, Griese Matthias, Li You, Lemke Kristi, Klena Nikolas, Liu Xiaoqin, Gabriel George, Tobita Kimimasa, Jaspers Martine, Morgan Lucy C, Shapiro Adam J, Letteboer Stef J F, Mans Dorus A, Carson Johnny L, Leigh Margaret W, Wolf Whitney E, Chen Serafine, Lucas Jane S, Onoufriadis Alexandros, Plagnol VincentORCID, Schmidts Miriam, Boldt Karsten, Roepman Ronald, Zariwala Maimoona A, Lo Cecilia W, Mitchison Hannah M, Knowles Michael R, Burdine Rebecca D, LoTurco Joseph J, Omran Heymut
Publisher
Springer Science and Business Media LLC
Reference61 articles.
1. Fliegauf, M., Benzing, T. & Omran, H. When cilia go bad: cilia defects and ciliopathies. Nat. Rev. Mol. Cell Biol. 8, 880–893 (2007). 2. Kennedy, M.P. et al. Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesia. Circulation 115, 2814–2821 (2007). 3. Ibañez-Tallon, I. et al. Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation. Hum. Mol. Genet. 13, 2133–2141 (2004). 4. Olbrich, H. et al. Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry. Nat. Genet. 30, 143–144 (2002). 5. Pennarun, G. et al. Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia. Am. J. Hum. Genet. 65, 1508–1519 (1999).
Cited by
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