A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome-Reference-Cited by-同舟云学术

A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome

Published:2016-04-11 Issue:1 Volume:5 Page:
ISSN:2046-2530
Container-title:Cilia
language:en
Short-container-title:Cilia

Author:

Oud Machteld M.,Bonnard Carine,Mans Dorus A.,Altunoglu Umut,Tohari Sumanty,Ng Alvin Yu Jin,Eskin Ascia,Lee Hane,Rupar C. Anthony,de Wagenaar Nathalie P.,Wu Ka Man,Lahiry Piya,Pazour Gregory J.,Nelson Stanley F.,Hegele Robert A.,Roepman Ronald,Kayserili Hülya,Venkatesh Byrappa,Siu Victoria M.,Reversade Bruno,Arts Heleen H.

Funder

Nierstichting (NL)

Nederlandse Organisatie voor Wetenschappelijk Onderzoek (NL)

A*STAR, Singapore

Türkiye Bilimsel ve Teknolojik Araştirma Kurumu (TR)

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology

Link

http://link.springer.com/content/pdf/10.1186/s13630-016-0029-1

Reference19 articles.

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2. Abe S, Yagi T, Ishiyama S, Hiroe M, Marumo F, Ikawa Y. Molecular cloning of a novel serine/threonine kinase, MRK, possibly involved in cardiac development. Oncogene. 1995;11(11):2187–95.

3. Bladt F, Birchmeier C. Characterization and expression analysis of the murine rck gene: a protein kinase with a potential function in sensory cells. Differentiation; research in biological diversity. 1993;53(2):115–22.

4. Gopalan G, Centanni JM, Moss S, Donovan PJ. A novel mammalian kinase, T/STK 30, is highly expressed in the germ line. Mol Reprod Dev. 1999;52(1):9–17. doi: 10.1002/(SICI)1098-2795(199901)52:1<9:AID-MRD2>3.0.CO;2-O .

5. Chaya T, Omori Y, Kuwahara R, Furukawa T. ICK is essential for cell type-specific ciliogenesis and the regulation of ciliary transport. EMBO J. 2014;33(11):1227–42. doi: 10.1002/embj.201488175 .

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