Citations for
1HYDIN, ICS19
Recessive HYDIN Mutations Cause Primary Ciliary Dyskinesia without Randomization of Left-Right Body Asymmetry.
Olbrich H, Schmidts M, Werner C, Onoufriadis A, Loges NT, Raidt J, Banki NF, Shoemark A, Burgoyne T, Al Turki S, Hurles ME; UK10K Consortium, Köhler G, Schroeder J, Nürnberg G, Nürnberg P, Chung EM, Reinhardt R, Marthin JK, Nielsen KG, Mitchison HM, Omran H.
Am J Hum Genet 91(4):672-84. doi: 10.1016/j.ajhg.2012.08.016. Epub 2012 Sep 27. 2012
2HYDIN
Mutations in Hydin impair ciliary motility in mice.
Lechtreck KF, Delmotte P, Robinson ML, Sanderson MJ, Witman GB.
J Cell Biol 180(3):633-43. Epub 2008 Feb 4. 2008
3HYDIN
The hydrocephalus inducing gene product, Hydin, positions axonemal central pair microtubules.
Dawe HR, Shaw MK, Farr H, Gull K.
BMC Biol 5:33. 2007
4HYDIN
Chlamydomonas reinhardtii hydin is a central pair protein required for flagellar motility.
Lechtreck KF, Witman GB.
J Cell Biol 176(4):473-82. 2007
5HYDIN
Hydin seek: finding a function in ciliary motility.
Smith EF.
J Cell Biol 176(4):403-4. Review. 2007
6HYDIN, HYDIN2
A 360-kb interchromosomal duplication of the human HYDIN locus.
Doggett NA, Xie G, Meincke LJ, Sutherland RD, Mundt MO, Berbari NS, Davy BE, Robinson ML, Rudd MK, Weber JL, Stallings RL, Han C.
Genomics 88(6):762-71. Epub 2006 Aug 30. 2006
7HYDIN
Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin, a large novel gene.
Davy BE, Robinson ML.
Hum Mol Genet 12(10):1163-70. 2003
8HYDIN
Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin, a large novel gene.
Davy BE, Robinson ML.
Hum Mol Genet 12(10):1163-70. 2003