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