Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice

By Dixon Michael J.   Gazzard James  

Human Molecular Genetics, Vol. 8, Iss. 8, 1999-08 ,pp. : 1579-1584

Oxford University Press

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Targeted disruption of the Epm2a gene causes formation of Lafora inclusion bodies, neurodegeneration, ataxia, myoclonus epilepsy and impaired behavioral response in mice

By Amano K.  

Human Molecular Genetics, Vol. 11, Iss. 11, 2002-05 ,pp. : 1251-1262

Oxford University Press

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Targeted disruption of Nphp1 causes male infertility due to defects in the later steps of sperm morphogenesis in mice

By Jiang Si-Tse   Chiou Yuan-Yow   Wang Ellian   Lin Hsiu-Kuan   Lee Sue-Ping   Lu Hsin-Yi   Wang Chi-Kuang Leo   Tang Ming-Jer   Li Hung  

Human Molecular Genetics, Vol. 17, Iss. 21, 2008-11 ,pp. : 3368-3379

Oxford University Press

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Disruption of the WFS1 gene in mice causes progressive -cell loss and impaired stimulus–secretion coupling in insulin secretion

By Ishihara Hisamitsu   Takeda Satoshi   Tamura Akira   Takahashi Rui   Yamaguchi Suguru   Takei Daisuke   Yamada Takahiro   Inoue Hiroshi   Soga Hiroyuki   Katagiri Hideki   Tanizawa Yukio   Oka Yoshitomo  

Human Molecular Genetics, Vol. 13, Iss. 11, 2004-06 ,pp. : 1159-1170

Oxford University Press

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Variation in the uric acid transporter gene ( SLC2A9 ) and memory performance

By Houlihan Lorna M.   Wyatt Niki D.   Harris Sarah E.   Hayward Caroline   Gow Alan J.   Marioni Riccardo E.   Strachan Mark W.J.   Price Jackie F.   Starr John M.   Wright Alan F.   Deary Ian J.  

Human Molecular Genetics, Vol. 19, Iss. 11, 2010-06 ,pp. : 2321-2330

Oxford University Press

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