Targeted disruption of Slc19a2 , the gene encoding the high-affinity thiamin transporter Thtr-1, causes diabetes mellitus, sensorineural deafness and megaloblastosis in mice

By Forrest D.  

Human Molecular Genetics, Vol. 11, Iss. 23, 2002-11 ,pp. : 2951-2960

Oxford University Press

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Caveolin-3 deficiency causes muscle degeneration in mice

By Hagiwara Yasuko   Sasaoka Toshikuni   Araishi Kenji   Imamura Michihiro   Yorifuji Hiroshi   Nonaka Ikuya   Ozawa Eijiro   Kikuchi Tateki  

Human Molecular Genetics, Vol. 9, Iss. 20, 2000-12 ,pp. : 3047-3054

Oxford University Press

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Secretin deficiency causes impairment in survival of neural progenitor cells in mice

By Jukkola Peter I.   Rogers Justin T.   Kaspar Brian K.   Weeber Edwin J.   Nishijima Ichiko  

Human Molecular Genetics, Vol. 20, Iss. 5, 2011-03 ,pp. : 1000-1007

Oxford University Press

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Connexin 31 ( GJB3 ) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment

By Avraham K.B.  

Human Molecular Genetics, Vol. 10, Iss. 9, 2001-04 ,pp. : 947-952

Oxford University Press

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Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression.

By Thönnissen Eva   Rabionet Raquel   Arbonès Maria   Estivill Xavier   Willecke Klaus   Ott Thomas  

Human Genetics, Vol. 111, Iss. 2, 2002-08 ,pp. : 190-197

Springer Publishing Company

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