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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Mutations in the gene for connexin 26 (GJB2) that cause hearing loss have a dominant negative effect on connexin 30

By Marziano N.K.  

Human Molecular Genetics, Vol. 12, Iss. 8, 2003-04 ,pp. : 805-812

Oxford University Press

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The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice

By Schtz Melanie   Scimemi Pietro   Majumder Paromita   De Siati Romolo Daniele   Crispino Giulia   Rodriguez Laura   Bortolozzi Mario   Santarelli Rosamaria   Seydel Anke   Sonntag Stephan   Ingham Neil   Steel Karen P.   Willecke Klaus   Mammano Fabio  

Human Molecular Genetics, Vol. 19, Iss. 24, 2010-12 ,pp. : 4759-4773

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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Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes

By Bi Weimin   Yan Jiong   Shi Xin   Yuva-Paylor Lisa A.   Antalffy Barbara A.   Goldman Alica   Yoo Jong W.   Noebels Jeffrey L.   Armstrong Dawna L.   Paylor Richard   Lupski James R.  

Human Molecular Genetics, Vol. 16, Iss. 15, 2007-08 ,pp. : 1802-1813

Oxford University Press

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