Loss of cIAP1 attenuates soleus muscle pathology and improves diaphragm function in mdx mice

By Enwere Emeka K.   Boudreault Louise   Holbrook Janelle   Timusk Kristen   Earl Nathalie   LaCasse Eric   Renaud Jean-Marc   Korneluk Robert G.  

Human Molecular Genetics, Vol. 22, Iss. 5, 2013-03 ,pp. : 867-878

Oxford University Press

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Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome

By Erway L.C.  

Human Molecular Genetics, Vol. 8, Iss. 4, 1999-04 ,pp. : 645-653

Oxford University Press

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Inverse correlation between expression of the Wolfs Hirschhorn candidate gene Letm1 and mitochondrial volume in C . elegans and in mammalian cells

By Hasegawa Ayako   van der Bliek Alexander M.  

Human Molecular Genetics, Vol. 16, Iss. 17, 2007-09 ,pp. : 2061-2071

Oxford University Press

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The recently identified type 2A juvenile haemochromatosis gene ( HJV ), a second candidate modifier of the C282Y homozygous phenotype

By Le Gac Gérald  

Human Molecular Genetics, Vol. 13, Iss. 17, 2004-09 ,pp. : 1913-1918

Oxford University Press

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Sequence of a cDNA Encoding Turtle High Mobility Group 1 Protein

By Zheng Jifang   Hu Bi   Wu Duansheng  

Russian Journal of Genetics, Vol. 41, Iss. 7, 2005-07 ,pp. : 755-759

MAIK Nauka/Interperiodica

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