Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome trafficking

By Hadano Shinji   Benn Susanna C.   Otomo Asako   Sudo Katsuko   Kunita Ryota   Suzuki-Utsunomiya Kyoko   Mizumura Hikaru   Shefner Jeremy M.   Cox Gregory A.   Iwakura Yoichiro   Brown Robert H.   Ikeda Joh-E  

Human Molecular Genetics, Vol. 15, Iss. 2, 2006-01 ,pp. : 233-250

Oxford University Press

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The R6/2 transgenic mouse model of Huntington's disease develops diabetes due to deficient -cell mass and exocytosis

By Björkqvist Maria  

Human Molecular Genetics, Vol. 14, Iss. 5, 2005-03 ,pp. : 565-574

Oxford University Press

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Hindlimb gait defects due to motor axon loss and reduced distal muscles in a transgenic mouse model of CharcotMarieTooth type 2A

By Detmer Scott A.   Velde Christine Vande   Cleveland Don W.   Chan David C.  

Human Molecular Genetics, Vol. 17, Iss. 3, 2008-02 ,pp. : 367-375

Oxford University Press

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Peripheral nerve pathology, including aberrant Schwann cell differentiation, is ameliorated by doxycycline in a laminin-α2-deficient mouse model of congenital muscular dystrophy

By Homma Sachiko   Beermann Mary Lou   Miller Jeffrey Boone  

Human Molecular Genetics, Vol. 20, Iss. 13, 2011-07 ,pp. : 2662-2672

Oxford University Press

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Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large myd mouse defines a natural model for glycosylation-deficient muscle – eye – brain disorders

By Holzfeind P.J.  

Human Molecular Genetics, Vol. 11, Iss. 21, 2002-10 ,pp. : 2673-2687

Oxford University Press

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