Hip14l -deficient mice develop neuropathological and behavioural features of Huntington disease

By Sutton Liza M.   Sanders Shaun S.   Butland Stefanie L.   Singaraja Roshni R.   Franciosi Sonia   Southwell Amber L.   Doty Crystal N.   Schmidt Mandi E.   Mui Katherine K.N.   Kovalik Vlad   Young Fiona B.   Zhang Weining   Hayden Michael R.  

Human Molecular Genetics, Vol. 22, Iss. 3, 2013-02 ,pp. : 452-465

Oxford University Press

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Genetic modifiers of the phenotype of mice deficient in mitochondrial superoxide dismutase

By Huang Ting-Ting   Naeemuddin Mohammed   Elchuri Sailaja   Yamaguchi Mutsuo   Kozy Heather M.   Carlson Elaine J.   Epstein Charles J.  

Human Molecular Genetics, Vol. 15, Iss. 7, 2006-04 ,pp. : 1187-1194

Oxford University Press

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Molybdenum cofactor-deficient mice resemble the phenotype of human patients

By Lee H-J.  

Human Molecular Genetics, Vol. 11, Iss. 26, 2002-12 ,pp. : 3309-3317

Oxford University Press

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Slc7a9 -deficient mice develop cystinuria non-I and cystine urolithiasis

By Feliubadaló Lídia  

Human Molecular Genetics, Vol. 12, Iss. 17, 2003-09 ,pp. : 2097-2108

Oxford University Press

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Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivo

By Mientjes Edwin J.   Willemsen Rob   Kirkpatrick Laura L.   Nieuwenhuizen Ingeborg M.   Hoogeveen-Westerveld Marianne   Verweij Marcel   Reis Surya   Bardoni Barbara   Hoogeveen Andre T.   Oostra Ben A.   Nelson David L.  

Human Molecular Genetics, Vol. 13, Iss. 13, 2004-07 ,pp. : 1291-1302

Oxford University Press

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