Loss of Uch-L1 and Uch-L3 leads to neurodegeneration, posterior paralysis and dysphagia

By Kikuchi T.  

Human Molecular Genetics, Vol. 10, Iss. 18, 2001-09 ,pp. : 1963-1970

Oxford University Press

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Selective neuroprotective effects of the S18Y polymorphic variant of UCH-L1 in the dopaminergic system

By Xilouri Maria   Kyratzi Elli   Pitychoutis Pothitos M.   Papadopoulou-Daifoti Zoi   Perier Celine   Vila Miquel   Maniati Matina   Ulusoy Ayse   Kirik Deniz   Park David S.   Wada Keiji   Stefanis Leonidas  

Human Molecular Genetics, Vol. 21, Iss. 4, 2012-02 ,pp. : 874-889

Oxford University Press

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Disease-associated mutations in L1 CAM interfere with ligand interactions and cell-surface expression

By Schäfer M.   Brümmendorf T.   de Angelis E.   Watkins A.   Kenwrick S.  

Human Molecular Genetics, Vol. 11, Iss. 1, 2002-01 ,pp. : 1-12

Oxford University Press

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Variation in the biochemical/biophysical properties of mutant superoxide dismutase 1 enzymes and the rate of disease progression in familial amyotrophic lateral sclerosis kindreds

By Ratovitski Tamara  

Human Molecular Genetics, Vol. 8, Iss. 8, 1999-08 ,pp. : 1451-1460

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Strong evidence that GNB1L is associated with schizophrenia

By Williams Nigel M.   Glaser Beate   Norton Nadine   Williams Hywel   Pierce Timothy   Moskvina Valentina   Monks Stephen   Del Favero Jurgen   Goossens Dirk   Rujescu Dan   Giegling Ina   Kirov George   Craddock Nicholas   Murphy Kieran C.   O'Donovan Michael C.   Owen Michael J.  

Human Molecular Genetics, Vol. 17, Iss. 4, 2008-02 ,pp. : 555-566

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