Aberrant molecular properties shared by familial Parkinsons disease-associated mutant UCH-L1 and carbonyl-modified UCH-L1

By Kabuta Tomohiro   Setsuie Rieko   Mitsui Takeshi   Kinugawa Aiko   Sakurai Mikako   Aoki Shunsuke   Uchida Kenko   Wada Keiji  

Human Molecular Genetics, Vol. 17, Iss. 10, 2008-05 ,pp. : 1482-1496

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

An engineered 800 kilobase deletion of Uchl3 and Lmo7 on mouse chromosome 14 causes defects in viability, postnatal growth and degeneration of muscle and retina

By Semenova Ekaterina  

Human Molecular Genetics, Vol. 12, Iss. 11, 2003-06 ,pp. : 1301-1312

Oxford University Press

Access to resources Recommend Favorite

Loss of thymidine kinase 2 alters neuronal bioenergetics and leads to neurodegeneration

By Bartesaghi Stefano   Betts-Henderson Joanne   Cain Kelvin   Dinsdale David   Zhou Xiaoshan   Karlsson Anna   Salomoni Paolo   Nicotera Pierluigi  

Human Molecular Genetics, Vol. 19, Iss. 9, 2010-05 ,pp. : 1669-1677

Oxford University Press

Access to resources Recommend Favorite

Palmitoyl-protein thioesterase-1 deficiency leads to the activation of caspase-9 and contributes to rapid neurodegeneration in INCL

By Kim Sung-Jo   Zhang Zhongjian   Lee Yi-Ching   Mukherjee Anil B.  

Human Molecular Genetics, Vol. 15, Iss. 10, 2006-05 ,pp. : 1580-1586

Oxford University Press

Access to resources Recommend Favorite