Pael receptor induces death of dopaminergic neurons in the substantia nigra via endoplasmic reticulum stress and dopamine toxicity, which is enhanced under condition of parkin inactivation

By Kitao Yasuko   Imai Yuzuru   Kataoka Ayane   Ikeda Toshio   Soda Mariko   Nakimawa Kazuhiko   Kiyama Hiroshi   Stern David M.   Hori Osamu   Wakamatsu Kazumasa   Ito Shosuke   Itohara Shigeyoshi  

Human Molecular Genetics, Vol. 16, Iss. 1, 2007-01 ,pp. : 50-60

Oxford University Press

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Deletion of the Parkin co-regulated gene causes defects in ependymal ciliary motility and hydrocephalus in the quaking viable mutant mouse

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Human Molecular Genetics, Vol. 19, Iss. 8, 2010-04 ,pp. : 1593-1602

Oxford University Press

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Combined kinase inhibition modulates parkin inactivation

By Rubio de la Torre Elena   Luzn-Toro Berta   Forte-Lago Irene   Minguez-Castellanos Adolfo   Ferrer Isidro   Hilfiker Sabine  

Human Molecular Genetics, Vol. 18, Iss. 5, 2009-03 ,pp. : 809-823

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Tsc2 gene inactivation causes a more severe epilepsy phenotype than Tsc1 inactivation in a mouse model of Tuberous Sclerosis Complex

By Zeng Ling-Hui   Rensing Nicholas R.   Zhang Bo   Gutmann David H.   Gambello Michael J.   Wong Michael  

Human Molecular Genetics, Vol. 20, Iss. 3, 2011-02 ,pp. : 445-454

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Parkin selectively alters the intrinsic threshold for mitochondrial cytochrome c release

By Berger Alison K.   Cortese Giuseppe P.   Amodeo Katherine D.   Weihofen Andreas   Letai Anthony   LaVoie Matthew J.  

Human Molecular Genetics, Vol. 18, Iss. 22, 2009-11 ,pp. : 4317-4328

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