A mutation in the saposin A domain of the sphingolipid activator protein (prosaposin) gene results in a late-onset, chronic form of globoid cell leukodystrophy in the mouse

By Matsuda J.  

Human Molecular Genetics, Vol. 10, Iss. 11, 2001-05 ,pp. : 1191-1199

Oxford University Press

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Targeted disruption of the mouse lysosomal acid lipase gene: long-term survival with massive cholesteryl ester and triglyceride storage

By Witte D.  

Human Molecular Genetics, Vol. 7, Iss. 9, 1998-09 ,pp. : 1347-1354

Oxford University Press

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Mutation in saposin D domain of sphingolipid activator protein gene causes urinary system defects and cerebellar Purkinje cell degeneration with accumulation of hydroxy fatty acid-containing ceramide in mouse

By Matsuda Junko  

Human Molecular Genetics, Vol. 13, Iss. 21, 2004-11 ,pp. : 2709-2723

Oxford University Press

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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

Oxford University Press

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Behavioral alterations associated with targeted disruption of exons 2 and 3 of the Disc1 gene in the mouse

By Kuroda Keisuke   Yamada Shinnosuke   Tanaka Motoki   Iizuka Michiro   Yano Hisashi   Mori Daisuke   Tsuboi Daisuke   Nishioka Tomoki   Namba Takashi   Iizuka Yukihiko   Kubota Shimpei   Nagai Taku   Ibi Daisuke   Wang Rui   Enomoto Atsushi   Isotani-Sakakibara Mayu   Asai Naoya   Kimura Kazushi   Kiyonari Hiroshi   Abe Takaya   Mizoguchi Akira   Sokabe Masahiro   Takahashi Masahide   Yamada Kiyofumi   Kaibuchi Kozo  

Human Molecular Genetics, Vol. 20, Iss. 23, 2011-12 ,pp. : 4666-4683

Oxford University Press

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