A mouse genetic model for familial cholestasis caused by ATP8B1 mutations reveals perturbed bile salt homeostasis but no impairment in bile secretion

By Pawlikowska Ludmila   Groen Annemiek   Eppens Elaine F.   Kunne Cindy   Ottenhoff Roelof   Looije Norbert   Knisely A.S.   Killeen Nigel P.   Bull Laura N.   Elferink Ronald P.J. Oude   Freimer Nelson B.  

Human Molecular Genetics, Vol. 13, Iss. 8, 2004-04 ,pp. : 881-892

Oxford University Press

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Two interactive genes responsible for a new inherited cataract (RCT) in the mouse

By Maeda Yukiko Y.   Funata Nobuaki   Takahama Sumiyo   Sugata Yasuo   Yonekawa Hiromichi  

Mammalian Genome, Vol. 12, Iss. 4, 2001-04 ,pp. : 278-283

Springer Publishing Company

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Dissection of behavior and psychiatric disorders using the mouse as a model

By Tarantino Lisa   Bucan Maja  

Human Molecular Genetics, Vol. 9, Iss. 6, 2000-04 ,pp. : 953-965

Oxford University Press

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A mouse model of Waardenburg syndrome type 4 with a new spontaneous mutation of the endothelin-B receptor gene

By Matsushima Yoshibumi   Shinkai Yusuke   Kobayashi Yasuhito   Sakamoto Michihiro   Kunieda Tetsuo   Tachibana Masayoshi  

Mammalian Genome, Vol. 13, Iss. 1, 2002-01 ,pp. : 30-35

Springer Publishing Company

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Survey of CAG/CTG Repeats in Human cDNAs Representing New Genes: Candidates for Inherited Neurological Disorders

By Néri Christian  

Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 1001-1009

Oxford University Press

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