Nf1/ mice have increased neointima formation via hyperactivation of a Gleevec sensitive molecular pathway

By Lasater Elisabeth A.   Bessler Waylan K.   Mead Laura E.   Horn Whitney E.   Clapp D. Wade   Conway Simon J.   Ingram David A.   Li Fang  

Human Molecular Genetics, Vol. 17, Iss. 15, 2008-08 ,pp. : 2336-2344

Oxford University Press

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The tuberous sclerosis proteins regulate formation of the primary cilium via a rapamycin-insensitive and polycystin 1-independent pathway

By Hartman Tiffiney R.   Liu Dongyan   Zilfou Jack T.   Robb Victoria   Morrison Tasha   Watnick Terry   Henske Elizabeth P.  

Human Molecular Genetics, Vol. 18, Iss. 1, 2009-01 ,pp. : 151-163

Oxford University Press

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Kidney-specific inactivation of the Pkd1 gene induces rapid cyst formation in developing kidneys and a slow onset of disease in adult mice

By Lantinga-van Leeuwen Irma S.   Leonhard Wouter N.   van der Wal Annemieke   Breuning Martijn H.   de Heer Emile   Peters Dorien J.M.  

Human Molecular Genetics, Vol. 16, Iss. 24, 2007-12 ,pp. : 3188-3196

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Molecular dissection of the events leading to inactivation of the FMR1 gene

By Pietrobono Roberta  

Human Molecular Genetics, Vol. 14, Iss. 2, 2005-01 ,pp. : 267-277

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Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1

By Griffin A.  

Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2509-2514

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