Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader–Willi syndrome

By Muscatelli Françoise   Abrous DjoherNora  

Human Molecular Genetics, Vol. 9, Iss. 20, 2000-12 ,pp. : 3101-3110

Oxford University Press

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An Imprinted Mouse Transcript Homologous to the Human Imprinted in Prader-Willi Syndrome ( IPW ) Gene

By Wevrick Rachel   Francke Uta  

Human Molecular Genetics, Vol. 6, Iss. 2, 1997-01 ,pp. : 325-332

Oxford University Press

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Necdin, a PraderWilli syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development

By Miller Nichol L.G.   Wevrick Rachel   Mellon Pamela L.  

Human Molecular Genetics, Vol. 18, Iss. 2, 2009-01 ,pp. : 248-260

Oxford University Press

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Essential role for the Prader–Willi syndrome protein necdin in axonal outgrowth

By Lee Syann  

Human Molecular Genetics, Vol. 14, Iss. 5, 2005-03 ,pp. : 627-637

Oxford University Press

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A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader–Willi syndrome critical region

By Jong M.T.C.  

Human Molecular Genetics, Vol. 8, Iss. 5, 1999-05 ,pp. : 783-793

Oxford University Press

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