Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader–Willi syndrome

By Tsai Ting-Fen   Jiang Yong-hui   Bressler Jan   Armstrong Dawna   Beaudet Arthur L.   Jiang Y.   Lalande M.   Nicholls R.D.   Malzac P.   Fang P.   Cassidy S.B.   Saitoh S.   Leff S.E.   Özçelik T.   Cattanach B.M.   Yang T.   McAllister G.   Schmauss C.   Sun Y.   Kuslich C.D.   Schulze A.   Conroy J.M.   Gabriel J.M.   Glenn C.C.   Shemer R.   Sutcliffe J.S.   Zeschnigk M.   Ramirez-Solis R.   Jiang Y.-H.   Watrin F.   Albrecht U.   Johnson D.K.   McMahon A.P.   Ramirez-Solis R.   Ramirez-Solis R.   Sambrook J.   Wevrick R.   Wagstaff J.  

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Oxford University Press

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3-Hydroxy-3-methylglutaryl-CoA lyase (HL): gene targeting causes prenatal lethality in HL-deficient mice

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Oxford University Press

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A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification

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Oxford University Press

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Protective effects of cardiotrophin-1 adenoviral gene transfer on neuromuscular degeneration in transgenic ALS mice

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Human Molecular Genetics, Vol. 10, Iss. 18, 2001-09 ,pp. : 1925-1933

Oxford University Press

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Tissue-specific and expression of porcine growth hormone gene in BAC transgenic mice

By Tong Jia  

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