An engineered 800 kilobase deletion of Uchl3 and Lmo7 on mouse chromosome 14 causes defects in viability, postnatal growth and degeneration of muscle and retina

Author： Semenova Ekaterina  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.12, Iss.11, 2003-06, pp. : 1301-1312

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Paternal deletion of Meg1/Grb10 DMR causes maternalization of the Meg1/Grb10 cluster in mouse proximal Chromosome 11 leading to severe pre- and postnatal growth retardation

By Shiura Hirosuke   Nakamura Kenji   Hikichi Takafusa   Hino Toshiaki   Oda Kanako   Suzuki-Migishima Rika   Kohda Takashi   Kaneko-Ishino Tomoko   Ishino Fumitoshi  

Human Molecular Genetics, Vol. 18, Iss. 8, 2009-04 ,pp. : 1424-1438

Oxford University Press

Access to resources Recommend Favorite

Caveolin-3 deficiency causes muscle degeneration in mice

By Hagiwara Yasuko   Sasaoka Toshikuni   Araishi Kenji   Imamura Michihiro   Yorifuji Hiroshi   Nonaka Ikuya   Ozawa Eijiro   Kikuchi Tateki  

Human Molecular Genetics, Vol. 9, Iss. 20, 2000-12 ,pp. : 3047-3054

Oxford University Press

Access to resources Recommend Favorite

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.  

Human Molecular Genetics, Vol. 8, Iss. 8, 1999-08 ,pp. : 1357-1364

Oxford University Press

Access to resources Recommend Favorite

Refinement of the postnatal growth restriction locus of chromosome 5q12‐13 deletion syndrome

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 11, 2015-11 ,pp. : 2737-2741

John Wiley & Sons Inc

Access to resources Recommend Favorite

Deletion of the Parkin co-regulated gene causes defects in ependymal ciliary motility and hydrocephalus in the quaking viable mutant mouse

By Wilson Gabrielle R.   Wang Hong X.   Egan Gary F.   Robinson Philip J.   Delatycki Martin B.   O'Bryan Moira K.   Lockhart Paul J.  

Human Molecular Genetics, Vol. 19, Iss. 8, 2010-04 ,pp. : 1593-1602

Oxford University Press

Access to resources Recommend Favorite