Mapping of genetic modifiers of Nr2e3 rd7/rd7 that suppress retinal degeneration and restore blue cone cells to normal quantity

By Haider Neena  

Mammalian Genome, Vol. 19, Iss. 3, 2008-03 ,pp. : 145-154

Springer Publishing Company

Access to resources Recommend Favorite

Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration

By Jacobson Samuel G.  

Human Molecular Genetics, Vol. 13, Iss. 17, 2004-09 ,pp. : 1893-1902

Oxford University Press

Access to resources Recommend Favorite

Lack of fibulin-3 causes early aging and herniation, but not macular degeneration in mice

By McLaughlin Precious J.   Bakall Benjamin   Choi Jiwon   Liu Zhonglin   Sasaki Takako   Davis Elaine C.   Marmorstein Alan D.   Marmorstein Lihua Y.  

Human Molecular Genetics, Vol. 16, Iss. 24, 2007-12 ,pp. : 3059-3070

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

In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development

By Cheng Hong   Aleman Tomas S.   Cideciyan Artur V.   Khanna Ritu   Jacobson Samuel G.   Swaroop Anand  

Human Molecular Genetics, Vol. 15, Iss. 17, 2006-09 ,pp. : 2588-2602

Oxford University Press

Access to resources Recommend Favorite