Lowe syndrome patient fibroblasts display Ocrl1-specific cell migration defects that cannot be rescued by the homologous Inpp5b phosphatase

By Coon Brian G.   Mukherjee Debarati   Hanna Claudia B.   Riese David J.   Lowe Martin   Aguilar R. Claudio  

Human Molecular Genetics, Vol. 18, Iss. 23, 2009-12 ,pp. : 4478-4491

Oxford University Press

Access to resources Recommend Favorite

Context-dependent robustness to 5′ splice site polymorphisms in human populations

By Lu Zhi-xiang   Jiang Peng   Cai James J.   Xing Yi  

Human Molecular Genetics, Vol. 20, Iss. 6, 2011-03 ,pp. : 1084-1096

Oxford University Press

Access to resources Recommend Favorite

A Point Mutation in the 5′ Splice Site of the Dystrophin Gene First Intron Responsible for X-Linked Dilated Cardiomyopathy

By Milasin Jelena  

Human Molecular Genetics, Vol. 5, Iss. 1, 1996-01 ,pp. : 73-79

Oxford University Press

Access to resources Recommend Favorite

Conserved use of a non-canonical 5′ splice site (/GA) in alternative splicing by fibroblast growth factor receptors 1, 2 and 3

By Twigg S.R.F.  

Human Molecular Genetics, Vol. 7, Iss. 4, 1998-04 ,pp. : 685-691

Oxford University Press

Access to resources Recommend Favorite

Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expression

By Korade-Mirnics Zeljka   Tarleton Jack  

Human Molecular Genetics, Vol. 8, Iss. 6, 1999-06 ,pp. : 1017-1023

Oxford University Press

Access to resources Recommend Favorite