Genetic analysis in mice identifies cysteamine as a novel partner for artemisinin in the treatment of malaria

By Min-Oo Gundula  

Mammalian Genome, Vol. 22, Iss. 7-8, 2011-08 ,pp. : 486-494

Springer Publishing Company

Access to resources Recommend Favorite

Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPAR pathway as a therapeutic target in Friedreichs ataxia

By Coppola Giovanni   Marmolino Daniele   Lu Daning   Wang Qing   Cnop Miriam   Rai Myriam   Acquaviva Fabio   Cocozza Sergio   Pandolfo Massimo   Geschwind Daniel H.  

Human Molecular Genetics, Vol. 18, Iss. 13, 2009-07 ,pp. : 2452-2461

Oxford University Press

Access to resources Recommend Favorite

Radiation-induced delayed cell death in a hypomorphic Artemis cell line

By Evans Paul M.   Woodbine Lisa   Riballo Enriquetta   Gennery Andrew R.   Hubank Michael  

Human Molecular Genetics, Vol. 15, Iss. 8, 2006-04 ,pp. : 1303-1311

Oxford University Press

Access to resources Recommend Favorite

Genetic interaction studies link autosomal dominant and recessive polycystic kidney disease in a common pathway

By Garcia-Gonzalez Miguel A.   Menezes Luis F.   Piontek Klaus B.   Kaimori Junya   Huso David L.   Watnick Terry   Onuchic Luiz F.   Guay-Woodford Lisa M.   Germino Gregory G.  

Human Molecular Genetics, Vol. 16, Iss. 16, 2007-08 ,pp. : 1940-1950

Oxford University Press

Access to resources Recommend Favorite

Linkage analysis of myelin oligodendrocyte glycoprotein-induced experimental autoimmune encephalomyelitis in the rat identifies a locus controlling demyelination on chromosome 18

By Dahlman Ingrid   Wallström Erik   Weissert Robert  

Human Molecular Genetics, Vol. 8, Iss. 12, 1999-11 ,pp. : 2183-2190

Oxford University Press

Access to resources Recommend Favorite