Related content

Novel glycogen synthase kinase 3 and ubiquitination pathways in progressive myoclonus epilepsy

By Lohi Hannes  

Human Molecular Genetics, Vol. 14, Iss. 18, 2005-09 ,pp. : 2727-2736

Oxford University Press

Access to resources Recommend Favorite

Identification of an N-terminal glycogen synthase kinase 3 phosphorylation site which regulates the functional localization of polycystin-2 in vivo and in vitro

By Streets Andrew J.   Moon David J.   Kane Michelle E.   Obara Tomoko   Ong Albert C.M.  

Human Molecular Genetics, Vol. 15, Iss. 9, 2006-05 ,pp. : 1465-1473

Oxford University Press

Access to resources Recommend Favorite

Overexpression of P104L mutant caveolin-3 in mice develops hypertrophic cardiomyopathy with enhanced contractility in association with increased endothelial nitric oxide synthase activity

By Ohsawa Yutaka  

Human Molecular Genetics, Vol. 13, Iss. 2, 2004-01 ,pp. : 151-157

Oxford University Press

Access to resources Recommend Favorite

Inhibition of GSK3β improves hippocampus-dependent learning and rescues neurogenesis in a mouse model of fragile X syndrome

By Guo Weixiang   Murthy Adeline C.   Zhang Li   Johnson Eric B.   Schaller Eric G.   Allan Andrea M.   Zhao Xinyu  

Human Molecular Genetics, Vol. 21, Iss. 3, 2012-02 ,pp. : 681-691

Oxford University Press

Access to resources Recommend Favorite

-Actinin-3 deficiency results in reduced glycogen phosphorylase activity and altered calcium handling in skeletal muscle

By Quinlan Kate G.R.   Seto Jane T.   Turner Nigel   Vandebrouck Aurelie   Floetenmeyer Matthias   Macarthur Daniel G.   Raftery Joanna M.   Lek Monkol   Yang Nan   Parton Robert G.   Cooney Gregory J.   North Kathryn N.  

Human Molecular Genetics, Vol. 19, Iss. 7, 2010-04 ,pp. : 1335-1346

Oxford University Press

Access to resources Recommend Favorite