Characterization of a monoclonal antibody panel shows that the myotonic dystrophy protein kinase, DMPK, is expressed almost exclusively in muscle and heart

By Lam L.T.   Pham Y.C.N.   Man Nguyenthi   Morris G.E.  

Human Molecular Genetics, Vol. 9, Iss. 14, 2000-09 ,pp. : 2167-2173

Oxford University Press

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Constitutive and regulated modes of splicing produce six major myotonic dystrophy protein kinase (DMPK) isoforms with distinct properties

By Groenen Patricia J.T.A.   Wansink Derick G.   Coerwinkel Marga   van den Broek Walther   Jansen Gert   Wieringa Bé  

Human Molecular Genetics, Vol. 9, Iss. 4, 2000-03 ,pp. : 605-616

Oxford University Press

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Skeletal muscle sodium channel gating in mice deficient in myotonic dystrophy protein kinase

By Mounsey J. Paul  

Human Molecular Genetics, Vol. 9, Iss. 15, 2000-09 ,pp. : 2313-2320

Oxford University Press

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Iraqi-Jewish Kindreds with Optic Atrophy Plus (3-Methylglutaconic Aciduria Type 3) Demonstrate Linkage Disequilibrium with the CTG Repeat in the 3′ Untranslated Region of the Myotonic Dystrophy Protein Kinase Gene

By Nystuen Arne   Costeff Hanan   Elpeleg Orly N.   Apter Naomi   Bonné-Tamir Batsheva   Mohrenweiser Harvey   Haider Neena   Stone Edwin M.   Sheffield Val C.  

Human Molecular Genetics, Vol. 6, Iss. 4, 1997-01 ,pp. : 563-569

Oxford University Press

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Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy

By O'Cochlain D. Fearghas  

Human Molecular Genetics, Vol. 13, Iss. 20, 2004-10 ,pp. : 2505-2518

Oxford University Press

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