Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (5) GO Terms (13) Nucleotides (96) Proteins (59) Interactants (75) Wiki
XB-GENEPAGE-949800

Papers associated with dmpk



???displayGene.coCitedPapers???

???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest Sort Oldest To Newest

Dominantly inherited myotonia congenita resulting from a mutation that increases open probability of the muscle chloride channel CLC-1., Richman DP, Yu Y, Lee TT, Tseng PY, Yu WP, Maselli RA, Tang CY, Chen TY., Neuromolecular Med. December 1, 2012; 14 (4): 328-37.

Molecular phylogeny of OVOL genes illustrates a conserved C2H2 zinc finger domain coupled by hypervariable unstructured regions., Kumar A, Bhandari A, Sinha R, Sardar P, Sushma M, Goyal P, Goswami C, Grapputo A., PLoS One. January 1, 2012; 7 (6): e39399.                

WNK2 kinase is a novel regulator of essential neuronal cation-chloride cotransporters., Rinehart J, Vázquez N, Kahle KT, Hodson CA, Ring AM, Gulcicek EE, Louvi A, Bobadilla NA, Gamba G, Lifton RP., J Biol Chem. August 26, 2011; 286 (34): 30171-80.              

Phospholemman is a substrate for myotonic dystrophy protein kinase., Mounsey JP, John JE, Helmke SM, Bush EW, Gilbert J, Roses AD, Perryman MB, Jones LR, Moorman JR., J Biol Chem. July 28, 2000; 275 (30): 23362-7.

Myotonic dystrophy kinase modulates skeletal muscle but not cardiac voltage-gated sodium channels., Chahine M, George AL., FEBS Lett. August 4, 1997; 412 (3): 621-4.

???pagination.result.page??? 1