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Journal Abstract Search
470 related items for PubMed ID: 12736199
1. Dystroglycan glycosylation and its role in matrix binding in skeletal muscle. Martin PT. Glycobiology; 2003 Aug; 13(8):55R-66R. PubMed ID: 12736199 [Abstract] [Full Text] [Related]
2. Deficiency of alpha-dystroglycan in muscle-eye-brain disease. Kano H, Kobayashi K, Herrmann R, Tachikawa M, Manya H, Nishino I, Nonaka I, Straub V, Talim B, Voit T, Topaloglu H, Endo T, Yoshikawa H, Toda T. Biochem Biophys Res Commun; 2002 Mar 15; 291(5):1283-6. PubMed ID: 11883957 [Abstract] [Full Text] [Related]
3. Localization of the dystrophin binding site at the carboxyl terminus of beta-dystroglycan. Rosa G, Ceccarini M, Cavaldesi M, Zini M, Petrucci TC. Biochem Biophys Res Commun; 1996 Jun 14; 223(2):272-7. PubMed ID: 8670271 [Abstract] [Full Text] [Related]
4. Towards an understanding of the dystrophin-glycoprotein complex: linkage between the extracellular matrix and the membrane cytoskeleton in muscle fibers. Ohlendieck K. Eur J Cell Biol; 1996 Jan 14; 69(1):1-10. PubMed ID: 8825019 [Abstract] [Full Text] [Related]
10. Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan. Longman C, Brockington M, Torelli S, Jimenez-Mallebrera C, Kennedy C, Khalil N, Feng L, Saran RK, Voit T, Merlini L, Sewry CA, Brown SC, Muntoni F. Hum Mol Genet; 2003 Nov 01; 12(21):2853-61. PubMed ID: 12966029 [Abstract] [Full Text] [Related]
11. Molecular recognition by LARGE is essential for expression of functional dystroglycan. Kanagawa M, Saito F, Kunz S, Yoshida-Moriguchi T, Barresi R, Kobayashi YM, Muschler J, Dumanski JP, Michele DE, Oldstone MB, Campbell KP. Cell; 2004 Jun 25; 117(7):953-64. PubMed ID: 15210115 [Abstract] [Full Text] [Related]
12. [Dystroglycan linkage and muscular dystrophy]. Shimizu T. Rinsho Shinkeigaku; 2002 Nov 25; 42(11):1091-4. PubMed ID: 12784674 [Abstract] [Full Text] [Related]
18. Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses. Côté PD, Moukhles H, Lindenbaum M, Carbonetto S. Nat Genet; 1999 Nov 25; 23(3):338-42. PubMed ID: 10610181 [Abstract] [Full Text] [Related]