These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
99 related articles for article (PubMed ID: 2668885)
21. Immunological identification of a high molecular weight protein as a candidate for the product of the Duchenne muscular dystrophy gene. Kao L; Krstenansky J; Mendell J; Rammohan KW; Gruenstein E Proc Natl Acad Sci U S A; 1988 Jun; 85(12):4491-5. PubMed ID: 3288996 [TBL] [Abstract][Full Text] [Related]
22. Brain- and muscle-type promoters of the dystrophin gene are selected in peripheral lymphocytes and Epstein Barr virus-transformed lymphoblastoid [correction of lymphoplastoid] cells. Nishio H; Matsuo M; Kitoh Y; Narita N; Shimmoto M; Suzuki Y; Nakamura H J Neurol; 1993 Dec; 241(2):81-6. PubMed ID: 8138829 [TBL] [Abstract][Full Text] [Related]
23. Duchenne muscular dystrophy: the gene and the protein. Love DR; Davies KE Mol Biol Med; 1989 Feb; 6(1):7-17. PubMed ID: 2666821 [No Abstract] [Full Text] [Related]
24. Duchenne/Becker muscular dystrophy: a short overview of the gene, the protein, and current diagnostics. Kunkel LM; Hoffman EP Br Med Bull; 1989 Jul; 45(3):630-43. PubMed ID: 2688821 [TBL] [Abstract][Full Text] [Related]
25. Dystrophin immunocytochemistry in muscle culture: detection of a carrier of Duchenne muscular dystrophy. Miranda AF; Francke U; Bonilla E; Martucci G; Schmidt B; Salviati G; Rubin M Am J Med Genet; 1989 Feb; 32(2):268-73. PubMed ID: 2648829 [TBL] [Abstract][Full Text] [Related]
27. Use of dystrophin genomic and cDNA probes for solving difficulties in carrier detection and prenatal diagnosis of Duchenne muscular dystrophy. Shomrat R; Driks N; Legum C; Shiloh Y Am J Med Genet; 1992 Feb; 42(3):281-7. PubMed ID: 1536162 [TBL] [Abstract][Full Text] [Related]
28. [The pathogenesis of Duchenne muscular dystrophy--defects of the membrane cytoskeleton "dystrophin"]. Arahata K; Sugita H Nihon Rinsho; 1989 Aug; 47(8):1857-64. PubMed ID: 2685400 [No Abstract] [Full Text] [Related]
29. A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patient. Prior TW; Papp AC; Snyder PJ; Burghes AH; Bartolo C; Sedra MS; Western LM; Mendell JR Nat Genet; 1993 Aug; 4(4):357-60. PubMed ID: 8401582 [TBL] [Abstract][Full Text] [Related]
31. Normal and dystrophin-deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophy. Bonilla E; Schmidt B; Samitt CE; Miranda AF; Hays AP; de Oliveira AB; Chang HW; Servidei S; Ricci E; Younger DS Am J Pathol; 1988 Dec; 133(3):440-5. PubMed ID: 3059802 [TBL] [Abstract][Full Text] [Related]
32. Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy. Narita N; Nishio H; Kitoh Y; Ishikawa Y; Ishikawa Y; Minami R; Nakamura H; Matsuo M J Clin Invest; 1993 May; 91(5):1862-7. PubMed ID: 8387534 [TBL] [Abstract][Full Text] [Related]
33. Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosome. Heilig R; Lemaire C; Mandel JL; Dandolo L; Amar L; Avner P Nature; 1987 Jul 9-15; 328(6126):168-70. PubMed ID: 3600794 [TBL] [Abstract][Full Text] [Related]
36. Nucleotide and corresponding amino acid sequence of human adult and fetal cDNA coding for portions of the Duchenne muscular dystrophy (DMD) gene. Rosenthal A; Speer A; Billwitz H; Cross GS; Forrest SM; Davies KE Biomed Biochim Acta; 1988; 47(2):K13-5. PubMed ID: 3178779 [No Abstract] [Full Text] [Related]
37. Expression of the putative Duchenne muscular dystrophy gene in differentiated myogenic cell cultures and in the brain. Nudel U; Robzyk K; Yaffe D Nature; 1988 Feb; 331(6157):635-8. PubMed ID: 3340214 [TBL] [Abstract][Full Text] [Related]
38. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene. Monaco AP; Neve RL; Colletti-Feener C; Bertelson CJ; Kurnit DM; Kunkel LM Nature; 1986 Oct 16-22; 323(6089):646-50. PubMed ID: 3773991 [TBL] [Abstract][Full Text] [Related]
39. High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridization. Blonden LA; den Dunnen JT; van Paassen HM; Wapenaar MC; Grootscholten PM; Ginjaar HB; Bakker E; Pearson PL; van Ommen GJ Nucleic Acids Res; 1989 Jul; 17(14):5611-21. PubMed ID: 2569720 [TBL] [Abstract][Full Text] [Related]
40. A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues. Lederfein D; Levy Z; Augier N; Mornet D; Morris G; Fuchs O; Yaffe D; Nudel U Proc Natl Acad Sci U S A; 1992 Jun; 89(12):5346-50. PubMed ID: 1319059 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]