160 related articles for article (PubMed ID: 11901990)
21. A novel cryptic exon in intron 2 of the human dystrophin gene evolved from an intron by acquiring consensus sequences for splicing at different stages of anthropoid evolution.
Dwi Pramono ZA; Takeshima Y; Surono A; Ishida T; Matsuo M
Biochem Biophys Res Commun; 2000 Jan; 267(1):321-8. PubMed ID: 10623618
[TBL] [Abstract][Full Text] [Related]
22. In vivo targeted repair of a point mutation in the canine dystrophin gene by a chimeric RNA/DNA oligonucleotide.
Bartlett RJ; Stockinger S; Denis MM; Bartlett WT; Inverardi L; Le TT; thi Man N; Morris GE; Bogan DJ; Metcalf-Bogan J; Kornegay JN
Nat Biotechnol; 2000 Jun; 18(6):615-22. PubMed ID: 10835598
[TBL] [Abstract][Full Text] [Related]
23. Two alternative exons can result from activation of the cryptic splice acceptor site deep within intron 2 of the dystrophin gene in a patient with as yet asymptomatic dystrophinopathy.
Yagi M; Takeshima Y; Wada H; Nakamura H; Matsuo M
Hum Genet; 2003 Feb; 112(2):164-70. PubMed ID: 12522557
[TBL] [Abstract][Full Text] [Related]
24. [The full sequence of intron 51 of dystrophin gene and its characteristic of sequence].
Pan S; Zhang C; Liu Z; Chen G; Sheng W; Lu X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Feb; 19(1):26-9. PubMed ID: 11836681
[TBL] [Abstract][Full Text] [Related]
25. Analysis of three deletion breakpoints in Xp21.1 and the further localization of RP3.
Brown J; Dry KL; Edgar AJ; Pryde FE; Hardwick LJ; Aldred MA; Lester DH; Boyle S; Kaplan J; Dufier JL; Ho MF; Monaco AM; Musarella MA; Wright AF
Genomics; 1996 Oct; 37(2):200-10. PubMed ID: 8921393
[TBL] [Abstract][Full Text] [Related]
26. Newly recognized exons induced by a splicing abnormality from an intronic mutation of the dystrophin gene resulting in Duchenne muscular dystrophy. Mutations in brief no. 213. Online.
Ikezawa M; Nishino I; Goto Y; Miike T; Nonaka I
Hum Mutat; 1999; 13(2):170. PubMed ID: 10094556
[TBL] [Abstract][Full Text] [Related]
27. A polymerase chain reaction screening strategy for the promoter of the canine dystrophin gene.
Schatzberg S; Olby N; Steingold S; Keene B; Atkins C; Meurs K; Solomon G; Goedegebuure SA; Wilton S; Sharp N
Am J Vet Res; 1999 Sep; 60(9):1040-6. PubMed ID: 10490068
[TBL] [Abstract][Full Text] [Related]
28. A novel cryptic exon in intron 3 of the dystrophin gene was incorporated into dystrophin mRNA with a single nucleotide deletion in exon 5.
Suminaga R; Takeshima Y; Adachi K; Yagi M; Nakamura H; Matsuo M
J Hum Genet; 2002; 47(4):196-201. PubMed ID: 12166656
[TBL] [Abstract][Full Text] [Related]
29. Investigating the mechanism of chromosomal deletion: characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene.
Toffolatti L; Cardazzo B; Nobile C; Danieli GA; Gualandi F; Muntoni F; Abbs S; Zanetti P; Angelini C; Ferlini A; Fanin M; Patarnello T
Genomics; 2002 Nov; 80(5):523-30. PubMed ID: 12408970
[TBL] [Abstract][Full Text] [Related]
30. [Combining approach with multiplex PCR and MLPA to detect deletion and duplication in DMD patients, carriers, and prenatal diagnosis].
Li H; Ding J; Wang W; Chen Y; Lu W; Shao H; Wu BL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):318-22. PubMed ID: 19504448
[TBL] [Abstract][Full Text] [Related]
31. Are there ethnic differences in deletions in the dystrophin gene?
Banerjee M; Verma IC
Am J Med Genet; 1997 Jan; 68(2):152-7. PubMed ID: 9028449
[TBL] [Abstract][Full Text] [Related]
32. [Single cell analysis of some deletion in dystrophin gene exons and gender determination by 3-plex nested PCR].
Huang W; Zhang C; Xie YM; Chen SL; Jiao ZX; Zhou CQ; Zhang WX; Lu XL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Aug; 21(4):389-91. PubMed ID: 15300642
[TBL] [Abstract][Full Text] [Related]
33. A cluster of transposon-like repetitive sequences in intron 7 of the human dystrophin gene.
McNaughton JC; Broom JE; Hill DF; Jones WA; Marshall CJ; Renwick NM; Stockwell PA; Petersen GB
J Mol Biol; 1993 Jul; 232(1):314-21. PubMed ID: 8392588
[TBL] [Abstract][Full Text] [Related]
34. Usefulness of dinucleotide polymorphism markers in genetic analysis of Duchenne's muscular dystrophy cases in Singapore.
Lai PS; Chiu LL; Low PS; Lee WL; Tay JS
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():175-8. PubMed ID: 8629101
[TBL] [Abstract][Full Text] [Related]
35. Mutation analysis in Duchenne and Becker muscular dystrophy patients from Bulgaria shows a peculiar distribution of breakpoints by intron.
Todoroya A; Bronzova J; Miorin M; Rosa M; Kremensky I; Danieli GA
Am J Med Genet; 1996 Oct; 65(1):40-3. PubMed ID: 8914739
[TBL] [Abstract][Full Text] [Related]
36. Detection of deletion in the dystrophin gene of a patient with quadriceps myopathy.
Kumari D; Gupta M; Goyle S
Neurol India; 2000 Mar; 48(1):68-71. PubMed ID: 10751817
[TBL] [Abstract][Full Text] [Related]
37. Novel cryptic exons identified in introns 2 and 3 of the human dystrophin gene with duplication of exons 8-11.
Ishibashi K; Takeshima Y; Yagi M; Nishiyama A; Matsuo M
Kobe J Med Sci; 2006; 52(3-4):61-75. PubMed ID: 16849873
[TBL] [Abstract][Full Text] [Related]
38. The evolution of an intron: analysis of a long, deletion-prone intron in the human dystrophin gene.
McNaughton JC; Hughes G; Jones WA; Stockwell PA; Klamut HJ; Petersen GB
Genomics; 1997 Mar; 40(2):294-304. PubMed ID: 9119397
[TBL] [Abstract][Full Text] [Related]
39. Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin gene.
McNaughton JC; Cockburn DJ; Hughes G; Jones WA; Laing NG; Ray PN; Stockwell PA; Petersen GB
Gene; 1998 Nov; 222(1):41-51. PubMed ID: 9813236
[TBL] [Abstract][Full Text] [Related]
40. The 5' region of intron 11 of the dystrophin gene contains target sequences for mobile elements and three overlapping ORFs.
Ferlini A; Muntoni F
Biochem Biophys Res Commun; 1998 Jan; 242(2):401-6. PubMed ID: 9446807
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]