181 related articles for article (PubMed ID: 12842431)
21. Encapsidated adenovirus minichromosomes allow delivery and expression of a 14 kb dystrophin cDNA to muscle cells.
Kumar-Singh R; Chamberlain JS
Hum Mol Genet; 1996 Jul; 5(7):913-21. PubMed ID: 8817325
[TBL] [Abstract][Full Text] [Related]
22. Fnip1 regulates skeletal muscle fiber type specification, fatigue resistance, and susceptibility to muscular dystrophy.
Reyes NL; Banks GB; Tsang M; Margineantu D; Gu H; Djukovic D; Chan J; Torres M; Liggitt HD; Hirenallur-S DK; Hockenbery DM; Raftery D; Iritani BM
Proc Natl Acad Sci U S A; 2015 Jan; 112(2):424-9. PubMed ID: 25548157
[TBL] [Abstract][Full Text] [Related]
23. Autotransplantation in mdx mice of mdx myoblasts genetically corrected by an HSV-1 amplicon vector.
Bujold M; Caron N; Camiran G; Mukherjee S; Allen PD; Tremblay JP; Wang Y
Cell Transplant; 2002; 11(8):759-67. PubMed ID: 12588108
[TBL] [Abstract][Full Text] [Related]
24. Adeno-associated virus vector gene transfer and sarcolemmal expression of a 144 kDa micro-dystrophin effectively restores the dystrophin-associated protein complex and inhibits myofibre degeneration in nude/mdx mice.
Fabb SA; Wells DJ; Serpente P; Dickson G
Hum Mol Genet; 2002 Apr; 11(7):733-41. PubMed ID: 11929846
[TBL] [Abstract][Full Text] [Related]
25. Intraarterial delivery of naked plasmid DNA expressing full-length mouse dystrophin in the mdx mouse model of duchenne muscular dystrophy.
Zhang G; Ludtke JJ; Thioudellet C; Kleinpeter P; Antoniou M; Herweijer H; Braun S; Wolff JA
Hum Gene Ther; 2004 Aug; 15(8):770-82. PubMed ID: 15319034
[TBL] [Abstract][Full Text] [Related]
26. Targeted inhibition of Ca2+ /calmodulin signaling exacerbates the dystrophic phenotype in mdx mouse muscle.
Chakkalakal JV; Michel SA; Chin ER; Michel RN; Jasmin BJ
Hum Mol Genet; 2006 May; 15(9):1423-35. PubMed ID: 16551657
[TBL] [Abstract][Full Text] [Related]
27. Expression of full-length and truncated dystrophin mini-genes in transgenic mdx mice.
Phelps SF; Hauser MA; Cole NM; Rafael JA; Hinkle RT; Faulkner JA; Chamberlain JS
Hum Mol Genet; 1995 Aug; 4(8):1251-8. PubMed ID: 7581361
[TBL] [Abstract][Full Text] [Related]
28. Overexpression of the cytotoxic T cell GalNAc transferase in skeletal muscle inhibits muscular dystrophy in mdx mice.
Nguyen HH; Jayasinha V; Xia B; Hoyte K; Martin PT
Proc Natl Acad Sci U S A; 2002 Apr; 99(8):5616-21. PubMed ID: 11960016
[TBL] [Abstract][Full Text] [Related]
29. Gene therapy in Duchenne muscular dystrophy.
Inui K; Okada S; Dickson G
Brain Dev; 1996; 18(5):357-61. PubMed ID: 8891229
[TBL] [Abstract][Full Text] [Related]
30. A highly functional mini-dystrophin/GFP fusion gene for cell and gene therapy studies of Duchenne muscular dystrophy.
Li S; Kimura E; Ng R; Fall BM; Meuse L; Reyes M; Faulkner JA; Chamberlain JS
Hum Mol Genet; 2006 May; 15(10):1610-22. PubMed ID: 16595609
[TBL] [Abstract][Full Text] [Related]
31. Adenovirus-mediated dystrophin minigene transfer improves muscle strength in adult dystrophic (MDX) mice.
Yang L; Lochmuller H; Luo J; Massie B; Nalbantoglu J; Karpati G; Petrof BJ
Gene Ther; 1998 Mar; 5(3):369-79. PubMed ID: 9614557
[TBL] [Abstract][Full Text] [Related]
32. AAV vector-mediated microdystrophin expression in a relatively small percentage of mdx myofibers improved the mdx phenotype.
Yoshimura M; Sakamoto M; Ikemoto M; Mochizuki Y; Yuasa K; Miyagoe-Suzuki Y; Takeda S
Mol Ther; 2004 Nov; 10(5):821-8. PubMed ID: 15509500
[TBL] [Abstract][Full Text] [Related]
33. Adeno-associated virus vector carrying human minidystrophin genes effectively ameliorates muscular dystrophy in mdx mouse model.
Wang B; Li J; Xiao X
Proc Natl Acad Sci U S A; 2000 Dec; 97(25):13714-9. PubMed ID: 11095710
[TBL] [Abstract][Full Text] [Related]
34. Branched fibers from old fast-twitch dystrophic muscles are the sites of terminal damage in muscular dystrophy.
Kiriaev L; Kueh S; Morley JW; North KN; Houweling PJ; Head SI
Am J Physiol Cell Physiol; 2018 Jun; 314(6):C662-C674. PubMed ID: 29412689
[TBL] [Abstract][Full Text] [Related]
35. Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for duchenne muscular dystrophy.
Ahmad A; Brinson M; Hodges BL; Chamberlain JS; Amalfitano A
Hum Mol Genet; 2000 Oct; 9(17):2507-15. PubMed ID: 11030755
[TBL] [Abstract][Full Text] [Related]
36. Comparative Label-Free Mass Spectrometric Analysis of Mildly versus Severely Affected mdx Mouse Skeletal Muscles Identifies Annexin, Lamin, and Vimentin as Universal Dystrophic Markers.
Holland A; Henry M; Meleady P; Winkler CK; Krautwald M; Brinkmeier H; Ohlendieck K
Molecules; 2015 Jun; 20(6):11317-44. PubMed ID: 26102067
[TBL] [Abstract][Full Text] [Related]
37. CD45 fraction bone marrow cells as potential delivery vehicles for genetically corrected dystrophin loci.
Kapsa RM; Wong SH; Bertoncello I; Quigley AF; Williams B; Sells K; Marotta R; Kita M; Simmons P; Byrne E; Kornberg AJ
Neuromuscul Disord; 2002 Oct; 12 Suppl 1():S61-6. PubMed ID: 12206798
[TBL] [Abstract][Full Text] [Related]
38. Stable micro-dystrophin gene transfer using an integrating adeno-retroviral hybrid vector ameliorates the dystrophic pathology in mdx mouse muscle.
Roberts ML; Wells DJ; Graham IR; Fabb SA; Hill VJ; Duisit G; Yuasa K; Takeda S; Cosset FL; Dickson G
Hum Mol Genet; 2002 Jul; 11(15):1719-30. PubMed ID: 12095914
[TBL] [Abstract][Full Text] [Related]
39. Making fast-twitch dystrophic muscles bigger protects them from contraction injury and attenuates the dystrophic pathology.
Gehrig SM; Koopman R; Naim T; Tjoakarfa C; Lynch GS
Am J Pathol; 2010 Jan; 176(1):29-33. PubMed ID: 19959813
[TBL] [Abstract][Full Text] [Related]
40. Contractile properties of diaphragm muscle segments from old mdx and old transgenic mdx mice.
Lynch GS; Rafael JA; Hinkle RT; Cole NM; Chamberlain JS; Faulkner JA
Am J Physiol; 1997 Jun; 272(6 Pt 1):C2063-8. PubMed ID: 9227435
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]