174 related articles for article (PubMed ID: 7808586)
1. Expression of utrophin (dystrophin-related protein) during regeneration and maturation of skeletal muscle in canine X-linked muscular dystrophy.
Wilson LA; Cooper BJ; Dux L; Dubowitz V; Sewry CA
Neuropathol Appl Neurobiol; 1994 Aug; 20(4):359-67. PubMed ID: 7808586
[TBL] [Abstract][Full Text] [Related]
2. Experimental regeneration in canine muscular dystrophy--1. Immunocytochemical evaluation of dystrophin and beta-spectrin expression.
Sewry CA; Wilson LA; Dux L; Dubowitz V; Cooper BJ
Neuromuscul Disord; 1992; 2(5-6):331-42. PubMed ID: 1300182
[TBL] [Abstract][Full Text] [Related]
3. Development of muscle pathology in canine X-linked muscular dystrophy. I. Delayed postnatal maturation of affected and normal muscle as revealed by myosin isoform analysis and utrophin expression.
Lanfossi M; Cozzi F; Bugini D; Colombo S; Scarpa P; Morandi L; Galbiati S; Cornelio F; Pozza O; Mora M
Acta Neuropathol; 1999 Feb; 97(2):127-38. PubMed ID: 9928823
[TBL] [Abstract][Full Text] [Related]
4. Correlation of Utrophin Levels with the Dystrophin Protein Complex and Muscle Fibre Regeneration in Duchenne and Becker Muscular Dystrophy Muscle Biopsies.
Janghra N; Morgan JE; Sewry CA; Wilson FX; Davies KE; Muntoni F; Tinsley J
PLoS One; 2016; 11(3):e0150818. PubMed ID: 26974331
[TBL] [Abstract][Full Text] [Related]
5. Utrophin is a regeneration-associated protein transiently present at the sarcolemma of regenerating skeletal muscle fibers in dystrophin-deficient hypertrophic feline muscular dystrophy.
Lin S; Gaschen F; Burgunder JM
J Neuropathol Exp Neurol; 1998 Aug; 57(8):780-90. PubMed ID: 9720493
[TBL] [Abstract][Full Text] [Related]
6. Reduced sarcolemmal dystrophin distribution and upregulation of utrophin in the cardiac and skeletal muscles of CHF-146 dystrophic hamsters.
Bhattacharya SK; Johnson PL; Li HJ; Handa RK; Adamec TA
Mol Chem Neuropathol; 1997 Jun; 31(2):187-206. PubMed ID: 9376024
[TBL] [Abstract][Full Text] [Related]
7. The dystrophin-related protein, utrophin, is expressed on the sarcolemma of regenerating human skeletal muscle fibres in dystrophies and inflammatory myopathies.
Helliwell TR; Man NT; Morris GE; Davies KE
Neuromuscul Disord; 1992; 2(3):177-84. PubMed ID: 1483043
[TBL] [Abstract][Full Text] [Related]
8. Experimental regeneration in canine muscular dystrophy--2. Expression of myosin heavy chain isoforms.
Wilson LA; Dux L; Cooper BJ; Dubowitz V; Sewry CA
Neuromuscul Disord; 1994 Jan; 4(1):25-37. PubMed ID: 7513568
[TBL] [Abstract][Full Text] [Related]
9. Embryonic myosin is a regeneration marker to monitor utrophin-based therapies for DMD.
Guiraud S; Edwards B; Squire SE; Moir L; Berg A; Babbs A; Ramadan N; Wood MJ; Davies KE
Hum Mol Genet; 2019 Jan; 28(2):307-319. PubMed ID: 30304405
[TBL] [Abstract][Full Text] [Related]
10. Expression of full-length utrophin prevents muscular dystrophy in mdx mice.
Tinsley J; Deconinck N; Fisher R; Kahn D; Phelps S; Gillis JM; Davies K
Nat Med; 1998 Dec; 4(12):1441-4. PubMed ID: 9846586
[TBL] [Abstract][Full Text] [Related]
11. Dystrophin-related protein, utrophin, in normal and dystrophic human fetal skeletal muscle.
Clerk A; Morris GE; Dubowitz V; Davies KE; Sewry CA
Histochem J; 1993 Aug; 25(8):554-61. PubMed ID: 8407365
[TBL] [Abstract][Full Text] [Related]
12. Differential effects of dystrophin and utrophin gene transfer in immunocompetent muscular dystrophy (mdx) mice.
Ebihara S; Guibinga GH; Gilbert R; Nalbantoglu J; Massie B; Karpati G; Petrof BJ
Physiol Genomics; 2000 Sep; 3(3):133-44. PubMed ID: 11015608
[TBL] [Abstract][Full Text] [Related]
13. Comparative analysis of Dp427-deficient mdx tissues shows that the milder dystrophic phenotype of extraocular and toe muscle fibres is associated with a persistent expression of beta-dystroglycan.
Dowling P; Lohan J; Ohlendieck K
Eur J Cell Biol; 2003 May; 82(5):222-30. PubMed ID: 12800977
[TBL] [Abstract][Full Text] [Related]
14. The abnormal expression of utrophin in Duchenne and Becker muscular dystrophy is age related.
Taylor J; Muntoni F; Dubowitz V; Sewry CA
Neuropathol Appl Neurobiol; 1997 Oct; 23(5):399-405. PubMed ID: 9364465
[TBL] [Abstract][Full Text] [Related]
15. Comparative evolution of muscular dystrophy in diaphragm, gastrocnemius and masseter muscles from old male mdx mice.
Muller J; Vayssiere N; Royuela M; Leger ME; Muller A; Bacou F; Pons F; Hugon G; Mornet D
J Muscle Res Cell Motil; 2001; 22(2):133-9. PubMed ID: 11519736
[TBL] [Abstract][Full Text] [Related]
16. Autosomal recessive distal muscular dystrophy: normal expression of dystrophin, utrophin and dystrophin-associated proteins in muscle fibers.
Yamanouchi Y; Ozawa E; Nonaka I
J Neurol Sci; 1994 Oct; 126(1):70-6. PubMed ID: 7836950
[TBL] [Abstract][Full Text] [Related]
17. Molecular mechanisms and putative signalling events controlling utrophin expression in mammalian skeletal muscle fibres.
Gramolini AO; Jasmin BJ
Neuromuscul Disord; 1998 Aug; 8(6):351-61. PubMed ID: 9713851
[TBL] [Abstract][Full Text] [Related]
18. A and B utrophin in human muscle and sarcolemmal A-utrophin associated with tumours.
Sewry CA; Nowak KJ; Ehmsen JT; Davies KE
Neuromuscul Disord; 2005 Nov; 15(11):779-85. PubMed ID: 16198105
[TBL] [Abstract][Full Text] [Related]
19. Distal mdx muscle groups exhibiting up-regulation of utrophin and rescue of dystrophin-associated glycoproteins exemplify a protected phenotype in muscular dystrophy.
Dowling P; Culligan K; Ohlendieck K
Naturwissenschaften; 2002 Feb; 89(2):75-8. PubMed ID: 12046625
[TBL] [Abstract][Full Text] [Related]
20. Brain dystrophin-glycoprotein complex: persistent expression of beta-dystroglycan, impaired oligomerization of Dp71 and up-regulation of utrophins in animal models of muscular dystrophy.
Culligan K; Glover L; Dowling P; Ohlendieck K
BMC Cell Biol; 2001; 2():2. PubMed ID: 11178104
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]