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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1946 1
1947 2
1950 1
1955 1
1958 3
1959 4
1960 7
1961 11
1962 9
1963 3
1964 6
1965 2
1966 8
1967 4
1968 12
1969 22
1970 36
1971 37
1972 47
1973 62
1974 69
1975 86
1976 76
1977 87
1978 83
1979 113
1980 78
1981 86
1982 96
1983 86
1984 91
1985 79
1986 87
1987 58
1988 75
1989 74
1990 74
1991 86
1992 79
1993 90
1994 74
1995 88
1996 76
1997 75
1998 94
1999 87
2000 81
2001 94
2002 108
2003 85
2004 105
2005 110
2006 127
2007 126
2008 164
2009 171
2010 190
2011 217
2012 199
2013 199
2014 220
2015 231
2016 221
2017 194
2018 237
2019 228
2020 255
2021 214
2022 152
2023 135
2024 164
2025 2

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6,240 results

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Page 1
Cardiomyopathy in animal models of muscular dystrophy.
Heydemann A, Wheeler MT, McNally EM. Heydemann A, et al. Curr Opin Cardiol. 2001 May;16(3):211-7. doi: 10.1097/00001573-200105000-00009. Curr Opin Cardiol. 2001. PMID: 11357018 Review.
Arrhythmia and cardiomyopathy frequently accompany muscular dystrophy. In the last year, the cardiovascular consequences of muscular dystrophy gene mutations have been established through studies of murine models. ...New findings have shown that cytosk …
Arrhythmia and cardiomyopathy frequently accompany muscular dystrophy. In the last year, the cardiovascular consequences of …
Animal models of Duchenne and Becker muscular dystrophy.
Cooper BJ. Cooper BJ. Br Med Bull. 1989 Jul;45(3):703-18. doi: 10.1093/oxfordjournals.bmb.a072353. Br Med Bull. 1989. PMID: 2688824 Review.
Two animal models have been shown to be related to Duchenne and Becker muscular dystrophy at the molecular level. ...Linkage studies, absence of dystrophin, and reduced levels of message indicate that the mutation in mdx lies in the gene for dystrophin, the g …
Two animal models have been shown to be related to Duchenne and Becker muscular dystrophy at the molecular level. ...Li …
Duchenne's muscular dystrophy: animal models used to investigate pathogenesis and develop therapeutic strategies.
Collins CA, Morgan JE. Collins CA, et al. Int J Exp Pathol. 2003 Aug;84(4):165-72. doi: 10.1046/j.1365-2613.2003.00354.x. Int J Exp Pathol. 2003. PMID: 14632630 Free PMC article. Review.
Duchenne's muscular dystrophy (DMD) is a lethal childhood disease caused by mutations of the dystrophin gene, the protein product of which, dystrophin, has a vital role in maintaining muscle structure and function. ...The most notable of these are the extensively st …
Duchenne's muscular dystrophy (DMD) is a lethal childhood disease caused by mutations of the dystrophin gene, the protein prod …
Behavioral Responses in Animal Model of Congenital Muscular Dystrophy 1D.
Comim CM, Schactae AL, Soares JA, Ventura L, Freiberger V, Mina F, Dominguini D, Vainzof M, Quevedo J. Comim CM, et al. Mol Neurobiol. 2016 Jan;53(1):402-407. doi: 10.1007/s12035-014-9024-y. Epub 2014 Dec 3. Mol Neurobiol. 2016. PMID: 25465243
However, in the animal model of CMD1D, the brain involvement remains unclear. Therefore, the objective of this study is to evaluate the cognitive involvement in the Large(myd) mice. ...This study shows the first evidence that abnormal glycosylation of alpha-DG may be affec …
However, in the animal model of CMD1D, the brain involvement remains unclear. Therefore, the objective of this study is to evaluate t …
Dystrophin-Deficient Muscular Dystrophy in Two Male Juvenile Brittanys.
Stevens R, Kanazono S, Petesch S, Guo LT, Shelton GD. Stevens R, et al. J Am Anim Hosp Assoc. 2022 Nov 1;58(6):292-296. doi: 10.5326/JAAHA-MS-7255. J Am Anim Hosp Assoc. 2022. PMID: 36315862
Immunofluorescence of biopsies confirmed dystrophin-deficient muscular dystrophy. This is the first report describing dystrophin-deficient muscular dystrophy in the Brittany breed. ...The location of the dogs in the United States and Japan suggests a w …
Immunofluorescence of biopsies confirmed dystrophin-deficient muscular dystrophy. This is the first report describing dystroph …
Inhibition of Rev-erbalpha ameliorates muscular dystrophy.
Xiong X, Gao H, Lin Y, Yechoor V, Ma K. Xiong X, et al. Exp Cell Res. 2021 Sep 15;406(2):112766. doi: 10.1016/j.yexcr.2021.112766. Epub 2021 Aug 6. Exp Cell Res. 2021. PMID: 34364881
Duchene muscular dystrophy leads to progressive muscle structural and functional decline due to chronic degenerative-regenerative cycles. ...Collectively, our findings revealed that the loss of Rev-erbalpha function protects dystrophic muscle from injury by promotin …
Duchene muscular dystrophy leads to progressive muscle structural and functional decline due to chronic degenerative-regenerat …
Canine X-linked muscular dystrophy. An animal model of Duchenne muscular dystrophy: clinical studies.
Valentine BA, Cooper BJ, de Lahunta A, O'Quinn R, Blue JT. Valentine BA, et al. J Neurol Sci. 1988 Dec;88(1-3):69-81. doi: 10.1016/0022-510x(88)90206-7. J Neurol Sci. 1988. PMID: 3225630 Free article.
The progression of clinical disease and serum creatine kinase (CK) levels in canine X-linked muscular dystrophy (CXMD) was studied in 7 dogs from birth to 12-14 months and in 18 dogs at varying intervals from birth to 8 weeks. ...These studies show that CXMD and Duc …
The progression of clinical disease and serum creatine kinase (CK) levels in canine X-linked muscular dystrophy (CXMD) was stu …
Oxidative stress and muscular dystrophy.
Murphy ME, Kehrer JP. Murphy ME, et al. Chem Biol Interact. 1989;69(2-3):101-73. doi: 10.1016/0009-2797(89)90075-6. Chem Biol Interact. 1989. PMID: 2649259 Review.
Oxidative stress may be the fundamental basis of many of the structural, functional and biochemical changes characteristic of the inherited muscular dystrophies in animals and humans. The presence of by-products of oxidative damage, and the compensatory increases in cellul …
Oxidative stress may be the fundamental basis of many of the structural, functional and biochemical changes characteristic of the inherited …
6,240 results