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

Year Number of Results
1970 2
1971 2
1972 1
1973 5
1974 5
1975 2
1976 5
1977 8
1978 4
1979 9
1980 15
1981 23
1982 18
1983 15
1984 28
1985 32
1986 24
1987 21
1988 26
1989 22
1990 29
1991 31
1992 28
1993 45
1994 24
1995 33
1996 41
1997 38
1998 46
1999 55
2000 55
2001 72
2002 57
2003 73
2004 71
2005 79
2006 98
2007 101
2008 129
2009 114
2010 112
2011 144
2012 144
2013 134
2014 137
2015 139
2016 144
2017 126
2018 132
2019 125
2020 114
2021 105
2022 29
2023 30
2024 12

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2,870 results

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Page 1
Muscular dystrophy in PTFR/cavin-1 null mice.
Ding SY, Liu L, Pilch PF. Ding SY, et al. JCI Insight. 2017 Mar 9;2(5):e91023. doi: 10.1172/jci.insight.91023. JCI Insight. 2017. PMID: 28289716 Free PMC article.
Thus, in addition to compromised adipocyte-related physiology, the absence of PTRF/cavin-1 in mice caused a unique form of muscular dystrophy with a phenotype similar or identical to that seen in humans lacking this protein. Further understanding of this muscular …
Thus, in addition to compromised adipocyte-related physiology, the absence of PTRF/cavin-1 in mice caused a unique form of muscular …
CD133+ cells derived from skeletal muscles of Duchenne muscular dystrophy patients have a compromised myogenic and muscle regenerative capability.
Meng J, Muntoni F, Morgan J. Meng J, et al. Stem Cell Res. 2018 Jul;30:43-52. doi: 10.1016/j.scr.2018.05.004. Epub 2018 May 12. Stem Cell Res. 2018. PMID: 29783100 Free PMC article.
Cell-mediated gene therapy is a possible means to treat muscular dystrophies like Duchenne muscular dystrophy. Autologous patient stem cells can be genetically-corrected and transplanted back into the patient, without causing immunorejection pro …
Cell-mediated gene therapy is a possible means to treat muscular dystrophies like Duchenne muscular dystrophy. A …
Expression of the Duchenne's muscular dystrophy gene in cultured muscle cells.
Lev AA, Feener CC, Kunkel LM, Brown RH Jr. Lev AA, et al. J Biol Chem. 1987 Nov 25;262(33):15817-20. J Biol Chem. 1987. PMID: 3680227 Free article.
A partial cDNA clone for the Duchenne's muscular dystrophy (DMD) locus was used to investigate the expression of this locus in human muscle in vitro. Hybridization to a 14-kilobase RNA transcript was demonstrated in both fetal and mature human skeletal muscle and fo …
A partial cDNA clone for the Duchenne's muscular dystrophy (DMD) locus was used to investigate the expression of this locus in …
Cell therapy in Duchenne muscular dystrophy treatment: clinical trials overview.
Bajek A, Porowinska D, Kloskowski T, Brzoska E, Ciemerych MA, Drewa T. Bajek A, et al. Crit Rev Eukaryot Gene Expr. 2015;25(1):1-11. doi: 10.1615/critreveukaryotgeneexpr.2015011074. Crit Rev Eukaryot Gene Expr. 2015. PMID: 25955813 Review.
Duchenne muscular dystrophy (DMD), the most common and most severe form of all muscular dystrophies, leads to progressive muscle fiber necrosis, fibroblast proliferation, and growth of fibrous tissue and fat. ...However, the results of intramuscular in …
Duchenne muscular dystrophy (DMD), the most common and most severe form of all muscular dystrophies, leads to pr …
Skin cells for use in an alternate diagnostic method for Duchenne muscular dystrophy.
Tyers L, Davids LM, Wilmshurst JM, Esterhuizen AI. Tyers L, et al. Neuromuscul Disord. 2018 Jul;28(7):553-563. doi: 10.1016/j.nmd.2018.05.001. Epub 2018 May 10. Neuromuscul Disord. 2018. PMID: 29958823
The importance of molecular diagnosis and identification of disease-associated variants for Duchenne muscular dystrophy (DMD) is evident in the age of gene-based therapies and personalised medicine. ...Biopsies were sampled, and tolerated without complications, usin …
The importance of molecular diagnosis and identification of disease-associated variants for Duchenne muscular dystrophy (DMD) …
Membrane Repair Deficit in Facioscapulohumeral Muscular Dystrophy.
Bittel AJ, Sreetama SC, Bittel DC, Horn A, Novak JS, Yokota T, Zhang A, Maruyama R, Rowel Q Lim K, Jaiswal JK, Chen YW. Bittel AJ, et al. Int J Mol Sci. 2020 Aug 4;21(15):5575. doi: 10.3390/ijms21155575. Int J Mol Sci. 2020. PMID: 32759720 Free PMC article.
Deficits in plasma membrane repair have been identified in dysferlinopathy and Duchenne Muscular Dystrophy, and contribute to progressive myopathy. Although Facioscapulohumeral Muscular Dystrophy (FSHD) shares clinicopathological features with these …
Deficits in plasma membrane repair have been identified in dysferlinopathy and Duchenne Muscular Dystrophy, and contribute to …
Gene Editing With CRISPR/Cas9 RNA-Directed Nuclease.
Doetschman T, Georgieva T. Doetschman T, et al. Circ Res. 2017 Mar 3;120(5):876-894. doi: 10.1161/CIRCRESAHA.116.309727. Circ Res. 2017. PMID: 28254804 Review.
Genetic engineering of model organisms and cultured cells has for decades provided important insights into the mechanisms underlying cardiovascular development and disease. ...We will also cover its use in iPSC for research and possible therapeutic purposes; and we …
Genetic engineering of model organisms and cultured cells has for decades provided important insights into the mechanisms unde …
Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention.
Moser H. Moser H. Hum Genet. 1984;66(1):17-40. doi: 10.1007/BF00275183. Hum Genet. 1984. PMID: 6365739 Review.
Duchenne muscular dystrophy (DMD) is the most common sex linked lethal disease in man (one case in about 4000 male live births). ...The results of studies on structural and functional membrane abnormalities in cells other than muscle tissue, e.g., erythrocyte …
Duchenne muscular dystrophy (DMD) is the most common sex linked lethal disease in man (one case in about 4000 male live births …
Dystrophin Expressing Chimeric (DEC) Human Cells Provide a Potential Therapy for Duchenne Muscular Dystrophy.
Siemionow M, Cwykiel J, Heydemann A, Garcia J, Marchese E, Siemionow K, Szilagyi E. Siemionow M, et al. Stem Cell Rev Rep. 2018 Jun;14(3):370-384. doi: 10.1007/s12015-018-9807-z. Stem Cell Rev Rep. 2018. PMID: 29546607 Free PMC article.
Duchenne Muscular Dystrophy (DMD) is a progressive and lethal disease caused by mutations of the dystrophin gene. ...This study establishes DEC as a potential therapy for DMD and other types of muscular dystrophies....
Duchenne Muscular Dystrophy (DMD) is a progressive and lethal disease caused by mutations of the dystrophin gene. ...This stud …
iMyoblasts for ex vivo and in vivo investigations of human myogenesis and disease modeling.
Guo D, Daman K, Chen JJ, Shi MJ, Yan J, Matijasevic Z, Rickard AM, Bennett MH, Kiselyov A, Zhou H, Bang AG, Wagner KR, Maehr R, King OD, Hayward LJ, Emerson CP Jr. Guo D, et al. Elife. 2022 Jan 25;11:e70341. doi: 10.7554/eLife.70341. Elife. 2022. PMID: 35076017 Free PMC article.
However, testing these ideas requires better ways to recreate human muscular dystrophy in the laboratory. One strategy for modelling muscular dystrophy involves coaxing skin or other cells from an individual into becoming 'induced pluripotent st …
However, testing these ideas requires better ways to recreate human muscular dystrophy in the laboratory. One strategy for mod …
2,870 results