Muscular Dystrophies, Limb-Girdle research, articles, guidelines & medical evidence database search.
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All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 18 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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Research
A two-segment model for thin filament architecture in skeletal muscle.
Gokhin David S, Fowler Velia M
Nature reviews. Molecular cell biology Vol 14(2)
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Date 01 Feb 2013
Research
Glia-to-Neuron Conversion by CRISPR-CasRx Alleviates Symptoms of Neurological Disease in Mice.
Zhou Haibo, Su Jinlin, Hu Xinde, Zhou Changyang, Li He ...
Cell Vol 181(3)
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Date 30 Apr 2020
Research
A Global Effort to Define the Human Genetics of Protective Immunity to SARS-CoV-2 Infection.
Casanova Jean-Laurent, Su Helen C
Cell Vol 181(6)
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Date 11 Jun 2020
Research
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A.
Richard I, Broux O, Allamand V, Fougerousse F, Chiannilkulchai N ...
Cell Vol 81(1)
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Date 07 Apr 1995
Research
Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy.
Brenman J E, Chao D S, Xia H, Aldape K, Bredt D S
Cell Vol 82(5)
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Date 08 Sep 1995
Research
Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: a model for Duchenne muscular dystrophy.
Grady R M, Teng H, Nichol M C, Cunningham J C, Wilkinson R S ...
Cell Vol 90(4)
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Date 22 Aug 1997
Research
Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface.
Bonilla E, Samitt C E, Miranda A F, Hays A P, Salviati G ...
Cell Vol 54(4)
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Date 12 Aug 1988
Research
A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy.
Cabianca Daphne S, Casa Valentina, Bodega Beatrice, Xynos Alexandros, Ginelli Enrico ...
Cell Vol 149(4)
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Date 11 May 2012
Research
Dystrophin: the protein product of the Duchenne muscular dystrophy locus.
Hoffman E P, Brown R H, Kunkel L M
Cell Vol 51(6)
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Date 24 Dec 1987
Research
Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member...
Brook J D, McCurrach M E, Harley H G, Buckler A J, Church D ...
Cell Vol 68(4)
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Date 21 Feb 1992
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