Myotonic Disorders 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 20 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
Temperature-sensitive mutations in the III-IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita.
McClatchey A I, Van den Bergh P, Pericak-Vance M A, Raskind W, Verellen C ...
Cell Vol 68(4)
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Date 21 Feb 1992
Research
VMA21 deficiency causes an autophagic myopathy by compromising V-ATPase activity and lysosomal acidification.
Ramachandran Nivetha, Munteanu Iulia, Wang Peixiang, Aubourg Pauline, Rilstone Jennifer J ...
Cell Vol 137(2)
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Date 17 Apr 2009
Research
Measles virus infection in a transgenic model: virus-induced immunosuppression and central nervous system disease.
Oldstone M B, Lewicki H, Thomas D, Tishon A, Dales S ...
Cell Vol 98(5)
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Date 03 Sep 1999
Research
Neurons under T Cell Attack Coordinate Phagocyte-Mediated Synaptic Stripping.
Di Liberto Giovanni, Pantelyushin Stanislav, Kreutzfeldt Mario, Page Nicolas, Musardo Stefano ...
Cell Vol 175(2)
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Date 04 Oct 2018
Research
VMA21 deficiency: a case of myocyte indigestion.
Hirano Michio, DiMauro Salvatore
Cell Vol 137(2)
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Date 17 Apr 2009
Research
Structure of the rigor actin-tropomyosin-myosin complex.
Behrmann Elmar, Müller Mirco, Penczek Pawel A, Mannherz Hans Georg, Manstein Dietmar J ...
Cell Vol 150(2)
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Date 20 Jul 2012
Research
Structural insight into processive human mitochondrial DNA synthesis and disease-related polymerase mutations.
Lee Young-Sam, Kennedy W Dexter, Yin Y Whitney
Cell Vol 139(2)
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Date 16 Oct 2009
Research
Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease.
Shoubridge E A, Karpati G, Hastings K E
Cell Vol 62(1)
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Date 13 Jul 1990
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