Access the latest scientific research and medical evidence related to Muscle Spasticity treatment, diagnosis and symptoms, quickly and easily with doctorAsyou.
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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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30786 Abstracts
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
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
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease.
Casari G, De Fusco M, Ciarmatori S, Zeviani M, Mora M ...
Cell Vol 93(6)
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Date 12 Jun 1998
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
Human CLP1 mutations alter tRNA biogenesis, affecting both peripheral and central nervous system function.
Karaca Ender, Weitzer Stefan, Pehlivan Davut, Shiraishi Hiroshi, Gogakos Tasos ...
Cell Vol 157(3)
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Date 24 Apr 2014
Research
Astrocytes Assemble Thalamocortical Synapses by Bridging NRX1α and NL1 via Hevin.
Singh Sandeep K, Stogsdill Jeff A, Pulimood Nisha S, Dingsdale Hayley, Kim Yong Ho ...
Cell Vol 164(1-2)
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Date 14 Jan 2016
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
Discovery of Human Signaling Systems: Pairing Peptides to G Protein-Coupled Receptors.
Foster Simon R, Hauser Alexander S, Vedel Line, Strachan Ryan T, Huang Xi-Ping ...
Cell Vol 179(4)
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Date 31 Oct 2019
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