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All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 19 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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16508 Abstracts
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 Genome-wide ER-phagy Screen Highlights Key Roles of Mitochondrial Metabolism and ER-Resident UFMylation.
Liang Jin Rui, Lingeman Emily, Luong Thao, Ahmed Saba, Muhar Matthias ...
Cell Vol 180(6)
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Date 19 Mar 2020
Research
Natural Killer Cells Degenerate Intact Sensory Afferents following Nerve Injury.
Davies Alexander J, Kim Hyoung Woo, Gonzalez-Cano Rafael, Choi Jahyang, Back Seung Keun ...
Cell Vol 176(4)
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Date 07 Feb 2019
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
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
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
Mitofusin 2 builds a bridge between ER and mitochondria.
Merkwirth Carsten, Langer Thomas
Cell Vol 135(7)
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Date 26 Dec 2008
Research
A Drosophila model for xeroderma pigmentosum and Cockayne's syndrome: haywire encodes the fly homolog of ERCC3, a human excision repair gene.
Mounkes L C, Jones R S, Liang B C, Gelbart W, Fuller M T
Cell Vol 71(6)
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Date 11 Dec 1992
Research
DNA deletion associated with hereditary neuropathy with liability to pressure palsies.
Chance P F, Alderson M K, Leppig K A, Lensch M W, Matsunami N ...
Cell Vol 72(1)
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Date 15 Jan 1993
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