Migraine with Aura 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
Stress-Induced Metabolic Disorder in Peripheral CD4+ T Cells Leads to Anxiety-like Behavior.
Fan Ke-Qi, Li Yi-Yuan, Wang Hao-Li, Mao Xin-Tao, Guo Jin-Xin ...
Cell Vol 179(4)
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Date 31 Oct 2019
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
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
Ophoff R A, Terwindt G M, Vergouwe M N, van Eijk R, Oefner P J ...
Cell Vol 87(3)
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Date 01 Nov 1996
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
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
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
Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse.
Burgess D L, Jones J M, Meisler M H, Noebels J L
Cell Vol 88(3)
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Date 07 Feb 1997
Research
Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms.
Walker Rebecca L, Ramaswami Gokul, Hartl Christopher, Mancuso Nicholas, Gandal Michael J ...
Cell Vol 179(3)
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Date 17 Oct 2019
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
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