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Science Signaling|October 26, 2021
Tyrosine phosphorylation of NLRP3 by the Src family kinase Lyn suppresses the activity of the NLRP3 inflammasomeJuan Tang, Yizhi Xiao, Guoxin Lin, et al.
Neurogenetics|September 7, 2014
Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathySenda Ajroud-Driss, Faisal Fecto, Kaouther Ajroud, et al.
Annals of Neurology|June 3, 2010
FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosisHan-Xiang Deng, Hong Zhai, Eileen H Bigio, et al.
Zhonghua Yi Xue Za Zhi|September 24, 2005
[Mutation analysis of PINK1 gene in Chinese patients with autosomal recessive early-onset parkinsonism type 6]Yu-hu Zhang, Bei-sha Tang, Ji-feng Guo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 4, 2019
Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humansYue-Qiu Tan, Chaofeng Tu, Lanlan Meng, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 11, 2019
Glutathione Reductase Promotes Fungal Clearance and Suppresses Inflammation during Systemic Candida albicans Infection in MiceVictoria Y Kim, Abel Batty, Jinhui Li, et al.
Neurology. Genetics|April 29, 2016
Compound heterozygote mutations in SPG7 in a family with adult-onset primary lateral sclerosisYi Yang, Lei Zhang, David R Lynch, et al.
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