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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.Current Medical Science|August 31, 2020
The Clinical Role of Changes of Maximum Expiratory Flow at 25% and 50% of Vital Capacity before and after Bronchodilator Reversibility Test in Diagnosing AsthmaXu-Xue Guo, Xiao-Fan Liu, Ai-Ling Wang, 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.Thyroid : Official Journal of the American Thyroid Association|August 13, 2020
A Comparative Analysis of Two Machine Learning-Based Diagnostic Patterns with Thyroid Imaging Reporting and Data System for Thyroid Nodules: Diagnostic Performance and Unnecessary Biopsy RateChong-Ke Zhao, Tian-Tian Ren, Yi-Fei Yin, et al.International Immunopharmacology|May 31, 2024
Dichotomous roles of ADAR1 in liver hepatocellular carcinoma and kidney renal cell carcinoma: Unraveling the complex tumor microenvironment and prognostic significanceJia-Xi Mao, Jing-Jing Li, Xin-Yi Lu, 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.Pageof 21