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Mitochondrion|October 17, 2021
Identification of a novel m.3955G > A variant in MT-ND1 associated with Leigh syndromeManting Xu, Robert Kopajtich, Matthias Elstner, et al.
Frontiers in Pharmacology|January 11, 2020
Clinical Assessments and EEG Analyses of Encephalopathies Associated With Dynamin-1 MutationHua Li, Fang Fang, Manting Xu, et al.
Current Pollution Reports|July 14, 2025
Arsenic and Human Health: New Molecular Mechanisms For Arsenic-Induced CancersAlexandra N Nail, Manting Xu, Jonathan C Bastick, et al.
World Journal of Gastroenterology|February 16, 2026
Mac-2 binding protein glycosylation isomer as a novel serum biomarker for recurrence in hepatocellular carcinomaKyle R Stephens, Megan Wilson, Manting Xu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 3, 2024
Genotype and Phenotype Characteristics of 58 Cases of Mitochondrial Epilepsy with Nuclear DNA Mutations in ChildrenXiaodi Han, Hua Li, Jie Deng, et al.
Frontiers in Pharmacology|October 25, 2021
Clinical Attributes and Electroencephalogram Analysis of Patients With Varying Alpers' Syndrome GenotypesHua Li, Wei Wang, Xiaodi Han, et al.
Archives of Toxicology|June 26, 2026
Deficient arsenic methylation and global proteomic reprogramming in human keratinocytes during arsenic-induced skin carcinogenesisAlexandra N Nail, Mayukh Banerjee, Manting Xu, et al.
Journal of Medical Genetics|April 3, 2021
Whole genome and exome sequencing identify NDUFV2 mutations as a new cause of progressive cavitating leukoencephalopathyZhimei Liu, Li Zhang, Changhong Ren, et al.
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