Xuebi Xu

发表

Bezafibrate Rescues Mitochondrial Encephalopathy in Mice via Induction of Daily Torpor and Hypometabolic State

Chuanzhu Yan, Yuying Zhao, Rui Zheng, 2022, Neurotherapeutics.

A novel nonsense variant in MT-CO3 causes MELAS syndrome

Yuan Sun, Dandan Zhao, Chuanzhu Yan, 2021, Neuromuscular Disorders.

Activated mTOR signaling pathway in myofibers with inherited metabolic defect might be an evidence for mTOR inhibition therapies

N. Zhang, Dandan Zhao, Yuying Zhao, 2019, Chinese medical journal.

Mitochondrial encephalopathy Due to a Novel Pathogenic Mitochondrial tRNAGln m.4349C>T Variant

Fuchen Liu, Chuanzhu Yan, Yuying Zhao, 2020, Annals of clinical and translational neurology.

Clinical, Neuroimaging, and Pathological Analyses of 13 Chinese Leigh Syndrome Patients with Mitochondrial DNA Mutations

T. Dai, Wei Li, Yuying Zhao, 2018, Chinese medical journal.

Leber’s hereditary optic neuropathy plus dystonia caused by the mitochondrial ND1 gene m.4160 T > C mutation

Chuanzhu Yan, Yuying Zhao, Xuebi Xu, 2022, Neurological Sciences.

C-reactive protein for predicting all-cause mortality in patients with acute ischemic stroke: a meta-analysis

Xuebi Xu, Lufei Shao, Ping Yang, 2019, Bioscience reports.

ETFDH Mutations and Flavin Adenine Dinucleotide Homeostasis Disturbance Are Essential for Developing Riboflavin‐Responsive Multiple Acyl–Coenzyme A Dehydrogenation Deficiency

Fuchen Liu, Dandan Zhao, P. Lin, 2018, Annals of neurology.

Bezafibrate Rescues Mitochondrial Encephalopathy in Mice via Induction of Daily Torpor and Hypometabolic State

Chuanzhu Yan, Yuying Zhao, Rui Zheng, 2022, Neurotherapeutics.

A mitochondrial myopathy-associated tRNASer(UCN) 7453G>A mutation alters tRNAmetabolismand mitochondrial function.

Fuchen Liu, Dandan Zhao, Chuanzhu Yan, 2020, Mitochondrion.

A novel m.11406T>A mutation in mitochondrial ND4 gene causes MELAS Syndrome.

Fuchen Liu, Dandan Zhao, Chuanzhu Yan, 2020, Mitochondrion.

Leber hereditary optic neuropathy and dystonia overlapping mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes due to m.14459G>A mutation

Jian-Qiang Lu, Chuanzhu Yan, Yuying Zhao, 2021, Neurological Sciences.

MELAS-associated m.5541C>T mutation caused instability of mitochondrial tRNATrp and remarkable mitochondrial dysfunction

Chuanzhu Yan, Chen Zhang, Wei Li, 2020, Journal of Medical Genetics.

A different pattern of clinical, muscle pathology and brain MRI findings in MELAS with mt‐ND variants

Yuan Sun, Fuchen Liu, Dandan Zhao, 2023, Annals of clinical and translational neurology.

Late-onset mitochondrial disease in a patient with MELAS and mitochondrial DNA T14487C mutation

Wei Li, Yuying Zhao, Shu Zhang, 2019, Chinese Medical Journal.

Reversible cerebral artery constriction accompanied with stroke-like episode in MELAS: A case series

Chuanzhu Yan, Yuying Zhao, Xuebi Xu, 2022, Journal of the Neurological Sciences.