Jinfan Zheng

发表

Skeletal muscle increases FGF21 expression in mitochondrial disorders to compensate for energy metabolic insufficiency by activating the mTOR-YY1-PGC1α pathway.

Chuanzhu Yan, Jingwen Xu, Wei Li, 2015, Free radical biology & medicine.

Increased muscle coenzyme Q10 in riboflavin responsive MADD with ETFDH gene mutations due to secondary mitochondrial proliferation.

Y. Gong, P. Lin, Chuanzhu Yan, 2013, Molecular genetics and metabolism.

Cleavage of potassium channel Kv2.1 by BACE2 reduces neuronal apoptosis

Fuchen Liu, Xiulian Sun, Weihong Song, 2018, Molecular Psychiatry.

Clinical and diagnostic features of anti‐neurofascin‐155 antibody‐positive neuropathy in Han Chinese

Chuanzhu Yan, Y. Shan, Wei Li, 2022, Annals of clinical and translational neurology.

Muscle injury induced by different types of contractions in dystrophic mdx mice

Wen-bo Bi, Chuanzhu Yan, Wei Li, 2012, Journal of Muscle Research and Cell Motility.

Oculopharyngeal Muscular Dystrophy: Phenotypic and Genotypic Studies in a Chinese Population

Yun Yuan, P. Lin, Chuanzhu Yan, 2014, NeuroMolecular Medicine.

Muscle injury induced by different types of contractions in dystrophic mdx mice

Wen-bo Bi, Chuanzhu Yan, Wei Li, 2012, Journal of Muscle Research and Cell Motility.

A novel Kir2.6 mutation associated with hypokalemic periodic paralysis

Fuchen Liu, P. Lin, Chuanzhu Yan, 2016, Clinical Neurophysiology.

Novel Mitochondrial C15620A Variant may Modulate the Phenotype of Mitochondrial G11778A Mutation in a Chinese Family with Leigh Syndrome

Fuchen Liu, Chuanzhu Yan, Yuying Zhao, 2014, NeuroMolecular Medicine.

Nickel-Atom Doping as a Potential Means to Enhance the Photoluminescence Performance of Carbon Dots

Zhongqi Sun, Fucheng Gao, Yanyan Jiang, 2023, Molecules.

Novel PANK2 gene mutations in two Chinese siblings with atypical pantothenate kinase-associated neurodegeneration

P. Lin, Chuanzhu Yan, Jun Zhu, 2013, Neurological Sciences.