Dandan Zhao

发表

Distal myopathy due to TCAP variants in four unrelated Chinese patients

Fuchen Liu, Xiaoqing Lv, F. Gao, 2020, neurogenetics.

Dysferlinopathy: mitochondrial abnormalities in human skeletal muscle

Fuchen Liu, Xiulian Sun, Dandan Zhao, 2015, The International journal of neuroscience.

A novel nonsense variant in MT-CO3 causes MELAS syndrome

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

Late-onset Pompe disease with complicated intracranial aneurysm: a Chinese case report

Dandan Zhao, Chuanzhu Yan, Ling Li, 2016, Neuropsychiatric disease and treatment.

Activation of the wnt/β-Catenin Signaling Pathway in Polymyositis, Dermatomyositis and Duchenne Muscular Dystrophy

Fuchen Liu, Dandan Zhao, Chuanzhu Yan, 2016, Journal of clinical neurology.

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.

TGM2 positively regulates myoblast differentiation via enhancing the mTOR signaling.

Fuchen Liu, T. Dai, Dandan Zhao, 2021, Biochimica et biophysica acta. Molecular cell research.

Cerebrotendinous xanthomatosis with peripheral neuropathy: a clinical and neurophysiological study in Chinese population

Dandan Zhao, Chuanzhu Yan, Wei Li, 2020, Annals of translational medicine.

Clinicopathologic Profiles of Sporadic Late-Onset Nemaline Myopathy

B. Zhao, Yuan Sun, Fuchen Liu, 2022, Neurology: Neuroimmunology & Neuroinflammation.

Clinical and molecular genetic analysis of a family with late-onset LAMA2-related muscular dystrophy

Feng Zhang, R. Du, Yuehua Zhang, 2016, Brain and Development.

Novel biallelic mutations in POLG gene: large deletion and missense variant associated with PEO

Fuchen Liu, Dandan Zhao, P. Lin, 2021, Neurological Sciences.

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.

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.

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.

Cylindrical Spirals in Skeletal Muscles Originate From the Longitudinal Sarcoplasmic Reticulum

Jian-Qiang Lu, Dandan Zhao, Wei Li, 2016, Journal of Neuropathology and Experimental Neurology.

DNM2 mutations in Chinese Han patients with centronuclear myopathy

Y. Gong, T. Dai, Dandan Zhao, 2016, Neurological Sciences.

A heterozygous deletion of PDGFB gene causes paroxysmal kinesigenic dyskinesia with primary familial brain calcification.

Dandan Zhao, R. Duan, Chuan-zhu Yan, 2021, Parkinsonism & related disorders.

Clinical, pathological, and molecular genetic analysis of 7 Chinese patients with hereditary myopathy with early respiratory failure

T. Dai, Dandan Zhao, Wei Jiang, 2021, Neurological Sciences.

Exon skipping caused by splicing mutation in TNNT1 nemaline myopathy

Dandan Zhao, P. Lin, Chuanzhu Yan, 2022, Journal of Human Genetics.

Insights into the mechanisms of telbivudine-induced myopathy associated with mitochondrial dysfunction.

Dandan Zhao, P. Lin, Chuanzhu Yan, 2023, Chemico-biological interactions.

Combining idebenone and rosuvastatin prevents atherosclerosis by suppressing oxidative stress and NLRP3 inflammasome activation.

Dandan Zhao, Wei Jiang, P. Lin, 2023, European journal of pharmacology.

A Missense Variant in AIFM1 Caused Mitochondrial Dysfunction and Intolerance to Riboflavin Deficiency.

Fuchen Liu, Dandan Zhao, Chuanzhu Yan, 2023, Neuromolecular medicine.

Establishment of an induced pluripotent stem cell (iPSC) line (INNDSUi001-A) from a healthy female Chinese Han.

Fuchen Liu, Rui Zhang, Dandan Zhao, 2022, Stem cell research.

Lysosomal dysfunction and overload of nucleosides in thymidine phosphorylase deficiency of MNGIE

Dandan Zhao, Chuanzhu Yan, Dongdong Wang, 2024, Journal of translational medicine.

Distinctive metabolic remodeling in TYMP deficiency beyond mitochondrial dysfunction

G. Shui, Fuchen Liu, Xihan Liu, 2023, Journal of Molecular Medicine.

Protein kinase R is highly expressed in dermatomyositis and promotes interferon-beta-induced muscle damage.

T. Dai, Dandan Zhao, Chuanzhu Yan, 2024, Annals of the rheumatic diseases.

Idebenone ameliorates statin-induced myotoxicity in atherosclerotic ApoE-/- mice by reducing oxidative stress and improving mitochondrial function.

Dandan Zhao, P. Lin, Chuanzhu Yan, 2024, Biochimica et biophysica acta. Molecular basis of disease.