Chuanzhu Yan

发表

Distal myopathy due to TCAP variants in four unrelated Chinese patients

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

Autophagic Vacuoles with Sarcolemmal Features Delineate Danon Disease and Related Myopathies

I. Nonaka, I. Nishino, K. von Figura, 2005, Journal of neuropathology and experimental neurology.

Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal Myopathy.

Y. Liang, H. Lv, Wei Zhang, 2020, American journal of human genetics.

Unfolded Protein Response and Activated Degradative Pathways Regulation in GNE Myopathy

Y. Gong, Fuchen Liu, Xuemei Zhang, 2013, PloS one.

Case Report: Two Chinese Infants of Sengers Syndrome Caused by Mutations in AGK Gene

V. Zhang, Chuanzhu Yan, Benzhen Wang, 2021, Frontiers in Pediatrics.

Novel compound heterozygous mutations in the TTN gene: elongation and truncation variants causing limb-girdle muscular dystrophy type 2J in a Han Chinese family

P. Lin, Chuanzhu Yan, Guangyu Wang, 2022, Neurological Sciences.

Apoptosis is suspended in muscle of mitochondrial encephalomyopathies

M. Nakagawa, J. Kira, I. Nonaka, 2002, Acta Neuropathologica.

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

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

Effects of intracerebral hemorrhage and subsequent minimally invasive hematoma aspiration on expression of apoptosisrelated genes in rats.

Chuanzhu Yan, Qianqian Tang, Xianghua Li, 2015, International journal of clinical and experimental pathology.

Accuracy of FGF‐21 and GDF‐15 for the diagnosis of mitochondrial disorders: A meta‐analysis

Chuanzhu Yan, Wei Li, Yuying Zhao, 2020, Annals of clinical and translational neurology.

Dysferlinopathy: mitochondrial abnormalities in human skeletal muscle

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

Serum metabolomic profiling in patients with Alzheimer Disease and Amnestic Mild Cognitive Impairment by GC/MS.

Xiulian Sun, Chuanzhu Yan, Congcong Sun, 2020, Biomedical chromatography : BMC.

A novel deletion mutation in GJB1 causes X‐linked Charcot–Marie–Tooth disease in a Han Chinese family

Y. Gong, C. Shao, Wanling Yang, 2010, Muscle & nerve.

A phase II randomized trial of sodium oligomannate in Alzheimer’s dementia

Wei Chen, Kewei Chen, Y. Guan, 2020, Alzheimer's research & therapy.

Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations

T. Dai, Chuanzhu Yan, Hong-hao Li, 2009, Journal of Neurology, Neurosurgery & Psychiatry.

A novel nonsense variant in MT-CO3 causes MELAS syndrome

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

Apoptotic muscle fiber degeneration in distal myopathy with rimmed vacuoles

I. Nonaka, Chuanzhu Yan, K. Ikezoe, 2000, Acta Neuropathologica.

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.

Mesenchymal stem cells transfer mitochondria into cerebral microvasculature and promote recovery from ischemic stroke.

Chuanzhu Yan, Mengxiong Pan, Liang Guo, 2019, Microvascular research.

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

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

Growth Differentiation Factor 15 Is a Novel Diagnostic Biomarker of Mitochondrial Diseases

Jian-Qiang Lu, Chuanzhu Yan, Wei Li, 2017, Molecular Neurobiology.

Novel PNPLA2 gene mutations in Chinese Han patients causing neutral lipid storage disease with myopathy

Y. Gong, P. Lin, Chuanzhu Yan, 2012, Journal of Human Genetics.

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.

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.

Role of Toll-like receptors and retinoic acid inducible gene I in endogenous production of type I interferon in dermatomyositis

T. Dai, Chuanzhu Yan, Ling Li, 2015, Journal of Neuroimmunology.

Amygdala Abnormalities Are Related to Anxiety in Patients With Sporadic Amyotrophic Lateral Sclerosis

G. Gong, Pei-yan Shan, T. Dai, 2021 .

Juvenile idiopathic inflammatory myopathies with anti‐3‐hydroxy‐3‐methylglutaryl‐coenzyme A reductase antibodies in a Chinese cohort

T. Dai, Chuanzhu Yan, Wei Li, 2021, CNS neuroscience & therapeutics.

Effect of low-dose rituximab treatment on autoimmune nodopathy with anti-contactin 1 antibody

Chuanzhu Yan, Anning Li, Xiao-lin Yu, 2022, Frontiers in Immunology.

A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).

Huili Hu, Y. Gong, C. Shao, 2008, American journal of human genetics.

Role of the chemokine receptors CXCR3, CXCR4 and CCR7 in the intramuscular recruitment of plasmacytoid dendritic cells in dermatomyositis

T. Dai, Chuanzhu Yan, Ling Li, 2018, Journal of Neuroimmunology.

Tcap Deficiency in Zebrafish Leads to ROS Production and Mitophagy, and Idebenone Improves its Phenotypes

P. Lin, Chuanzhu Yan, Guangyu Wang, 2022, Frontiers in Cell and Developmental Biology.

Hypothalamic subregion abnormalities are related to body mass index in patients with sporadic amyotrophic lateral sclerosis

G. Gong, Pei-yan Shan, Yuan Sun, 2021, Journal of Neurology.

CMAP decrement by low-frequency repetitive nerve stimulation in different hand muscles of ALS patients

Chuanzhu Yan, Yuying Zhao, Lili Cao, 2019, Neurological Sciences.

Reversible Neuropsychiatric Disturbances Caused by Nitrous Oxide Toxicity: Clinical, Imaging and Electrophysiological Profiles of 21 Patients with 6–12 Months Follow-up

B. Zhao, Yuan Sun, Fuchen Liu, 2020, Neuropsychiatric disease and treatment.

Novel SEPN1 Mutations in Exon 1 Are Common in Rigid Spine With Muscular Dystrophy Type 1 in Chinese Patients

Zhaoxia Wang, Yun Yuan, C. Que, 2022, Frontiers in Genetics.

Amygdala abnormalities across disease stages in patients with sporadic amyotrophic lateral sclerosis

Pei-yan Shan, T. Dai, P. Lin, 2022, Human brain mapping.

Multiple acyl-CoA dehydrogenation deficiency as decreased acyl-carnitine profile in serum

Chuanzhu Yan, Wei Li, Yuying Zhao, 2015, Neurological Sciences.

TGM2 positively regulates myoblast differentiation via enhancing the mTOR signaling.

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

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.

Whole-Genome Linkage Analysis with Whole-Exome Sequencing Identifies a Novel Frameshift Variant in NEFH in a Chinese Family with Charcot-Marie-Tooth 2: A Novel Variant in NEFH for Charcot-Marie-Tooth 2

Shang Gao, Y. Gong, F. Gao, 2018, Neurodegenerative Diseases.

A Chinese case of Susac syndrome mimicking encephalitis

Chuanzhu Yan, Yuying Zhao, Qinzhou Wang, 2017 .

The clinical and histopathological features of idiopathic inflammatory myopathies with asymmetric muscle involvement

Q. Fang, T. Dai, Chuanzhu Yan, 2019, Journal of Clinical Neuroscience.

Revisiting Pathological Classification Criteria for Adult Idiopathic Inflammatory Myopathies: In-Depth Analysis of Muscle Biopsies and Correlation Between Pathological Diagnosis and Clinical Manifestations

Jian-Qiang Lu, T. Dai, Chuanzhu Yan, 2018, Journal of neuropathology and experimental neurology.

Expression of adenosine receptors in muscle tissues from patients with idiopathic inflammatory myopathies

Fuchen Liu, Chuanzhu Yan, Hong-hao Li, 2016 .

Neutral lipid storage disease with myopathy in China: a large multicentric cohort study

Wei Zhang, Zhaoxia Wang, Yun Yuan, 2019, Orphanet Journal of Rare Diseases.

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.

Characteristics of Pompe disease in China: a report from the Pompe registry

Zhaoxia Wang, Xuefan Gu, Chuanzhu Yan, 2019, Orphanet Journal of Rare Diseases.

Indole-3-acetic acid improves the hepatic mitochondrial respiration defects by PGC1a up-regulation.

Xiao-dong Zhang, Chuanzhu Yan, Qingsong Fu, 2022, Cellular signalling.

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

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

Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency

P. Lin, Chuanzhu Yan, S. Luo, 2014, Journal of Inherited Metabolic Disease.

Increased intra-mitochondrial lipofuscin aggregates with spherical dense body formation in mitochondrial myopathy

M. Tarnopolsky, T. Hawke, Jian-Qiang Lu, 2020, Journal of the Neurological Sciences.

A novel mutation in HINT1 gene causes autosomal recessive axonal neuropathy with neuromyotonia, effective treatment with carbamazepine and review of the literature

P. Lin, Chuanzhu Yan, Guangyu Wang, 2022, Acta Neurologica Belgica.

Clinicopathologic Profiles of Sporadic Late-Onset Nemaline Myopathy

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

Identification of miRNA, lncRNA and mRNA-associated ceRNA networks and potential biomarker for MELAS with mitochondrial DNA A3243G mutation

Wei Li, Wei Wang, Wei Li, 2017, Scientific Reports.

Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients

Yun Yuan, Ning Wang, T. Toda, 2020, Clinical genetics.

Molecular landscape of DYSF mutations in dysferlinopathy: From a Chinese multicenter analysis to a worldwide perspective

H. Lv, Wei Zhang, Zhaoxia Wang, 2021, Human mutation.

Efficacy and safety of rituximab treatment in patients with idiopathic inflammatory myopathies: A systematic review and meta-analysis

T. Dai, Chuanzhu Yan, Chao Zhen, 2022, Frontiers in Immunology.

A novel congenital myopathy with apoptotic changes

I. Nonaka, K. Nihei, N. Minami, 2000, Annals of neurology.

Mesenchymal stem cells rescue injured endothelial cells in an in vitro ischemia-reperfusion model via tunneling nanotube like structure-mediated mitochondrial transfer.

Huixia Lu, Pei-yan Shan, Kaiming Liu, 2014, Microvascular research.

Tacrolimus in the treatment of myasthenia gravis in patients with an inadequate response to glucocorticoid therapy: randomized, double-blind, placebo-controlled study conducted in China

H. Shang, B. Bu, Q. Fang, 2017, Therapeutic advances in neurological disorders.

Identification of IFRD1 variant in a Han Chinese family with autosomal dominant hereditary spastic paraplegia associated with peripheral neuropathy and ataxia

P. Lin, Chuanzhu Yan, Guangrun Xu, 2018, Journal of Human Genetics.

The CGG repeat expansion in RILPL1 is associated with oculopharyngodistal myopathy type 4.

H. Lv, Wei Zhang, Zhaoxia Wang, 2022, American journal of human genetics.

The GGC repeat expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy type 3

H. Lv, Wei Zhang, Zhaoxia Wang, 2021, Brain : a journal of neurology.

Molecular landscape of CAPN3 mutations in limb-girdle muscular dystrophy type R1: from a Chinese multicentre analysis to a worldwide perspective

H. Lv, Wei Zhang, Zhaoxia Wang, 2020, Journal of Medical Genetics.

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.

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.

MERRF/MELAS overlap syndrome due to the m.3291T>C mutation

Chuanzhu Yan, Hui Zhao, K. Ji, 2014, Metabolic Brain Disease.

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

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

The clinical and myopathological features of oculopharyngodistal myopathy in a Chinese family

Yun Yuan, Chuanzhu Yan, Weiping Sun, 2008, Neuropathology : official journal of the Japanese Society of Neuropathology.

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

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

Response to Eura et al.

H. Lv, Wei Zhang, Zhaoxia Wang, 2022, American journal of human genetics.

Gasdermine E-Dependent Mitochondrial Pyroptotic Pathway in Dermatomyositis: A Possible Mechanism of Perifascicular Atrophy.

T. Dai, Chuanzhu Yan, Ling Li, 2020, Journal of neuropathology and experimental neurology.

Neuroinflammation and cell therapy for Parkinson's disease.

Chuanzhu Yan, Feng Li, Chengyuan Wu, 2011, Frontiers in bioscience.

Clinical, pathological and genetic characteristics of autosomal dominant inherited dynamin 2 centronuclear myopathy.

Chuanzhu Yan, Xinhong Liu, Huamin Wu, 2016, Molecular medicine reports.

Clinical, pathological and genetic characteristics of autosomal dominant inherited dynamin 2 centronuclear myopathy.

Chuanzhu Yan, Xinhong Liu, Huamin Wu, 2016, Molecular medicine reports.

Somatic and germinal mosaicism in a Han Chinese family with laminopathies

P. Lin, Chuanzhu Yan, Guangyu Wang, 2022, European Journal of Human Genetics.

Agrypnia excitata and obstructive apnea in a patient with fatal familial insomnia from China

Y. Liu, Chuanzhu Yan, Guoyong Jia, 2017, 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.

Metabolic disorder and intestinal microflora dysbiosis in chronic inflammatory demyelinating polyradiculoneuropathy

Jinxiang Han, Guangxiang Cao, Yazhou Cui, 2023, Cell & Bioscience.

Idiopathic inflammatory myopathies with anti-mitochondrial antibodies: Clinical features and treatment outcomes in a Chinese cohort

Yuan Sun, T. Dai, Chuanzhu Yan, 2019, Neuromuscular Disorders.

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.

Idebenone protects against oxidized low density lipoprotein induced mitochondrial dysfunction in vascular endothelial cells via GSK3β/β-catenin signalling pathways.

Y. Gong, P. Lin, Chuanzhu Yan, 2015, Biochemical and biophysical research communications.

Reduced Serum Level of Interleukin-10 is Associated with Cerebral Infarction: A Case-Control and Meta-Analysis Study

Yifei Zhu, Haiqing Yang, Chuanzhu Yan, 2015, Molecular Neurobiology.

Hypertension modifies the short-term effects of temperature on morbidity of hemorrhagic stroke.

Hualiang Lin, Chuanzhu Yan, Wei Li, 2017, The Science of the total environment.

Idebenone Protects against Atherosclerosis in Apolipoprotein E-Deficient Mice Via Activation of the SIRT3-SOD2-mtROS Pathway

Fuchen Liu, Xiaoqing Lv, Wei Jiang, 2020, Cardiovascular Drugs and Therapy.

Mutation in CUL4B, which encodes a member of cullin-RING ubiquitin ligase complex, causes X-linked mental retardation.

Xiyu Zhang, Y. Gong, C. Shao, 2007, American journal of human genetics.

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

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

“Myo-neuropathy” is commonly associated with mitochondrial tRNALysine mutation

Fuchen Liu, Chuanzhu Yan, Wei Li, 2020, Journal 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.

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.

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.

Unique genotype-phenotype correlations within LAMA2-related limb girdle muscular dystrophy in Chinese patients

Yun Yuan, Xiuli Huang, Hui Xiong, 2023, Frontiers in Neurology.

Polyglucosan bodies in intramuscular nerves: Association with muscle fiber denervation atrophy

D. Zochodne, Jian-Qiang Lu, Chuanzhu Yan, 2016, Journal of the Neurological Sciences.

Anti-HMGCR myopathy overlaps with dermatomyositis-like rash: a distinct subtype of idiopathic inflammatory myopathy

G. Norman, Jian-Qiang Lu, T. Dai, 2021, Journal of Neurology.

Late-Onset Leukodystrophy Mimicking Hereditary Spastic Paraplegia without Diffuse Leukodystrophy on Neuroimaging

Chuanzhu Yan, Yuying Zhao, Lingyi Chi, 2021, Neuropsychiatric disease and treatment.

Correlation between depression and quality of life in patients with Parkinson's disease

Yanyan Jiang, Haibo Chen, Chuanzhu Yan, 2021, Clinical Neurology and Neurosurgery.

Adult-onset Krabbe disease in two generations of a Chinese family.

Xiuhe Zhao, P. Lin, Chuanzhu Yan, 2018, Annals of translational medicine.

NDT_A_296424 1451..1458

Chuanzhu Yan, Yuying Zhao, Lingyi Chi, 2021 .

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.

Migratory Rolandic Encephalopathy Caused by the Mitochondrial ND3 Variant

H. Ren, Xiuhe Zhao, Chuanzhu Yan, 2021, Neurology.

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.

Anti-rituximab antibodies in patients with refractory autoimmune nodopathy with anti-neurofascin-155 antibody

Wei Li, Chuanzhu Yan, Wei Li, 2023, Frontiers in Immunology.

Clinical and molecular genetic analysis in Chinese patients with distal myopathy with rimmed vacuoles

T. Liu, Y. Gong, Fuchen Liu, 2011, Journal of Human Genetics.

Hippocampal subfield and anterior-posterior segment volumes in patients with sporadic amyotrophic lateral sclerosis

G. Gong, B. Zhao, Pei-yan Shan, 2021, NeuroImage: Clinical.

Neurogenic Muscle Biopsy Findings Are Common in Mitochondrial Myopathy.

M. Tarnopolsky, Jian-Qiang Lu, Chuanzhu Yan, 2019, Journal of neuropathology and experimental neurology.

Fluctuating ataxia caused by mitochondrial tRNA (Lys) gene m.8363G > A variant

Chuanzhu Yan, K. Ji, Bing Zhao, 2022, Neurological Sciences.

Aspirin plus Clopidogrel as Secondary Prevention after Stroke or Transient Ischemic Attack: A Systematic Review and Meta-Analysis

Chuanzhu Yan, Qinghua Zhang, Jincun Li, 2014, Cerebrovascular Diseases.

DNM2 mutations in Chinese Han patients with centronuclear myopathy

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

Reduced Serum Level of Interleukin-10 is Associated with Cerebral Infarction: A Case-Control and Meta-Analysis Study

Yifei Zhu, Haiqing Yang, Chuanzhu Yan, 2016, Molecular Neurobiology.

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.

Aberrant mRNA processing caused by splicing mutations in TTN-related neuromuscular disorders

P. Lin, Chuanzhu Yan, Guangyu Wang, 2023, Journal of Human Genetics.

Exon skipping caused by splicing mutation in TNNT1 nemaline myopathy

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

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

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

Twinkle mutations in two Chinese families with autosomal dominant progressive external ophthalmoplegia

P. Lin, Chuanzhu Yan, Yuying Zhao, 2014, Neurological Sciences.

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

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

A female carrier of spinal and bulbar muscular atrophy diagnosed with DNAJB6-related distal myopathy

Hongzhi Geng, P. Lin, Chuanzhu Yan, 2022, Journal of human genetics.

A female carrier of spinal and bulbar muscular atrophy diagnosed with DNAJB6-related distal myopathy

Hongzhi Geng, P. Lin, Chuanzhu Yan, 2022, Journal of Human Genetics.

Posterior reversible encephalopathy in a pregnant woman without preeclampsia or eclampsia: A case report

Yi Zhang, Chuanzhu Yan, Cuiping Zhao, 2022, Medicine.

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.

CD8/MHC-I Complex is Specific but Not Sensitive for the Diagnosis of Polymyositis

Wei Li, W. Li, T. Dai, 2010, The Journal of international medical research.

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.

Shedding Light on Lysosomal Malondialdehyde Affecting Vitamin B12 Transport during Cerebral Ischemia/Reperfusion Injury.

Ping Li, Xin Wang, Zhenzhen Liu, 2023, Journal of the American Chemical Society.

Defect in degradation of glycogenin-exposed residual glycogen in lysosomes is the fundamental pathomechanism of Pompe disease.

Fuchen Liu, Chuanzhu Yan, Na Zhang, 2024, The Journal of pathology.

Myofascial edema of gastrocnemius: A prominent MRI characteristic in dermatomyositis patients with anti‐transcriptional intermediate factor 1‐γ antibody

T. Dai, Chuanzhu Yan, Ying Hou, 2024, CNS neuroscience & therapeutics.

A case report of long-delayed diagnosis of pseudorabies virus encephalitis with endophthalmitis: lessons from metagenomic next generation sequencing

Chuanzhu Yan, Ling Li, Bing Liang, 2023, BMC Neurology.

CMAP decrement by low-frequency repetitive nerve stimulation in different hand muscles of ALS patients

Chuanzhu Yan, Yuying Zhao, Lili Cao, 2019, Neurological Sciences.

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

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

Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG42) caused by SLC33A1 mutation in a Chinese kindred

Y. Gong, C. Shao, P. Lin, 2010, Prenatal diagnosis.

Distinctive metabolic remodeling in TYMP deficiency beyond mitochondrial dysfunction

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

[Retracted] Clinical, pathological and genetic characteristics of autosomal dominant inherited dynamin 2 centronuclear myopathy.

Chuanzhu Yan, Huamin Wu, Jian Gong, 2016, Molecular medicine reports.

Choroid plexus enlargement in amyotrophic lateral sclerosis patients and its correlation with clinical disability and blood-CSF barrier permeability

T. Dai, P. Lin, Chuanzhu Yan, 2024, Fluids and barriers of the CNS.

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.

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, 2013, NeuroMolecular Medicine.

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.