Yanmin Song

发表

Genetically proxied gut microbiota, gut metabolites with risk of epilepsy and the subtypes: A bi-directional Mendelian randomization study

L. Long, Yan-min Song, Zhuanyi Yang, 2022, Frontiers in Molecular Neuroscience.

Neurological complications and risk factors of cardiopulmonary failure of EV-A71-related hand, foot and mouth disease

Li Feng, B. Xiao, K. Luo, 2016, Scientific Reports.

DNA methyltransferase 3, a target of microRNA-29c, contributes to neuronal proliferation by regulating the expression of brain-derived neurotrophic factor.

S. Pan, Guoshuai Yang, Guohu Weng, 2015, Molecular medicine reports.

Correlation of Seizure Increase and COVID-19 Outbreak in Adult Patients with Epilepsy: Findings and Suggestions from a Nationwide Multi-centre Survey in China

M. Zhang, Li Feng, Chang Zeng, 2021, Seizure.

A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions

K. Xia, Q. Pan, B. Tang, 2003, Epilepsy Research.

The circular RNA 001971/miR-29c-3p axis modulates colorectal cancer growth, metastasis, and angiogenesis through VEGFA

Mu Zhang, Chen Chen, Xiangmin Li, 2020, Journal of experimental & clinical cancer research : CR.

RETRACTED ARTICLE: The circular RNA 001971/miR-29c-3p axis modulates colorectal cancer growth, metastasis, and angiogenesis through VEGFA

C. Chen, Mu Zhang, Xiangmin Li, 2020, Journal of Experimental & Clinical Cancer Research.

Expression levels of TGF-β1 and CTGF are associated with the severity of Duchenne muscular dystrophy

L. Long, Huan Yang, Xinxin Li, 2017, Experimental and therapeutic medicine.

Mutation Detection in Candidate Genes for Benign Familial Infantile Seizures on a Novel Locus

K. Xia, Q. Pan, Zhengmao Hu, 2010, The International journal of neuroscience.

TTTCA Repeat Expansion of SAMD12 in a New Benign Adult Familial Myoclonic Epilepsy Pedigree

B. Xiao, Ying Peng, H. Long, 2020, Frontiers in Neurology.

Genetic analysis in a Chinese BAFME pedigree indicates the possibility of an unidentified locus

Hongyu, Lingqian Wu, B. Xiao, 2016 .

Polymorphism Ala54Thr of Fatty Acid-Binding Protein 2 Gene is Not Associated with Stroke Risk in Han Population of Hunan China

L. Long, Yan-min Song, Yun-hai Liu, 2014, Medical science monitor : international medical journal of experimental and clinical research.

MicroRNA-29c targets β-site amyloid precursor protein-cleaving enzyme 1 and has a neuroprotective role in vitro and in vivo.

S. Pan, Guoshuai Yang, Guohu Weng, 2015, Molecular medicine reports.

MicroRNA-29 c targets β-site amyloid precursor protein-cleaving enzyme 1 and has a neuroprotective role in vitro and in vivo

S. Pan, Guoshuai Yang, Guohu Weng, 2015 .

Adenylate Kinase Fused to Spidroin as a Catalyst for Decreasing Leakage out of 3D-Bioprinted Hydrogels and for ATP Regeneration.

Dongyi Zhang, Lei Wu, Tianhao Hu, 2023, Biomacromolecules.

Altered cerebellar‐cerebral functional connectivity in benign adult familial myoclonic epilepsy

D. Hu, H. Shen, L. Zeng, 2016, Epilepsia.

A case-control proton magnetic resonance spectroscopy study confirms cerebellar dysfunction in benign adult familial myoclonic epilepsy

B. Xiao, H. Long, L. Long, 2015, Neuropsychiatric disease and treatment.

Altered cerebellar‐motor loop in benign adult familial myoclonic epilepsy type 1: The structural basis of cortical tremor

D. Hu, H. Shen, L. Zeng, 2022, Epilepsia.

Gray Matter Loss and Related Functional Connectivity Alterations in A Chinese Family With Benign Adult Familial Myoclonic Epilepsy

D. Hu, H. Shen, L. Zeng, 2015, Medicine.

Shared hippocampal abnormalities in sporadic temporal lobe epilepsy patients and their siblings

S. Vos, M. Koepp, F. Xiao, 2020, Epilepsia.

Shared functional network abnormality in patients with temporal lobe epilepsy and their siblings

F. Chen, F. Xie, Haiyun Tang, 2023, CNS neuroscience & therapeutics.

Spinocerebellar ataxia type 3/Machado-Joseph disease manifested as spastic paraplegia: A clinical and genetic study

L. Long, Ning Zhang, Yanmin Song, 2014, Experimental and Therapeutic Medicine.

[Clinical and mutational analysis of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions].

K. Xia, B. Tang, Ji-feng Guo, 2006, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

ExosomesHBO-based therapy: A promising strategy for therapeutic angiogenesis.

Xiangmin Li, Yanmin Song, Honghua Yang, 2021, International Journal of Cardiology.

Relationship between polymorphism Ser 89 Asn of UTS 2 gene and atherosclerotic cerebral infarction in Chinese Hunan Han population

L. Long, Xiaogang Li, Yan-min Song, 2016 .

Lack of Association of Urotensin II Gene Polymorphism with Atherosclerotic Cerebral Infarction Risk in the Southern Han Population Research

Ning Zhang, Ruoli Tan, Yanmin Song, 2014 .

Inhibitory effects of hydroxysafflor yellow A on PDGF‑BB‑induced proliferation and migration of vascular smooth muscle cells via mediating Akt signaling.

Ning Zhang, Yanmin Song, Lili Long, 2014, Molecular medicine reports.

Hydroxysafflor yellow A inhibits lipopolysaccharide-induced proliferation and migration of vascular smooth muscle cells via Toll-like receptor-4 pathway.

S. Pan, Tao Chen, Yan-min Song, 2015, International journal of clinical and experimental medicine.

Aberrant neuronal synaptic connectivity in CA1 area of the hippocampus from pilocarpine-induced epileptic rats observed by fluorogold.

Li Feng, B. Xiao, H. Long, 2014, International journal of clinical and experimental medicine.

TLR4 rs1927911, but Not TLR2 rs5743708, Is Associated With Atherosclerotic Cerebral Infarction in the Southern Han Population

Ning Zhang, Yanmin Song, Huarong Liu, 2015, Medicine.

TLR 4 rs 1927911 , but Not TLR 2 rs 5743708 , Is Associated With Atherosclerotic Cerebral Infarction in the Southern Han Population ontrol Study

Li-Jan Lo, Yanmin Song, Huarong Liu, 2015 .