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1دورية أكاديمية
المؤلفون: Miao Zhao, Hui-Zhen Su, Yi-Heng Zeng, Yuan Sun, Xin-Xin Guo, Yun-Lu Li, Chong Wang, Zhi-Yuan Zhao, Xue-Jing Huang, Kai-Jun Lin, Zi-Ling Ye, Bi-Wei Lin, Shunyan Hong, Jitan Zheng, Yao-Bin Liu, Xiang-Ping Yao, Dehao Yang, Ying-Qian Lu, Hai-Zhu Chen, Erwei Zuo, Guang Yang, Hong-Tao Wang, Chen-Wei Huang, Xiao-Hong Lin, Zhidong Cen, Lu-Lu Lai, Yan-Ke Zhang, Xi Li, Tianmin Lai, Jingjing Lin, Dan-Dan Zuo, Min-Ting Lin, Chia-Wei Liou, Qing-Xia Kong, Chuan-Zhu Yan, Zhi-Qi Xiong, Ning Wang, Wei Luo, Cui-Ping Zhao, Xuewen Cheng, Wan-Jin Chen
المصدر: Cell Discovery, Vol 8, Iss 1, Pp 1-17 (2022)
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2056-5968
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2دورية أكاديمية
المؤلفون: Lu‐Lu Lai, Yi‐Jun Chen, Yun‐Lu Li, Xiao‐Hong Lin, Meng‐Wen Wang, En‐Lin Dong, Ning Wang, Wan‐Jin Chen, Xiang Lin
المصدر: Annals of Clinical and Translational Neurology, Vol 7, Iss 10, Pp 1862-1869 (2020)
مصطلحات موضوعية: Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571, Neurology. Diseases of the nervous system, RC346-429
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2328-9503
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3دورية أكاديمية
المؤلفون: Yi-Heng Zeng, Bi-Wei Lin, Hui-Zhen Su, Xin-Xin Guo, Yun-Lu Li, Lu-Lu Lai, Wan-Jin Chen, Miao Zhao, Xiang-Ping Yao
المصدر: Frontiers in Genetics, Vol 12 (2021)
مصطلحات موضوعية: primary familial brain calcification, MYORG, mutations, parkinsonism, phenotype, Genetics, QH426-470
وصف الملف: electronic resource
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4
المؤلفون: Yun‐Lu Li, Wen‐Qi Lv, Yi‐Heng Zeng, Yi‐Kun Chen, Xian‐Long Wang, Kang Yang, Yuan‐Liang Ding, Ru‐Kai Chen, Ning Wang, Wan‐Jin Chen
المصدر: Movement disorders : official journal of the Movement Disorder SocietyReferences. 37(3)
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5
المؤلفون: Yun-Lu Li, Hui-Zhen Su, Yao Xiangping, Lu-Lu Lai, Miao Zhao, Wan-Jin Chen, Yi-Heng Zeng, Bi-Wei Lin, Xin-Xin Guo
المصدر: Frontiers in Genetics, Vol 12 (2021)
Frontiers in Geneticsمصطلحات موضوعية: Ataxia, phenotype, Neurological disorder, QH426-470, symbols.namesake, medicine, Genetics, Missense mutation, Family history, Genetics (clinical), parkinsonism, Original Research, Dystonia, Sanger sequencing, business.industry, Parkinsonism, primary familial brain calcification, medicine.disease, mutations, symbols, Molecular Medicine, medicine.symptom, MYORG, business, Calcification
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ecf7d561ce2c3ee786bd1bcff3b64b1
https://www.frontiersin.org/articles/10.3389/fgene.2021.732389/full -
6دورية أكاديمية
المؤلفون: Tao Yao, Yun-Lu Lin, Yu-Qing Wu, Xin-Ge Qian, Zhe-Ning Wang, Sang Qian, Ting Jiang, Jing-Chen Liu, Luo-Xiang Fang, Cheng Zhen, Chun-Hui Wu
المصدر: Frontiers in Oncology, Vol 14 (2024)
مصطلحات موضوعية: breast cancer, drug targets, Mendelian randomization, single-nucleotide polymorphism, genetic approaches, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
وصف الملف: electronic resource
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7
المؤلفون: Yi-Heng Zeng, Yi-Jun Chen, Xiang Lin, Zhi-Yuan Zhao, Yun-Lu Li, Hai-Zhu Chen, Yi Lin, Gui-He Li, Xiao-Hong Lin, Lu-Lu Lai, Wan-Jin Chen, Qi-Qi Wang, Ji-Ting Zhu, Ying Fu, Guanghou Shui, Meng-Wen Wang, Sin Man Lam, Ning Wang, Xue-Jing Huang
المصدر: SSRN Electronic Journal.
مصطلحات موضوعية: Clinical trial, medicine.medical_specialty, Evolocumab, business.industry, Informed consent, Internal medicine, PCSK9, medicine, Biomarker (medicine), Prospective cohort study, Institutional review board, business, Adverse effect
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::8a331d21040f78d98dff78bc7b7e6206
https://doi.org/10.2139/ssrn.3569873 -
8
المؤلفون: Lu-Lu Lai, Jie Lin, Jing-Mei Hong, Yun-Lu Li, Kun-Xin Lin, Chong Wang, Ying-Qian Lu, Miao Zhao, Wan-Jin Chen, Ning Wang, Yao Xiangping, Hui-Zhen Su, Xiao-Huan Zou, Xin-Xin Guo, Yi-Heng Zeng
المصدر: Clinical genetics. 96(1)
مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Adolescent, Genotype, PDGFRB, 030105 genetics & heredity, Biology, 03 medical and health sciences, Exon, Young Adult, Basal Ganglia Diseases, Genetics, Coding region, Missense mutation, Humans, Genetic Predisposition to Disease, Copy-number variation, Child, Gene, Genetics (clinical), Alleles, Genetic Association Studies, Aged, Sequence Deletion, PDGFB, Sodium-Phosphate Cotransporter Proteins, Type III, Calcinosis, High-Throughput Nucleotide Sequencing, Neurodegenerative Diseases, Sequence Analysis, DNA, Middle Aged, Pedigree, 030104 developmental biology, Real-time polymerase chain reaction, Phenotype, Female, Xenotropic and Polytropic Retrovirus Receptor, Microsatellite Repeats
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9
المؤلفون: Lu-Lu Lai, Ying-Qian Lu, Shuang Wu, En-Lin Dong, Chong Wang, Ning-Yi Cheng, Jin-Jing Li, Ning Wang, Xin-Xin Guo, Xiang Lin, Zhi-Wei Liu, Yun-Lu Li, Wan-Jin Chen
المصدر: Journal of molecular neuroscience : MN. 65(2)
مصطلحات موضوعية: 0301 basic medicine, Male, RNA Splicing, SMN1, Biology, Compound heterozygosity, Muscular Atrophy, Spinal, 03 medical and health sciences, Cellular and Molecular Neuroscience, Exon, 0302 clinical medicine, Cell Line, Tumor, medicine, Humans, Genetic disorder, Infant, General Medicine, Spinal muscular atrophy, Motor neuron, medicine.disease, SMA, Molecular biology, Survival of Motor Neuron 1 Protein, Exon skipping, nervous system diseases, 030104 developmental biology, medicine.anatomical_structure, HEK293 Cells, Mutation, 030217 neurology & neurosurgery
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10
المؤلفون: Yun-lu Li, Zhen Liu, Da-zhi Wang
المصدر: DEStech Transactions on Engineering and Technology Research.
مصطلحات موضوعية: Engineering, business.industry, 020208 electrical & electronic engineering, 020206 networking & telecommunications, 02 engineering and technology, Least mean squares filter, Active power filter, Control theory, 0202 electrical engineering, electronic engineering, information engineering, Electronic engineering, Harmonic, Current (fluid), business, Voltage
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::cfd13857caa4011f701ac5bb6c018979
https://doi.org/10.12783/dtetr/iceea2016/6641