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1دورية أكاديمية
المؤلفون: Yang Zhang, Zhixian Ye, Binghua Li, Lan Xie, Jianfeng Zou, Yao Zheng
المصدر: Advances in Aerodynamics, Vol 4, Iss 1, Pp 1-28 (2022)
مصطلحات موضوعية: Riblets control, Drag reduction, Turbulent boundary layer, Large-scale simulation, Engineering (General). Civil engineering (General), TA1-2040, Motor vehicles. Aeronautics. Astronautics, TL1-4050
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2524-6992
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2دورية أكاديمية
المؤلفون: Qianqian Lin, Ying Liu, Zhixian Ye, Jianping Hu, Wenjie Cai, Qiang Weng, Wan-Jin Chen, Ning Wang, Dairong Cao, Yi Lin, Ying Fu
المصدر: Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
مصطلحات موضوعية: Spastic paraplegia, Hereditary, Magnetic resonance imaging, Biomarkers, Sample size, Medicine
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1750-1172
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3دورية أكاديمية
المؤلفون: Fuze Zheng, Long Chen, Liangliang Qiu, Lin Lin, Xin Lin, Qifang He, Lili Wang, Zhixian Ye, Minting Lin, Zhiqiang Wang
المصدر: Stem Cell Research, Vol 60, Iss , Pp 102678- (2022)
مصطلحات موضوعية: Biology (General), QH301-705.5
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Zhiqiang Wang, Liangliang Qiu, Minting Lin, Long Chen, Fuze Zheng, Lin Lin, Feng Lin, Zhixian Ye, Xiaodan Lin, Junjie He, Lili Wang, Xin Lin, Qifang He, Wanjin Chen, Yi Lin, Ying Fu, Ning Wang
المصدر: The Lancet Regional Health. Western Pacific, Vol 18, Iss , Pp 100323- (2022)
مصطلحات موضوعية: FSHD1, Prevalence, Independent ambulation loss, Public aspects of medicine, RA1-1270
وصف الملف: electronic resource
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5دورية أكاديميةCorrection to: Potential markers for sample size estimations in hereditary spastic paraplegia type 5
المؤلفون: Qianqian Lin, Ying Liu, Zhixian Ye, Jianping Hu, Wenjie Cai, Qiang Weng, Wan-Jin Chen, Ning Wang, Dairong Cao, Yi Lin, Ying Fu
المصدر: Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-1 (2021)
مصطلحات موضوعية: Medicine
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1750-1172
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6
المؤلفون: Qiangqiang Guo, Zhixian Ye, Liyang Wang, Liangjun Zhang
المصدر: 2022 IEEE/RSJ International Conference on Intelligent Robots and Systems (IROS).
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::5ba52b7ffaea4cd9e4196be149dbfce1
https://doi.org/10.1109/iros47612.2022.9981220 -
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المؤلفون: Liangliang Qiu, Long Chen, Fuze Zheng, Ying Zheng, Xin Lin, Qifang He, Lin Lin, Lili Wang, Zhixian Ye, Minting Lin, Yi Lin, Ying Fu, Zhi-qiang Wang, Ning Wang
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::89329baf05b32291c0832364a28962fc
https://doi.org/10.21203/rs.3.rs-2006739/v1 -
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المؤلفون: Ruitao Song, Zhixian Ye, Liyang Wang, Tianyi He, Liangjun Zhang
مصطلحات موضوعية: Computer Science::Systems and Control, FOS: Electrical engineering, electronic engineering, information engineering, Systems and Control (eess.SY), Astrophysics::Cosmology and Extragalactic Astrophysics, Electrical Engineering and Systems Science - Systems and Control, GeneralLiterature_MISCELLANEOUS
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0dffdc226d7eb174a3e806a18ae0fd2
http://arxiv.org/abs/2203.08944 -
9
المؤلفون: Hai-Zhu Chen, Min-Ting Lin, Lin Lin, Liangliang Qiu, Guo-Rong Xu, Lili Wang, Feng Lin, Zhixian Ye, Nai-Qing Cai, Xiao-Dan Lin, Ming Jin, Zhi-Qiang Wang, Ning Wang, Jun-Jie He
المصدر: Journal of Medical Genetics. 57:777-785
مصطلحات موضوعية: Adult, Male, musculoskeletal diseases, 0301 basic medicine, Oncology, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Neuromuscular disease, Adolescent, Genotype, Chromosomal translocation, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Disease severity, Internal medicine, Genetics, medicine, Humans, Genetic Association Studies, Genetics (clinical), Aged, Mosaicism, business.industry, Dystrophy, Chromosome, DNA Methylation, Middle Aged, medicine.disease, Muscular Dystrophy, Facioscapulohumeral, Pedigree, Phenotype, 030104 developmental biology, Somatic mosaicism, Cohort, Female, Chromosomes, Human, Pair 4, business, 030217 neurology & neurosurgery
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10
المؤلفون: Min-Ting Lin, Hai-Zhu Chen, Nai-Qing Cai, Zhixian Ye, Ning Wang, Feng Lin, Guo-Rong Xu, Lili Wang, Liangliang Qiu, Ming Jin
المصدر: Neuromuscular Disorders. 30:137-143
مصطلحات موضوعية: Adult, Male, musculoskeletal diseases, 0301 basic medicine, China, Pathology, medicine.medical_specialty, Proximal muscle weakness, Telethonin, Muscle disorder, 03 medical and health sciences, 0302 clinical medicine, medicine, Humans, Connectin, Progressive proximal muscle weakness, Age of Onset, Muscular dystrophy, Muscle, Skeletal, Genetics (clinical), Pelvic girdle, business.industry, Middle Aged, medicine.disease, Magnetic Resonance Imaging, Muscle atrophy, Pedigree, 030104 developmental biology, Muscular Dystrophies, Limb-Girdle, Neurology, Pediatrics, Perinatology and Child Health, Female, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery, Limb-girdle muscular dystrophy