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1دورية أكاديمية
المؤلفون: Hao Lv, Kunyu Liu, Yulie Xie, Yunfei Wang, Siyuan Chen, Peiqiang Liu, Mengting Guan, Jianchao Cong, Yu Xu
المصدر: European Journal of Medical Research, Vol 29, Iss 1, Pp 1-11 (2024)
مصطلحات موضوعية: Mendelian randomization, Allergic rhinitis, Migraine, Causal relationship, Genetic correlation, Medicine
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2047-783X
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2دورية أكاديمية
المؤلفون: Ziang Gao, Hao Lv, Yunfei Wang, Yulie Xie, Mengting Guan, Yu Xu
المصدر: Molecular Medicine, Vol 29, Iss 1, Pp 1-18 (2023)
مصطلحات موضوعية: Allergic rhinitis, Anxiety and depression-like behavior, TET2, NLRP3/IL-1β, Microglia, Metformin, Therapeutics. Pharmacology, RM1-950, Biochemistry, QD415-436
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1528-3658
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3دورية أكاديمية
المؤلفون: Xander Wang, Yurui Fan, Shan Zhao, Yulie Xie, Hans Von Storch
المصدر: Frontiers in Environmental Science, Vol 10 (2022)
مصطلحات موضوعية: regional climate projections, climate change monitoring, hydrological modeling, climate change impacts and adaptation, climate modeling, Environmental sciences, GE1-350
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Cong Qiu, Chengyan Li, Xiaoyun Tong, Luoyang Dai, Wenda Liu, Yulie Xie, Qimei Zhang, Guohua Yang, Tao Li
المصدر: Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
مصطلحات موضوعية: frameshift mutation, MINI‐gene, NMD, PTC, TSC1, tuberous sclerosis complex, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2324-9269
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5
المؤلفون: Xiaoyun Tong, Yulie Xie, Chengyan Li, Guohua Yang, Wenda Liu, Qimei Zhang, Luoyang Dai, Tao Li, Cong Qiu
المصدر: Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)مصطلحات موضوعية: 0301 basic medicine, Adult, congenital, hereditary, and neonatal diseases and abnormalities, lcsh:QH426-470, frameshift mutation, RNA Splicing, Mutant, tuberous sclerosis complex, 030105 genetics & heredity, Biology, medicine.disease_cause, Tuberous Sclerosis Complex 1 Protein, Frameshift mutation, 03 medical and health sciences, Tuberous Sclerosis, Genetics, medicine, Humans, NMD, Molecular Biology, Gene, Genetics (clinical), Mutation, Messenger RNA, Original Articles, Molecular biology, Nonsense Mediated mRNA Decay, Pedigree, TSC1, lcsh:Genetics, 030104 developmental biology, medicine.anatomical_structure, HEK293 Cells, PTC, RNA splicing, UPF1, Trans-Activators, Female, Original Article, TSC2, MINI‐gene, RNA Helicases, HeLa Cells