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1دورية أكاديمية
المؤلفون: Young-Keol Cho, Jung-Eun Kim, Jinny Lee
المصدر: Journal of Ginseng Research, Vol 46, Iss 6, Pp 731-737 (2022)
مصطلحات موضوعية: Gross deletion, HIV-1 subtype B, Korean Red Ginseng, Nef gene, Non-B subtypes, Botany, QK1-989
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Hairong Wang, Yang Wan, Yun Yang, Hao Li, Liangwei Mao, Shuyang Gao, Jingjing Xu, Jing Wang
المصدر: BMC Medical Genetics, Vol 20, Iss 1, Pp 1-6 (2019)
مصطلحات موضوعية: Oculocutaneous albinism, OCA2, Non-syndromic, Gross deletion, Targeted NGS, Internal medicine, RC31-1245, Genetics, QH426-470
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Young-Keol Cho, Jung-Eun Kim, Jun-Hee Woo
المصدر: Journal of Ginseng Research, Vol 41, Iss 2, Pp 144-150 (2017)
مصطلحات موضوعية: AIDS/HIV-1, genetic defects, gross deletion, Korean Red Ginseng, nef, Botany, QK1-989
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Wang, HairongAff1, Wan, YangAff2, Yang, YunAff1, Aff3, Li, HaoAff1, Mao, LiangweiAff1, Aff4, Gao, ShuyangAff5, Xu, JingjingAff6, Wang, JingAff6
المصدر: BMC Medical Genetics. 20(1)
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5دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
6دورية أكاديمية
المؤلفون: Wei, Xiao-Feng, Shang, Xuan, He, De-Qin, Huang, Ji-Wei, Zhang, Xin-Hua, Xu, Xiang-Min
المصدر: Annals of Hematology. January 2011 90(1):17-22
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7دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
8
المؤلفون: Jing Wang, Jingjing Xu, Yang Wan, Yun Yang, Liangwei Mao, Shuyang Gao, Hai-rong Wang, Hao Li
المصدر: BMC Medical Genetics, Vol 20, Iss 1, Pp 1-6 (2019)
BMC Medical Geneticsمصطلحات موضوعية: Male, Models, Molecular, 0301 basic medicine, Proband, genetic structures, Protein Conformation, Usher syndrome, Case Report, Gross deletion, 030105 genetics & heredity, medicine.disease_cause, Compound heterozygosity, Sequence Analysis, Protein, Genetics (clinical), Sequence Deletion, Genetics, OCA2, Sanger sequencing, Mutation, Targeted NGS, High-Throughput Nucleotide Sequencing, Exons, Oculocutaneous albinism, Albinism, Oculocutaneous, Myosin VIIa, symbols, Heterozygote, lcsh:Internal medicine, lcsh:QH426-470, Genetic Counseling, Myosins, Biology, 03 medical and health sciences, symbols.namesake, Non-syndromic, Asian People, medicine, Humans, Genetic Predisposition to Disease, lcsh:RC31-1245, Genetic heterogeneity, Infant, Membrane Transport Proteins, medicine.disease, lcsh:Genetics, 030104 developmental biology
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9
المؤلفون: Yanzhou Wang, Bin Mao, Xue Zhang, Xiu Zhi Ren, Yanshan Liu, Yun Guan, Xiuli Zhao, Xingzhu Geng
المصدر: Molecular Pain
مصطلحات موضوعية: 0301 basic medicine, Proband, Male, Adolescent, DNA Mutational Analysis, Alu element, NTRK1, Compound heterozygosity, medicine.disease_cause, Genetic analysis, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, Congenital insensitivity to pain with anhidrosis, Asian People, Gene Frequency, deep intronic mutation, medicine, Humans, Hereditary Sensory and Autonomic Neuropathies, Receptor, trkA, Child, Allele frequency, Gene, Sequence Deletion, Genetics, Mutation, gross deletion, Base Sequence, business.industry, Infant, medicine.disease, Introns, 030104 developmental biology, Anesthesiology and Pain Medicine, Child, Preschool, Molecular Medicine, Female, business, 030217 neurology & neurosurgery, Research Article
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10
المؤلفون: Young-Keol, Cho, Jung-Eun, Kim, Jun-Hee, Woo
المصدر: Journal of Ginseng Research
مصطلحات موضوعية: gross deletion, Korean Red Ginseng, nef, AIDS/HIV-1, Research Article, genetic defects