يعرض 1 - 10 نتائج من 10 نتيجة بحث عن '"Guangqing Sun"', وقت الاستعلام: 0.90s تنقيح النتائج
  1. 1
    مؤتمر
    Architecture of Intelligent Operation Center for Thermal Power Unit

    المؤلفون: Yaokui, Gao, Haidong, Gao, Lin, Wang, Linjuan, Gong, Wenyu, Wang, Yangxiang, Lei, Jianguo, Wu, Xinbo, Yu, Guangqing, Sun

    المصدر: 2022 IEEE 2nd International Conference on Digital Twins and Parallel Intelligence (DTPI) Digital Twins and Parallel Intelligence (DTPI), 2022 IEEE 2nd International Conference on. :1-4 Oct, 2022

    Relation: 2022 IEEE 2nd International Conference on Digital Twins and Parallel Intelligence (DTPI)

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  2. 2
    دورية أكاديمية
    Whole-exome sequencing for the identification of susceptibility genes of Kashin-Beck disease.

    المؤلفون: Zhenxing Yang, Yu Xu, Hongrong Luo, Xiaohong Ma, Qiang Wang, Yingcheng Wang, Wei Deng, Tao Jiang, Guangqing Sun, Tingting He, Jingchu Hu, Yingrui Li, Jun Wang, Tao Li, Xun Hu

    المصدر: PLoS ONE, Vol 9, Iss 4, p e92298 (2014)

    مصطلحات موضوعية: Medicine, Science

    وصف الملف: electronic resource

    Relation: http://europepmc.org/articles/PMC4002427?pdf=render; https://doaj.org/toc/1932-6203

    URL الوصول: https://doaj.org/article/12c620063a4349258dd2f675ffa79c86

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  3. 3
    A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes

    المؤلفون: Nikolaj T. Krarup, Thorfinn Sand Korneliussen, Jumana Y. Al-Aama, Anette P. Gjesing, Knut Borch-Johnsen, Niels Grarup, Xin Jin, Allan Linneberg, Torben Hansen, Jonas T. Treebak, Ida Moltke, Jun Wang, Xueli Wu, Marianne A. Andersen, Oluf Pedersen, Anders Albrechtsen, Peter Bjerregaard, Juleen R. Zierath, Marit E. Jørgensen, Rasmus Nielsen, Guangqing Sun, Thomas Nielsen, Matteo Fumagalli

    المصدر: Moltke, I, Grarup, N, Jørgensen, M E, Bjerregaard, P, Treebak, J T, Fumagalli, M, Korneliussen, T S, Andersen, M A, Nielsen, T S, Krarup, N T, Gjesing, A P, Zierath, J R, Linneberg, A, Wu, X, Sun, G, Jin, X, Al-Aama, J, Wang, J, Borch-Johnsen, K, Pedersen, O, Nielsen, R, Albrechtsen, A & Hansen, T 2014, ' A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes ', Nature, vol. 512, no. 7513, pp. 190–193 . https://doi.org/10.1038/nature13425

    مصطلحات موضوعية: Adult, Blood Glucose, medicine.medical_specialty, Genotype, Glucose uptake, Greenland, Population, Type 2 diabetes, Biology, Impaired glucose tolerance, Insulin resistance, Gene Frequency, Diabetes mellitus, Internal medicine, medicine, Humans, Insulin, Muscle, Skeletal, education, education.field_of_study, Multidisciplinary, GTPase-Activating Proteins, Glucose transporter, Genetic Variation, Middle Aged, medicine.disease, Endocrinology, Diabetes Mellitus, Type 2, Codon, Nonsense, biology.protein, Insulin Resistance, GLUT4, Genome-Wide Association Study

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad993ecfdb4f468726c2ff24d7a654e8
    https://doi.org/10.1038/nature13425

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  4. 4
    Exome sequencing identified a missense mutation ofEPS8L3in Marie Unna hereditary hypotrichosis

    المؤلفون: Qibin Li, Yingrui Li, Xianfa Tang, Huayang Tang, Xiaodong Zheng, Yong Cui, Pei-Guang Wang, Jun Wang, Yuan Liu, Liangdan Sun, Ping Li, Hui Cheng, Min Li, Jun Zhu, Jian Wang, Guangqing Sun, Sen Yang, Li-Qiong Cai, Tao Jiang, Xin Zhang, Bi-Rong Guo, Xu Yang, Min Gao, Jing-Chu Hu, Xianbo Zuo, Jianjun Liu, Xuejun Zhang, Gang Chen

    المصدر: Journal of medical genetics, vol 49, iss 12
    Journal of Medical Genetics

    مصطلحات موضوعية: Male, Genotype, DNA Mutational Analysis, Mutation, Missense, Locus (genetics), Biology, Hypotrichosis, Medical and Health Sciences, symbols.namesake, Exome Sequencing, Genetics, medicine, Humans, Missense mutation, Exome, Genetics (clinical), Exome sequencing, Adaptor Proteins, Signal Transducing, Genetics & Heredity, Sanger sequencing, Base Sequence, Genetic heterogeneity, Signal Transducing, New Loci, Adaptor Proteins, Biological Sciences, medicine.disease, Molecular biology, Marie Unna Hereditary Hypotrichosis, Pedigree, Mutation, symbols, Female, Marie Unna hereditary hypotrichosis, Missense

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7cbe0d54a75e0b42d9018dbfb5249f7
    https://doi.org/10.1136/jmedgenet-2012-101134

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  5. 5
    Exome sequencing identifies MVK mutations in disseminated superficial actinic porokeratosis

    المؤلفون: Ping Li, Yantao Ding, Xuejun Zhang, Jinping Gao, Liangdan Sun, Min Li, Kun Xia, You-Wen Zhou, Xin Zhang, Bo Liang, Jian Wang, Pan Li, Yuan Liu, Yingrui Li, Wen Wang, Xiaodong Zheng, Ming Zeng, Ke Yang, Pei-Guang Wang, Jianjun Liu, Tingting He, Jun Zhu, Sheng-Quan Zhang, Bi-Rong Guo, Hui Li, Gang Chen, Fusheng Zhou, Jingchu Hu, Jun-Sheng Hou, Guangqing Sun, Hui Cheng, Xing Fan, Xin Hu, Xianyong Yin, Yujun Sheng, Huanming Yang, Feng-Li Xiao, Xiang-Feng Yuan, Sen Yang, Shi-Xiang Zhao, Wei-Dong Du, Yu-Juan Zhai, Tao Jiang, Zhen-Ying Wang, Jun Wang, Zhong-Yi Yu, Zheng-Mao Hu, Li Zhang, Songke Shen, Wei-Wei Ha, Huayang Tang, Wen Ju Wang, Hui-Feng Zhang, Yong Cui, Bao-Yu Wu, Yu Xu, Xianfa Tang, Jian-Bo Wang, Yang Li, Yunqing Ren, Jing Wang, Shengcai Wei, Min Gao, Fang-Fang Qian, Jie Wang, Xianbo Zuo, Shengxiu Liu

    المصدر: Nature Genetics. 44:1156-1160

    مصطلحات موضوعية: Keratinocytes, Male, Candidate gene, DNA Mutational Analysis, Apoptosis, Disseminated superficial actinic porokeratosis, symbols.namesake, Genetics, medicine, Humans, Point Mutation, Exome, 1000 Genomes Project, Cells, Cultured, Genetic Association Studies, Exome sequencing, Cell Proliferation, Sanger sequencing, biology, Point mutation, Mevalonate kinase, Cell Differentiation, medicine.disease, Pedigree, Porokeratosis, Phosphotransferases (Alcohol Group Acceptor), Case-Control Studies, symbols, biology.protein, Female, RNA Splice Sites

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1be35a7df88956b14b72b643bd5c609
    https://doi.org/10.1038/ng.2409

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  6. 6
    Excess of rare variants in genes that are key epigenetic regulators of spermatogenesis in the patients with non-obstructive azoospermia

    المؤلفون: Xiao Liu, Guangwu Guo, Zheguang Lin, Tao Jiang, Chengliang Dong, Qiang Feng, Jingxiao Lu, Jian Wang, Guangqing Sun, Wei Zhao, Chengliang Xiong, Jun Wang, Yingrui Li, Tingting He, Yaoting Gui, Zesong Li, Shengjie Gao, Jun Xie, Song Wu, Yu Xu, Yong Zeng, Lisha Mou, Huanming Yang, Xiaojuan Sun, Weiping Qian, Zhiming Cai, Jingchu Hu, Xiuqing Zhang, Honggang Li, Qunlong Liu, Aifa Tang, Yi Huang

    المصدر: Scientific reports, vol 5, iss 1
    Scientific Reports

    مصطلحات موضوعية: Genetic Markers, Male, Epigenomics, DNMT3B, Biology, Bioinformatics, Article, Male infertility, Epigenesis, Genetic, Genetic, Gene Frequency, Clinical Research, Genetic variation, medicine, Genetics, 2.1 Biological and endogenous factors, Humans, Gene Regulatory Networks, Epigenetics, Genetic Testing, Allele, Spermatogenesis, Alleles, Genetic testing, Azoospermia, Multidisciplinary, medicine.diagnostic_test, Gene Expression Profiling, Human Genome, Genetic Variation, medicine.disease, Infertility, Biotechnology, Epigenesis

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a9b08db16d46a0d290b2f67b460a911
    https://escholarship.org/uc/item/9b40w69k

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  7. 7
    Control System Based on PLC for Winding Machine

    المؤلفون: Mei Wang, Wei Mo, Jzau-Sheng Lin, Hongyang Zan, Guangqing Sun

    المصدر: 2014 International Symposium on Computer, Consumer and Control.

    مصطلحات موضوعية: Engineering, Winding machine, business.industry, Circuit design, Computation, Control engineering, Servomechanism, Impulse (physics), Servomotor, law.invention, law, Control system, Software design, business

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::4e29a9bf3e0830c25702d47da793d122
    https://doi.org/10.1109/is3c.2014.31

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  8. 8
    Whole-exome sequencing for the identification of susceptibility genes of Kashin-Beck disease

    المؤلفون: Guangqing Sun, Yingrui Li, Xun Hu, Hongrong Luo, Tao Jiang, Yingcheng Wang, Jingchu Hu, Tao Li, Yu Xu, Wei Deng, Xiaohong Ma, Qiang Wang, Jun Wang, Tingting He, Zhenxing Yang

    المساهمون: Palmer, Nicholette D

    المصدر: PLoS ONE
    PLoS ONE, Vol 9, Iss 4, p e92298 (2014)
    PloS one, vol 9, iss 4

    مصطلحات موضوعية: Male, Genotyping Techniques, lcsh:Medicine, Medicine and Health Sciences, 2.1 Biological and endogenous factors, Exome, Genome Sequencing, Aetiology, lcsh:Science, Exome sequencing, Genetics, Kashin-Beck Disease, Multidisciplinary, Transmission disequilibrium test, Genomics, Middle Aged, Asians, Female, Sequence Analysis, Biotechnology, Research Article, Asian Continental Ancestry Group, Adult, Adolescent, General Science & Technology, Immunology, Single-nucleotide polymorphism, Biology, Autoimmune Disease, Autoimmune Diseases, Young Adult, Genetic, Asian People, Rheumatology, medicine, Humans, Genetic Predisposition to Disease, Genetic Testing, KEGG, Polymorphism, Sports and Exercise Medicine, Molecular Biology Techniques, Sequencing Techniques, Molecular Biology, Aged, Clinical Genetics, Kashin–Beck disease, Evolutionary Biology, Polymorphism, Genetic, Arthritis, Inflammatory and immune system, Human Genome, lcsh:R, Biology and Life Sciences, Computational Biology, medicine.disease, Actin cytoskeleton, Case-Control Studies, Genetic Polymorphism, lcsh:Q, Clinical Immunology, Population Genetics

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15734e7e5110331dbcb6f1202179a115
    https://pubmed.ncbi.nlm.nih.gov/24776925

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  9. 9
    دورية أكاديمية
    Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing.

    المؤلفون: O'Rawe, Jason, Tao Jiang, Guangqing Sun, Yiyang Wu, Wei Wang, Jingchu Hu, Bodily, Paul, Lifeng Tian, Hakonarson, Hakon, Johnson, W. Evan, Zhi Wei, Kai Wang, Lyon, Gholson J.

    المصدر: Genome Medicine; 2013, Vol. 5 Issue 3, p1-18, 18p, 1 Diagram, 3 Charts, 4 Graphs

    مصطلحات موضوعية: GENOMES, GENOMICS, SINGLE nucleotide polymorphisms, FAMILIES, COMPUTER software, MEDICAL research

    Find this article in full text from Springer Verlag. Full Text Finder
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  10. 10
    Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing

    المؤلفون: Tao Jiang, Kai Wang, Lifeng Tian, Gholson J. Lyon, Jason O'Rawe, Jingchu Hu, Wei Min Wang, W. Evan Johnson, Hakon Hakonarson, Zhi Wei, Yiyang Wu, Guangqing Sun, Paul Bodily

    المصدر: Genome medicine, vol 5, iss 3
    Genome Medicine

    مصطلحات موضوعية: Whole genome sequencing, Genetics, 0303 health sciences, Research, Clinical Sciences, Genomics, Biology, Genome, Human genetics, DNA sequencing, 3. Good health, 03 medical and health sciences, 0302 clinical medicine, 030220 oncology & carcinogenesis, Molecular Medicine, Genetics(clinical), Indel, Exome, Molecular Biology, Genetics (clinical), Exome sequencing, 030304 developmental biology

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e21222048807a5096280f3a52ca7745

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