Arama Sonuçları - Sha Tang

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  1. 1
    Characterization of Mitochondrial DNA Heteroplasmy Using a Parallel Sequencing System

    Characterization of Mitochondrial DNA Heteroplasmy Using a Parallel Sequencing System Yazar: Sha Tang, Taosheng Huang

    Baskı/Yayın Bilgisi 2010
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  2. 2
    PLA2G6-Associated Neurodegeneration (PLAN): Review of Clinical Phenotypes and Genotypes

    PLA2G6-Associated Neurodegeneration (PLAN): Review of Clinical Phenotypes and Genotypes Yazar: Yu-pei Guo, Bei-sha Tang, Jifeng Guo

    Baskı/Yayın Bilgisi 2018
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  3. 3
    Patient decisions for disclosure of secondary findings among the first 200 individuals undergoing clinical diagnostic exome sequencing

    Patient decisions for disclosure of secondary findings among the first 200 individuals undergoing clinical diagnostic exome sequencing Yazar: Layla Shahmirzadi, Elizabeth Chao, Erika Palmaer, Melissa Parra, Sha Tang, Kelly Gonzalez

    Baskı/Yayın Bilgisi 2013
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  4. 4
    Heterozygous Mutation of Opa1 in Drosophila Shortens Lifespan Mediated through Increased Reactive Oxygen Species Production

    Heterozygous Mutation of Opa1 in Drosophila Shortens Lifespan Mediated through Increased Reactive Oxygen Species Production Yazar: Sha Tang, Phung Khanh Le, Stephanie Tse, Douglas C. Wallace, Taosheng Huang

    Baskı/Yayın Bilgisi 2009
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  5. 5
    Loose Panicle1 encoding a novel WRKY transcription factor, regulates panicle development, stem elongation, and seed size in foxtail millet [Setaria italica (L.) P. Beauv.]

    Loose Panicle1 encoding a novel WRKY transcription factor, regulates panicle development, stem elongation, and seed size in foxtail millet [Setaria italica (L.) P. Beauv.] Yazar: Jishan Xiang, Sha Tang, Hui Zhi, Guanqing Jia, Huajun Wang, Xianmin Diao

    Baskı/Yayın Bilgisi 2017
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  6. 6
    Mutation in<i>SNAP25</i>as a novel genetic cause of epilepsy and intellectual disability

    Mutation in<i>SNAP25</i>as a novel genetic cause of epilepsy and intellectual disability Yazar: Luis Rohena, Julie Neidich, Megan Truitt Cho, Kelly Gonzalez, Sha Tang, Orrin Devinsky, Wendy K. Chung

    Baskı/Yayın Bilgisi 2013
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  7. 7
    Genome-wide identification and functional prediction of novel and drought-responsive lincRNAs in Populus trichocarpa

    Genome-wide identification and functional prediction of novel and drought-responsive lincRNAs in Populus trichocarpa Yazar: Peng Shuai, Dan Liang, Sha Tang, Zhoujia Zhang, Chuyu Ye, Yanyan Su, Xinli Xia, Weilun Yin

    Baskı/Yayın Bilgisi 2014
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  8. 8
    VPS35-deficiency results in an impaired AMPA receptor trafficking and decreased dendritic spine maturation

    VPS35-deficiency results in an impaired AMPA receptor trafficking and decreased dendritic spine maturation Yazar: Yun Tian, Fu‐Lei Tang, Xiang-Dong Sun, Lei Wen, Lin Mei, Bei-sha Tang, Wen‐Cheng Xiong

    Baskı/Yayın Bilgisi 2015
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  9. 9
    MDSi: Multi-omics Database for Setaria italica

    MDSi: Multi-omics Database for Setaria italica Yazar: Xukai Li, Siyu Hou, Mengmeng Feng, Rui Xia, Jiawei Li, Sha Tang, Yuanhuai Han, Jianhua Gao, Xingchun Wang

    Baskı/Yayın Bilgisi 2023
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  10. 10
    Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy

    Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy Yazar: Katherine L. Helbig, Kelly D. Farwell Hagman, Deepali N. Shinde, Cameron Mroske, Zöe Powis, Shuwei Li, Sha Tang, Ingo Helbig

    Baskı/Yayın Bilgisi 2016
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  11. 11
    Association between shift work and risk of prostate cancer: a systematic review and meta-analysis of observational studies

    Association between shift work and risk of prostate cancer: a systematic review and meta-analysis of observational studies Yazar: Yong Gan, Liqing Li, Liangwen Zhang, Shijiao Yan, Chao Gao, Sai Hu, Yan Qiao, Sha Tang, Chao Wang, Zuxun Lu

    Baskı/Yayın Bilgisi 2017
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  12. 12
    4-Nonylphenol induces autophagy and attenuates mTOR-p70S6K/4EBP1 signaling by modulating AMPK activation in Sertoli cells

    4-Nonylphenol induces autophagy and attenuates mTOR-p70S6K/4EBP1 signaling by modulating AMPK activation in Sertoli cells Yazar: Peng Duan, Chunhui Hu, Chao Quan, Tingting Yu, Wenting Huang, Wei Chen, Sha Tang, Yuqin Shi, Francis L. Martin, Kedi Yang

    Baskı/Yayın Bilgisi 2016
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  13. 13
    Diagnostic Exome Sequencing Identifies Two Novel <i>IQSEC2</i> Mutations Associated with X‐Linked Intellectual Disability with Seizures: Implications for Genetic Counseling and Clinical Diagnosis

    Diagnostic Exome Sequencing Identifies Two Novel <i>IQSEC2</i> Mutations Associated with X‐Linked Intellectual Disability with Seizures: Implications for Genetic Counseling and Cli... Yazar: Stephanie Gandomi, Kelly Gonzalez, M. Parra, Layla Shahmirzadi, James J. Mancuso, Pavel N. Pichurin, Renee Temme, Sarah Dugan, Wenqi Zeng, Sha Tang

    Baskı/Yayın Bilgisi 2013
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  14. 14
    Exome sequencing covers &gt;98% of mutations identified on targeted next generation sequencing panels

    Exome sequencing covers &gt;98% of mutations identified on targeted next generation sequencing panels Yazar: Holly LaDuca, Kelly D. Farwell, Huy Gia Vuong, Hsiao‐Mei Lu, Wenbo Mu, Layla Shahmirzadi, Sha Tang, Jefferey Chen, Shruti Bhide, Elizabeth Chao

    Baskı/Yayın Bilgisi 2017
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  15. 15
    Characterization of a caveolin‐1 mutation associated with both pulmonary arterial hypertension and congenital generalized lipodystrophy

    Characterization of a caveolin‐1 mutation associated with both pulmonary arterial hypertension and congenital generalized lipodystrophy Yazar: Bing Han, Courtney A. Copeland, Yumeko Kawano, Erika B. Rosenzweig, Eric D. Austin, Layla Shahmirzadi, Sha Tang, Krishnan Raghunathan, Wendy K. Chung, Anne K. Kenworthy

    Baskı/Yayın Bilgisi 2016
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  16. 16
    Interpretation of mitochondrial tRNA variants

    Interpretation of mitochondrial tRNA variants Yazar: Lee‐Jun C. Wong, Ting Chen, Jing Wang, Sha Tang, Eric Schmitt, Megan Landsverk, Fangyuan Li, Yue Wang, Shulin Zhang, Victor Wei Zhang, William J. Craigen

    Baskı/Yayın Bilgisi 2020
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  17. 17
    Autonomic ganglionic injection of α-synuclein fibrils as a model of pure autonomic failure α-synucleinopathy

    Autonomic ganglionic injection of α-synuclein fibrils as a model of pure autonomic failure α-synucleinopathy Yazar: Xue-Jing Wang, Ming-ming Ma, Le-Bo Zhou, Xiao-Yi Jiang, Miao-Miao Hao, Robert K. F. Teng, Erxi Wu, Bei-sha Tang, Jiayi Li, J Teng, Xuebing Ding

    Baskı/Yayın Bilgisi 2020
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  18. 18
    Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications

    Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications Yazar: Erica D. Smith, Kelly Radtke, Mari Rossi, Deepali N. Shinde, Sourat Darabi, Dima El‐Khechen, Zöe Powis, Katherine L. Helbig, Kendra Waller, Dorothy K. Grange, Sha Tang, Kelly D. Farwell Hagman

    Baskı/Yayın Bilgisi 2017
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  19. 19
    Exome sequencing positively identified relevant alterations in more than half of cases with an indication of prenatal ultrasound anomalies

    Exome sequencing positively identified relevant alterations in more than half of cases with an indication of prenatal ultrasound anomalies Yazar: Christina L. Alamillo, Zöe Powis, Kelly D. Farwell, Layla Shahmirzadi, Elaine Weltmer, John Turocy, Thomas W. Lowe, Christine Kobelka, Emily Chen, Donald Basel, Elena Ashkinadze, Lisa D'Augelli, Elizabeth Chao, Sha Tang

    Baskı/Yayın Bilgisi 2015
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  20. 20
    Novel mutations in the mitochondrial complex I assembly gene NDUFAF5 reveal heterogeneous phenotypes

    Novel mutations in the mitochondrial complex I assembly gene NDUFAF5 reveal heterogeneous phenotypes Yazar: Mariella Simon, Shaya S. Eftekharian, Alexander E. Stover, Aaron Fletcher Osborne, Bruce H. Braffman, Richard Chang, Raymond Wang, Maija Steenari, Sha Tang, Wuh‐Liang Hwu, Ryan J. Taft, Paul J. Benke, José E. Abdenur

    Baskı/Yayın Bilgisi 2018
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