Hasil Pencarian - Xueya Zhou

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  1. 1
    Co-occurring protein phosphorylation are functionally associated.

    Co-occurring protein phosphorylation are functionally associated. oleh Ying Li, Xueya Zhou, Zichao Zhai, Tingting Li

    Diterbitkan 2017-05-01
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  2. 2
    Soil water response to rainfall in a dune-interdune landscape in Horqin Sand Land, northern China

    Soil water response to rainfall in a dune-interdune landscape in Horqin Sand Land, northern China oleh Xueya Zhou, Dexin Guan, Jiabing Wu, Fenghui Yuan, Anzhi Wang, Cangjie Jin, Yushu Zhang

    Diterbitkan 2019-12-01
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  3. 3
    Environmental Regulation, Promotion Pressure of Officials, and Enterprise Environmental Protection Investment

    Environmental Regulation, Promotion Pressure of Officials, and Enterprise Environmental Protection Investment oleh Ke-Chiun Chang, Di Wang, Yangyang Lu, Wen Chang, Guangqian Ren, Li Liu, Xueya Zhou

    Diterbitkan 2021-08-01
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  4. 4
    Phase separation as a possible mechanism for dosage sensitivity

    Phase separation as a possible mechanism for dosage sensitivity oleh Liang Yang, Jiali Lyu, Xi Li, Gaigai Guo, Xueya Zhou, Taoyu Chen, Yi Lin, Tingting Li

    Diterbitkan 2024-01-01
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  5. 5
    Trans-Ethnic Polygenic Analysis Supports Genetic Overlaps of Lumbar Disc Degeneration With Height, Body Mass Index, and Bone Mineral Density

    Trans-Ethnic Polygenic Analysis Supports Genetic Overlaps of Lumbar Disc Degeneration With Height, Body Mass Index, and Bone Mineral Density oleh Xueya Zhou, Xueya Zhou, Ching-Lung Cheung, Ching-Lung Cheung, Tatsuki Karasugi, Jaro Karppinen, Dino Samartzis, Yi-Hsiang Hsu, Yi-Hsiang Hsu, Yi-Hsiang Hsu, Timothy Shin-Heng Mak, You-Qiang Song, You-Qiang Song, Kazuhiro Chiba, Yoshiharu Kawaguchi, Yan Li, Danny Chan, Kenneth Man-Chee Cheung, Shiro Ikegawa, Kathryn Song-Eng Cheah, Pak Chung Sham, Pak Chung Sham

    Diterbitkan 2018-08-01
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  6. 6
    De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders.

    De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders. oleh Hongjian Qi, Lan Yu, Xueya Zhou, Julia Wynn, Haoquan Zhao, Yicheng Guo, Na Zhu, Alexander Kitaygorodsky, Rebecca Hernan, Gudrun Aspelund, Foong-Yen Lim, Timothy Crombleholme, Robert Cusick, Kenneth Azarow, Melissa E Danko, Dai Chung, Brad W Warner, George B Mychaliska, Douglas Potoka, Amy J Wagner, Mahmoud ElFiky, Jay M Wilson, Debbie Nickerson, Michael Bamshad, Frances A High, Mauro Longoni, Patricia K Donahoe, Wendy K Chung, Yufeng Shen

    Diterbitkan 2018-12-01
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  7. 7
    Correction to: Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

    Correction to: Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH oleh Na Zhu, Emilia M. Swietlik, Carrie L. Welch, Michael W. Pauciulo, Jacob J. Hagen, Xueya Zhou, Yicheng Guo, Johannes Karten, Divya Pandya, Tobias Tilly, Katie A. Lutz, Jennifer M. Martin, Carmen M. Treacy, Erika B. Rosenzweig, Usha Krishnan, Anna W. Coleman, Claudia Gonzaga-Jauregui, Allan Lawrie, Richard C. Trembath, Martin R. Wilkins, Regeneron Genetics Center, PAH Biobank Enrolling Centers’ Investigators, NIHR BioResource for Translational Research - Rare Diseases, National Cohort Study of Idiopathic and Heritable PAH, Nicholas W. Morrell, Yufeng Shen, Stefan Gräf, William C. Nichols, Wendy K. Chung

    Diterbitkan 2021-06-01
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  8. 8
    Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

    Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH oleh Na Zhu, Emilia M. Swietlik, Carrie L. Welch, Michael W. Pauciulo, Jacob J. Hagen, Xueya Zhou, Yicheng Guo, Johannes Karten, Divya Pandya, Tobias Tilly, Katie A. Lutz, Jennifer M. Martin, Carmen M. Treacy, Erika B. Rosenzweig, Usha Krishnan, Anna W. Coleman, Claudia Gonzaga-Juaregui, Allan Lawrie, Richard C. Trembath, Martin R. Wilkins, Regeneron Genetics Center, PAH Biobank Enrolling Centers’ Investigators, NIHR BioResource for Translational Research - Rare Diseases, National Cohort Study of Idiopathic and Heritable PAH, Nicholas W. Morrell, Yufeng Shen, Stefan Gräf, William C. Nichols, Wendy K. Chung

    Diterbitkan 2021-05-01
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