Ngā hua rapu - Shen Gu

Whakamahine hua
  1. 1
    Flexible and Versatile as a Chameleon—Sophisticated Functions of microRNA-199a

    Flexible and Versatile as a Chameleon—Sophisticated Functions of microRNA-199a mā Shen Gu, Wai‐Yee Chan

    I whakaputaina 2012
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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  2. 2
    Survey of Solvents for the Conrad–Limpach Synthesis of 4-Hydroxyquinolones

    Survey of Solvents for the Conrad–Limpach Synthesis of 4-Hydroxyquinolones mā Jean‐Cristophe Brouet, Shen Gu, Norton P. Peet, John D. Williams

    I whakaputaina 2009
    Whiwhi kuputuhi katoa
    Artigo
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  3. 3
    microRNA-199a-3p, DNMT3A, and aberrant DNA methylation in testicular cancer

    microRNA-199a-3p, DNMT3A, and aberrant DNA methylation in testicular cancer mā Bifeng Chen, Shen Gu, Yick-Keung Suen, Lu Li, Wai‐Yee Chan

    I whakaputaina 2013
    Whiwhi kuputuhi katoa
    Artigo
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  4. 4
    A miR-199a/miR-214 Self-Regulatory Network via PSMD10, TP53 and DNMT1 in Testicular Germ Cell Tumor

    A miR-199a/miR-214 Self-Regulatory Network via PSMD10, TP53 and DNMT1 in Testicular Germ Cell Tumor mā Bifeng Chen, Yick-Keung Suen, Shen Gu, Lu Li, Wai‐Yee Chan

    I whakaputaina 2014
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  5. 5
    miR-877-3p targets Smad7 and is associated with myofibroblast differentiation and bleomycin-induced lung fibrosis

    miR-877-3p targets Smad7 and is associated with myofibroblast differentiation and bleomycin-induced lung fibrosis mā Cong Wang, Shen Gu, Honghui Cao, Zutong Li, Zou Xiang, Kebin Hu, Xiaodong Han

    I whakaputaina 2016
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  6. 6
    Epigenetic Control of circHNRNPH1 in Postischemic Myocardial Fibrosis through Targeting of TGF-β Receptor Type I

    Epigenetic Control of circHNRNPH1 in Postischemic Myocardial Fibrosis through Targeting of TGF-β Receptor Type I mā Li, Weifeng, Wang, Yue, Deng, Yunfei, Ni, Huaner, Shen, Gu, Liu, Xiaoqiang, Li, Jun, Wang, Fang

    I whakaputaina 2020
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    Text
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  7. 7
    Down-regulation of Dicer1 promotes cellular senescence and decreases the differentiation and stem cell-supporting capacities of mesenchymal stromal cells in patients with myelodysplastic syndrome

    Down-regulation of Dicer1 promotes cellular senescence and decreases the differentiation and stem cell-supporting capacities of mesenchymal stromal cells in patients with myelodysp... mā Youshan Zhao, Dongwei Wu, Fei Cao, Jian‐Rong Guo, Shen Gu, Yanling Zhu, Feng Xu, Z. Zhang, Lifang Wu, X. Li, Chunkang Chang

    I whakaputaina 2014
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  8. 8
    Predicting human genes susceptible to genomic instability associated with <i>Alu</i>/<i>Alu</i>-mediated rearrangements

    Predicting human genes susceptible to genomic instability associated with <i>Alu</i>/<i>Alu</i>-mediated rearrangements mā Xiaofei Song, Christine R. Beck, Renqian Du, Ian M. Campbell, Zeynep Coban‐Akdemir, Shen Gu, Amy M. Breman, Paweł Stankiewicz, Grzegorz Ira, Chad A. Shaw, James R. Lupski

    I whakaputaina 2018
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  9. 9
    The near-infrared dye IR-61 restores erectile function in a streptozotocin-induced diabetes modelvia mitochondrial protection

    The near-infrared dye IR-61 restores erectile function in a streptozotocin-induced diabetes modelvia mitochondrial protection mā Yue, Xiao-Feng, Shen, Chong-Xing, Wang, Jian-Wu, Dai, Lin-Yong, Fang, Qiang, Long, Lei, Zhi, Yi, Li, Xue-Ru, Wang, Ya-Wei, Shen, Gu-Fang, Liu, Zu-Juan, Shi, Chun-Meng, Li, Wei-Bing

    I whakaputaina 2021
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Text
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  10. 10
    Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3

    Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3 mā Shen Gu, Bo Yuan, Ian M. Campbell, Christine R. Beck, Claudia M.B. Carvalho, Sandesh C.S. Nagamani, Ayelet Erez, Ankita Patel, Carlos A. Bacino, Chad A. Shaw, Paweł Stankiewicz, Sau Wai Cheung, Weimin Bi, James R. Lupski

    I whakaputaina 2015
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  11. 11
    Mechanisms for Complex Chromosomal Insertions

    Mechanisms for Complex Chromosomal Insertions mā Shen Gu, Przemysław Szafrański, Zeynep Coban‐Akdemir, Bo Yuan, M. Lance Cooper, Maria A. Magriñá, Carlos A. Bacino, Seema R. Lalani, Amy M. Breman, Janice Smith, Ankita Patel, Rodger Song, Weimin Bi, Sau Wai Cheung, Claudia M.B. Carvalho, Paweł Stankiewicz, James R. Lupski

    I whakaputaina 2016
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  12. 12
    Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohort

    Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohort mā Tomasz Gambin, Zeynep Coban‐Akdemir, Bo Yuan, Shen Gu, Theodore Chiang, Claudia M.B. Carvalho, Chad A. Shaw, Shalini N. Jhangiani, Philip M. Boone, Mohammad K. Eldomery, Ender Karaca, Yavuz Bayram, Asbjørg Stray‐Pedersen, Donna M. Muzny, Wu‐Lin Charng, Vahid Bahrambeigi, John W. Belmont, Eric Boerwinkle, Arthur L. Beaudet, Richard A. Gibbs, James R. Lupski

    I whakaputaina 2016
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  13. 13
    Whole-Exome Sequencing in Familial Parkinson Disease

    Whole-Exome Sequencing in Familial Parkinson Disease mā Janice L. Farlow, Laurie Robak, Kurt N. Hetrick, Kevin M. Bowling, Eric Boerwinkle, Zeynep Coban‐Akdemir, Tomasz Gambin, Richard A. Gibbs, Shen Gu, Preti Jain, Joseph Jankovic, Shalini N. Jhangiani, Kaveeta Kaw, Dongbing Lai, Hai Lin, Hua Ling, Yunlong Liu, James R. Lupski, Donna M. Muzny, Paula Porter, Elizabeth Pugh, Janson J. White, Kimberly F. Doheny, R Myers, Joshua Shulman, Tatiana Foroud

    I whakaputaina 2015
    Whiwhi kuputuhi katoa
    Artigo
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  14. 14
    Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate

    Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate mā Wu‐Lin Charng, Ender Karaca, Zeynep Coban‐Akdemir, Tomasz Gambin, Mehmed M. Atik, Shen Gu, Jennifer E. Posey, Shalini N. Jhangiani, Donna M. Muzny, HarshaVardhan Doddapaneni, Jianhong Hu, Eric Boerwinkle, Richard A. Gibbs, Jill A. Rosenfeld, Hong Cui, Fan Xia, Kandamurugu Manickam, Yaping Yang, Eissa Faqeih, Ali Al Asmari, Mohammed A. Saleh, Ayman W. El‐Hattab, James R. Lupski

    I whakaputaina 2016
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  15. 15
    Epidemiological and Clinical Characteristics and Risk Factors for Death of Patients with Avian Influenza A H7N9 Virus Infection from Jiangsu Province, Eastern China

    Epidemiological and Clinical Characteristics and Risk Factors for Death of Patients with Avian Influenza A H7N9 Virus Infection from Jiangsu Province, Eastern China mā Ji, Hong, Gu, Qin, Chen, Li-ling, Xu, Ke, Ling, Xia, Bao, Chang-jun, Tang, Fen-yang, Qi, Xian, Wu, Ying-qiu, Ai, Jing, Shen, Gu-yu, Dong, Dan-jiang, Yu, Hui-yan, Huang, Mao, Cao, Quan, Xu, Ying, Zhao, Wei, Xu, Yang-ting, Xia, Yu, Chen, Shan-hui, Yang, Gen-lin, Gu, Cai-ling, Xie, Guo-xiang, Zhu, Ye-fei, Zhu, Feng-cai, Zhou, Ming-hao

    I whakaputaina 2014
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    Text
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  16. 16
    Developmental genomics of limb malformations: Allelic series in association with gene dosage effects contribute to the clinical variability

    Developmental genomics of limb malformations: Allelic series in association with gene dosage effects contribute to the clinical variability mā Ruizhi Duan, Hadia Hijazi, Elif Yılmaz Güleç, Hatice Koçak Eker, Silvia R. Costa, Yavuz Şahin, Zeynep Ocak, Sedat Işıkay, Özge Özalp, Sevcan Tuğ Bozdoğan, Hüseyin Aslan, Nursel Elçioǧlu, Débora Romeo Bertola, Alper Gezdirici, Haowei Du, Jawid M. Fatih, Christopher M. Grochowski, Gülsen Akay, Shalini N. Jhangiani, Ender Karaca, Shen Gu, Zeynep Coban‐Akdemir, Jennifer E. Posey, Yavuz Bayram, V. Reid Sutton, Claudia M.B. Carvalho, Davut Pehli̇van, Richard A. Gibbs, James R. Lupski

    I whakaputaina 2022
    Whiwhi kuputuhi katoa
    Artigo
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  17. 17
    Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypes

    Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypes mā Bo Yuan, Davut Pehli̇van, Ender Karaca, Nisha Patel, Wu‐Lin Charng, Tomasz Gambin, Claudia Gonzaga‐Jauregui, V. Reid Sutton, Gözde Yeşil, Sevcan Tuğ Bozdoğan, Tülay Tos, Asuman Koparır, Erkan Koparir, Christine R. Beck, Shen Gu, Hüseyin Aslan, Özge Özalp Yüreğir, Khalid Al Rubeaan, Dhekra Alnaqeb, Muneera J. Alshammari, Yavuz Bayram, Mehmed M. Atik, Hatip Aydın, Bilgen Bilge Geçkinli, Mehmet Seven, Hakan Ulucan, Elif Fenercioğlu, Mustafa Özen, Shalini N. Jhangiani, Donna M. Muzny, Eric Boerwinkle, Beyhan Tüysüz, Fowzan S. Alkuraya, Richard A. Gibbs, James R. Lupski

    I whakaputaina 2015
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  18. 18
    MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death

    MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death mā Mohammad K. Eldomery, Zeynep Coban‐Akdemir, F.‐Nora Vögtle, Wu‐Lin Charng, Patrycja Mulica, Jill A. Rosenfeld, Tomasz Gambin, Shen Gu, Lindsay C. Burrage, Aisha Al Shamsi, Samantha Penney, Shalini N. Jhangiani, Holly H. Zimmerman, Donna M. Muzny, Xia Wang, Jia Tang, Ravi Medikonda, Prasanna Venkatesh Ramachandran, Lee-Jun Wong, Eric Boerwinkle, Richard A. Gibbs, Christine M. Eng, Seema R. Lalani, Jozef Hertecant, Richard J. Rodenburg, Omar Abdul‐Rahman, Yaping Yang, Fan Xia, Meng C. Wang, James R. Lupski, Chris Meisinger, V. Reid Sutton

    I whakaputaina 2016
    Whiwhi kuputuhi katoa
    Artigo
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  19. 19
    Genetic architecture of laterality defects revealed by whole exome sequencing

    Genetic architecture of laterality defects revealed by whole exome sequencing mā Alexander Li, Neil A. Hanchard, Mahshid S. Azamian, Lisa C.A. D’Alessandro, Zeynep Coban‐Akdemir, Keila N. Lopez, Nancy J. Hall, Heather A. Dickerson, Annarita Nicosia, Susan Fernbach, Philip M. Boone, Tomasz Gambin, Ender Karaca, Shen Gu, Bo Yuan, Shalini N. Jhangiani, HarshaVardhan Doddapaneni, Jianhong Hu, Huyen Dinh, Joy C. Jayaseelan, Donna M. Muzny, Seema R. Lalani, Jeffrey A. Towbin, Daniel J. Penny, Charles D. Fraser, James F. Martin, James R. Lupski, Richard A. Gibbs, Eric Boerwinkle, Stephanie M. Ware, John W. Belmont

    I whakaputaina 2019
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  20. 20
    Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases

    Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases mā Avinash V. Dharmadhikari, Rajarshi Ghosh, Bo Yuan, Pengfei Liu, Hongzheng Dai, Sami Al Masri, Jennifer Scull, Jennifer E. Posey, Allen H. Jiang, Weimin He, Francesco Vetrini, Alicia Braxton, Patricia A. Ward, Theodore Chiang, Chunjing Qu, Shen Gu, Chad A. Shaw, Janice Smith, Seema R. Lalani, Paweł Stankiewicz, Sau Wai Cheung, Carlos A. Bacino, Ankita Patel, Amy M. Breman, Xia Wang, Linyan Meng, Rui Xiao, Fan Xia, Donna M. Muzny, Richard A. Gibbs, Arthur L. Beaudet, Christine M. Eng, James R. Lupski, Yaping Yang, Weimin Bi

    I whakaputaina 2019
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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