Výsledky vyhledávání - Shen Gu
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Down-regulation of Dicer1 promotes cellular senescence and decreases the differentiation and stem cell-supporting capacities of mesenchymal stromal cells in patients with myelodysp... Autor Youshan Zhao, Dongwei Wu, Fei Cao, Jian‐Rong Guo, Shen Gu, Yanling Zhu, Feng Xu, Z. Zhang, Lifang Wu, X. Li, Chunkang Chang
Vydáno 2014Artigo -
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Predicting human genes susceptible to genomic instability associated with <i>Alu</i>/<i>Alu</i>-mediated rearrangements Autor 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
Vydáno 2018Artigo -
9
The near-infrared dye IR-61 restores erectile function in a streptozotocin-induced diabetes modelvia mitochondrial protection Autor 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
Vydáno 2021Text -
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Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3 Autor 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
Vydáno 2015Artigo -
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Mechanisms for Complex Chromosomal Insertions Autor 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
Vydáno 2016Artigo -
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Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohort Autor 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
Vydáno 2016Artigo -
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Whole-Exome Sequencing in Familial Parkinson Disease Autor 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
Vydáno 2015Artigo -
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Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate Autor 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
Vydáno 2016Artigo -
15
Epidemiological and Clinical Characteristics and Risk Factors for Death of Patients with Avian Influenza A H7N9 Virus Infection from Jiangsu Province, Eastern China Autor 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
Vydáno 2014Text -
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Developmental genomics of limb malformations: Allelic series in association with gene dosage effects contribute to the clinical variability Autor 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
Vydáno 2022Artigo -
17
Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypes Autor 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
Vydáno 2015Artigo -
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MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death Autor 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
Vydáno 2016Artigo -
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Genetic architecture of laterality defects revealed by whole exome sequencing Autor 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
Vydáno 2019Artigo -
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Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases Autor 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
Vydáno 2019Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Exome sequencing
Genome
Medicine
Copy-number variation
Phenotype
Bioinformatics
Exome
Mutation
Gene expression
Pathology
Cancer research
Comparative genomic hybridization
Breakpoint
Cell biology
Chromosome
Genomics
Mendelian inheritance
Proband
microRNA
Cancer
Candidate gene
Computational biology
DNA
DNA damage
Disease
Genetic heterogeneity
Genome instability