Výsledky vyhledávání - Zhishuo, Ou

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  1. 1
    Single-cell analysis identifies MKI67+ microglia as drivers of neovascularization in proliferative diabetic retinopathy

    Single-cell analysis identifies MKI67+ microglia as drivers of neovascularization in proliferative diabetic retinopathy Autor Kang Zou, Xue Li, Bibo Ren, Fu Cheng, Jian Ye, Zhishuo Ou

    Vydáno 2025
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  2. 2
    Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses

    Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses Autor Zhishuo Ou, Sung‐Hae Kang, Chad A. Shaw, Condie E. Carmack, Lisa D. White, Ankita Patel, Arthur L. Beaudet, Sau Wai Cheung, A. Craig Chinault

    Vydáno 2008
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  3. 3
    The projection from the rostral anterior cingulate cortex to the ventral tegmental area regulates 5-HT-induced itch aversion and scratching in rats

    The projection from the rostral anterior cingulate cortex to the ventral tegmental area regulates 5-HT-induced itch aversion and scratching in rats Autor Jun-Fei Teng, Xingyu Lu, Jun-hui Long, Ying Shi, Xueqiang Hu, Jian-Feng Sui, Ping Wang, Ling Zeng, Xuan Li, Jiansong Xu, Zhishuo Ou, Kang-Quan Hu, Shulei Liu

    Vydáno 2025
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  4. 4
    Development and validation of a CGH microarray for clinical cytogenetic diagnosis

    Development and validation of a CGH microarray for clinical cytogenetic diagnosis Autor Sau Wai Cheung, Chad A. Shaw, Wei Yu, Jiangzham Li, Zhishuo Ou, Ankita Patel, Svetlana A. Yatsenko, M. Lance Cooper, Patti Furman, P Stankiewicz, James R. Lupski, A. Craig Chinault, Arthur L. Beaudet

    Vydáno 2005
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  5. 5
    Insertional translocation detected using FISH confirmation of array‐comparative genomic hybridization (aCGH) results

    Insertional translocation detected using FISH confirmation of array‐comparative genomic hybridization (aCGH) results Autor Sung‐Hae Kang, Chad A. Shaw, Zhishuo Ou, Patricia A. Eng, M. Lance Cooper, Amber N. Pursley, Trilochan Sahoo, Carlos A. Bacino, A. Craig Chinault, Paweł Stankiewicz, Ankita Patel, James R. Lupski, Sau Wai Cheung

    Vydáno 2010
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  6. 6
    Identification of critical regions for clinical features of distal 10q deletion syndrome

    Identification of critical regions for clinical features of distal 10q deletion syndrome Autor S A Yatsenko, M.D. and Colin M. Roberts Michael C. Kruer, PI Bader, D Corzo, Jane L. Schuette, CE Keegan, Beata Nowakowska, Sandra Peacock, WW Cai, DA Peiffer, KL Gunderson, Zhishuo Ou, AC Chinault, SW Cheung

    Vydáno 2009
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  7. 7
    Selective Antitumor Activity of Ibrutinib in EGFR-Mutant Non–Small Cell Lung Cancer Cells

    Selective Antitumor Activity of Ibrutinib in EGFR-Mutant Non–Small Cell Lung Cancer Cells Autor Wen Gao, Michael Wang, Li Wang, Haibo Lu, Shuhong Wu, Bingbing Dai, Zhishuo Ou, Liang Zhang, John V. Heymach, Kathryn A. Gold, John D. Minna, Jack A. Roth, Wayne L. Hofstetter, Stephen G. Swisher, Bingliang Fang

    Vydáno 2014
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  8. 8
    Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes

    Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes Autor Zhishuo Ou, Jonathan S. Berg, Hagith Yonath, Victoria B. Enciso, David T. Miller, Jonathan Picker, Tiffanee Lenzi, Catherine E. Keegan, V. Reid Sutton, John W. Belmont, A. Craig Chinault, James R. Lupski, Sau Wai Cheung, Elizabeth Roeder, Ankita Patel

    Vydáno 2008
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  9. 9
    22q11.2 Distal Deletion: A Recurrent Genomic Disorder Distinct from DiGeorge Syndrome and Velocardiofacial Syndrome

    22q11.2 Distal Deletion: A Recurrent Genomic Disorder Distinct from DiGeorge Syndrome and Velocardiofacial Syndrome Autor Shay Ben‐Shachar, Zhishuo Ou, Chad A. Shaw, John W. Belmont, Millan S. Patel, Marybeth Hummel, Stephen Amato, Nicole Tartaglia, Jonathan S. Berg, V. Reid Sutton, Seema R. Lalani, A. Craig Chinault, Sau Wai Cheung, James R. Lupski, Ankita Patel

    Vydáno 2008
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  10. 10
    Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping

    Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping Autor Ayman W. El‐Hattab, Teresa A. Smolarek, Martha E. Walker, Elizabeth K. Schorry, LaDonna Immken, Gayle Patel, Mary‐Alice Abbott, Brendan C. Lanpher, Zhishuo Ou, Sung‐Hae Kang, Ankita Patel, Fernando Scaglia, James R. Lupski, Sau Wai Cheung, Paweł Stankiewicz

    Vydáno 2009
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  11. 11
    Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE

    Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE Autor Patrícia B. S. Celestino-Soper, Chad A. Shaw, Stephan Sanders, Jian Li, Michael T. Murtha, A. Gulhan Ercan‐Sencicek, Lea K. Davis, Susanne Thomson, Tomasz Gambin, A. Craig Chinault, Zhishuo Ou, Jennifer R. German, Aleksandar Milosavljevic, James S. Sutcliffe, Edwin H. Cook, Paweł Stankiewicz, Matthew W. State, Arthur L. Beaudet

    Vydáno 2011
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  12. 12
    Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes

    Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes Autor Zhishuo Ou, Paweł Stankiewicz, Zhilian Xia, Amy M. Breman, Brian Dawson, Joanna Wiszniewska, Przemysław Szafrański, M. Lance Cooper, Mitchell Rao, Lina Shao, Sarah T. South, Karlene Coleman, Paul M. Fernhoff, Marcel J. Deray, Sally Rosengren, Elizabeth Roeder, Victoria B. Enciso, A. Craig Chinault, Ankita Patel, Sung-Hae L. Kang, Chad A. Shaw, James R. Lupski, Sau Wai Cheung

    Vydáno 2011
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  13. 13
    Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder

    Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder Autor Przemysław Szafrański, Avinash V. Dharmadhikari, Erwin Brosens, Priyatansh Gurha, Katarzyna Kołodziejska, Zhishuo Ou, Piotr Dittwald, Tadeusz Majewski, K. Naga Mohan, Bo Chen, Richard Person, Dick Tibboel, Annelies de Klein, Jason Pinner, Maya Chopra, Girvan Malcolm, Gregory B. Peters, Susan Arbuckle, Sixto F. Guiang, Virginia A. Hustead, José Jessurun, Russel Hirsch, David P. Witte, Isabelle Maystadt, Neil J. Sebire, Richard Fisher, Claire Langston, Partha Sen, Paweł Stankiewicz

    Vydáno 2012
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  14. 14
    Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder

    Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder Autor Szafranski, Przemyslaw, Dharmadhikari, Avinash V., Brosens, Erwin, Gurha, Priyatansh, Kołodziejska, Katarzyna E., Zhishuo, Ou, Dittwald, Piotr, Majewski, Tadeusz, Mohan, K. Naga, Chen, Bo, Person, Richard E., Tibboel, Dick, de Klein, Annelies, Pinner, Jason, Chopra, Maya, Malcolm, Girvan, Peters, Gregory, Arbuckle, Susan, Guiang, Sixto F., Hustead, Virginia A., Jessurun, Jose, Hirsch, Russel, Witte, David P., Maystadt, Isabelle, Sebire, Neil, Fisher, Richard, Langston, Claire, Sen, Partha, Stankiewicz, Paweł

    Vydáno 2013
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  15. 15
    Rare DNA copy number variants in cardiovascular malformations with extracardiac abnormalities

    Rare DNA copy number variants in cardiovascular malformations with extracardiac abnormalities Autor Seema R. Lalani, Chad A. Shaw, Xueqing Wang, Ankita Patel, Lance W Patterson, Katarzyna Kołodziejska, Przemysław Szafrański, Zhishuo Ou, Qi Tian, Sung-Hae L. Kang, Amina Jinnah, Sophia Ali, A. H. Malik, Patricia Hixson, Lorraine Potocki, James R. Lupski, Paweł Stankiewicz, Carlos A. Bacino, Brian Dawson, Arthur L. Beaudet, Fatima Boricha, Runako Whittaker, Chumei Li, Stephanie M. Ware, Sau Wai Cheung, Daniel J. Penny, John L. Jefferies, John W. Belmont

    Vydáno 2012
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  16. 16
    Targeting BTK with Ibrutinib in Relapsed or Refractory Mantle-Cell Lymphoma

    Targeting BTK with Ibrutinib in Relapsed or Refractory Mantle-Cell Lymphoma Autor Michael Wang, Simon Rule, Peter Martin, André Goy, Rebecca Auer, Brad S. Kahl, Wojciech Jurczak, Ranjana H. Advani, Jorge Romaguera, Michael E. Williams, Jacqueline C. Barrientos, Ewa Chmielowska, John Radford, Stephan Stilgenbauer, Martin Dreyling, W Wiktor-Jędrzejczak, Peter Johnson, Stephen E. Spurgeon, Lei Li, Liang Zhang, Kate J. Newberry, Zhishuo Ou, Nancy Cheng, Bingliang Fang, Jesse McGreivy, Fong Clow, Joseph J. Buggy, Betty Chang, Darrin M. Beaupre, Lori Kunkel, Kristie A. Blum

    Vydáno 2013
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  17. 17
    20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits

    20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits Autor Seema R. Lalani, Joseph V. Thakuria, Gerald F. Cox, X. Wang, Weimin Bi, Molly S. Bray, Chad A. Shaw, Sau Wai Cheung, A. Craig Chinault, Barbara A. Boggs, Zhishuo Ou, Ellen K. Brundage, James R. Lupski, Jennifer Gentile, Susan E. Waisbren, Amber N. Pursley, Ling Ma, Mehrdad Khajavi, Gladys Zapata, Richard A. Friedman, J J Kim, Jeffrey A. Towbin, Paweł Stankiewicz, Susanne Schnittger, I. Hansmann, Tomohiko Ai, Subeena Sood, Xander H.T. Wehrens, James F. Martin, John W. Belmont, Lorraine Potocki

    Vydáno 2008
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  18. 18
    Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations

    Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations Autor Paweł Stankiewicz, Partha Sen, Samarth Bhatt, Mekayla A. Storer, Zhilian Xia, Bassem A. Bejjani, Zhishuo Ou, Joanna Wiszniewska, Daniel J. Driscoll, Juan M. Bolívar, Mislen Bauer, Elaine H. Zackai, Donna M. McDonald‐McGinn, Małgorzata M.J. Nowaczyk, Mitzi L. Murray, Tamim H. Shaikh, Vicki Martin, Matthew Tyreman, Ingrid Simonic, Lionel Willatt, Joan Paterson, Sarju Mehta, Diana Rajan, Tomas Fitzgerald, Susan Gribble, Elena Prigmore, Ankita Patel, Lisa G. Shaffer, Nigel P. Carter, Sau Wai Cheung, Claire Langston, Charles Shaw‐Smith

    Vydáno 2009
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  19. 19
    Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations

    Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations Autor Paweł Stankiewicz, Partha Sen, Samarth Bhatt, Mekayla A. Storer, Zhilian Xia, Bassem A. Bejjani, Zhishuo Ou, Joanna Wiszniewska, Daniel J. Driscoll, Melissa K. Maisenbacher, Juan M. Bolívar, Mislen Bauer, Elaine H. Zackai, Donna M. McDonald‐McGinn, Małgorzata M.J. Nowaczyk, Mitzi L. Murray, Virginia A. Hustead, Kristin Mascotti, Regina Schultz, Lavinia Hallam, D. Harold McRae, Andrew G. Nicholson, Robert Newbury, Jane Durham-O'Donnell, G. R. Knight, Usha Kini, Tamim H. Shaikh, Vicki Martin, Matthew Tyreman, Ingrid Simonic, Lionel Willatt, Joan Paterson, Sarju Mehta, C. Jones, Diana Rajan, Tomas Fitzgerald, Susan Gribble, Elena Prigmore, Ankita Patel, Lisa G. Shaffer, Nigel P. Carter, Sau Wai Cheung, Claire Langston, Charles Shaw‐Smith

    Vydáno 2009
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