Resultados da pesquisa - Lifeng Tian

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  1. 1
    Acetylation and nuclear receptor action

    Acetylation and nuclear receptor action Por Chenguang Wang, Lifeng Tian, Vladimir M. Popov, Richard G. Pestell

    Publicado em 2010
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  2. 2
    Expression Pattern of the SARS-CoV-2 Entry Genes ACE2 and TMPRSS2 in the Respiratory Tract

    Expression Pattern of the SARS-CoV-2 Entry Genes ACE2 and TMPRSS2 in the Respiratory Tract Por Yichuan Liu, Hui‐Qi Qu, Jingchun Qu, Lifeng Tian, Hákon Hákonarson

    Publicado em 2020
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  3. 3
    Transcriptome of the human retina, retinal pigmented epithelium and choroid

    Transcriptome of the human retina, retinal pigmented epithelium and choroid Por Lifeng Tian, Krista L. Kazmierkiewicz, Anita S. Bowman, Mingyao Li, Christine A. Curcio, Dwight Stambolian

    Publicado em 2015
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  4. 4
    Vertebrate OTOP1 is also an alkali-activated channel

    Vertebrate OTOP1 is also an alkali-activated channel Por Lifeng Tian, Hao Zhang, Shilong Yang, Anna Luo, Peter Muiruri Kamau, Jingmei Hu, Lei Luo, Ren Lai

    Publicado em 2023
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  5. 5
    The Cell Fate Determination Factor Dachshund Inhibits Androgen Receptor Signaling and Prostate Cancer Cellular Growth

    The Cell Fate Determination Factor Dachshund Inhibits Androgen Receptor Signaling and Prostate Cancer Cellular Growth Por Kongming Wu, Sanjay Katiyar, Agnes Witkiewicz, Anping Li, Peter A. McCue, Liang‐Nian Song, Lifeng Tian, Ming Jin, Richard G. Pestell

    Publicado em 2009
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  6. 6
    EYA1 Phosphatase Function Is Essential to Drive Breast Cancer Cell Proliferation through Cyclin D1

    EYA1 Phosphatase Function Is Essential to Drive Breast Cancer Cell Proliferation through Cyclin D1 Por Kongming Wu, Zhaoming Li, Shaoxin Cai, Lifeng Tian, Ke Chen, Jing Wang, Junbo Hu, Ye Sun, Xue Li, Adam Ertel, Richard G. Pestell

    Publicado em 2013
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  7. 7
    No Effect of Inactivated SARS-CoV-2 Vaccination on in vitro Fertilization Outcomes: A Propensity Score-Matched Study

    No Effect of Inactivated SARS-CoV-2 Vaccination on in vitro Fertilization Outcomes: A Propensity Score-Matched Study Por Jialyu Huang, Leizhen Xia, Jiaying Lin, Bangdong Liu, Yan Zhao, Cai-Lin Xin, Xiaoyan Ai, Wen-Ting Cao, Xiaocui Zhang, Lifeng Tian, Qiongfang Wu

    Publicado em 2022
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  8. 8
    PD1 Expression in EGFRvIII-Directed CAR T Cell Infusion Product for Glioblastoma Is Associated with Clinical Response

    PD1 Expression in EGFRvIII-Directed CAR T Cell Infusion Product for Glioblastoma Is Associated with Clinical Response Por Oliver Y. Tang, Lifeng Tian, Todd Yoder, Rong Xu, Irina Kulikovskaya, Minnal Gupta, J. Joseph Melenhorst, Simon F. Lacey, Donald M. O’Rourke, Zev A. Binder

    Publicado em 2022
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  9. 9
    Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing

    Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing Por Jason O'Rawe, Tao Jiang, Guangqing Sun, Yiyang Wu, Wei Wang, Jingchu Hu, Paul Bodily, Lifeng Tian, Hákon Hákonarson, W. Evan Johnson, Zhi Wei, Kai Wang, Gholson J. Lyon

    Publicado em 2013
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  10. 10
    Foxp1 is an essential transcriptional regulator for the generation of quiescent naive T cells during thymocyte development

    Foxp1 is an essential transcriptional regulator for the generation of quiescent naive T cells during thymocyte development Por Xiaoming Feng, Gregory C. Ippolito, Lifeng Tian, Karla R. Wiehagen, Soyoung Oh, Arivazhagan Sambandam, Jessica Willen, Ralph M. Bunte, Shanna D. Maika, June V. Harriss, Andrew J. Caton, Avinash Bhandoola, Philip W. Tucker, Hui Hu

    Publicado em 2009
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  11. 11
    Inherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1

    Inherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1 Por Yiran Guo, Melissa Kartawinata, Jiankang Li, Hilda A. Pickett, Juliana Teo, Tatjana Kilo, Pasquale Barbaro, Brendan J. Keating, Yulan Chen, Lifeng Tian, Ahmad Alodaib, Roger R. Reddel, John Christodoulou, Xun Xu, Hákon Hákonarson, Tracy M. Bryan

    Publicado em 2014
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  12. 12
    Comprehensive analysis of gene expression in human retina and supporting tissues

    Comprehensive analysis of gene expression in human retina and supporting tissues Por Mingyao Li, Jia Cheng, Krista L. Kazmierkiewicz, Anita S. Bowman, Lifeng Tian, Yichuan Liu, Neel Gupta, Harini V. Gudiseva, Stephanie S. Yee, Mijin Kim, Tzvete Dentchev, James A. Kimble, John S. Parker, Jeffrey D. Messinger, Hákon Hákonarson, Christine A. Curcio, Dwight Stambolian

    Publicado em 2014
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  13. 13
    Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder

    Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder Por Michael D. Keller, Rahul Pandey, Dong Li, Joseph Glessner, Lifeng Tian, Sarah E. Henrickson, Iván K. Chinn, Linda Monaco-Shawver, Jennifer Heimall, Cuiping Hou, F. George Otieno, Soma Jyonouchi, Leonard H. Calabrese, Joris van Montfrans, Jordan S. Orange, Hákon Hákonarson

    Publicado em 2016
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  14. 14
    Fresh versus Frozen Embryos for Infertility in the Polycystic Ovary Syndrome

    Fresh versus Frozen Embryos for Infertility in the Polycystic Ovary Syndrome Por Zi‐Jiang Chen, Yuhua Shi, Yun Sun, Bo Zhang, Xiaoyan Liang, Yunxia Cao, Jing Yang, Jiayin Liu, Daimin Wei, Ning Weng, Lifeng Tian, Cuifang Hao, Dongzi Yang, Feng Zhou, Juanzi Shi, Yongle Xu, Jing Li, Junhao Yan, Yingying Qin, Han Zhao, Heping Zhang, Richard S. Legro

    Publicado em 2016
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  15. 15
    AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate

    AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate Por Marni J. Falk, Dong Li, Xiaowu Gai, Elizabeth M. McCormick, Emily Place, Francesco M. Lasorsa, F. George Otieno, Cuiping Hou, Chong Ae Kim, Nada Abdelmagid, Lyam Vazquez, Frank Mentch, Rosetta Chiavacci, Jinlong Liang, Xuanzhu Liu, Hui Jiang, Giulia Giannuzzi, Eric D. Marsh, Guo Yiran, Lifeng Tian, Ferdinando Palmieri, Hákon Hákonarson

    Publicado em 2014
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  16. 16
    Phase I Study of Lentiviral-Transduced Chimeric Antigen Receptor-Modified T Cells Recognizing Mesothelin in Advanced Solid Cancers

    Phase I Study of Lentiviral-Transduced Chimeric Antigen Receptor-Modified T Cells Recognizing Mesothelin in Advanced Solid Cancers Por Andrew R. Haas, János L. Tanyi, Mark H. O’Hara, Whitney L. Gladney, Simon F. Lacey, Drew A. Torigian, Michael C. Soulen, Lifeng Tian, Maureen McGarvey, Anne Marie Nelson, Caitlin S. Farabaugh, Edmund K. Moon, Bruce L. Levine, J. Joseph Melenhorst, Gabriela Plesa, Carl H. June, Steven Μ. Albelda, Gregory L. Beatty

    Publicado em 2019
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  17. 17
    Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly

    Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly Por Dong Li, Tara Wenger, Christoph Seiler, Michael March, Álvaro Gutiérrez-Uzquiza, Charlly Kao, Elizabeth Bhoj, Lifeng Tian, Misha Rosenbach, Yichuan Liu, Nora Robinson, Mechenzie Behr, Rosetta Chiavacci, Cuiping Hou, Tiancheng Wang, Marina Bakay, Renata Pellegrino da Silva, Jonathan A. Perkins, Patrick Sleiman, Michael A. Levine, Patricia J. Hicks, Maxim Itkin, Yoav Dori, Hákon Hákonarson

    Publicado em 2018
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  18. 18
    The transcription factor Foxp1 is a critical negative regulator of the differentiation of follicular helper T cells

    The transcription factor Foxp1 is a critical negative regulator of the differentiation of follicular helper T cells Por Haikun Wang, Jianlin Geng, Xiaomin Wen, Enguang Bi, Andrew V. Kossenkov, Amaya I. Wolf, Jeroen M. J. Tas, Youn Soo Choi, Hiroshi Takata, Timothy J Day, Li-Yuan Chang, Stephanie L Sprout, Emily K Becker, Jessica Willen, Lifeng Tian, Xinxin Wang, Changchun Xiao, Ping Jiang, Shane Crotty, Gabriel D. Victora, Louise C. Showe, Haley O. Tucker, Jan Erikson, Hui Hu

    Publicado em 2014
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  19. 19
    GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers

    GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers Por Dong Li, Hongjie Yuan, Xilma R. Ortiz‐González, Eric D. Marsh, Lifeng Tian, Elizabeth M. McCormick, Gabrielle J. Kosobucki, Wenjuan Chen, Anthony J. Schulien, Rosetta Chiavacci, Anel Tankovic, Claudia Naase, F Brueckner, Celina von Stülpnagel-Steinbeis, Chun Hu, Hirofumi Kusumoto, Ulrike B. S. Hedrich, Gina E. Elsen, Konstanze Hörtnagel, Elias Aizenman, Johannes R. Lemke, Hákon Hákonarson, Stephen F. Traynelis, Marni J. Falk

    Publicado em 2016
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  20. 20
    Genetic predisposition to neuroblastoma mediated by a LMO1 super-enhancer polymorphism

    Genetic predisposition to neuroblastoma mediated by a LMO1 super-enhancer polymorphism Por Derek A. Oldridge, Andrew Wood, Nina Weichert‐Leahey, Ian Crimmins, Robyn T. Sussman, Cynthia Winter, Lee McDaniel, Maura Diamond, Lori S. Hart, Shizhen Zhu, Adam D. Durbin, Brian J. Abraham, Lars Anders, Lifeng Tian, Shile Zhang, Jun S. Wei, Javed Khan, Kelli Bramlett, Nazneen Rahman, Mario Capasso, Achille Iolascon, Daniela S. Gerhard, Jaime M. Guidry Auvil, Richard A. Young, Hákon Hákonarson, Sharon J. Diskin, A. Thomas Look, John M. Maris

    Publicado em 2015
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