Search Results - Weimin He

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  1. 1
    Single-cell RNA-sequencing reveals cellular heterogeneity and immune microenvironment characteristics between ocular adnexal mucosa-associated lymphoid lymphoma and IgG4−related ophthalmic disease

    Single-cell RNA-sequencing reveals cellular heterogeneity and immune microenvironment characteristics between ocular adnexal mucosa-associated lymphoid lymphoma and IgG4−related op... by Yu Yang, Yujiao Wang, Xuelian Jin, Weimin He

    Published 2025
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  2. 2
    Distinct Modes of Interaction of SHC and Insulin Receptor Substrate-1 with the Insulin Receptor NPEY Region via Non-SH2 Domains

    Distinct Modes of Interaction of SHC and Insulin Receptor Substrate-1 with the Insulin Receptor NPEY Region via Non-SH2 Domains by Weimin He, Thomas J. O’Neill, Thomas A. Gustafson

    Published 1995
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  3. 3
    Grb10 Interacts Differentially with the Insulin Receptor, Insulin-like Growth Factor I Receptor, and Epidermal Growth Factor Receptor via the Grb10 Src Homology 2 (SH2) Domain and a Second Novel Domain Located between the Pleckstrin Homology and SH2 Domains

    Grb10 Interacts Differentially with the Insulin Receptor, Insulin-like Growth Factor I Receptor, and Epidermal Growth Factor Receptor via the Grb10 Src Homology 2 (SH2) Domain and... by Weimin He, David W. Rose, Jerrold M. Olefsky, Thomas A. Gustafson

    Published 1998
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  4. 4
    Phosphotyrosine-Dependent Interaction of SHC and Insulin Receptor Substrate 1 with the NPEY Motif of the Insulin Receptor via a Novel Non-SH2 Domain

    Phosphotyrosine-Dependent Interaction of SHC and Insulin Receptor Substrate 1 with the NPEY Motif of the Insulin Receptor via a Novel Non-SH2 Domain by Thomas A. Gustafson, Weimin He, Ann Craparo, Charles D. Schaub, Thomas J. O’Neill

    Published 1995
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  5. 5
    Clinical presentation and treatment outcome of retinoblastoma in children of South Western China

    Clinical presentation and treatment outcome of retinoblastoma in children of South Western China by Jingge Gao, Jihong Zeng, Bo Guo, Weimin He, Jun Chen, Fang Lü, Danian Chen

    Published 2016
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  6. 6
    Selective modulation of promoter recruitment and transcriptional activity of PPARγ

    Selective modulation of promoter recruitment and transcriptional activity of PPARγ by Dorothy D. Sears, Albert Hsiao, Jachelle M. Ofrecio, Justin Chapman, Weimin He, Jerrold M. Olefsky

    Published 2007
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  7. 7
    Nuclear Receptor Expression Links the Circadian Clock to Metabolism

    Nuclear Receptor Expression Links the Circadian Clock to Metabolism by Xiaoyong Yang, Michael Downes, Ruth T. Yu, Angie L. Bookout, Weimin He, Marty Straume, David J. Mangelsdorf, Ronald M. Evans

    Published 2006
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  8. 8
    Interaction of Insulin Receptor Substrate-2 (IRS-2) with the Insulin and Insulin-like Growth Factor I Receptors

    Interaction of Insulin Receptor Substrate-2 (IRS-2) with the Insulin and Insulin-like Growth Factor I Receptors by Weimin He, Ann Craparo, Youyan Zhu, Thomas J. O’Neill, Ling-Mei Wang, Jacalyn H. Pierce, Thomas A. Gustafson

    Published 1996
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  9. 9
    Effects of peroxisome proliferator-activated receptor δ on placentation, adiposity, and colorectal cancer

    Effects of peroxisome proliferator-activated receptor δ on placentation, adiposity, and colorectal cancer by Yaacov Barak, Debbie Liao, Weimin He, Estelita S. Ong, Michael C. Nelson, Jerrold M. Olefsky, Richard Boland, Ronald M. Evans

    Published 2001
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  10. 10
    PPARδ is a very low-density lipoprotein sensor in macrophages

    PPARδ is a very low-density lipoprotein sensor in macrophages by Ajay Chawla, Chih‐Hao Lee, Yaacov Barak, Weimin He, John M. Rosenfeld, Debbie Liao, Jungyeob Han, Heonjoong Kang, Ronald M. Evans

    Published 2003
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  11. 11
    Adipose-specific peroxisome proliferator-activated receptor γ knockout causes insulin resistance in fat and liver but not in muscle

    Adipose-specific peroxisome proliferator-activated receptor γ knockout causes insulin resistance in fat and liver but not in muscle by Weimin He, Yaacov Barak, Andrea L. Hevener, Peter Olson, Debbie Liao, Jamie Le, Michael C. Nelson, Estelita S. Ong, Jerrold M. Olefsky, Ronald M. Evans

    Published 2003
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  12. 12
    ERRγ Directs and Maintains the Transition to Oxidative Metabolism in the Postnatal Heart

    ERRγ Directs and Maintains the Transition to Oxidative Metabolism in the Postnatal Heart by William A. Alaynick, Richard P. Kondo, Wen Xie, Weimin He, Catherine R. Dufour, Michael Downes, Johan W. Jonker, Wayne R. Giles, Robert K. Naviaux, Vincent Giguère, Ronald M. Evans

    Published 2007
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  13. 13
    <i>KIF5A</i> mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction

    <i>KIF5A</i> mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction by Jessica Duis, Shannon L. Dean, Carolyn Applegate, Amy Harper, Rui Xiao, Weimin He, James D. Dollar, Lisa R. Sun, Marta Biderman Waberski, Thomas O. Crawford, Ada Hamosh, Carl E. Stafstrom

    Published 2016
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  14. 14
    Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder

    Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder by Elizabeth A. Normand, Alicia Braxton, Salma Nassef, Patricia A. Ward, Francesco Vetrini, Weimin He, Vipulkumar Patel, Chunjing Qu, Lauren Westerfield, Samantha Stover, Avinash V. Dharmadhikari, Donna M. Muzny, Richard A. Gibbs, Hongzheng Dai, Linyan Meng, Xia Wang, Rui Xiao, Pengfei Liu, Weimin Bi, Fan Xia, Magdalena Walkiewicz, Ignatia B. Van den Veyver, Christine M. Eng, Yaping Yang

    Published 2018
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  15. 15
    Mutations in the nuclear bile acid receptor FXR cause progressive familial intrahepatic cholestasis

    Mutations in the nuclear bile acid receptor FXR cause progressive familial intrahepatic cholestasis by Natalia Gomez‐Ospina, Carol Potter, Rui Xiao, Kandamurugu Manickam, Mi-Sun Kim, Kang Ho Kim, Benjamin L. Shneider, Jennifer Picarsic, Theodora A. Jacobson, Jing Zhang, Weimin He, Pengfei Liu, Alexander S. Knisely, Milton J. Finegold, Donna M. Muzny, Eric Boerwinkle, James R. Lupski, Sharon E. Plon, Richard A. Gibbs, Christine M. Eng, Yaping Yang, Gabriel C. Washington, Matthew H. Porteus, William E. Berquist, Neeraja Kambham, Ravinder J. Singh, Fan Xia, Gregory M. Enns, David D. Moore

    Published 2016
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  16. 16
    CNVs cause autosomal recessive genetic diseases with or without involvement of SNV/indels

    CNVs cause autosomal recessive genetic diseases with or without involvement of SNV/indels by Bo Yuan, Lei Wang, Pengfei Liu, Chad A. Shaw, Hongzheng Dai, Lance Cooper, Wenmiao Zhu, Stephanie A. Anderson, Linyan Meng, Xia Wang, Yue Wang, Fan Xia, Rui Xiao, Alicia Braxton, Sandra Peacock, Eric Schmitt, Patricia A. Ward, Francesco Vetrini, Weimin He, Theodore Chiang, Donna M. Muzny, Richard A. Gibbs, Arthur L. Beaudet, Amy M. Breman, Janice Smith, Sau Wai Cheung, Carlos A. Bacino, Christine M. Eng, Yaping Yang, James R. Lupski, Weimin Bi

    Published 2020
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  17. 17
    Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing

    Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing by Yaping Yang, Donna M. Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia A. Ward, Alicia Braxton, Min Wang, Christian Buhay, Narayanan Veeraraghavan, Alicia Hawes, Theodore Chiang, Magalie S. Leduc, Joke Beuten, Jing Zhang, Weimin He, Jennifer Scull, Alecia Willis, Megan Landsverk, William J. Craigen, Mir Reza Bekheirnia, Asbjørg Stray‐Pedersen, Pengfei Liu, Shu Wen, Wendy Alcaraz, Hong Cui, Magdalena Walkiewicz, Jeffrey G. Reid, Matthew N. Bainbridge, Ankita Patel, Eric Boerwinkle, Arthur L. Beaudet, James R. Lupski, Sharon E. Plon, Richard A. Gibbs, Christine M. Eng

    Published 2014
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  18. 18
    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 by 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

    Published 2019
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  19. 19
    Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

    Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features by Jing Zhang, Tomasz Gambin, Bo Yuan, Przemysław Szafrański, Jill A. Rosenfeld, Mohammed Al Balwi, Abdulrahman Alswaid, Lihadh Al‐Gazali, Aisha M. Al Shamsi, Makanko Komara, Bassam R. Ali, Elizabeth Roeder, Laura McAuley, Daniel Roy, David K. Manchester, Pilar Magoulas, Lauren E. King, Vickie Hannig, Dominique Bonneau, Anne‐Sophie Denommé‐Pichon, Majida Charif, Thomas Besnard, Stéphane Bézieau, Benjamin Cogné, Joris Andrieux, Wenmiao Zhu, Weimin He, Francesco Vetrini, Patricia A. Ward, Sau Wai Cheung, Weimin Bi, Christine M. Eng, James R. Lupski, Yaping Yang, Ankita Patel, Seema R. Lalani, Fan Xia, Paweł Stankiewicz

    Published 2017
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  20. 20
    Phenotypic expansion in <i><scp>DDX</scp>3X</i> – a common cause of intellectual disability in females

    Phenotypic expansion in <i><scp>DDX</scp>3X</i> – a common cause of intellectual disability in females by Xia Wang, Jennifer E. Posey, Jill A. Rosenfeld, Carlos A. Bacino, Fernando Scaglia, LaDonna Immken, Jill M. Harris, Scott E. Hickey, Theresa Mihalic Mosher, Anne Slavotinek, Jing Zhang, Joke Beuten, Magalie S. Leduc, Weimin He, Francesco Vetrini, Magdalena Walkiewicz, Weimin Bi, Rui Xiao, Pengfei Liu, Yunru Shao, Alper Gezdirici, Elif Yılmaz Güleç, Yunyun Jiang, Sandra Darilek, Adam Hansen, Michael M. Khayat, Davut Pehli̇van, Juliette Piard, Donna M. Muzny, Neil A. Hanchard, John W. Belmont, Lionel Van Maldergem, Richard A. Gibbs, Mohammad K. Eldomery, Zeynep Coban‐Akdemir, Adekunle M. Adesina, Shan Chen, Yi‐Chien Lee, Brendan Lee, James R. Lupski, Christine M. Eng, Fan Xia, Yaping Yang, Brett H. Graham, Paolo Moretti

    Published 2018
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