Search Results - Michael March

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  1. 1
    A signaling network stimulated by β <sub>2</sub> integrin promotes the polarization of lytic granules in cytotoxic cells

    A signaling network stimulated by β <sub>2</sub> integrin promotes the polarization of lytic granules in cytotoxic cells by Minggang Zhang, Michael March, William S. Lane, Eric O. Long

    Published 2014
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  2. 2
    Synergy among receptors on resting NK cells for the activation of natural cytotoxicity and cytokine secretion

    Synergy among receptors on resting NK cells for the activation of natural cytotoxicity and cytokine secretion by Yenan T. Bryceson, Michael March, Hans‐Gustaf Ljunggren, Eric O. Long

    Published 2005
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  3. 3
    Activation, coactivation, and costimulation of resting human natural killer cells

    Activation, coactivation, and costimulation of resting human natural killer cells by Yenan T. Bryceson, Michael March, Hans‐Gustaf Ljunggren, Eric O. Long

    Published 2006
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  4. 4
    Cytolytic granule polarization and degranulation controlled by different receptors in resting NK cells

    Cytolytic granule polarization and degranulation controlled by different receptors in resting NK cells by Yenan T. Bryceson, Michael March, Domingo F. Barber, Hans‐Gustaf Ljunggren, Eric O. Long

    Published 2005
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  5. 5
    The Role of Autophagy in Skeletal Muscle Diseases

    The Role of Autophagy in Skeletal Muscle Diseases by Qianghua Xia, Xubo Huang, Jieru Huang, Yongfeng Zheng, Michael March, Jin Li, Yongjie Wei

    Published 2021
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  6. 6
    Kaposiform lymphangiomatosis effectively treated with <scp>MEK</scp> inhibition

    Kaposiform lymphangiomatosis effectively treated with <scp>MEK</scp> inhibition by Jessica Foster, Dong Li, Michael March, Sarah E. Sheppard, Denise M. Adams, Hákon Hákonarson, Yoav Dori

    Published 2020
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  7. 7
    Severe Lymphatic Disorder Resolved With MEK Inhibition in a Patient With Noonan Syndrome and SOS1 Mutation

    Severe Lymphatic Disorder Resolved With MEK Inhibition in a Patient With Noonan Syndrome and SOS1 Mutation by Yoav Dori, Christopher L. Smith, Erin Pinto, Kristen Snyder, Michael March, Hákon Hákonarson, Jean B. Belasco

    Published 2020
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  8. 8
    Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders

    Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders by Joseph Glessner, Jin Li, Dai Wang, Michael March, Leandro Lima, Akshatha Desai, Dexter Hadley, Charlly Kao, Raquel E. Gur, Nadine Cohen, Patrick Sleiman, Qingqin S. Li, Hákon Hákonarson

    Published 2017
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  9. 9
    Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders

    Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders by Xueming Yao, Joseph Glessner, Junyi Li, Xiaohui Qi, Xiaoyuan Hou, Chonggui Zhu, Xiaoge Li, Michael March, Liu Yang, Frank Mentch, Heather S. Hain, Xinyi Meng, Qianghua Xia, Hákon Hákonarson, Jin Li

    Published 2021
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  10. 10
    A genome-wide association meta-analysis identifies new eosinophilic esophagitis loci

    A genome-wide association meta-analysis identifies new eosinophilic esophagitis loci by Xiao Chang, Michael March, Frank Mentch, Kenny Nguyen, Joseph Glessner, Hui‐Qi Qu, Yichuan Liu, G.T. Furuta, Seema S. Aceves, Nirmala Gonsalves, Kari C. Nadeau, Antonella Cianferoni, Jonathan M. Spergel, Patrick Sleiman, Hákon Hákonarson

    Published 2021
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  11. 11
    Treatment of severe Kaposiform lymphangiomatosis positive for NRAS mutation by MEK inhibition

    Treatment of severe Kaposiform lymphangiomatosis positive for NRAS mutation by MEK inhibition by Guy Chowers, Gadi Abebe‐Campino, Hana Golan, Asaf Vivante, Shoshana Greenberger, Michalle Soudack, Galia Barkai, Ilana Fox-Fisher, Dong Li, Michael March, Mark R. Battig, Hákon Hákonarson, Denise M. Adams, Yoav Dori, Adi Dagan

    Published 2022
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  12. 12
    Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly

    Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly by 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

    Published 2018
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  13. 13
    Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene

    Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene by Gijs van Ingen, Jin Li, André Goedegebure, Rahul Pandey, Leslie A. Lange, Michael March, Vincent W. V. Jaddoe, Marina Bakay, Frank Mentch, Kelly Thomas, Zhi Wei, Xiao Chang, Heather S. Hain, André G. Uitterlinden, Henriëtte A. Moll, Cornelia M. van Duijn, Fernando Rivadeneira, Hein Raat, Robert J. Baatenburg de Jong, Patrick Sleiman, Marc P. van der Schroeff, Hákon Hákonarson

    Published 2016
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  14. 14
    Detecting multiple differentially methylated CpG sites and regions related to dimensional psychopathology in youths

    Detecting multiple differentially methylated CpG sites and regions related to dimensional psychopathology in youths by Letícia Spíndola, Marcos Santoro, Pedro Mário Pan, Vanessa Kiyomi Ota, Gabriela Xavier, Carolina Muniz Carvalho, Fernanda Talarico, Patrick Sleiman, Michael March, Renata Pellegrino, Elisa Brietzke, Rodrigo Grassi‐Oliveira, Jair de Jesus Mari, Ary Gadelha, Eurípedes C. Miguel, Luís Augusto Rohde, Rodrigo A. Bressan, Diego R. Mazzotti, João Ricardo Sato, Giovanni Abrahão Salum, Hákon Hákonarson, Síntia Belangero

    Published 2019
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  15. 15
    Bi-allelic variants in the ER quality-control mannosidase gene EDEM3 cause a congenital disorder of glycosylation

    Bi-allelic variants in the ER quality-control mannosidase gene EDEM3 cause a congenital disorder of glycosylation by D.L. Polla, Andrew C. Edmondson, Sandrine Duvet, Michael March, Ana Berta Sousa, Anna Lehman, Dmitriy Niyazov, Fleur van Dijk, Serwet Demirdas, Marjon A. van Slegtenhorst, Anneke J.A. Kievit, Céline Schulz, Linlea Armstrong, Xin Bi, Daniel J. Rader, Kosuke Izumi, Elaine H. Zackai, Elisa De Franco, Paula Jorge, Sophie C. Huffels, Marina P. Hommersom, Sian Ellard, Dirk J. Lefeber, Avni Santani, Nicholas J. Hand, Hans van Bokhoven, Miao He, Arjan P.M. de Brouwer

    Published 2021
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  16. 16
    Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genes

    Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genes by Joseph Glessner, Mylarappa Ningappa, Kim A. Ngo, Maliha Zahid, Juhoon So, Brandon W. Higgs, Patrick Sleiman, Tejaswini Narayanan, Sarangarajan Ranganathan, Michael March, Krishna Prasadan, Courtney Vaccaro, Miguel Reyes‐Múgica, Jeremy J. Velazquez, Cláudia Salgado, Mo R. Ebrahimkhani, Lori Schmitt, Dhivyaa Rajasundaram, Paul Morgan, Renata Pellegrino, George K. Gittes, Dong Li, Xiang Wang, Jonathan Billings, Robert H. Squires, Chethan Ashokkumar, Khalid Sharif, Déirdre Kelly, Anil Dhawan, Simon Horslen, Cecilia Lo, Donghun Shin, Shankar Subramaniam, Hákon Hákonarson, Rakesh Sindhi

    Published 2023
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  17. 17
    Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibition

    Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibition by Sarah E. Sheppard, Michael March, Christoph Seiler, Leticia S. Matsuoka, S Kim, Charlly Kao, Adam I. Rubin, Mark R. Battig, Nahla Khalek, Erica Schindewolf, Nora O’Connor, Erin Pinto, Jessica Priestley, Victoria R. Sanders, Rojeen Niazi, Arupa Ganguly, Cuiping Hou, Diana J. Slater, Ilona J. Frieden, Thy Huynh, Joseph T.C. Shieh, Ian D. Krantz, Jessenia Guerrero, Lea F. Surrey, David M. Biko, Pablo Laje, Leslie Castelo‐Soccio, Taizo A. Nakano, Kristen Snyder, Christopher L. Smith, Dong Li, Yoav Dori, Hákon Hákonarson

    Published 2023
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  18. 18
    Phenome-wide association studies across large population cohorts support drug target validation

    Phenome-wide association studies across large population cohorts support drug target validation by Dorothée Diogo, Chao Tian, Christopher S. Franklin, Mervi Alanne-Kinnunen, Michael March, Chris C. A. Spencer, Ciara Vangjeli, Michael E. Weale, Hannele Mattsson, Elina Kilpeläinen, Patrick Sleiman, Dermot F. Reilly, Joshua McElwee, Joseph Maranville, Arnaub K. Chatterjee, Aman Bhandari, Khanh‐Dung H. Nguyen, Karol Estrada, Mary-Pat Reeve, Janna Hutz, Nan Bing, Sally John, Daniel G. MacArthur, Veikko Salomaa, Samuli Ripatti, Hákon Hákonarson, Mark J. Daly, Aarno Palotie, David A. Hinds, Peter Donnelly, Caroline S. Fox, Aaron Day-Williams, Robert M. Plenge, Heiko Runz

    Published 2018
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  19. 19
    Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

    Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations by Leslie A. Lange, Joseph Glessner, Bradley P. Coe, Jin Li, Maedeh Mohebnasab, Xiao Chang, John J. Connolly, Charlly Kao, Zhi Wei, Jonathan P. Bradfield, Cecilia Kim, Cuiping Hou, Munir Khan, Frank Mentch, Haijun Qiu, Marina Bakay, Christopher J. Cardinale, Maria Lemma, Debra Abrams, Andrew Bridglall-Jhingoor, Meckenzie Behr, Shanell Harrison, George Otieno, Alexandria Thomas, Fengxiang Wang, Rosetta Chiavacci, Lawrence Shih-Hsin Wu, Dexter Hadley, Elizabeth Goldmuntz, Josephine Elia, John M. Maris, Robert W. Grundmeier, Marcella Devoto, Brendan J. Keating, Michael March, Renata Pellagrino, Struan F.A. Grant, Patrick Sleiman, Mingyao Li, Evan E. Eichler, Hákon Hákonarson

    Published 2020
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  20. 20
    Genomic profiling informs diagnoses and treatment in vascular anomalies

    Genomic profiling informs diagnoses and treatment in vascular anomalies by Dong Li, Sarah E. Sheppard, Michael March, Mark R. Battig, Lea F. Surrey, Abhay Srinivasan, Leticia S. Matsuoka, Lifeng Tian, Fengxiang Wang, Christoph Seiler, Jill Dayneka, Alexandra J. Borst, Mary C. Matos, Scott M. Paulissen, Ganesh Krishnamurthy, Bede N. Nriagu, Tamjeed Sikder, Melissa Casey, Lydia Williams, Sneha Rangu, Nora O’Connor, Alexandria Thomas, Erin Pinto, Cuiping Hou, Kenny Nguyen, Renata Pellegrino da Silva, Samar Nasser Chehimi, Charlly Kao, Lauren Biroc, Allison Britt, Maria Queenan, Janet R. Reid, Joseph A. Napoli, D.M. Low, Seth Vatsky, James R. Treat, Christopher L. Smith, Anne Marie Cahill, Kristen Snyder, Denise M. Adams, Yoav Dori, Hákon Hákonarson

    Published 2023
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