檢索結果 - Lisa R. Forbes
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Signal transducer and activator of transcription 3 由 Lisa R. Forbes, Josh Milner, Élie Haddad
出版 2015Revisão -
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High-resolution phenotyping identifies NK cell subsets that distinguish healthy children from adults 由 Sanjana Mahapatra, Emily M. Mace, Charles G. Minard, Lisa R. Forbes, Alexander Vargas‐Hernández, Teresa Duryea, George Makedonas, Pinaki P. Banerjee, William T. Shearer, Jordan S. Orange
出版 2017Artigo -
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Association of Rituximab Use With Adverse Events in Children, Adolescents, and Young Adults 由 Casey L. McAtee, Joseph Lubega, Kristen Underbrink, Kristen Curry, Pavlos Msaouel, M.E.H. BARROW, Eyal Muscal, Timothy Lotze, Poyyapakkam Srivaths, Lisa R. Forbes, Carl E. Allen, M. Brooke Bernhardt
出版 2021Artigo -
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Copa Syndrome: a Novel Autosomal Dominant Immune Dysregulatory Disease 由 Timothy J. Vece, Levi B. Watkin, Sarah K. Nicholas, Debra Canter, Michael Braun, R. Paul Guillerman, Karen W. Eldin, Grant Bertolet, Scott McKinley, Marietta De Guzman, Lisa R. Forbes, Iván K. Chinn, Jordan S. Orange
出版 2016Revisão -
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Ruxolitinib reverses dysregulated T helper cell responses and controls autoimmunity caused by a novel signal transducer and activator of transcription 1 (STAT1) gain-of-function mu... 由 Katja G. Weinacht, Louis‐Marie Charbonnier, Fayhan Alroqi, Ashley Plant, Qi Qiao, Hao Wu, Clement Ma, Troy R. Torgerson, Sergio D. Rosenzweig, Thomas A. Fleisher, Luigi D. Notarangelo, I. Celine Hanson, Lisa R. Forbes, Talal A. Chatila
出版 2017Artigo -
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Mutations in PI3K110δ cause impaired natural killer cell function partially rescued by rapamycin treatment 由 Raquel Ruiz‐García, Alexander Vargas‐Hernández, Iván K. Chinn, Laura S. Angelo, Tram N. Cao, Zeynep Coban‐Akdemir, Shalini N. Jhangiani, Qingchang Meng, Lisa R. Forbes, Donna M. Muzny, Luís M. Allende, M S Ehlayel, Richard A. Gibbs, James R. Lupski, Gülbû Uzel, Jordan S. Orange, Emily M. Mace
出版 2018Artigo -
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Ruxolitinib partially reverses functional natural killer cell deficiency in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 由 Alexander Vargas‐Hernández, Emily M. Mace, Ofer Zimmerman, Christa S. Zerbe, Alexandra F. Freeman, Sergio D. Rosenzweig, Jennifer W. Leiding, Troy R. Torgerson, Matthew C. Altman, Edith Schussler, Charlotte Cunningham‐Rundles, Iván K. Chinn, Alexandre F. Carisey, I. Celine Hanson, Nicholas L. Rider, Steven M. Holland, Jordan S. Orange, Lisa R. Forbes
出版 2017Artigo -
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Failing to Make Ends Meet: The Broad Clinical Spectrum of DNA Ligase IV Deficiency. Case Series and Review of the Literature 由 Aidé Tamara Staines Boone, Iván K. Chinn, Carmen Aláez‐Verson, Marco Antonio Yamazaki‐Nakashimada, Karol Carrillo‐Sánchez, María de la Luz Hortensia García-Cruz, M. Cecilia Poli, María Edith González Serrano, Edgar Alejandro Medina Torres, David Muzquiz Zermeño, Lisa R. Forbes, Francisco Espinosa‐Rosales, Sara Elva Espinosa‐Padilla, Jordan S. Orange, Saúl Oswaldo Lugo Reyes
出版 2019Artigo -
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Vaccine-associated varicella and rubella infections in severe combined immunodeficiency with isolated CD4 lymphocytopenia and mutations in <i>IL 7 R</i> detected by tandem whole ex... 由 Diana K. Bayer, Caridad Martinez, Hanne Sørmo Sorte, Lisa R. Forbes, Gail J. Demmler‐Harrison, I. Celine Hanson, Nathaniel M. Pearson, Lenora M. Noroski, Sherif R. Zaki, William J. Bellini, Magalie S. Leduc, Yuan Yang, Christine M. Eng, Ankita Patel, Olaug K. Rødningen, Donna M. Muzny, Richard A. Gibbs, Ian M. Campbell, Chad A. Shaw, Mei Baker, V Zhang, James R. Lupski, Jordan S. Orange, Filiz O. Seeborg, Asbjørg Stray‐Pedersen
出版 2014Artigo -
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Jakinibs for the treatment of immune dysregulation in patients with gain-of-function signal transducer and activator of transcription 1 (STAT1) or STAT3 mutations 由 Lisa R. Forbes, Tiphanie P. Vogel, Megan A. Cooper, Johana B Castro-Wagner, Edith Schussler, Katja G. Weinacht, Ashley Plant, Helen C. Su, Eric J. Allenspach, Mary Slatter, Mario Abinun, Desa Lilić, Charlotte Cunningham‐Rundles, Olive S. Eckstein, Peter Olbrich, R. Paul Guillerman, Niraj Patel, Yeşim Yılmaz Demirdağ, Christa S. Zerbe, Alexandra F. Freeman, Steven M. Holland, Paul Szabolcs, Andrew R. Gennery, Troy R. Torgerson, Joshua D. Milner, Jennifer W. Leiding
出版 2018Carta -
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Heterozygous Truncating Variants in POMP Escape Nonsense-Mediated Decay and Cause a Unique Immune Dysregulatory Syndrome 由 M. Cecilia Poli, Frédéric Ebstein, Sarah K. Nicholas, Marietta M. de Guzman, Lisa R. Forbes, Iván K. Chinn, Emily M. Mace, Tiphanie P. Vogel, Alexandre F. Carisey, Felipe Benavides, Zeynep Coban‐Akdemir, Richard A. Gibbs, Shalini N. Jhangiani, Donna M. Muzny, Claudia M.B. Carvalho, Deborah Schady, Mahim Jain, Jill A. Rosenfeld, Lisa Emrick, Richard A. Lewis, Brendan Lee, Barbara A. Zieba, Sébastien Küry, Elke Krüger, James R. Lupski, Bret L. Bostwick, Jordan S. Orange
出版 2018Artigo -
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IFN-γ signature in the plasma proteome distinguishes pediatric hemophagocytic lymphohistiocytosis from sepsis and SIRS 由 Howard Lin, Brooks Scull, Baruch R. Goldberg, Harshal Abhyankar, Olive E. Eckstein, Daniel Zinn, Joseph Lubega, Jennifer E. Agrusa, Nader El Mallawaney, Nitya Gulati, Lisa R. Forbes, Iván K. Chinn, Rikhia Chakraborty, Jessica Velasquez, Jordana Goldman, Dalia Bashir, Fong Lam, Eyal Muscal, M M Henry, Jay Greenberg, Stephan Ladisch, Michelle L. Hermiston, Lauren K. Meyer, Michael Jeng, Ahmed Naqvi, Kenneth L. McClain, Trung Nguyen, Hector R. Wong, Tsz‐Kwong Man, Michael B. Jordan, Carl E. Allen
出版 2021Artigo -
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Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosis 由 Iván K. Chinn, Olive S. Eckstein, Erin C. Peckham‐Gregory, Baruch R. Goldberg, Lisa R. Forbes, Sarah K. Nicholas, Emily M. Mace, Tiphanie P. Vogel, Harshal Abhyankar, María I. Díaz, Helen E. Heslop, Robert A. Krance, Caridad Martinez, Trung C. Nguyen, Dalia Bashir, Jordana Goldman, Asbjørg Stray‐Pedersen, Luis Alberto Pedroza, M. Cecilia Poli, Juan Carlos Aldave Becerra, Sean McGhee, Waleed Al‐Herz, Aghiad Chamdin, Zeynep Coban‐Akdemir, Shalini N. Jhangiani, Donna M. Muzny, Tram N. Cao, Diana N. Hong, Richard A. Gibbs, James R. Lupski, Jordan S. Orange, Kenneth L. McClain, Carl E. Allen
出版 2018Artigo -
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PGM3 Mutations Cause a Congenital Disorder of Glycosylation with Severe Immunodeficiency and Skeletal Dysplasia 由 Asbjørg Stray‐Pedersen, Paul Hoff Backe, Hanne Sørmo Sorte, Lars Mørkrid, Niti Chokshi, Hans Christian Erichsen, Tomasz Gambin, Katja Benedikte Prestø Elgstøen, Magnar Bjørås, Marcin W. Włodarski, Marcus Krüger, Shalini N. Jhangiani, Donna M. Muzny, Ankita Patel, Kimiyo Raymond, Ghadir Sasa, Robert A. Krance, Caridad Martinez, Shirley Abraham, Carsten Speckmann, Stephan Ehl, Patricia Hall, Lisa R. Forbes, Else Merckoll, Jostein Westvik, Gen Nishimura, Cecilie F. Rustad, Tore G. Abrahamsen, Arild Rønnestad, Liv Osnes, Torstein Egeland, Olaug K. Rødningen, Christine R. Beck, Eric Boerwinkle, Richard A. Gibbs, James R. Lupski, Jordan S. Orange, Ekkehart Lausch, I. Celine Hanson
出版 2014Artigo
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