نتائج البحث - Lisa R. Forbes
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Signal transducer and activator of transcription 3 حسب Lisa R. Forbes, Josh Milner, Élie Haddad
منشور في 2015Revisão -
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Human immunodeficiency-causing mutation defines CD16 in spontaneous NK cell cytotoxicity حسب Jennifer T. Grier, Lisa R. Forbes, Linda Monaco-Shawver, Jennifer Oshinsky, T. Prescott Atkinson, Curtis Moody, Rahul Pandey, Kerry S. Campbell, Jordan S. Orange
منشور في 2012Artigo -
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Clinical Aspects of STAT3 Gain-of-Function Germline Mutations: A Systematic Review حسب Alexandre Fabre, Sarah Marchal, Vincent Barlogis, Bernard Mari, Pascal Barbry, Pierre‐Simon Rohrlich, Lisa R. Forbes, Tiphanie P. Vogel, Lisa Giovannini‐Chami
منشور في 2019Revisão -
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High-resolution phenotyping identifies NK cell subsets that distinguish healthy children from adults حسب 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
منشور في 2017Artigo -
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Association of Rituximab Use With Adverse Events in Children, Adolescents, and Young Adults حسب 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
منشور في 2021Artigo -
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Copa Syndrome: a Novel Autosomal Dominant Immune Dysregulatory Disease حسب 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
منشور في 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... حسب 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
منشور في 2017Artigo -
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Mutations in PI3K110δ cause impaired natural killer cell function partially rescued by rapamycin treatment حسب 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
منشور في 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 حسب 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
منشور في 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 حسب 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
منشور في 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... حسب 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
منشور في 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 حسب 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
منشور في 2018Carta -
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Heterozygous Truncating Variants in POMP Escape Nonsense-Mediated Decay and Cause a Unique Immune Dysregulatory Syndrome حسب 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
منشور في 2018Artigo -
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IFN-γ signature in the plasma proteome distinguishes pediatric hemophagocytic lymphohistiocytosis from sepsis and SIRS حسب 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
منشور في 2021Artigo -
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Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosis حسب 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
منشور في 2018Artigo -
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PGM3 Mutations Cause a Congenital Disorder of Glycosylation with Severe Immunodeficiency and Skeletal Dysplasia حسب 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
منشور في 2014Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Immunology
Medicine
Genetics
Immune system
Gene
Internal medicine
Disease
Mutation
Primary immunodeficiency
Cell biology
Phenotype
Autoimmunity
Cancer research
Immune dysregulation
T cell
Cell
Immunodeficiency
Pediatrics
Antibody
Biochemistry
Hematopoietic stem cell transplantation
In vitro
Intensive care medicine
Natural killer cell
Pathology
STAT protein
STAT3
Severe combined immunodeficiency
Signal transduction