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Science Immunology
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August 12, 2022
Immunodeficiency, autoimmunity, and increased risk of B cell malignancy in humans with <i>TRAF3</i> mutations
William Rae, John M Sowerby, Dorit Verhoeven, et al.
The New England Journal of Medicine
|
January 13, 2012
Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions
Michael J Ombrello, Elaine F Remmers, Guangping Sun, et al.
Nature Genetics
|
October 28, 2017
Corrigendum: Germline hypomorphic CARD11 mutations in severe atopic disease
Chi A Ma, Jeffrey R Stinson, Yuan Zhang, et al.
Nature Genetics
|
December 8, 2015
Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease
Qing Zhou, Hongying Wang, Daniella M Schwartz, et al.
Nature Genetics
|
June 20, 2017
Germline hypomorphic CARD11 mutations in severe atopic disease
Chi A Ma, Jeffrey R Stinson, Yuan Zhang, et al.
The New England Journal of Medicine
|
May 31, 2023
Variant <i>STAT4</i> and Response to Ruxolitinib in an Autoinflammatory Syndrome
Hratch Baghdassarian, Sarah A Blackstone, Owen S Clay, et al.
Blood Advances
|
September 28, 2022
Genetically defined individual reference ranges for tryptase limit unnecessary procedures and unmask myeloid neoplasms
Jack Chovanec, Ilker Tunc, Jason Hughes, et al.
The Journal of Allergy and Clinical Immunology
|
May 27, 2026
Guidance on JAK inhibitor treatment for inborn errors of JAK-STAT signaling (2026). An international consensus statement on behalf of the ESID/EBMT-IEWP and ERN-RITA
Peter Olbrich, M Fischer, A Deyà-Martinez, et al.
Blood
|
November 1, 2014
Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations
Joshua D Milner, Tiphanie P Vogel, Lisa Forbes, et al.
JAMA
|
October 24, 2024
Expanded Newborn Screening Using Genome Sequencing for Early Actionable Conditions
Alban Ziegler, Carrie Koval-Burt, Denise M Kay, et al.
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of 66
Search research articles
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Showing results (631-640 of 658) with videos related to
Sort By:
Page
of 66
Science Immunology
|
August 12, 2022
Immunodeficiency, autoimmunity, and increased risk of B cell malignancy in humans with <i>TRAF3</i> mutations
William Rae, John M Sowerby, Dorit Verhoeven, et al.
The New England Journal of Medicine
|
January 13, 2012
Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions
Michael J Ombrello, Elaine F Remmers, Guangping Sun, et al.
Nature Genetics
|
October 28, 2017
Corrigendum: Germline hypomorphic CARD11 mutations in severe atopic disease
Chi A Ma, Jeffrey R Stinson, Yuan Zhang, et al.
Nature Genetics
|
December 8, 2015
Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease
Qing Zhou, Hongying Wang, Daniella M Schwartz, et al.
Nature Genetics
|
June 20, 2017
Germline hypomorphic CARD11 mutations in severe atopic disease
Chi A Ma, Jeffrey R Stinson, Yuan Zhang, et al.
The New England Journal of Medicine
|
May 31, 2023
Variant <i>STAT4</i> and Response to Ruxolitinib in an Autoinflammatory Syndrome
Hratch Baghdassarian, Sarah A Blackstone, Owen S Clay, et al.
Blood Advances
|
September 28, 2022
Genetically defined individual reference ranges for tryptase limit unnecessary procedures and unmask myeloid neoplasms
Jack Chovanec, Ilker Tunc, Jason Hughes, et al.
The Journal of Allergy and Clinical Immunology
|
May 27, 2026
Guidance on JAK inhibitor treatment for inborn errors of JAK-STAT signaling (2026). An international consensus statement on behalf of the ESID/EBMT-IEWP and ERN-RITA
Peter Olbrich, M Fischer, A Deyà-Martinez, et al.
Blood
|
November 1, 2014
Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations
Joshua D Milner, Tiphanie P Vogel, Lisa Forbes, et al.
JAMA
|
October 24, 2024
Expanded Newborn Screening Using Genome Sequencing for Early Actionable Conditions
Alban Ziegler, Carrie Koval-Burt, Denise M Kay, et al.
Page
of 66