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The Journal of Experimental Medicine
|
December 17, 2019
Activated PI3Kδ breaches multiple B cell tolerance checkpoints and causes autoantibody production
Anthony Lau, Danielle T Avery, Katherine Jackson, et al.
The Journal of Allergy and Clinical Immunology
|
January 15, 2017
Disease-associated mutations identify a novel region in human STING necessary for the control of type I interferon signaling
Isabelle Melki, Yoann Rose, Carolina Uggenti, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
March 30, 2019
Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome
Davide Montin, Agostina Marolda, Francesco Licciardi, et al.
Molecular Genetics and Metabolism
|
March 23, 2026
Efficacy of JAK1/2 inhibitors in AGS genes-related interferonopathies: A multicenter retrospective observational study with treated vs untreated comparison
Gemma Marinella, Ylenia Vaia, Davide Politano, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 26, 2022
Epigenetic analysis of cell-free DNA by fragmentomic profiling
Qing Zhou, Guannan Kang, Peiyong Jiang, et al.
Nature Communications
|
November 2, 2023
ARF1 prevents aberrant type I interferon induction by regulating STING activation and recycling
Maximilian Hirschenberger, Alice Lepelley, Ulrich Rupp, et al.
American Journal of Human Genetics
|
October 6, 2020
Plasma DNA Profile Associated with DNASE1L3 Gene Mutations: Clinical Observations, Relationships to Nuclease Substrate Preference, and In Vivo Correction
Rebecca W Y Chan, Lee Serpas, Meng Ni, et al.
Frontiers in Immunology
|
August 15, 2022
Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait?
Maria Chiriaco, Giorgiana Madalina Ursu, Donato Amodio, et al.
American Journal of Human Genetics
|
May 2, 2025
Plasma DNA Profile Associated with DNASE1L3 Gene Mutations: Clinical Observations, Relationships to Nuclease Substrate Preference, and In Vivo Correction
Rebecca W Y Chan, Lee Serpas, Meng Ni, et al.
American Journal of Human Genetics
|
December 12, 2025
Plasma DNA Profile Associated with DNASE1L3 Gene Mutations: Clinical Observations, Relationships to Nuclease Substrate Preference, and In Vivo Correction
Rebecca W Y Chan, Lee Serpas, Meng Ni, et al.
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of 17
Search research articles
Search
Showing results (131-140 of 166) with videos related to
Sort By:
Page
of 17
The Journal of Experimental Medicine
|
December 17, 2019
Activated PI3Kδ breaches multiple B cell tolerance checkpoints and causes autoantibody production
Anthony Lau, Danielle T Avery, Katherine Jackson, et al.
The Journal of Allergy and Clinical Immunology
|
January 15, 2017
Disease-associated mutations identify a novel region in human STING necessary for the control of type I interferon signaling
Isabelle Melki, Yoann Rose, Carolina Uggenti, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
March 30, 2019
Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome
Davide Montin, Agostina Marolda, Francesco Licciardi, et al.
Molecular Genetics and Metabolism
|
March 23, 2026
Efficacy of JAK1/2 inhibitors in AGS genes-related interferonopathies: A multicenter retrospective observational study with treated vs untreated comparison
Gemma Marinella, Ylenia Vaia, Davide Politano, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 26, 2022
Epigenetic analysis of cell-free DNA by fragmentomic profiling
Qing Zhou, Guannan Kang, Peiyong Jiang, et al.
Nature Communications
|
November 2, 2023
ARF1 prevents aberrant type I interferon induction by regulating STING activation and recycling
Maximilian Hirschenberger, Alice Lepelley, Ulrich Rupp, et al.
American Journal of Human Genetics
|
October 6, 2020
Plasma DNA Profile Associated with DNASE1L3 Gene Mutations: Clinical Observations, Relationships to Nuclease Substrate Preference, and In Vivo Correction
Rebecca W Y Chan, Lee Serpas, Meng Ni, et al.
Frontiers in Immunology
|
August 15, 2022
Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait?
Maria Chiriaco, Giorgiana Madalina Ursu, Donato Amodio, et al.
American Journal of Human Genetics
|
May 2, 2025
Plasma DNA Profile Associated with DNASE1L3 Gene Mutations: Clinical Observations, Relationships to Nuclease Substrate Preference, and In Vivo Correction
Rebecca W Y Chan, Lee Serpas, Meng Ni, et al.
American Journal of Human Genetics
|
December 12, 2025
Plasma DNA Profile Associated with DNASE1L3 Gene Mutations: Clinical Observations, Relationships to Nuclease Substrate Preference, and In Vivo Correction
Rebecca W Y Chan, Lee Serpas, Meng Ni, et al.
Page
of 17