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Open Forum Infectious Diseases
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July 30, 2024
Opportunistic Infections, Mortality Risk, and Prevention Strategies in Patients With Vacuoles, E1 Enzyme, X-Linked, Autoinflammatory, Somatic (VEXAS) Syndrome
Mary Czech, Jennifer Cuellar-Rodriguez, Bhavisha A Patel, et al.
Journal of Clinical Immunology
|
July 9, 2020
Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual Inheritance
Oskar Schnappauf, Qing Zhou, Natalia Sampaio Moura, et al.
The Journal of Allergy and Clinical Immunology
|
May 28, 2021
Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXAS
Caspar I van der Made, Judith Potjewijd, Annemiek Hoogstins, et al.
Blood
|
May 24, 2022
Ruxolitinib is more effective than other JAK inhibitors to treat VEXAS syndrome: a retrospective multicenter study
Maël Heiblig, Marcela A Ferrada, Matthew J Koster, et al.
Biorxiv : the Preprint Server for Biology
|
June 5, 2026
Cell autonomous inflammation in VEXAS is mediated by cGAS-STING
Samuel J Magaziner, Jason C Collins, Brecca Miller, et al.
Science Advances
|
February 1, 2021
Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation
David B Beck, Mohammed A Basar, Anthony J Asmar, et al.
American Journal of Human Genetics
|
January 14, 2020
Delineation of a Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 Deficiency
David B Beck, Ana Petracovici, Chongsheng He, et al.
American Journal of Human Genetics
|
July 7, 2018
Bi-allelic Mutations in Phe-tRNA Synthetase Associated with a Multi-system Pulmonary Disease Support Non-translational Function
Zhiwen Xu, Wing-Sze Lo, David B Beck, et al.
Blood
|
April 21, 2023
Spectrum of clonal hematopoiesis in VEXAS syndrome
Fernanda Gutierrez-Rodrigues, Yael Kusne, Jenna Fernandez, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
March 29, 2021
Somatic Mutations in UBA1 Define a Distinct Subset of Relapsing Polychondritis Patients With VEXAS
Marcela A Ferrada, Keith A Sikora, Yiming Luo, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 83) with videos related to
Sort By:
Page
of 9
Open Forum Infectious Diseases
|
July 30, 2024
Opportunistic Infections, Mortality Risk, and Prevention Strategies in Patients With Vacuoles, E1 Enzyme, X-Linked, Autoinflammatory, Somatic (VEXAS) Syndrome
Mary Czech, Jennifer Cuellar-Rodriguez, Bhavisha A Patel, et al.
Journal of Clinical Immunology
|
July 9, 2020
Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual Inheritance
Oskar Schnappauf, Qing Zhou, Natalia Sampaio Moura, et al.
The Journal of Allergy and Clinical Immunology
|
May 28, 2021
Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXAS
Caspar I van der Made, Judith Potjewijd, Annemiek Hoogstins, et al.
Blood
|
May 24, 2022
Ruxolitinib is more effective than other JAK inhibitors to treat VEXAS syndrome: a retrospective multicenter study
Maël Heiblig, Marcela A Ferrada, Matthew J Koster, et al.
Biorxiv : the Preprint Server for Biology
|
June 5, 2026
Cell autonomous inflammation in VEXAS is mediated by cGAS-STING
Samuel J Magaziner, Jason C Collins, Brecca Miller, et al.
Science Advances
|
February 1, 2021
Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation
David B Beck, Mohammed A Basar, Anthony J Asmar, et al.
American Journal of Human Genetics
|
January 14, 2020
Delineation of a Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 Deficiency
David B Beck, Ana Petracovici, Chongsheng He, et al.
American Journal of Human Genetics
|
July 7, 2018
Bi-allelic Mutations in Phe-tRNA Synthetase Associated with a Multi-system Pulmonary Disease Support Non-translational Function
Zhiwen Xu, Wing-Sze Lo, David B Beck, et al.
Blood
|
April 21, 2023
Spectrum of clonal hematopoiesis in VEXAS syndrome
Fernanda Gutierrez-Rodrigues, Yael Kusne, Jenna Fernandez, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
March 29, 2021
Somatic Mutations in UBA1 Define a Distinct Subset of Relapsing Polychondritis Patients With VEXAS
Marcela A Ferrada, Keith A Sikora, Yiming Luo, et al.
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of 9