A novel XNA-based Luminex assay to detect UBA1 somatic mutations associated with VEXAS syndrome-Reference-Cited by-同舟云学术

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A novel XNA-based Luminex assay to detect UBA1 somatic mutations associated with VEXAS syndrome

Published:2024-03 Issue: Volume:39 Page:e00380
ISSN:2352-5517
Container-title:Practical Laboratory Medicine
language:en
Short-container-title:Practical Laboratory Medicine

Author:

Ma Yunqing^ORCID,Hu ShianPin,Ni Rui,Liu Wei,Fu Andrew,Sha Michael,Zhang Aiguo,Lu Chuanyi M.

Publisher

Elsevier BV

Reference15 articles.

1. Somatic mutations in UBA1 and severe adult-onset autoinflammatory disease;Beck;N. Engl. J. Med.,2020

2. How to treat VEXAS syndrome: a systematic review on effectiveness and safety of current treatment strategies;Boyadzhieva;Rheumatology,2023

3. Translation of cytoplasmic UBA1 contributes to VEXAS syndrome pathogenesis;Ferrada;Blood,2022

4. Novel somatic mutations in UBA1 as a cause of VEXAS syndrome;Poulter;Blood,2021

5. Novel causative variants of VEXAS in UBA1 detected through whole genome transcriptome sequencing in a large cohort of hematological malignancies;Sakuma;Leukemia,2023

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