Genetic Variants of the BAFF Gene and Risk of Fatigue Among Patients With Primary Sjögren’s Syndrome
Background/PurposePrimary Sjögren’s Syndrome (SS) is characterized by B lymphocyte hyperactivity with B cell activating factor (BAFF) acting as an important regulator. Single Nucleotide Polymorphisms (SNPs) of the BAFF gene have been implicated in the pathogenesis of several autoimmune diseases char...
Main Authors: | Christina-Maria Flessa, Evangelia Zampeli, Maria-Eleftheria Evangelopoulos, Vasilis Natsis, Iris L. A. Bodewes, Erika Huijser, Marjan A. Versnel, Haralampos M. Moutsopoulos, Clio P. Mavragani |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2022-03-01
|
Series: | Frontiers in Immunology |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fimmu.2022.836824/full |
Similar Items
-
Association of BAFF and BAFF-R polymorphisms with sarcoidosis in a Greek patient cohort
by: Maria Martinou, et al.
Published: (2022-10-01) -
Editorial: Demyelinating neurological syndromes: The role of autoimmunity
by: Maria Eleftheria Evangelopoulos, et al.
Published: (2023-03-01) -
Editorial: Management of Sjögren's Syndrome
by: Alessia Alunno, et al.
Published: (2022-01-01) -
Musculoskeletal Manifestations in Sjogren’s Syndrome: An Orthopedic Point of View
by: Meletios Rozis, et al.
Published: (2021-04-01) -
A case of antisynthetase syndrome
by: Clio P. Mavragani, et al.
Published: (2020-08-01)