TNFRSF13B VARIANTS ACT AS MODIFIERS TO CLINICAL PHENOTYPES IN COMMON VARIABLE IMMUNE DEFICIENCY DISORDERS
Objective: The TNF receptor gene 13B (TNFSRF13B) is a member of the TNF superfamily which is crucial for B cell maturation, plasma cell differentiation, and antibody response. Impaired expression of the TNFRSF13B gene is associated with common variable immune deficiency (CVID), autoimmunity, and lym...
Saved in:
| Main Authors: | Sinem Fırtına, Aslı Kutlu, Begüm Işıkgil, Medinenur Yozlu, Beyza Nur Cepeci, Hülya Yılmaz, Yuk Yin Ng, Özden Hatırnaz Ng, Ayça Kıykım, Esra Özek Yücel, Elif Karakoç Aydıner, Safa Barış, Ahmet Oğuzhan Özen, Serdar Nepesov, Yıldız Çamcıoğlu, İsmail Reisli, Muhlis Cem Ar, Müge Sayitoğlu |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Istanbul University Press
2023-10-01
|
| Series: | Sabiad |
| Subjects: | |
| Online Access: | https://cdn.istanbul.edu.tr/file/JTA6CLJ8T5/E2CF0E56089245BFAA286E3C6775A853 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
麝鼠TNFRSF13C和TNFRSF4基因表达分析
by: 廖光珍, et al.
Published: (2020-01-01) -
TNFRSF11B promotes the progression of bladder cancer through PI3K/AKT signaling pathway
by: Hao Deng, et al.
Published: (2024-12-01) -
HETEROZYGOUS PATHOGENIC MASP2 VARIANT ASSOCIATED WITH INFANTILE GIANT CELL HEPATITIS WITH AUTOIMMUNE HAEMOLYTIC ANAEMIA IN A CHILD
by: Merve Sarıtaş, et al.
Published: (2024-10-01) -
TNFRSF11B-modified umbilical cord mesenchymal stem cells as a novel strategy for bone-related diseases by suppressing osteoclast activity
by: Mina Ding, et al.
Published: (2025-05-01) -
Juvenile Paget disease with unique compound heterozygous sequence variants in the TNFRSF11B gene
by: Jana Horackova, et al.
Published: (2025-08-01)