Multi-Omics Profiling in PGM3 and STAT3 Deficiencies: A Tale of Two Patients
Hyper-IgE Syndrome (HIES) is a heterogeneous group of primary immune-deficiency disorders characterized by elevated levels of IgE, eczema, and recurrent skin and lung infections. HIES that is autosomally dominant in the signal transducer and activator of transcription 3 (STAT3), and autosomal recess...
Main Authors: | Minnie Jacob, Afshan Masood, Anas M. Abdel Rahman |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2023-01-01
|
Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/1422-0067/24/3/2406 |
Similar Items
-
Hyper-IgE syndrome. Lessons from function and defects of STAT-3 or DOCK-8
by: Julio César Alcántara-Montiel, et al.
Published: (2016-10-01) -
Dominant-negative signal transducer and activator of transcription (STAT)3 variants in adult patients: A single center experience
by: Oded Shamriz, et al.
Published: (2022-12-01) -
In Vitro Skeletal Muscle Model of PGM1 Deficiency Reveals Altered Energy Homeostasis
by: Federica Conte, et al.
Published: (2023-05-01) -
REC8 regulates neuroblastoma cell proliferation, migration, invasion, and angiogenesis via STAT3/VEGF signaling
by: Qiang Wang, et al.
Published: (2023-12-01) -
Astragalus polysaccharide ameliorates CD8+ T cell dysfunction through STAT3/Gal-3/LAG3 pathway in inflammation‐induced colorectal cancer
by: Qiuyi Li, et al.
Published: (2024-02-01)