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Frontiers in Immunology|May 21, 2020
Clinical, Immunological, and Genetic Features in 49 Patients With ZAP-70 Deficiency: A Systematic ReviewNiusha Sharifinejad, Mahnaz Jamee, Majid Zaki-Dizaji, et al.
Frontiers in Immunology|February 10, 2025
MUC2 expression modulates immune infiltration in colorectal cancerChristophe M Raynaud, Ayesha Jabeen, Eiman I Ahmed, et al.
The Journal of Allergy and Clinical Immunology. in Practice|May 20, 2020
Clinical, Immunological, and Genetic Features in Patients with Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked (IPEX) and IPEX-like SyndromeMahnaz Jamee, Majid Zaki-Dizaji, Bernice Lo, et al.
Scientific Reports|July 9, 2021
In vitro Interleukin-7 treatment partially rescues MAIT cell dysfunction caused by SARS-CoV-2 infectionSatanay Hubrack, Maryam Ali Al-Nesf, Nourhen Agrebi, et al.
The Journal of Allergy and Clinical Immunology. in Practice|April 18, 2019
Clinical, Immunologic, and Molecular Spectrum of Patients with LPS-Responsive Beige-Like Anchor Protein Deficiency: A Systematic ReviewSima Habibi, Majid Zaki-Dizaji, Hosein Rafiemanesh, et al.
BMC Medical Genetics|November 19, 2016
Two hits in one: whole genome sequencing unveils LIG4 syndrome and urofacial syndrome in a case report of a child with complex phenotypeAbeer Fadda, Fiza Butt, Sara Tomei, et al.
Frontiers in Immunology|September 22, 2025
A novel homozygous frameshift mutation likely causing nonsense-mediated mRNA decay in an Algerian kindred with CD19 complex deficiencyBrahim Belaid, Koon-Wing Chan, Lydia Lamara Mahammed, et al.
Cellular and Molecular Gastroenterology and Hepatology|July 8, 2021
Human AGR2 Deficiency Causes Mucus Barrier Dysfunction and Infantile Inflammatory Bowel DiseaseAhmad A Al-Shaibi, Ussama M Abdel-Motal, Satanay Z Hubrack, et al.
Journal of Human Immunity|June 11, 2026
A homozygous CTLA-4 variant causes CTLA-4 deficiency with severe immune dysregulationMehmet Cihangir Catak, Salim Can, Satanay Hubrack, et al.
The Journal of Allergy and Clinical Immunology|May 16, 2024
Loss of the TRPM4 channel in humans causes immune dysregulation with defective monocyte migrationFang Yu, Satanay Hubrack, Christophe M Raynaud, et al.
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