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Nature|August 7, 2007
Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndromeYoshiyuki Minegishi, Masako Saito, Shigeru Tsuchiya, et al.
The Journal of Experimental Medicine|February 14, 2007
WASP regulates suppressor activity of human and murine CD4(+)CD25(+)FOXP3(+) natural regulatory T cellsFrancesco Marangoni, Sara Trifari, Samantha Scaramuzza, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|February 16, 2020
The evaluation of malignancies in Turkish primary immunodeficiency patients; a multicenter studySukru Cekic, Ayse Metin, Caner Aytekin, et al.
Clinical and Experimental Immunology|May 5, 2022
Increased radiosensitivity and impaired DNA repair in patients with STAT3-LOF and ZNF341 deficiency, potentially contributing to malignant transformationsSukru Cekic, Huzeyfe Huriyet, Melika Hortoglu, et al.
Scientific Reports|May 24, 2026
Evaluation of bone mineral density in patients with severe congenital neutropenia: experience of six centers in TurkeyYasin Karali, Deniz Cagdas Ayvaz, Deniz Yilmaz Karapinar, et al.
Pediatric Hematology and Oncology|March 14, 2022
Clinical Profile and Outcomes of Primary Immunodeficiency and Malignancy in Childhood at a Tertiary Oncology Center in Developing CountryDerya Özyörük, Zeliha Güzelküçük, Ayse Metin, et al.
BMC Immunology|February 8, 2008
Screening of functional and positional candidate genes in families with common variable immunodeficiencyUlrich Salzer, Carla Neumann, Jens Thiel, et al.
The Journal of Experimental Medicine|January 23, 2013
Wiskott-Aldrich syndrome protein-mediated actin dynamics control type-I interferon production in plasmacytoid dendritic cellsFrancesca Prete, Marco Catucci, Mayrel Labrada, et al.
Journal of Clinical Immunology|October 21, 2025
Beyond the Classical Triad: Atypical Presentations and Regulatory T Cell Phenotyping in a Cohort of IPEX PatientsIsmail Yaz, Sevil Oskay Halacli, Canberk Ipsir, et al.
Human Molecular Genetics|June 22, 2019
A purely quantitative form of partial recessive IFN-γR2 deficiency caused by mutations of the initiation or second codonCarmen Oleaga-Quintas, Caroline Deswarte, Marcela Moncada-Vélez, et al.
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