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The Journal of Allergy and Clinical Immunology|September 10, 2013
High-content cytometry and transcriptomic biomarker profiling of human B-cell activationChristian Hennig, Claudia Ilginus, Kaan Boztug, 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|July 26, 2021
Clinical and laboratory findings in patients with leukocyte adhesion deficiency type I: A multicenter study in TurkeyIsmail Yaz, Begum Ozbek, Hacer Neslihan Bildik, 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.
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.
Blood|July 21, 2009
Loss of Kindlin-3 in LAD-III eliminates LFA-1 but not VLA-4 adhesiveness developed under shear flow conditionsEugenia Manevich-Mendelson, Sara W Feigelson, Ronit Pasvolsky, et al.
The Journal of Experimental Medicine|June 20, 2007
A LAD-III syndrome is associated with defective expression of the Rap-1 activator CalDAG-GEFI in lymphocytes, neutrophils, and plateletsRonit Pasvolsky, Sara W Feigelson, Sara Sebnem Kilic, et al.
Brain : a Journal of Neurology|August 5, 2009
Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlationAnnelies Rotthier, Jonathan Baets, Els De Vriendt, et al.
Immunologic Research|April 21, 2024
Primary immune regulatory disorders (PIRD): expanding the mutation spectrum in Turkey and identification of sixteen novel variantsAyca Aykut, Asude Durmaz, Neslihan Karaca, et al.
Haematologica|September 11, 2016
Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosisAmanda J Walne, Laura Collopy, Shirleny Cardoso, et al.
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