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International Journal of Rheumatic Diseases|July 1, 2025
Patients With IgA Vasculitis and Kawasaki Disease Show Dysregulated Interferon SignatureSevki Erdem Varol, Cisem Cinar, Nihan Burtecene, et al.
Immunologic Research|May 16, 2025
Identification of nonsense variants in the ATM gene mimicking SCID phenotype: a brief reportSinem Firtina, Merve Saritas, Yuk Yin Ng, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|April 8, 2023
Impact of <i>TP53</i> gene variants on prognosis and survival of childhood acute lymphoblastic leukemiaSinem Firtina, Yucel Erbilgin, Ozden Hatirnaz Ng, et al.
Immunogenetics|June 10, 2017
A novel pathogenic frameshift variant of CD3E gene in two T-B+ NK+ SCID patients from TurkeySinem Firtina, Yuk Yin Ng, Ozden Hatirnaz Ng, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|October 22, 2020
G-protein Coupled Estrogen Receptor Expression in Growth Hormone Secreting and Non-Functioning AdenomasHande Mefkure Ozkaya, Muge Sayitoglu, Nil Comunoglu, et al.
Leukemia Research|June 23, 2019
Prognostic gene alterations and clonal changes in childhood B-ALLYucel Erbilgin, Sinem Firtina, Sevcan Mercan, et al.
Journal of Clinical Immunology|July 5, 2020
Lymphoma Predisposing Gene in an Extended Family: CD70 Signaling DefectKhusan Khodzhaev, Sema Buyukkapu Bay, Rejin Kebudi, et al.
Biochemical Genetics|January 9, 2025
Status of IKZF1 Deletions in Diagnose and Relapsed Pediatric B-ALL PatientsYücel Erbilgin, Sinem Firtina, Elif Kirat, et al.
Leukemia & Lymphoma|July 3, 2018
Deep sequencing of BCR-ABL1 kinase domain mutations in chronic myeloid leukemia patients with resistance to tyrosine kinase inhibitorsYucel Erbilgin, Ahmet Emre Eskazan, Ozden Hatirnaz Ng, et al.
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