Found: 29
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Differential Expression of LEF1 Isoforms in Adult Lymphoid and Myeloid Malignancies.
- Published in:
- Experimed, 2021, v. 11, n. 3, p. 184, doi. 10.26650/experimed.2021.993743
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- Article
Prognostic evidence of LEF1 isoforms in childhood acute lymphoblastic leukemia.
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- International Journal of Laboratory Hematology, 2021, v. 43, n. 5, p. 1093, doi. 10.1111/ijlh.13513
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- Article
Mutational landscape of severe combined immunodeficiency patients from Turkey.
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- International Journal of Immunogenetics, 2020, v. 47, n. 6, p. 529, doi. 10.1111/iji.12496
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- Article
Comparison of plasma viscosity as a marker of endothelial dysfunction with nitric oxide and asymmetric dimethylarginine in subjects with dyslipidemia.
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- Clinical Hemorheology & Microcirculation, 2014, v. 57, n. 4, p. 315, doi. 10.3233/CH-131706
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- Article
Somatic hypermutation defects in two adult hyper immunoglobulin M patients.
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- Immunologic Research, 2022, v. 70, n. 6, p. 811, doi. 10.1007/s12026-022-09310-y
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- Article
Correction to: Primary antibody deficiencies in Turkey: molecular and clinical aspects.
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- 2022
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- Publication type:
- Correction Notice
Primary antibody deficiencies in Turkey: molecular and clinical aspects.
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- Immunologic Research, 2022, v. 70, n. 1, p. 44, doi. 10.1007/s12026-021-09242-z
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- Publication type:
- Article
Germline mutations of aryl hydrocarbon receptor-interacting protein (AIP) gene and somatostatin receptor 1-5 and AIP immunostaining in patients with sporadic acromegaly with poor versus good response to somatostatin analogues.
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- Pituitary, 2018, v. 21, n. 4, p. 335, doi. 10.1007/s11102-018-0876-4
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- Article
Familial acromegaly due to aryl hydrocarbon receptor-interacting protein (AIP) gene mutation in a Turkish cohort.
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- Pituitary, 2014, v. 17, n. 3, p. 220, doi. 10.1007/s11102-013-0493-1
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- Publication type:
- Article
Clinical features, severity, and immunological changes during venom immunotherapy in children and adults.
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- Allergy & Asthma Proceedings, 2024, v. 45, n. 4, p. 276, doi. 10.2500/aap.2024.45.240017
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- Article
Dysregulation of the DKK1 gene in pediatric B-cell acute lymphoblastic leukemia.
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- Turkish Journal of Medical Sciences, 2017, v. 47, n. 1, p. 357, doi. 10.3906/sag-1507-106
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- Article
Detection of genetic variations in severe combined immunodeficiency (SCID) patients by targeted amplicon sequencing.
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- Turkish Journal of Immunology, 2016, v. 4, p. 64
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- Article
A case with TACI mutation.
- Published in:
- Turkish Journal of Immunology, 2016, v. 4, p. 57
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- Publication type:
- Article
Artemis deficiency: A large cohort including a novel variant with increased radiosensitivity.
- Published in:
- Pediatric Allergy & Immunology, 2024, v. 35, n. 6, p. 1, doi. 10.1111/pai.14171
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- Publication type:
- Article
Serum brain-derived neurotrophic factor, nerve growth factor and neurotrophin-3 levels in dementia.
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- Acta Neurologica Belgica, 2012, v. 112, n. 3, p. 255, doi. 10.1007/s13760-012-0101-6
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- Article
Lymphoma Predisposing Gene in an Extended Family: CD70 Signaling Defect.
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- Journal of Clinical Immunology, 2020, v. 40, n. 6, p. 883, doi. 10.1007/s10875-020-00816-4
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- Publication type:
- Article
Invasive Saprochaete capitata Infection in a Patient with Autosomal Recessive CARD9 Deficiency and a Review of the Literature.
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- Journal of Clinical Immunology, 2020, v. 40, n. 3, p. 466, doi. 10.1007/s10875-020-00759-w
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- Article
Biallelic Form of a Known CD3E Mutation in a Patient with Severe Combined Immunodeficiency.
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- 2020
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- Publication type:
- Letter
A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency.
- Published in:
- 2019
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- Publication type:
- Letter
Aberrant Hypermethylation of APC Tumor Supressor Gene in Acute Leukemia Patients.
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- UHOD: International Journal of Hematology & Oncology / Uluslararasi Hematoloji Onkoloji Dergisi, 2017, v. 27, n. 1, p. 1, doi. 10.4999/uhod.171663
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- Article
Diagnosis of primary immunodeficiency diseases in pediatric patients hospitalized for recurrent, severe, or unusual infections.
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- Allergologia & Immunopathologia, 2022, v. 50, n. 4, p. 50, doi. 10.15586/aei.v50i4.605
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- Publication type:
- Article
Inflammatory hypothesis as a link between Alzheimer's disease and diabetes mellitus.
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- Geriatrics & Gerontology International, 2016, v. 16, n. 10, p. 1161, doi. 10.1111/ggi.12602
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- Article
Determining T and B Cell development by TREC/KREC analysis in primary immunodeficiency patients and healthy controls.
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- Scandinavian Journal of Immunology, 2022, v. 95, n. 3, p. 1, doi. 10.1111/sji.13130
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- Publication type:
- Article
A novel pathogenic frameshift variant of CD3E gene in two T-B+ NK+ SCID patients from Turkey.
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- Immunogenetics, 2017, v. 69, n. 10, p. 653, doi. 10.1007/s00251-017-1005-7
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- Publication type:
- Article
PTEN and AKT1 Variations in Childhood T-Cell Acute Lymphoblastic Leukemia.
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- Turkish Journal of Hematology, 2020, v. 37, n. 2, p. 98, doi. 10.4274/tjh.galenos.2019.2019.0282
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- Article
A Possible Role for WNT5A Hypermethylation in Pediatric Acute Lymphoblastic Leukemia.
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- Turkish Journal of Hematology, 2015, v. 32, n. 2, p. 127, doi. 10.4274/tjh.2013.0296
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- Article
TNFRSF13B VARIANTS ACT AS MODIFIERS TO CLINICAL PHENOTYPES IN COMMON VARIABLE IMMUNE DEFICIENCY DISORDERS.
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- Journal of Advanced Research in Health Sciences (JARHS) / Sağlık Bilimlerinde İleri Araştırmalar Dergisi (SABİAD), 2023, v. 6, n. 3, p. 210, doi. 10.26650/JARHS2023-1346155
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- Article
GENETIC AND CLINICAL PROFILING OF MENDELIAN SUSCEPTIBILITY TO MYCOBACTERIAL DISEASE PATIENTS; SINGLECENTER EXPERIENCE.
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- Journal of Advanced Research in Health Sciences (JARHS) / Sağlık Bilimlerinde İleri Araştırmalar Dergisi (SABİAD), 2022, v. 5, n. 3, p. 140, doi. 10.26650/JARHS2022-1119899
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- Article
Relationship among plasma secretory phospholipase A<sub>2</sub>, oxidized low density lipoprotein & paraoxonase activities in hypertensive subjects treated with angiotensin converting enzyme inhibitors.
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- Indian Journal of Medical Research, 2009, v. 129, n. 4, p. 390
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- Article