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Lenfoma ve İmmünyetmezliğe Sahip İndeks Olguda Somatik ve Germline Varyasyonların Ekzom Dizi Analizi ile Analizi.
- Published in:
- Experimed, 2022, v. 12, n. 1, p. S17
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- Publication type:
- Article
Candidate Variant Detection by Whole Exome Sequencing in Two Cases with Congenital Hemolytic Anemia.
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- Experimed, 2022, v. 12, n. 1, p. S16
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- Publication type:
- Article
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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- Publication type:
- Article
Metformin reverses the effects of high glucose on human dermal fibroblasts of aged skin via downregulating RELA/p65 expression.
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- Journal of Physiology & Biochemistry, 2021, v. 77, n. 3, p. 443, doi. 10.1007/s13105-021-00823-y
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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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- Publication type:
- Article
High TUBB2A expression in childhood T‐ALL is correlated with the clinical outcome.
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- International Journal of Laboratory Hematology, 2020, v. 42, n. 5, p. 581, doi. 10.1111/ijlh.13235
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- Publication type:
- Article
A Genetic Assessment of Dopamine Agonist-Induced Impulse Control Disorder in Patients With Prolactinoma.
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- Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 6, p. e275, doi. 10.1210/clinem/dgac718
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- Article
Novel RUNX1 Variation in B-cell Acute Lymphoblastic Leukemia.
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- Mediterranean Journal of Hematology & Infectious Diseases, 2023, v. 15, n. 1, p. 1, doi. 10.4084/MJHID.2023.036
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- Publication type:
- 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
Sequence variations of NKX2-5 and HAND1 genes in patients with atrial isomerism.
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- Anatolian Journal of Cardiology / Anadolu Kardiyoloji Dergisi, 2011, v. 11, n. 4, p. 319, doi. 10.5152/akd.2011.083
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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
Local hematopoietic renin-angiotensin system in myeloid versus lymphoid hematological neoplastic disorders.
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- Journal of the Renin-Angiotensin-Aldosterone System, 2013, v. 14, n. 4, p. 308, doi. 10.1177/1470320312464677
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- Publication type:
- 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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- Publication type:
- Article
Common Cytochrome p4503A (CYP3A4 and CYP3A5) and Thiopurine S-Methyl Transferase (TPMT) Polymorphisms In Turkish Population.
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- Turkish Journal of Medical Sciences, 2006, v. 36, n. 1, p. 11
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- Publication type:
- 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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- Publication type:
- Article
Prognostic significance of NOTCH1 and FBXW7 mutations in pediatric T-ALL.
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- Disease Markers, 2010, v. 28, n. 6, p. 353, doi. 10.1155/2010/740140
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- Publication type:
- Article
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations.
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- Journal of Clinical Immunology, 2021, v. 41, n. 4, p. 756, doi. 10.1007/s10875-021-00967-y
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- Publication type:
- 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
A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency.
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- 2019
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- Publication type:
- Letter
Analysis of MYH Tyr165Cys and Gly382Asp variants in childhood leukemias.
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- Journal of Cancer Research & Clinical Oncology, 2003, v. 129, n. 10, p. 604, doi. 10.1007/s00432-003-0483-1
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- Publication type:
- Article
Prevalence and Effect Evaluation of FLT3 and NPM1 Mutations in Acute Myeloid Leukemia Patients in Eastern Algeria.
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- UHOD: International Journal of Hematology & Oncology / Uluslararasi Hematoloji Onkoloji Dergisi, 2018, v. 28, n. 3, p. 169, doi. 10.4999/uhod.182822
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- Publication type:
- Article
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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- Publication type:
- Article
Renin-Angiotensin System (RAS) Expressions in Myeloid Leukemic Cell Lines.
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- UHOD: International Journal of Hematology & Oncology / Uluslararasi Hematoloji Onkoloji Dergisi, 2013, v. 23, n. 4, p. 264, doi. 10.4999/uhod.13014
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- Publication type:
- Article
Perception and management of cancer predisposition in pediatric cancer centers: A European‐wide questionnaire‐based survey.
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- Pediatric Blood & Cancer, 2023, v. 70, n. 5, p. 1, doi. 10.1002/pbc.30229
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- Publication type:
- Article
Minimal residual disease (MRD) detection with translocations and T-cell receptor and immunoglobulin gene rearrangements in adult acute lymphoblastic leukemia patients: a pilot study.
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- Turkish Journal of Hematology, 2008, v. 25, n. 3, p. 124
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- Publication type:
- Article
Role of CYP2D6, CYP1A1, CYP2E1, GSTT1, and GSTM1 genes in the susceptibility to acute leukemias.
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- American Journal of Hematology, 2006, v. 81, n. 3, p. 162, doi. 10.1002/ajh.20434
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- Publication type:
- Article
Elevated TRIB2 with NOTCH1 activation in paediatric/adult T- ALL.
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- British Journal of Haematology, 2012, v. 158, n. 5, p. 626, doi. 10.1111/j.1365-2141.2012.09222.x
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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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- Publication type:
- Article
The Role of the Local Bone Marrow Renin-Angiotensin System in Multiple Myeloma.
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- Turkish Journal of Hematology, 2019, v. 36, n. 3, p. 178, doi. 10.4274/tjh.galenos.2019.2018.0420
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- Publication type:
- Article
Clinical Interpretation of Genomic Variations.
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- Turkish Journal of Hematology, 2016, v. 33, n. 3, p. 172, doi. 10.4274/tjh.2016.0149
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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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- Publication type:
- Article
Local Renin-Angiotensin System in Normal Hematopoietic and Multiple Myeloma-Related Progenitor Cells.
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- Turkish Journal of Hematology, 2014, v. 31, n. 2, p. 136, doi. 10.4274/tjh.2013.0011
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- Publication type:
- Article
Upregulation of T-Cell-Specific Transcription Factor Expression in Pediatric T-Cell Acute Lymphoblastic Leukemia (T-ALL)
- Published in:
- 2012
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- Publication type:
- Journal Article
Upregulation of T-Cell-Specific Transcription Factor Expression in Pediatric T-Cell Acute Lymphoblastic Leukemia (T-ALL).
- Published in:
- Turkish Journal of Hematology, 2012, v. 29, n. 4, p. 325, doi. 10.5505/tjh.2012.13540
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- Publication type:
- 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