Mehmet Burak DURMAZ

Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Tıbbi Genetik Anabilim Dalı

Araştırma alanları: Sağlık Bilimleri, Tıp, Dahili Tıp Bilimleri, Tıbbi Genetik, Temel Bilimler, Yaşam Bilimleri, Temel Tıp Bilimleri, Moleküler Biyoloji ve Genetik, Çocuk Sağlığı ve Hastalıkları, İç Hastalıkları

Yayınlar

• Prenatal ve Preimplantasyon Genetik Tanı (2026)
• A Novel MPIG6B Gene Variant Identified in a Patient with Congenital Thrombocytopenia from Turkey (2026)
• Pyrimidine-5′-Nucleotidase Deficiency: a New Homozygous NT5C3A Mutation (c.693+1G>A variant) (2025)
• Anti-miRNA- 155 - 5p enhances the cytotoxic efficacy of temozolomide in brain cancer stem cells (2025)
• Elucidating the genetic mechanism of anti-cancer efficacy of prednisolone in acute lymphoblastic leukemia through anti-miRNA treatments (2025)
• Dao (Diaminoxidase) Purification from Natural Sources and Enzyme-Enriched Food Production (2025)
• The cytotoxic effects of bio-transformed propolis on healthy and colon cancer cell lines (2025)
• Elucidating the genetic mechanism of anti-cancer efficacy of prednisolone in acute lymphoblastic leukemia through anti-miRNA treatments (2025)
• MALIGNANCY IN FANCONI APLASTIC ANEMIA; SINGLE CENTER EXPERIENCE (2025)
• Next generation sequence-based targeted somatic mutation analysis in thyroid nodules with pathologically diagnosed as indeterminate cytology (2024)
• Next Generation Sequence-Based Targeted Somatic Mutation Analysis in Thyroid Nodules with Pathologically Diagnosed as Indeterminate Cytology (2024)
• A complex t(15;22;17)(q22;q11.2;q21) variant of APL (2024)
• Biallelic variants in <i>ADAMTS15</i> cause a novel form of distal arthrogryposis (vol 24, pg 2187, 2022) (2023)
• Glycosaminoglycan-induced proinflammatory cytokine levels as disease marker in mucopolysaccharidosis (2023)
• The association of plasma pancreastatin levels with insulin resistance in patients with gestational diabetes mellitus (2023)
• Successful Treatment of a Child with Hemoglobin Hammersmith with Hematopoietic Stem Cell Transplantation (2023)
• The association of plasma pancreastatin levels with insulin resistance in patients with gestational diabetes mellitus (2023)
• Kordosentezde mozaik tetrazomi 9p olan olguya yaklaşım (2022)
• Gestasyonel diabetes mellitus saptanan olgularda plazma pankreastatin düzeyinin insülin direnci ve fetal doğum kilosu üzerine etkileri (2022)
• Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium (2022)
• Prenatal diagnosis of a case with tetrasomy 9p confirmed by cytogenetics, FISH, microarray analysis and review (2022)
• Complex karyotype with double Philadelphia chromosome and T315I mutation results in blastic phase and extensive extramedullary infiltration in a chronic myeloid leukemia patient (2022)
• Clinicopathological characteristics, genetics and prognosis of patients with myeloid sarcoma: a single-center study. (2022)
• Biallelic variants in ADAMTS15 cause a novel form of distal arthrogryposis. (2022)
• The Effect of Radiofrequency Waves on Pregnant Mice in Association with Genes Involved in Neuronal Migration (2022)
• Clinical and molecular evaluation of <i>MEFV</i> gene variants in the Turkish population: a study by the National Genetics Consortium (2022)
• Biallelic variants in ADAMTS15 cause a novel phenotype characterized by congenital contractures of the hands and feet with absent palmar creases (2022)
• Biallelic variants in ADAMTS15 cause a novel form of distal arthrogryposis (2022)
• Propolis Extract Regulates microRNA Expression in Glioblastoma and Brain Cancer Stem Cells. (2022)
• The Effect of Radiofrequency Waves on Pregnant Mice in Association with Genes Involved in Neuronal Migration (2022)
• In vitro fertilization and preimplantation genetic diagnosis outcomes in mosaic Turners syndrome: A retrospective cohort study from a single referral center experience (2022)
• Propolis Extract Regulates microRNA Expression in Glioblastoma and Brain Cancer Stem Cells. (2022)
• The association between genetic polymorphisms in matrix metalloproteinases and caries experience (2021)
• 20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey (2021)
• 11Q Oktozomisi Saptanan Nadir Aml Olgusu (2021)
• Karyotip Analizi 46,xy,der(21)T(1;21)(Q11-12;p11-13) Saptanan Mds Tanılı Olgu (2021)
• The Effect of Maximal Exercise on Matrix Metalloproteinase, its Inhibitor (MMP9 and TIMP1), and the Role of MMP9 -1562 C/T and TIMP1 372 T/C Polymorphisms (2021)
• Biallelic variants in ADAMTS15 cause a novel phenotype characterized by congenital contractures of the hands and feet with absent palmar creases (2021)
• A Novel Homozygous TRNT1 Mutation in a Child With an Early Diagnosis of Common Variable Immunodeficiency Leading to Mild Hypogammaglobulinemia and Hemolytic Anemia. (2021)
• X-linked agammaglobulinemia: ınvestigation of clinical and laboratory findings, novel gene mutations and prevention of ınfective complications in long-term follow-up. (2021)
• Does the TMPRSS6 C >T Polymorphism Modify the Endurance Training Effects on Hematological Parameters? (2021)
• Biallelic variants in ADAMTS15 cause a novel phenotype characterized by congenital contractures of the hands and feet with absent palmar creases (2021)
• Miyelodisplastik Sendromda Kromozomal Yeniden Düzenlemelerin Tespiti: Standart Karyotip Ve Fish Yöntemleri Arasinda Karşilaştirma (2021)
• Association of mutation in PTPN14 gene and gingival fibromatosis with distinctive facies: a novel finding in whole exome sequencing (2021)
• Antileukemic Effects of Anti-miR-146a, Anti-miR-155, Anti-miR-181a, and Prednisolone on Childhood Acute Lymphoblastic Leukemia. (2021)
• Does Mannose-Binding Lectin Gene Polymorphism in Pediatric Patients Undergoing Peritoneal Dialysis Cause Susceptibility to the Development of Peritonitis? (2021)
• The association between genetic polymorphisms in matrix metalloproteinases and caries experience. (2021)
• Does MCT1-T1470A Polymorphism Modify Lactate Kinetics and Training Status? (2021)
• Investigation of genotype–phenotype correlation in patients with AZF microdeletion in a single‐reference centre (2021)
• NF1 TÜM GEN DELESYONU SAPTANAN DİSMORFİK BİR NÖROFİBROMATOZİS OLGUSU (2020)
• Co-occurrences of polymorphic heterochromatin regions of chromosomes and effect on reproductive failure (2020)
• Akut miyeloid lösemi (AML) hastalarında sitogenetik, moleküler sitogenetik, moleküler genetik ve klinik sonuçların retrospektif analizi; tek merkezden 4 yıllık veri analizi (2020)
• The effects of regular aerobic exercise training on blood nitric oxide levels and oxidized LDL and the role of eNOS intron 4a/b polymorphism (2020)
• Co-occurrences of polymorphic heterochromatin regions of chromosomes and effect on reproductive failure. (2020)
• The effects of IGF-1 and erythropoietin on apoptosis and telomerase activity in necrotizing enterocolitis model (2020)
• Co-occurrences of polymorphic heterochromatin regions of chromosomes and effect on reproductive failure (2020)
• Submicroscopic insertion of PML segment into RARA on chromosome 17q resulting a very rare variant of PML-RARA fusion in acute promyelocytic leukemia (2020)
• The effects of IGF-1 and erythropoietin on apoptosis and telomerase activity in necrotizing enterocolitis model (2020)
• Akut miyeloid lösemi (AML) hastalarında sitogenetik, moleküler sitogenetik, moleküler genetik ve klinik sonuçların retrospektif analizi; tek merkezden 4 yıllık veri analizi (2020)
• Çocukluk çağı akut lenfoblastik lösemide FISH yöntemi ile kromozomal yeniden düzenlenmelerin tespiti (2020)
• Mitokondri ve İlaçlar (2020)
• Propolis prevents inhibition of apoptosis by potassium bromate in CCD 841 human colon cell (2020)
• SURF1 related Leigh syndrome: Clinical and molecular findings of 16 patients from Turkey (2020)
• Topraksız çilek yetiştiriciliğinde mikoriza ve yetiştirme ortamı hacminin bitki gelişimi üzerine etkileri (2020)
• Antiproliferative effect of rosehip tea phenolics in prostate cancer cell lines (2020)
• The effects of regular aerobic exercise training on blood nitric oxide levels and oxidized LDL and the role of eNOS intron 4a/b polymorphism. (2020)
• The effects of IGF-1 and erythropoietin on apoptosis and telomerase activity in necrotizing enterocolitis model. (2020)
• ACTN3 R577X Polymorphism Does Not Influence Explosive Leg Muscle Power in Elite Turkish Volleyball Players (2020)
• Determination of Lymphocyte Cytokinesis-Block Micronucleus Values in Apparently Healthy Children by means of Age and Sex (2019)
• The relationship between ACTN3 R577X gene polymorphism and physical performance in amateur soccer players and sedentary individuals (2019)
• Boy kısalıklarında sitogenetik, moleküler sitogenetik ve moleküler genetik testler hangi olgularda ne zaman istenir (2019)
• Klinik, Muayene ve Laboratuvar Bulguları Belirgin Olan İskelet Displazileri (2019)
• Akut Myeloblastik Lösemi’de Kromozomal Yeniden Düzenlemelerin Tespiti: Standart Sitogenetik ve FISH Yöntemleri Arasında Bir Karşılaştırma (2019)
• mitokondri ve reaktif oksien türleri (2019)
• Cytogenetic analysis of miscarriage materials of couples with recurrent pregnancy loss in a tertiary center (2019)
• Fetal Gene Therapy Using a Single Injection of Recombinant AAV9 Rescued SMA Phenotype in Mice (2019)
• Hematolojik malignitelerde moleküler sitogenetik belirteçler (2019)
• Myelodisplastik Sendrom Tanısında Karyotip ve FISH Analizlerinin Kullanımının Değerlendirilmesi (2019)
• Gain of 1q21 locus in a multiple myeloma patient (2019)
• PREIMPLANTASYON GENETIK TARAMA ILE MONOZOMI SAPTANAN EMBRYOLARIN IVF SONUÇLARI (2019)
• Co-occurrences of polymorphic heterochromatin regions of chromosomes and effect on reproductive failure (2019)
• Evaluation of 22q11.2 anomalies via two pediatric patients (2019)
• Cytogenetic analysis of miscarriage materials of couples with recurrent pregnancy loss at a high-volume tertiary center (2019)
• Genetic factors associated with the predisposition to late onset Alzheimer's disease (2019)
• Futbol hakemlerİnde düzenlİ aerobİk egzersİzİn hepsİdİn ve hematolojİk parametreler üzerine etkİsİ ve TMPRSS6 rs855791 polİmorfİzmİnİn rolü (2018)
• MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome (2018)
• Erkek Sporcularda Monokarboksilat Taşıyıcı 1–T1470A Polimorfizminin Kan Laktat Birikimi Ve Laktat Eliminasyon Hızı Üzerine Etkileri (2018)
• DÜZENLİ AEROBİK EGZERSİZİN KAN NİTRİK OKSİT VE ENDOTELYAL NİTRİK OKSİT SENTAZ (ENOS) PROTEİN DÜZEYİ ÜZERİNE ETKİLERİ VE ENOS İNTRON 4A/B POLİMOFİZMİNİN ROLÜ (2018)
• Kardiyovasküler Sistem (Kalp-Dolaşım Sistemi) (2018)
• MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome (2018)
• Dilşah (2018)
• – Deri ve Ekleri (2018)
• Düzenli Aerobik Egzersizin Paraoksonaz 3 (PON3) ve Paraoksonaz 2 (PON2) Protein Düzeyleri Üzerine Etkisi Ve PON3-746Ve PON2-S311C Polimorfizminin Rolü (2018)
• The relationship between ACTN3 R577X gene polymorphism and physical performance in amateur soccer players and sedentary individuals (2018)
• Neuronal ceroid lipofuscinosis: Twofamilies, two forms, two new mutations. (2017)
• Nörolojik Genetik Hastalıklar (2017)
• Hastalıklara Yatkınlıklar (2017)
• TIBBİ GENETİĞİN TARİHÇESİ (2017)
• PRADER-WILLI VE ANGELMAN SENDROMU’NDA METİLASYON VE FISH SONUÇLARININ DEĞERLENDİRİLMESİ (2017)
• Tıbbi Genetiğin Tarihçesi (2017)

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