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Burak Durmaz

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Citations 461
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Recent Articles
31.
Karaca E, Aykut A, Erturk B, Durmaz B, Guler A, Buke B, et al.
Balkan Med J . 2017 Dec; 35(2):163-166. PMID: 29219113
Background: Down syndrome, which is the most common human chromosomal anomaly that can affect people of any race and age, can be diagnosed prenatally in most cases. Prenatal diagnosis via...
32.
Yilmaz U, Bagca B, Karaca E, Durmaz A, Durmaz B, Aykut A, et al.
Biomed Pharmacother . 2016 Nov; 84:1266-1273. PMID: 27810783
Acute lymphoblastic leukemia (ALL) is one of the most frequent causes of death from cancer. Since the discovery of chemotherapeutic agents, ALL has become a model for improvement of survival....
33.
Durmaz B, Alpman Durmaz A, Karaca E, Saydam G, Cogulu O, Ozkinay F
Turk J Haematol . 2016 Jun; 27(4):299-302. PMID: 27263746
We report herein a very rare case of acute lymphoblastic leukemia having a chromosomal constitution of 48,XY,+X,+5,t(9;22)(q34;q11) in the bone marrow. A patient with additional chromosomes X and 5 with...
34.
Erturk B, Karaca E, Aykut A, Durmaz B, Guler A, Buke B, et al.
Biomed Res Int . 2016 Apr; 2016:5312674. PMID: 27110565
Background: Currently, the data available on the utility of miRNAs in noninvasive prenatal testing is insufficient in the literature. We evaluated the expression levels of 14 miRNAs located on chromosome...
35.
Karaca E, Harel T, Pehlivan D, Jhangiani S, Gambin T, Akdemir Z, et al.
Neuron . 2015 Nov; 88(3):499-513. PMID: 26539891
Development of the human nervous system involves complex interactions among fundamental cellular processes and requires a multitude of genes, many of which remain to be associated with human disease. We...
36.
Duyu M, Durmaz B, Gunduz C, Vergin C, Karapinar D, Aksoylar S, et al.
Biomed Res Int . 2014 Jun; 2014:967585. PMID: 24955371
Dysregulation of microRNA (miRNA) expression contributes to the pathogenesis of several clinical conditions. The aim of this study is to evaluate the associations between miRNAs and childhood acute lymphoblastic leukemia...
37.
Durmaz B, Aykut A, Hursitoglu G, Bak M, Serdaroglu E, Onay H, et al.
Int J Rheum Dis . 2014 Mar; 17(3):317-20. PMID: 24576294
Aim: Immune and inflammatory response activation is a common feature of systemic vasculitis. There is a protein called mannose binding lectin (MBL) that was reported to play an important role...
38.
Schreml J, Durmaz B, Cogulu O, Keupp K, Beleggia F, Pohl E, et al.
Hum Genet . 2013 Aug; 133(1):29-39. PMID: 23982343
Proteoglycan (PG) synthesis begins with the sequential addition of a "linker chain", made up of four sugar residues, to a specific region of a core protein. Defects in the enzymes...
39.
Pohl E, Aykut A, Beleggia F, Karaca E, Durmaz B, Keupp K, et al.
Hum Genet . 2013 Jul; 132(11):1311-20. PMID: 23851939
Otofaciocervical syndrome (OFCS) is an autosomal recessively inherited disorder characterized by facial dysmorphism, external ear anomalies with preauricular pits and hearing impairment, branchial cysts or fistulas, anomalies of the vertebrae...
40.
Isleten B, Durmaz B, Durmaz B, Onay H, Ozkinay F, Durmaz A, et al.
Arch Gynecol Obstet . 2013 Apr; 288(4):917-23. PMID: 23553199
Purpose: To investigate the association between C421T polymorphism within exon 4, C575T polymorphism within exon 6 of the RANK gene and bone mineral density (BMD) variations in postmenopausal Turkish women....