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Akademický článek

Il‐6 and UGT1A1 variations may related to furosemide resistance in heart failure patients.

Autor: Koprululu Kucuk, G., Guney, A. I., Sunbul, M., Guctekin, T., Koç, G., Kirac, D.

Publikováno v: IUBMB Life; Oct2023, Vol. 75 Issue 10, p830-843, 14p

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Akademický článek

Predictors of atopic dermatitis phenotypes and severity: Roles of serum immunoglobulins and filaggrin gene mutation R501X

Autor: Ercan, H., Ispir, T., Kirac, D., Baris, S., Ozen, A., Oztezcan, S., Cengizlier, M.R.

Publikováno v: In Allergologia et Immunopathologia March-April 2013 41(2):86-93

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Male infertility in Sertoli cell-only syndrome: An investigation of autosomal gene defects

Autor: Koc, G., Ozdemir, A.A., Girgin, G., Akbal, C., Kirac, D., Avcilar, T., Guney, A.I.

Objectives: To detect autosomal genetic defects and to determine candidate genes in Sertoli cell-only syndrome infertile men. Methods: Single-nucleotide polymorphism + comparative genomic hybridization microarray technology was carried out on 39 Sert

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10007::a732a382e864a01402ea53522a5a5c8f
https://hdl.handle.net/20.500.11831/361

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VDBP, VDR mutations and other factors related with vitamin D metabolism may be associated with type 1 diabetes mellitus

Autor: Kirac, D., Yazan, C.D., Gezmis, H., Yaman, A., Haklar, G., Sirikci, O., Deyneli, O.

Type 1 diabetes mellitus (T1DM) is an insulin dependent autoimmune disorder resulting the progressive destruction of pancreatic beta cells. Another possible factor considered to be related with T1DM is vitamin D deficiency. Therefore in this study it

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10007::546cc00f99d04557c24b2e3ffdee8980
https://hdl.handle.net/20.500.11831/3665

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HMGCR and ApoE mutations may cause different responses to lipid lowering statin therapy

Autor: Kirac, D., Bayam, E., Dagdelen, M., Gezmis, H., Sarikaya, S., Pala, S., Genc, E.

Coronary artery disease (CAD) and its complications are the major causes of death in the world. Although statins have been used to lower lipid levels in CAD patients, this goal can not be attained in 1/3 of the patients. The objective of this study w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10007::d4fef3f5c486ab20cc55e930d449662b
https://hdl.handle.net/20.500.11831/3650

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The Effect of Different ApoE Genotypes and Other Risk Factors on Obstructive Sleep Apnea Syndrome Formation

Autor: Kirac, D, Yassa, OY, Gezmis, H, Domac, SFM, Altunok, EC, Genc, E

Objective: Obstructive sleep apnea syndrome (OSAS) is a disorder characterized by partial or complete narrowing of the pharyngeal airway during sleep. In this study it was aimed to investigate the relation between OSAS and different variants of the A

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10007::e838899f2f5b193b5a5ab57b187c4a0a
https://hdl.handle.net/20.500.11831/4878

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Investigation of the association between mitochondrial DNA and p53 gene mutations in transitional cell carcinoma of the bladder

Autor: Avcilar, T., Kirac, D., Ergec, D., Koc, G., Ulucan, K., Kaya, Z., Guney, A.I.

Bladder carcinoma is the most common malignancy of the urinary tract. The major aim of the present study is to investigate the association between mitochondrial DNA (mtDNA) and p53 gene mutations in bladder carcinoma. A total of 30 patients with tran

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10007::127ff62ad03c527add8b62936533f4db
https://hdl.handle.net/20.500.11831/2563

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