Lista de obras -

Association between genetic polymorphism in DNA repair genes and risk of B-cell lymphoma.

artículo científico publicado en 2009

Association of three SNPs in the PARP-1 gene with Hashimoto's thyroiditis.

artículo científico publicado en 2014

DNA Repair Gene Polymorphisms and Their Relation With DNA Damage, DNA Repair, and Total Antioxidant Capacity in Childhood Acute Lymphoblastic Leukemia Survivors

artículo científico publicado en 2015

DNA repair XRCC1 Arg399Gln polymorphism is associated with the risk of development of end-stage renal disease.

artículo científico publicado en 2012

DNA repair and apoptosis: Roles in radiotherapy-related acute reactions in breast cancer patients.

artículo científico publicado en 2018

DNA repair gene XPD and XRCC1 polymorphisms and the risk of childhood acute lymphoblastic leukemia

artículo científico publicado en 2008

DNA repair gene XRCC1 and XPD polymorphisms and their association with coronary artery disease risks and micronucleus frequency

scientific article published on 26 November 2007

DNA repair gene XRCC1 polymorphisms and the risk of asthma in a Turkish population

artículo científico publicado el 1 de julio de 2010

Decreased DNA repair gene XRCC1 expression is associated with radiotherapy-induced acute side effects in breast cancer patients.

artículo científico publicado en 2016

Fhit and Wwox loss-associated genome instability: A genome caretaker one-two punch

artículo científico publicado en 2016

Fhit loss-associated initiation and progression of neoplasia in vitro

artículo científico publicado en 2016

Fragile Genes That Are Frequently Altered in Cancer: Players Not Passengers

artículo científico publicado en 2017

Glutathione S transferase M1 and T1 genetic polymorphisms are related to the risk of primary open-angle glaucoma: a study in a Turkish population.

artículo científico publicado en 2006

Glutathione-S-transferase M1 and T1 genetic polymorphisms and the risk of cataract development: a study in the Turkish population

artículo científico publicado en 2007

Polymorphism of the NFKB1 affects the serum inflammatory levels of IL-6 in Hashimoto thyroiditis in a Turkish population

artículo científico publicado en 2014

Polymorphisms of DNA repair genes XPD and XRCC1 and risk of cataract development

artículo científico publicado en 2007

Polymorphisms of DNA repair genes XRCC1 and XPD and risk of primary open angle glaucoma (POAG)

artículo científico publicado en 2007

Polymorphisms of the DNA repair genes XPD and XRCC1 and the risk of age-related macular degeneration.

artículo científico publicado en 2010

Relationship between genomic damage and clinical features in dialysis patients.

artículo científico publicado en 2013

Relationship between two estrogen receptor-alpha gene polymorphisms and angiographic coronary artery disease.

artículo científico publicado en 2009

Rheumatoid arthritis risk associates with DNA repair gene XRCC1 Arg399Gln polymorphism in Turkish patients ⬇️

artículo científico publicado el 26 de enero de 2011

Role of glutathione S-transferase M1, T1 and P1 gene polymorphisms in childhood acute lymphoblastic leukemia susceptibility in a Turkish population.

artículo científico publicado en 2015

The association of MDR1 C3435T and G2677T/A polymorphisms with plasma platelet-activating factor levels and coronary artery disease risk in Turkish population

artículo científico publicado en 2013

The difference between pre-B cell acute lymphoblastic leukemia and Burkitt lymphoma in relation to DNA damage repair gene polymorphisms in childhood

scientific article published on 01 August 2008

The drug-transporter gene MDR1 C3435T and G2677T/A polymorphisms and the risk of multidrug-resistant epilepsy in Turkish children

artículo científico publicado en 2013

The effect of genetic polymorphisms of TLR2 and TLR4 in Turkish patients with coronary artery disease.

artículo científico publicado en 2014

The effect of genetic polymorphisms of cytochrome P450 CYP2C9, CYP2C19, and CYP2D6 on drug-resistant epilepsy in Turkish children

artículo científico publicado en 2014

The role of TMPRSS6 gene variants in iron-related hematological parameters in Turkish patients with iron deficiency anemia

article

Lista de obras de

Association between genetic polymorphism in DNA repair genes and risk of B-cell lymphoma.

Association of three SNPs in the PARP-1 gene with Hashimoto's thyroiditis.

DNA Repair Gene Polymorphisms and Their Relation With DNA Damage, DNA Repair, and Total Antioxidant Capacity in Childhood Acute Lymphoblastic Leukemia Survivors

DNA repair XRCC1 Arg399Gln polymorphism is associated with the risk of development of end-stage renal disease.

DNA repair and apoptosis: Roles in radiotherapy-related acute reactions in breast cancer patients.

DNA repair gene XPD and XRCC1 polymorphisms and the risk of childhood acute lymphoblastic leukemia

DNA repair gene XRCC1 and XPD polymorphisms and their association with coronary artery disease risks and micronucleus frequency

DNA repair gene XRCC1 polymorphisms and the risk of asthma in a Turkish population

Decreased DNA repair gene XRCC1 expression is associated with radiotherapy-induced acute side effects in breast cancer patients.

Fhit and Wwox loss-associated genome instability: A genome caretaker one-two punch

Fhit loss-associated initiation and progression of neoplasia in vitro

Fragile Genes That Are Frequently Altered in Cancer: Players Not Passengers

Glutathione S transferase M1 and T1 genetic polymorphisms are related to the risk of primary open-angle glaucoma: a study in a Turkish population.

Glutathione-S-transferase M1 and T1 genetic polymorphisms and the risk of cataract development: a study in the Turkish population

Polymorphism of the NFKB1 affects the serum inflammatory levels of IL-6 in Hashimoto thyroiditis in a Turkish population

Polymorphisms of DNA repair genes XPD and XRCC1 and risk of cataract development

Polymorphisms of DNA repair genes XRCC1 and XPD and risk of primary open angle glaucoma (POAG)

Polymorphisms of the DNA repair genes XPD and XRCC1 and the risk of age-related macular degeneration.

Relationship between genomic damage and clinical features in dialysis patients.

Relationship between two estrogen receptor-alpha gene polymorphisms and angiographic coronary artery disease.

Rheumatoid arthritis risk associates with DNA repair gene XRCC1 Arg399Gln polymorphism in Turkish patients ⬇️

Role of glutathione S-transferase M1, T1 and P1 gene polymorphisms in childhood acute lymphoblastic leukemia susceptibility in a Turkish population.

The association of MDR1 C3435T and G2677T/A polymorphisms with plasma platelet-activating factor levels and coronary artery disease risk in Turkish population

The difference between pre-B cell acute lymphoblastic leukemia and Burkitt lymphoma in relation to DNA damage repair gene polymorphisms in childhood

The drug-transporter gene MDR1 C3435T and G2677T/A polymorphisms and the risk of multidrug-resistant epilepsy in Turkish children

The effect of genetic polymorphisms of TLR2 and TLR4 in Turkish patients with coronary artery disease.

The effect of genetic polymorphisms of cytochrome P450 CYP2C9, CYP2C19, and CYP2D6 on drug-resistant epilepsy in Turkish children

The role of TMPRSS6 gene variants in iron-related hematological parameters in Turkish patients with iron deficiency anemia