Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Duygu Erhan"'
Publikováno v:
International Journal of Breast Cancer, Vol 2022 (2022)
Background. Breast cancer is the most common malignancy in women. Genetic risk factors associated with breast cancer incidence have been identified. Aims. This study is aimed at determining the association of XRCC3 Thr241Met (rs861539), XRCC4 G(-1394
Externí odkaz:
https://doaj.org/article/b6aa6a93a9fb4c668f076f42d73b27b4
Autor:
Tuba Mutlu, Emre Ozoran, Didem Can Trabulus, Canan Kelten Talu, Duygu Erhan, Meltem Mete, Mehmet Guven
Publikováno v:
Molecular Biology Reports. 50:5157-5163
Background: The dysfunctions in the metabolism of iron has an important role in many pathological conditions, ranging from disease with iron deposition to cancer. Studies on malignant diseases of the breast reported irregular expression in genes asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfe92a3fc146ca64a3819ea449b73e61
https://doi.org/10.1007/s11033-023-08433-1
https://doi.org/10.1007/s11033-023-08433-1
Background Breast cancer is the most common malignancy in women. Genetic risk factors associated with breast cancer incidence have been identified. Aims The aim of this study was to determine the association of XRCC3 Thr241Met (rs861539), XRCC4 G(-13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0da6328b566be41207446406c442b1be
https://doi.org/10.21203/rs.3.rs-896763/v1
https://doi.org/10.21203/rs.3.rs-896763/v1
Publikováno v:
Human Gene. 33:201074
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f656f754d5b9972c46bf3d1492c78bb3
https://doi.org/10.1016/j.humgen.2022.201074
https://doi.org/10.1016/j.humgen.2022.201074
Publikováno v:
International Journal of Breast Cancer
Background: breast cancer is the most common malignancy in women. Genetic risk factors associated with breast cancer incidence have been identified. Aims: this study is aimed at determining the association of XRCC3 Thr241Met (rs861539), XRCC4 G(-1394
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef98717346207411942f860f05387a80
https://pubmed.ncbi.nlm.nih.gov/35320970
https://pubmed.ncbi.nlm.nih.gov/35320970
Publikováno v:
Meta Gene. 29:100941
Mutations in TMPRSS6 gene encoding matriptase-2 result in Iron refractory iron deficiency anemia (IRIDA). Polymorphisms in the TMPRSS6 gene have been found to be more common in comparison with mutations in this gene. These polymorphisms were reported
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d00b65186882a276d2a5429897e63479
https://doi.org/10.1016/j.mgene.2021.100941
https://doi.org/10.1016/j.mgene.2021.100941
Autor:
Hakan Yavuzer, Isil Bavunoglu, Dilek Cuhadar Ercelebi, Aydın Tunçkale, Tuba Mutlu, Selin Unal, Yalcin Hacioglu, Serap Yavuzer, Bahadir Batar, Mahir Cengiz, Duygu Erhan, Mehmet Güven
Publikováno v:
Gene. 673
TMPRSS6 gene mutations can result in iron deficiency anemia (IDA) and cause an increased iron-regulatory hormone, hepcidin, levels. TMPRSS6 encodes a serine protease, matriptase-2, which functions as negative regulatory protein of hepcidin transcript
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e16ef632750c50731c1180a2ab78fccf
https://pubmed.ncbi.nlm.nih.gov/29928945
https://pubmed.ncbi.nlm.nih.gov/29928945
Autor:
Mehmet Güven, Bahadir Batar, Safa Baris, Duygu Erhan, Selin Unal, Nihal Özdemir, Merve Bostancı, Tiraje Celkan
Publikováno v:
Meta Gene
The variations between different individuals in the xenobiotic metabolizing enzymes' activity were shown to modify susceptibility to childhood acute lymphoblastic leukemia (ALL). Polymorphisms associated with genes coding for the glutathione S-transf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcce8f6b3575c25321e00d5e55941c29
https://pubmed.ncbi.nlm.nih.gov/26137447
https://pubmed.ncbi.nlm.nih.gov/26137447