Zobrazeno 1 - 10
of 318
pro vyhledávání: '"XRCC1 Gene"'
Autor:
Wenjing Zhang, Yubo Su, Genquan Yue, Lingyan Zhao, Hailing Li, Min Jia, Yuqi Wang, Dongyang Liu, Haisheng Wang, Yumin Gao
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-12 (2024)
Abstract To study the relationships between stromal cell-derived factor-1 (SDF-1ɑ) and renal cell carcinoma (RCC) susceptibility and the presence of single nucleotide polymorphisms in the human X-ray cross-complementary repair gene (XRCC1). Compare
Externí odkaz:
https://doaj.org/article/d8a0aead3e1b47a5a96350598c21b9ec
Autor:
T. M. Zavarykina, P. K. Lomskova, M. A. Kapralova, O. O. Gordeeva, I. P. Ganshina, D. S. Khodyrev, S. V. Khokhlova, I. V. Kolyadina
Publikováno v:
Опухоли женской репродуктивной системы, Vol 18, Iss 4, Pp 69-80 (2023)
Background. Breast cancer is the most common cancer among women. Triple negative breast cancer (TNBC) is the most aggressive subtype of breast cancer, in which there are no special targets for therapy. Therefore chemotherapy is still leading treatmen
Externí odkaz:
https://doaj.org/article/5ed10ee33c6541e192682c3fd761a34a
Akademický článek
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Publikováno v:
Balkan Journal of Medical Genetics, Vol 24, Iss 1, Pp 73-80 (2021)
Differentiated thyroid carcinomas (DTC) are the most common form of endocrine malignancies. The role of genetic variations in the development of papillary thyroid carcinoma (PTC) is approximately 60.0-70.0%. The X-ray repair cross-complementing group
Externí odkaz:
https://doaj.org/article/60621fb3bc724622ae39040f590f9d2e
Autor:
Nuntiput Putthanachote, Supannee Promthet, Cameron Hurst, Krittika Suwanrungruang, Peechanika Chopjitt, Surapon Wiangnon, Sam Li-Sheng Chen, Amy Ming-Fang Yen, Tony Hsiu-Hsi Chen
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-7 (2017)
Abstract Background Previous studies have found that polymorphisms of the DNA repair gene X-ray repair cross-complementing group 1(XRCC1) and environmental factors are both associated with an increased risk of stomach cancer, but no study has reporte
Externí odkaz:
https://doaj.org/article/a6d095365f0448e992d2f978e1b7bf95
Autor:
Neslihan Bascil Tutuncu, Hpb Cebi, Fatma Belgin Ataç, T Tutuncu, Nazli Gulsoy Kirnap, Hasibe Verdi, Yaprak Yılmaz Yalçın, Asli Nar
Publikováno v:
Balkan Journal of Medical Genetics, Vol 24, Iss 1, Pp 73-80 (2021)
Differentiated thyroid carcinomas (DTC) are the most common form of endocrine malignancies. The role of genetic variations in the development of papillary thyroid carcinoma (PTC) is approximately 60.0-70.0%. The X-ray repair cross-complementing group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e28fdf2035b2291ccf28c5fe915a3a3
https://doaj.org/article/60621fb3bc724622ae39040f590f9d2e
https://doaj.org/article/60621fb3bc724622ae39040f590f9d2e
Publikováno v:
Molecular Biology Reports. 48:405-412
Gastric cancer (GC) is a multistep process characterized by a gradual accumulation of genetic and epigenetic alterations in genes at various stages of progression. Epigenetic alterations like DNA methylation play an important role in cancer and may s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca81811f400c68550d30d0b4ccb0e74a
https://doi.org/10.1007/s11033-020-06064-4
https://doi.org/10.1007/s11033-020-06064-4
Publikováno v:
Brazilian Journal of Medical and Biological Research, Vol 46, Iss 12, Pp 1028-1032 (2013)
Esophageal cancer (EC) is a common malignancy worldwide. The X-ray repair cross-complementing 1 gene (XRCC1) is one of the most important candidate genes for influencing susceptibility to EC. This study aimed to investigate the effect of XRCC1 geneti
Externí odkaz:
https://doaj.org/article/ff2082c4897b46679b8d1ef3564bfadc
Publikováno v:
Research in Molecular Medicine, Vol 8, Iss 4, Pp 171-178 (2020)
Background: Gastric cancer is one of the most common malignancies in the world. It may result from a defect in the genes involved in DNA repair. One of the essential genes in the repair pathway is the XRCC1 gene that its polymorphisms in the human po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba5357c2072d245c08acc0c011eec6d4
https://doi.org/10.32598/rmm.8.4.2
https://doi.org/10.32598/rmm.8.4.2
Publikováno v:
Archivos de la Sociedad Española de Oftalmología (English Edition). 95:439-446
Background Keratoconus is a progressive disorder distinguished by thinning of the corneal tissue and bulging forward into a cone-shaped fashion. Yet its aetiology, which is multifactorial, despite intensive research remains elusive. Corneal exposure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e9b0a0562bdd1469956a1057a45a968
https://doi.org/10.1016/j.oftale.2020.03.002
https://doi.org/10.1016/j.oftale.2020.03.002