Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Shahpour Omidvari"'
Autor:
Mohammad Mohammadianpanah, Amir Abbas Kani, Hamid Nasrolahi, Mansour Ansari, Seyed Hasan Hamedi, Niloofar Ahmadloo, Shahpour Omidvari, Ahmad Mosalaei, Samira Razzaghi
Publikováno v:
Lymphoma. 2013:1-9
Introduction. This study aimed to report the characteristics, prognostic factors, and treatment outcomes of 54 patients with primary gastric lymphoma. Materials and Methods. This retrospective study was carried out by reviewing the medical records of
Publikováno v:
Scopus-Elsevier
Glutathione S-transferases class zeta (GSTζ) is involved in the detoxification of xenobiotic compounds and catalyzes the biotransformation of a variety of α-haloacids including dichloroacetic acid and chlorofluoroacetic acid. It has been reported t
Publikováno v:
Molecular Biology Reports. 38:4309-4313
Expression pattern analysis has been revealed that glutathione S-transferase omega 2 (GSTO2, a member of class omega) is ubiquitously expressed. Over expression of GSTO2 induced apoptosis. The gene encoding GSTO2 was localized to human chromosome 10q
Publikováno v:
Comparative Clinical Pathology. 19:345-349
DNA in most cells is regularly damaged by endogenous and exogenous mutagens. Among DNA repair systems, the base excision repair pathway is responsible for the repair of oxidative DNA damage and single-strand breaks. The X-ray repair cross-complementa
Publikováno v:
Molecular Biology Reports. 36:781-784
Objective The glutathione S-transferases (GSTs) are a superfamily of proteins that participates in detoxification. The GSTs were dividing into several classes including omega (GSTO), mu (GSTM) and theta (GSTT) classes. In human GSTO2, GSTM1, and GSTT
Publikováno v:
Gene. 505:195-197
The human XRCC7 is a DNA double-strand break (DSBs) repair gene, involved in non-homologous end joining (NHEJ). It is speculated that DNA DSBs repair have an important role during development of breast cancer. The human XRCC7 is a NHEJ DSBs repair ge
Publikováno v:
Pathology oncology research : POR. 21(4)
The X-ray complementing group 4 (XRCC4, OMIM: 194363) plays a key role in non-homologous end-joining DNA repair pathway in mammalian cells. This pathway is believed to help maintain genomic stability. In the present study, it is hypothesized that gen
Publikováno v:
Breast Cancer Research and Treatment. 120:263-265
Association between polymorphisms of X-ray repair crosscomplementation group 1 (XRCC1, at codons 194 and 399) and also several classes of glutathione S-transferases (GSTs such as GSTS1, GSTL1) and risk of breast cancer have been studied extensively [
Publikováno v:
Medical oncology (Northwood, London, England). 31(4)
Variation in DNA repair genes is one of the mechanisms that may lead to variation in DNA repair capacity. Ku, a heterodimeric DNA-binding complex, is directly involved in repair of DNA double-strand breaks. Ku consists of two subunits, Ku70 and Ku80,