Zobrazeno 1 - 10
of 72
pro vyhledávání: '"An, Semiachkina"'
Autor:
Zh M, Shagirova, L A, Kurbatova, L V, Shulenina, A N, Semiachkina, V F, Mikhaĭlov, G D, Zasukhina
Publikováno v:
Radiatsionnaia biologiia, radioecologiia. 51(4)
Codon 312 and 751 polymorphisms ofXPD gene and codon 399 polymorphism of XRCC1 gene of peripheral blood lymphocytes in patients with Down syndrome (DS) (46 individuals), Ehlers-Danlo syndrome (EDS) (47 individuals) and in a group of healthy donors (c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4de5e1ae720d17bb6dde520d5bd5b831
https://pubmed.ncbi.nlm.nih.gov/21950097
https://pubmed.ncbi.nlm.nih.gov/21950097
Autor:
Zh M, Shagirova, L N, Ushenkova, V F, Mikhaĭlov, L A, Kurbatova, N S, Kuz'mina, A N, Semiachkina, I M, Vasil'eva, V K, Mazurik, G D, Zasukhina
Publikováno v:
Radiatsionnaia biologiia, radioecologiia. 50(2)
The genes of detoxication, MTHFR and p53 were studied in Down' and Ehlers-Danlos syndrome cells. The frequency GSTM1(0/0) genotype in Down syndrome patients was in 1.5 times higher than in control cells (p0.069). Opposite the frequency GSTM1(0/0) gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::03c1d327b3eee60436f2551a6c3f7e52
https://pubmed.ncbi.nlm.nih.gov/20464958
https://pubmed.ncbi.nlm.nih.gov/20464958
Publikováno v:
Radiatsionnaia biologiia, radioecologiia. 48(2)
The action of natural (garlick extract, retinol) and of synthetic (crown-compound) antimutagenes in lymphotytes with gamma-radiation-induced inhibition of DNA-damages repair in cases of Elers-Danlos, syndrom, progeria and gomocystinurea was studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::94953c3804066fdfe5ffb76c8137de79
https://pubmed.ncbi.nlm.nih.gov/18666652
https://pubmed.ncbi.nlm.nih.gov/18666652
Autor:
N S, Kuz'mina, I M, Vasil'eva, T A, Sinelshchikova, A N, Semiachkina, G I, Kuznetsova, V A, Shevchenko, G D, Zasukhina
Publikováno v:
Radiatsionnaia biologiia, radioecologiia. 46(4)
A complex investigation of different cell defence systems, such as: DNA repair, antioxidant system (SOD), xenobiotic detoxification system (glutathione-S-transferases M1 and T1), radioadaptive response (RAR) in lymphocytes of patients with hereditary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6922efb9c380f9383d19518612e18c7d
https://pubmed.ncbi.nlm.nih.gov/17020091
https://pubmed.ncbi.nlm.nih.gov/17020091
Publikováno v:
Radiatsionnaia biologiia, radioecologiia. 45(2)
DNA repair synthesis (RS) was investigated in lymphocytes of healty donors and repair-deficient cells (Marfan's syndrome), treated with inhibitor of superoxidedismutase (SOD)--TRIEN--after gamma-irradiation. Significant difference was revealed in cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::301ac2e95f79738be89167b124030e3e
https://pubmed.ncbi.nlm.nih.gov/15906854
https://pubmed.ncbi.nlm.nih.gov/15906854
Publikováno v:
Genetika. 39(12)
The superoxide dismutase (SOD) inhibitor, TRIEN, which enhanced the formation of gamma-induced DNA breaks in cells of healthy donors and patients with Marfan syndrome and Bloom syndrome (repair-defective hereditary diseases), had virtually no effect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::297aa06dbe3580f316e36bb96861feca
https://pubmed.ncbi.nlm.nih.gov/14964829
https://pubmed.ncbi.nlm.nih.gov/14964829
Publikováno v:
Voprosy meditsinskoi khimii. 48(6)
The data on biochemical and molecular-genetic diagnostics of a hereditary lisosomal storage disease, late infantile neuronal ceroid lipofuscinosis (CLN2) are presented. The disease is associated with a hereditary deficiency of pepstatin-unsensitive p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7cad0fb5d6cee7a3a05397705d722a94
https://pubmed.ncbi.nlm.nih.gov/12698559
https://pubmed.ncbi.nlm.nih.gov/12698559
Publikováno v:
Radiatsionnaia biologiia, radioecologiia. 40(5)
The evidence for independency of DNA repair and radioadaptive response (RAR) was obtained in cells of patients with Bloom syndrome. The cells of patients with Bloom syndrome (human autosomal recessive disorder) are characterized by chromosomal instab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c2acd6d7df0e6566f3809514ad37f291
https://pubmed.ncbi.nlm.nih.gov/11252227
https://pubmed.ncbi.nlm.nih.gov/11252227
Publikováno v:
Europe PubMed Central
The radioadaptive response was assessed by the chromosome aberration test in lymphocytes of humans with hereditary diseases of connective tissue, which were earlier characterized as repair-deficient: Marfan syndrome (SM), Elers-Danlos syndrome (E-D),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::c6f9dde78bb90be91e7f369d1c0f4ce6
https://pubmed.ncbi.nlm.nih.gov/10779916
https://pubmed.ncbi.nlm.nih.gov/10779916
Autor:
G P, Makedonov, L V, Tskhovrebova, S V, Unzhakov, A N, Semiachkina, I M, Vasil'eva, G D, Zasukhina
Publikováno v:
Radiatsionnaia biologiia, radioecologiia. 37(4)
The radioadaptive response and antimutagenic action of lymphoblastoid interferon in the human blood lymphocytes of the children from polluted after Chernobyl accident Bryansk region were studied. Cells pretreated with tritiated thymidine with 2 Gy of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::550ca658f7211fad823c89ba25643ed1
https://pubmed.ncbi.nlm.nih.gov/9599623
https://pubmed.ncbi.nlm.nih.gov/9599623