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Страница 6 из 100502

Oncogenic aspects in breast cancer
Kharchenko V.P., Keshelava V.V., Shajkhaev G.O., Khodorovich O.S.
of genes BRCA 1 и BRCA2. There were revealed hereditary and sporadic cancer groups. 2 patients are under
The nature of Rec+ revertants isolated from the E. coli K 12 cultures mutant by the Rec A gene (Russian)
Naumova O.B.
The nature of Rec+ revertants isolated from the E. coli K 12 cultures mutant by the Rec A gene
Genetic Modification of Human Embryos: Limits
Savvina O.V.
The article analyses the moral justification of human germline editing and the tendency to its
Cost-Effectiveness Analysis of Cancer Risk Reduction Strategies for BRCA Mutation Carriers
Деркач Е.В., Солодкий В.А., Ходорович О.С.
Cost-Effectiveness Analysis of Cancer Risk Reduction Strategies for BRCA Mutation Carriers
Genetics of cardiomyopathies [Genetika kardiomiopatii.]
Moiseev V.I.
gene therapy
Determination of EGFR gene somatic mutations in tissues and plasma of patients with advanced non-small cell lung cancer
Brovkina O., Gordiev M., Toropovskiy A., Khodyrev D., Enikeev R., Gusev O., Shigapova L., Nikitin A.
The presence of activating mutations in the EGFR gene influences cell proliferation, angiogenesis
RRM2B Is Frequently Amplified Across Multiple Tumor Types: Implications for DNA Repair, Cellular Survival, and Cancer Therapy
Iqbal W., Demidova E.V., Serrao S., ValizadehAslani T., Rosen G., Arora S.
RRM2B plays a crucial role in DNA replication, repair and oxidative stress. While germline RRM2B
Comparative preclinical pharmacokinetics study of 3,3′-diindolylmethane formulations: is personalized treatment and targeted chemoprevention in the horizon?
Paltsev Mikhail, Kiselev Vsevolod, Muyzhnek Ekaterina, Drukh Vadim, Kuznetsov Igor, Pchelintseva Olga
to prevent breast and ovarian cancer development in patients with heterozygous inherited and sporadic BRCA1
Autism spectrum disorder development factors - between gene mutations and vitamin D deficiency
El Makhour M., Zaytseva P.N.
In this article, various gene mutations associated with the development of autism spectrum disorder
THE FANCM:P.ARG658* TRUNCATING VARIANT IS ASSOCIATED WITH RISK OF TRIPLE-NEGATIVE BREAST CANCER
Bogliolo, M., Catucci, I., Caleca, L., Lasheras, S.V., Pujol, R., Kiiski, J.I., Muranen, T.A., Barnes, D.R., Dennis, J., Michailidou, K., Bolla, M.K., Leslie, G., Figlioli, G.
variants in DNA repair genes BRCA1, BRCA2, PALB2, ATM, and CHEK2 are associated with breast cancer risk

Страница 6 из 100502

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