Примери за използване на Human lymphocytes на Английски и техните преводи на Български
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Chaga was evaluated for its potential for protecting against oxidative damage to DNA in human lymphocytes.
An in vitro micronucleus(MN)test in primary culture of human lymphocytes with the aglycone metabolite(SL59.0955), with centromere staining(Whitwell J., 2012);
One study showed it can help reduce the side effects of chemotherapy in human lymphocytes!
The in vitro MN test in human lymphocytes showed that M2 induced micronuclei in cultured human peripheral blood lymphocytes in all treatment conditions.
One study showed that it can help reduce the side effects of chemotherapy on human lymphocytes.
In vitro(bacterial, mammalian cells, human lymphocytes) and in vivo studies(micronucleus test) for genotoxic effects have not produced any evidence for a mutagenic potential.
Cladribine and/or its phosphorylated metabolites are substantially accumulated and retained in human lymphocytes.
A major immune-supporting activity of vitamin C is boosting glutathione levels in human lymphocytes, cells that make up about 25% of all white cells in the blood.
Lamivudine was mutagenic in an L5178Y mouse lymphoma assay andclastogenic in a cytogenetic assay using cultured human lymphocytes.
However, sapropterin has not been shown to be genotoxic in the in vitro test with human lymphocytes as well as in in vivo micronucleus mouse tests.
Various studies andresearches have found out that consumption of Chaga mushrooms offers protection against damage of an oxidative kind to the human lymphocytes DNA.
Pixuvri was mutagenic in the Ames test,increased the number of chromosomal aberrations in human lymphocytes, and increased the frequency of micronuclei in vivo.
Peginterferon beta-1a was not mutagenic when tested in an in vitro bacterial reverse mutation(Ames) test andwas not clastogenic in an in vitro assay in human lymphocytes.
Paclitaxel has been shown to be clastogenic in vitro(chromosome aberrations in human lymphocytes) and in vivo(micronucleus test in mice).
It was not clastogenic in an in vitro test in human lymphocytes(no induction of structural chromosomal aberration but it increased number of polyploid cells) and induced an increase of micronuclei in the in vivo test in rats.
Resulting from its mechanism of action, topotecan is genotoxic to mammalian cells(mouse lymphoma cells and human lymphocytes) in vitro and mouse bone marrow cells in vivo.
In vitro(bacterial mutation, human lymphocytes, mouse lymphoma, Syrian Hamster Embryo cell transformation) and in vivo(rat micronucleus) mutagenicity studies revealed no drug related effects at either the gene or chromosomal level.
Darunavir was not mutagenic or genotoxic in a battery of in vitro and in vivo assays including bacterial reverse mutation(Ames),chromosomal aberration in human lymphocytes and in vivo micronucleus test in mice.
Thiocolchicoside itself did not induce gene mutation in bacteria(Ames test),in vitro chromosomal damage(chromosome aberration test in human lymphocytes) and in vivo chromosomal damage(in vivo micronucleus in mouse bone marrow administered intraperitoneally).
Collagenase clostridium histolyticum was not mutagenic in Salmonella typhimurium(AMES test) and was not clastogenic in both an in vivo mouse micronucleus assay andan in vitro chromosomal aberration assay in human lymphocytes.
In fact, a major immune-supporting activity of vitamin C is boosting glutathione levels(a potent internal antioxidant) in human lymphocytes, cells that make up about 25% of all white blood cells in the blood.
Lopinavir/ ritonavir was not found to be mutagenic or clastogenic in a battery of in vitro and in vivo assays including the Ames bacterial reverse mutation assay, the mouse lymphoma assay, the mouse micronucleus test andchromosomal aberration assays in human lymphocytes.
Ertugliflozin was not mutagenic or clastogenic with or without metabolic activation in the microbial reverse mutation,in vitro cytogenetic(human lymphocytes), and in vivo rat micronucleus assays.
Ritonavir was not found to be mutagenic or clastogenic in a battery of in vitro and in vivo assays including the Ames bacterial reverse mutation assay using S. typhimurium and E. coli, the mouse lymphoma assay, the mouse micronucleus test andchromosomal aberration assays in human lymphocytes.
Maraviroc was not mutagenic or genotoxic in a battery of in vitro and in vivo assays including bacterial reverse mutation,chromosome aberrations in human lymphocytes and mouse bone marrow micronucleus.
Alitretinoin was studied for genotoxic potential using the Ames test, the in vivo mouse micronucleus assay,the chromosomal aberration test in human lymphocytes, and the CHO cell mutation test.
Genotoxicity Alitretinoin was studied for genotoxic potential using the Ames test, the in vivo mouse micronucleus assay,the chromosomal aberration test in human lymphocytes, and the CHO cell mutation test.
However, the mutagenic potential has been evaluated, and alitretinoin has tested negative in the Ames test, the in vivo mouse micronucleus assay,the chromosomal aberration test in human lymphocytes, and the CHO cell mutation test.
Allogeneic transplant is more complicated because of proteins called human lymphocyte antigens(HLA) that are on the surface of the bone marrow cells.
Dacomitinib was clastogenic in the in vitro human lymphocyte chromosome aberration assay at cytotoxic concentrations.