Примери за използване на Chromosomal aberrations на Английски и техните преводи на Български
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These are chromosomal aberrations.
Chromosomal aberrations were categorized according to Döhner' s hierarchical model.
Gilteritinib did not induce gene mutation or chromosomal aberrations in vitro.
Chromosomal aberrations have also been detected in in vivo studies in mice and monkeys.
If left unrepaired,this damage can create serious and even lethal chromosomal aberrations.
Rucaparib induced structural chromosomal aberrations in the in vitro human lymphocyte chromosomal aberration assay.
Radiofrequency radiation can increase the local temperature of living tissues and provoke chromosomal aberrations of cells.
Adefovir induced chromosomal aberrations in the in vitro human peripheral blood lymphocyte assay without metabolic activation.
Mercaptopurine, in common with other antimetabolites,is mutagenic and causes chromosomal aberrations in vitro and in vivo in mice and rats.
Arsenic compounds induce chromosomal aberrations and morphological transformations of mammalian cells in vitro and in vivo.
Upadacitinib was not mutagenic or genotoxic based on the results of in vitro andin vivo tests for gene mutations and chromosomal aberrations.
Azacitidine induces both gene mutations and chromosomal aberrations in bacterial and mammalian cell systems in vitro.
Tofacitinib is not mutagenic or genotoxic based on the results of a series of in vitro andin vivo tests for gene mutations and chromosomal aberrations.
Cidofovir induced chromosomal aberrations in human peripheral blood lymphocytes in vitro without metabolic activation(S-9 fraction).
In vitro studies using different cell systems have shown paclitaxel to be clastogenic inducing chromosomal aberrations, micronuclei and DNA damage.
Cytoplasmic factors, polygenic inheritance, chromosomal aberrations, and environmental influences(eg, teratogens) have all been considered as possible causes.
Mutagenicity studies were negative in bacterial gene mutation,bacterial DNA repair, mammalian cell gene mutation and mouse in vivo bone marrow chromosomal aberrations.
Pixuvri was mutagenic in the Ames test,increased the number of chromosomal aberrations in human lymphocytes, and increased the frequency of micronuclei in vivo.
Two genotoxicity assays(in vitro mouse lymphoma assay and in vivo mouse bone marrow micronucleus test)showed a potential of mycophenolate mofetil to cause chromosomal aberrations.
Trametinib was not genotoxic in studies evaluating reverse mutations in bacteria, chromosomal aberrations in mammalian cells and micronuclei in the bone marrow of rats.
The genotoxicity of GM corn and soy, as explained by the researchers, was demonstrated in germ cells,for which there was a considerable increase in the number of cells with chromosomal aberrations.
Atazanavir was negative in an Ames reverse-mutation assay butdid induce chromosomal aberrations in vitro in both the absence and presence of metabolic activation.
Stavudine was genotoxic in in vitro tests in human lymphocytes possessing triphosphorylating activity(in which no no-effect level was established), in mouse fibroblasts, andin an in vivo test for chromosomal aberrations.
Palbociclib was not mutagenic in a bacterial reverse mutation(Ames) assay anddid not induce structural chromosomal aberrations in the in vitro human lymphocyte chromosome aberration assay.
In the presence of metabolite activation rasagiline induced an increase of chromosomal aberrations at concentrations with excessive cytotoxicity which are unattainable at the clinical conditions of use.
Craniofacial abnormalities, in particular morphological changes in the teeth,can be caused by chromosomal aberrations, gene mutation, as well as joint actions of many genes and environmental factors.
Hereditary chromosomal aberration.
This error is often caused by a chromosomal aberration.
Genotoxicity(Chromosomal aberration and mouse lymphoma mutation assay) studies with aztreonam were negative.
Dimethyl fumarate and mono-methylfumarate were negative in a battery of in vitro assays(Ames, chromosomal aberration in mammalian cells).