Busque entre los 168426 recursos disponibles en el repositorio
Mostrar el registro sencillo del ítem
dc.date.accessioned | 2019-10-29T13:20:16Z | |
dc.date.available | 2019-10-29T13:20:16Z | |
dc.date.issued | 2000 | |
dc.identifier.uri | http://sedici.unlp.edu.ar/handle/10915/84279 | |
dc.description.abstract | The induction of aneuploidy by physical and chemical agents using different test systems was evaluated. The effect of X-rays, caffeine, acetaldehyde, ethanol, diethylstilbestrol, propionaldehyde, and chloral hydrate was studied by chromosome counting in Chinese hamster embryonic diploid cells. Aneugenic ability of cadmium chloride, cadmium sulfate, potassium dichromate, chromium chloride, nickel chloride, and nickel sulfate was assessed by means of anaphase-telophase analysis in Chinese hamster ovary cells. Chromosome counting in human fibroblasts (MRC-5 cell line) was employed to evaluate the effect of cacodilic acid, cadmium chloride, cadmium sulfate, and potassium dichromate. Finally, the induction of kinetochore-positive and kinetochore negative micronuclei by cadmium chloride, cadmium sulfate, potassium dichromate, chromium chloride, and nickel chloride was studied using CREST antibodies. When the effect of different agents was determined by chromosome counting, an increase of hypoploid but not of hyperploid cells was observed. Anaphase-telophase analysis showed that metal salts increased the frequency of lagging chromosomes. This finding has been confirmed by the increment of kinetochore-positive micronuclei using CREST antibodies. Therefore, chromosome loss could be considered as the main cause of induced aneuploidy. | en |
dc.format.extent | 1077-1082 | es |
dc.language | en | es |
dc.subject | induction of aneuploidy | es |
dc.subject | chromosome loss | es |
dc.title | Mechanisms involved in the induction of aneuploidy: The significance of chromosome loss | en |
dc.type | Articulo | es |
sedici.identifier.other | doi:10.1590/S1415-47572000000400054 | es |
sedici.identifier.other | eid:2-s2.0-0034431929 | es |
sedici.identifier.issn | 1415-4757 | es |
sedici.creator.person | Seoane, Analía Isabel | es |
sedici.creator.person | Güerci, Alba Mabel | es |
sedici.creator.person | Dulout, Fernando Noel | es |
sedici.subject.materias | Ciencias Veterinarias | es |
sedici.description.fulltext | true | es |
mods.originInfo.place | Facultad de Ciencias Veterinarias | es |
mods.originInfo.place | Instituto de Genética Veterinaria | es |
sedici.subtype | Articulo | es |
sedici.rights.license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) | |
sedici.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | |
sedici.description.peerReview | peer-review | es |
sedici.relation.journalTitle | Genetics and Molecular Biology | es |
sedici.relation.journalVolumeAndIssue | vol. 23, no. 4 | es |
sedici.rights.sherpa | * RoMEO: gray* Pre-print del autor: unknown* Post-print del autor: unknown* Versión de editor/PDF:unknown* Condiciones:>>Las políticas de este editor no han sido verificadas por RoMEO.>>DOAJ dice que es una revista de acceso abierto, pero esto puede que signifique sólo que está libremente disponible para leerla>>La mayor parte de las editoriales de acceso abierto permiten también el autoarchivo y la reutilización, pero algunos no lo hacen.>>No debe asumirse que el autoarchivo está autorizado, salvo que se publique bajo una licencia Creative Commons.>>Contacte por favor con la editorial para mayor información si es necesaria>>Email romeo@jisc.ac.uk if you wish to suggest adding this publisher properly to RoMEO.* Link a Sherpa: http://sherpa.ac.uk/romeo/issn/1415-4757/es/ |