About: The assessment of array comparative genomic hybridization in complex karyotype analyses

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An Entity of Type : http://linked.opendata.cz/ontology/domain/vavai/Vysledek, within Data Space : linked.opendata.cz associated with source document(s)

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rdf:type	skos:Concept http://linked.opendata.cz/ontology/domain/vavai/Vysledek
Description	Molecular-cytogenetic methods were used for analyses of complex genome rearrangements of malignant cells to specify them in more detail. Twelve samples of bone marrow cells of patients with myelodysplastic syndromes (MDS) and complex karyotype were examined by multicolor fluorescence in situ hybridization (mFISH), high-resolution multicolor banding (mBAND) and array comparative genomic hybridization (aCGH). Combination of both approaches brought more detailed description of complex karyotypes and is highly recommended. Molecular-cytogenetic methods were used for analyses of complex genome rearrangements of malignant cells to specify them in more detail. Twelve samples of bone marrow cells of patients with myelodysplastic syndromes (MDS) and complex karyotype were examined by multicolor fluorescence in situ hybridization (mFISH), high-resolution multicolor banding (mBAND) and array comparative genomic hybridization (aCGH). Combination of both approaches brought more detailed description of complex karyotypes and is highly recommended. (en)
Title	The assessment of array comparative genomic hybridization in complex karyotype analyses The assessment of array comparative genomic hybridization in complex karyotype analyses (en)
skos:prefLabel	The assessment of array comparative genomic hybridization in complex karyotype analyses The assessment of array comparative genomic hybridization in complex karyotype analyses (en)
skos:notation	RIV/00023736:_____/10:00008831!RIV11-MZ0-00023736
http://linked.open...avai/riv/aktivita	P Z
http://linked.open...avai/riv/aktivity	P(LC535), P(NR9227), Z(MSM0021620808), Z(MZ0VFN2005)
http://linked.open...iv/cisloPeriodika	5
http://linked.open...vai/riv/dodaniDat	2011
http://linked.open...aciTvurceVysledku	Šárová, Iveta Březinová, Jana Izáková, Silvia
http://linked.open.../riv/druhVysledku	J - Článek v odborném periodiku
http://linked.open...iv/duvernostUdaju	S - Úplné a pravdivé údaje nepodléhající ochraně podle zvláštních právních předpisů
http://linked.open...titaPredkladatele	Ústav hematologie a krevní transfúze
http://linked.open...dnocenehoVysledku	247892
http://linked.open...ai/riv/idVysledku	RIV/00023736:_____/10:00008831
http://linked.open...riv/jazykVysledku	eng - angličtina
http://linked.open.../riv/klicovaSlova	array comparative genomic hybridization; multicolor fluorescence in situ hybridization; myelodysplastic syndromes; complex karyotype (en)
http://linked.open.../riv/klicoveSlovo	myelodysplastic syndromes array comparative genomic hybridization multicolor fluorescence in situ hybridization complex karyotype
http://linked.open...odStatuVydavatele	CZ - Česká republika
http://linked.open...ontrolniKodProRIV	[AF9FF9AEB8AE]
http://linked.open...i/riv/nazevZdroje	Folia Biologica
http://linked.open...in/vavai/riv/obor	FD
http://linked.open...ichTvurcuVysledku	3 (xsd:int)
http://linked.open...cetTvurcuVysledku	9 (xsd:int)
http://linked.open...vavai/riv/projekt	Chromosome dynamics and organization during the cell cycle in normal and pathologic conditions Molecular cytogenetic analysis of complex chromosomal aberrations in bone marrow cells of patients with myelodysplastic syndrome (MDS) and/or acute myeloid leukemia (AML) and AND its contribution for prognosis.
http://linked.open...UplatneniVysledku	2010
http://linked.open...v/svazekPeriodika	56
http://linked.open...iv/tvurceVysledku	Březinová, Jana Berková, A. Zemanová, Z. Michalová, K. Bystřická, D. Šárová, Iveta Izáková, Sylvia Gančarčíková, M. Grosová, L.
http://linked.open...ain/vavai/riv/wos	000284254900006
http://linked.open...n/vavai/riv/zamer	Molekulárně biologické, genetické a epigenetické aspekty vzniku a rozvoje modelových tumorů dospělého věku. Význam pro epidemiologii, časnou diagnostiku a léčbu Diagnosis and treatment of inherited disorders II
issn	0015-5500
number of pages	8 (xsd:int)

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