An optimized, fully automated system for fast and accurate identification of chromosomal rearrangements by multiplex-FISH (M-FISH).
about
Three-dimensional maps of all chromosomes in human male fibroblast nuclei and prometaphase rosettes.Molecular and phenotypic characterisation of paediatric glioma cell lines as models for preclinical drug developmentSequential application of interphase-FISH and CGH to single cells.Towards many colors in FISH on 3D-preserved interphase nuclei.Pooling strategy and chromosome painting characterize a living zebroid for the first timeFamilial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3).Classification of multicolor fluorescence in situ hybridization (M-FISH) images with sparse representation.Multiplex-FISH for pre- and postnatal diagnostic applications.An optimized probe set for the detection of small interchromosomal aberrations by use of 24-color FISH.Molecular cytogenetic analysis of telomere rearrangements.Telomere dysfunction as a cause of genomic instability in Werner syndrome.A hybrid approach of using wavelets and fuzzy clustering for classifying multispectral florescence in situ hybridization imagesHodgkin's lymphoma cell lines are characterized by frequent aberrations on chromosomes 2p and 9p including REL and JAK2.Identification of de novo chromosome rearrangements: five cases analyzed with differential chromosome painting.New concepts to improve resolution and sensitivity of molecular cytogenetic diagnostics by multicolor fluorescence in situ hybridization.A classification efficiency test of spectral karyotyping and multiplex fluorescence in situ hybridization: identification of chromosome homologies between Homo sapiens and Hylobates leucogenys.Limitations of chromosome classification by multicolor karyotyping.INK4a-deficient human diploid fibroblasts are resistant to RAS-induced senescenceA patch-based tensor decomposition algorithm for M-FISH image classification.Analysis of chromosomal alterations in non-small cell lung cancer by multiplex-FISH, comparative genomic hybridization, and multicolor bar coding.Twenty-four-color spectral karyotyping reveals chromosome aberrations in cytogenetically normal acute myeloid leukemia.Fourier transformed spectral bio-imaging for studying the intracellular fate of liposomes.Usefulness of high-resolution comparative genomic hybridization (CGH) for detecting and characterizing constitutional chromosome abnormalities.Multicolor karyotypic interpretation of a heterochromatin-associated marker chromosome in a dysmorphic girl with developmental delay.Additional dark G-band in the p-arm of chromosome 19 due to a paracentric inversion with a breakpoint in the pericentromeric heterochromatin
P2860
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P2860
An optimized, fully automated system for fast and accurate identification of chromosomal rearrangements by multiplex-FISH (M-FISH).
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
An optimized, fully automated ...... ts by multiplex-FISH (M-FISH).
@ast
An optimized, fully automated ...... ts by multiplex-FISH (M-FISH).
@en
type
label
An optimized, fully automated ...... ts by multiplex-FISH (M-FISH).
@ast
An optimized, fully automated ...... ts by multiplex-FISH (M-FISH).
@en
prefLabel
An optimized, fully automated ...... ts by multiplex-FISH (M-FISH).
@ast
An optimized, fully automated ...... ts by multiplex-FISH (M-FISH).
@en
P2093
P356
P1476
An optimized, fully automated ...... nts by multiplex-FISH (M-FISH)
@en
P2093
I Petersen
J Chassery
K Saracoglu
P304
P356
10.1159/000015092
P577
1998-01-01T00:00:00Z