Ploidy analysis of paraffin-embedded breast fibroadenomas with flow cytometry and fluorescence in situ hybridization. 1997

M G Grollino, and P Eleuteri, and D Pomponi, and G Calugi, and M Rocchi, and R De Vita
Unità di Epidemiologia Ambientale, ENEA Casaccia, Roma, Italy.

UI MeSH Term Description Entries
D001943 Breast Neoplasms Tumors or cancer of the human BREAST. Breast Cancer,Breast Tumors,Cancer of Breast,Breast Carcinoma,Cancer of the Breast,Human Mammary Carcinoma,Malignant Neoplasm of Breast,Malignant Tumor of Breast,Mammary Cancer,Mammary Carcinoma, Human,Mammary Neoplasm, Human,Mammary Neoplasms, Human,Neoplasms, Breast,Tumors, Breast,Breast Carcinomas,Breast Malignant Neoplasm,Breast Malignant Neoplasms,Breast Malignant Tumor,Breast Malignant Tumors,Breast Neoplasm,Breast Tumor,Cancer, Breast,Cancer, Mammary,Cancers, Mammary,Carcinoma, Breast,Carcinoma, Human Mammary,Carcinomas, Breast,Carcinomas, Human Mammary,Human Mammary Carcinomas,Human Mammary Neoplasm,Human Mammary Neoplasms,Mammary Cancers,Mammary Carcinomas, Human,Neoplasm, Breast,Neoplasm, Human Mammary,Neoplasms, Human Mammary,Tumor, Breast
D002879 Chromosomes, Human, Pair 10 A specific pair of GROUP C CHROMOSOMES of the human chromosome classification. Chromosome 10
D002898 Chromosomes, Human, Pair 8 A specific pair of GROUP C CHROMOSOMES of the human chromosome classification. Chromosome 8
D005240 Feasibility Studies Studies to determine the advantages or disadvantages, practicability, or capability of accomplishing a projected plan, study, or project. Feasibility Study,Studies, Feasibility,Study, Feasibility
D005260 Female Females
D005434 Flow Cytometry Technique using an instrument system for making, processing, and displaying one or more measurements on individual cells obtained from a cell suspension. Cells are usually stained with one or more fluorescent dyes specific to cell components of interest, e.g., DNA, and fluorescence of each cell is measured as it rapidly transverses the excitation beam (laser or mercury arc lamp). Fluorescence provides a quantitative measure of various biochemical and biophysical properties of the cell, as well as a basis for cell sorting. Other measurable optical parameters include light absorption and light scattering, the latter being applicable to the measurement of cell size, shape, density, granularity, and stain uptake. Cytofluorometry, Flow,Cytometry, Flow,Flow Microfluorimetry,Fluorescence-Activated Cell Sorting,Microfluorometry, Flow,Cell Sorting, Fluorescence-Activated,Cell Sortings, Fluorescence-Activated,Cytofluorometries, Flow,Cytometries, Flow,Flow Cytofluorometries,Flow Cytofluorometry,Flow Cytometries,Flow Microfluorometries,Flow Microfluorometry,Fluorescence Activated Cell Sorting,Fluorescence-Activated Cell Sortings,Microfluorimetry, Flow,Microfluorometries, Flow,Sorting, Fluorescence-Activated Cell,Sortings, Fluorescence-Activated Cell
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000782 Aneuploidy The chromosomal constitution of cells which deviate from the normal by the addition or subtraction of CHROMOSOMES, chromosome pairs, or chromosome fragments. In a normally diploid cell (DIPLOIDY) the loss of a chromosome pair is termed nullisomy (symbol: 2N-2), the loss of a single chromosome is MONOSOMY (symbol: 2N-1), the addition of a chromosome pair is tetrasomy (symbol: 2N+2), the addition of a single chromosome is TRISOMY (symbol: 2N+1). Aneuploid,Aneuploid Cell,Aneuploid Cells,Aneuploidies,Aneuploids,Cell, Aneuploid,Cells, Aneuploid
D016612 Paraffin Embedding The infiltrating of tissue specimens with paraffin, as a supporting substance, to prepare for sectioning with a microtome. Embedding, Paraffin
D017404 In Situ Hybridization, Fluorescence A type of IN SITU HYBRIDIZATION in which target sequences are stained with fluorescent dye so their location and size can be determined using fluorescence microscopy. This staining is sufficiently distinct that the hybridization signal can be seen both in metaphase spreads and in interphase nuclei. FISH Technique,Fluorescent in Situ Hybridization,Hybridization in Situ, Fluorescence,FISH Technic,Hybridization in Situ, Fluorescent,In Situ Hybridization, Fluorescent,FISH Technics,FISH Techniques,Technic, FISH,Technics, FISH,Technique, FISH,Techniques, FISH

Related Publications

M G Grollino, and P Eleuteri, and D Pomponi, and G Calugi, and M Rocchi, and R De Vita
July 1994, Human pathology,
M G Grollino, and P Eleuteri, and D Pomponi, and G Calugi, and M Rocchi, and R De Vita
April 1995, Analytical and quantitative cytology and histology,
M G Grollino, and P Eleuteri, and D Pomponi, and G Calugi, and M Rocchi, and R De Vita
January 1998, Cancer genetics and cytogenetics,
M G Grollino, and P Eleuteri, and D Pomponi, and G Calugi, and M Rocchi, and R De Vita
October 1992, Cancer genetics and cytogenetics,
M G Grollino, and P Eleuteri, and D Pomponi, and G Calugi, and M Rocchi, and R De Vita
January 1997, Cancer,
M G Grollino, and P Eleuteri, and D Pomponi, and G Calugi, and M Rocchi, and R De Vita
July 1995, Human pathology,
M G Grollino, and P Eleuteri, and D Pomponi, and G Calugi, and M Rocchi, and R De Vita
January 2013, Methods in molecular biology (Clifton, N.J.),
M G Grollino, and P Eleuteri, and D Pomponi, and G Calugi, and M Rocchi, and R De Vita
August 1998, Nucleic acids research,
M G Grollino, and P Eleuteri, and D Pomponi, and G Calugi, and M Rocchi, and R De Vita
October 1990, Nihon Sanka Fujinka Gakkai zasshi,
M G Grollino, and P Eleuteri, and D Pomponi, and G Calugi, and M Rocchi, and R De Vita
September 1997, Cancer letters,
Copied contents to your clipboard!