Preferred Label : flow cytometry;
MeSH definition : 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.;
MeSH synonym : flow microfluorometry; flow cytometries; cytofluorometries, flow; flow cytofluorometry; cytometry, flow; cytometries, flow; flow cytofluorometries; microfluorimetry, flow; microfluorometry, flow; flow microfluorometries; microfluorometries, flow; flow microfluorimetry; cytofluorometry, flow;
MeSH hyponym : Fluorescence-Activated cell sorting; Cell Sorting, Fluorescence-Activated; Cell Sortings, Fluorescence-Activated; Fluorescence Activated Cell Sorting; Fluorescence-Activated Cell Sortings; Sorting, Fluorescence-Activated Cell; Sortings, Fluorescence-Activated Cell;
MeSH annotation : flow cell sorting & FLUORESCENCE-ACTIVATED CELL SORTING: coord with CELL SEPARATION;
Wikipedia link : https://en.wikipedia.org/wiki/Flow cytometry;
Origin ID : D005434;
UMLS CUI : C0016263;
- Allowable qualifiers
- Automatic exact mappings (from CISMeF team)
- Currated CISMeF NLP mapping
- Indexing information
- Record concept(s)
- Semantic type(s)
- UMLS correspondences (same concept)
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.
https://dumas.ccsd.cnrs.fr/dumas-01932674/document
2018
France
dissertations, academic
leukaemia
burkitt lymphoma
Child
Diseases
Child
leukemia, B-Cell
lymphoblast
child, nos
neoplasm, residual
symptom assessment
acute disease
precursor cell lymphoblastic Leukemia-Lymphoma
hospitals, university
Child
Acute lymphocytic leukemia
flow cytometry
Child
child
acute disease, nos
flow cytometry, nos
leukemia, b-cell
child
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http://afcytometrie.fr/
France
French
flow cytometry
image cytometry
scientific society
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