Flow Cytometric Determination of Micronucleus Frequency

2013 ◽  
pp. 209-235 ◽  
Author(s):  
Azeddine Elhajouji ◽  
Magdalena Lukamowicz-Rajska
Keyword(s):  
Micronucleus Frequency ◽  
Flow Cytometric

Determination of the Developmental Origin of Seeds Containing Endosperm Using Flow Cytometric Analysis

BIO-PROTOCOL ◽  
2015 ◽  
Vol 5 (11) ◽  
Author(s):  
Christian Sailer ◽  
Anja Schmidt ◽  
Ueli Grossniklaus
Keyword(s):  
Flow Cytometric Analysis ◽  
Developmental Origin ◽  
Flow Cytometric

Correlation between flow cytometric determination of nuclear DNA content and chromosome number in somatic hybrids within Brassicaceae

1988 ◽  
Vol 7 (1) ◽  
pp. 74-77 ◽  
Author(s):  
Jan Fahleson ◽  
Johan Dixelius ◽  
Eva Sundberg ◽  
Kristina Glimelius
Keyword(s):  
Chromosome Number ◽  
Dna Content ◽  
Nuclear Dna ◽  
Somatic Hybrids ◽  
Nuclear Dna Content ◽  
Flow Cytometric

Flow cytometric determination of metastatic spread during fractionated radiation therapy of the rat rhabdomyosarcoma R1H

1989 ◽  
Vol 17 ◽  
pp. 242-243
Author(s):  
Michael Baumann ◽  
Hans-Peter Beck-Bornholdt ◽  
Sibylle Becker ◽  
Hubert Vogler ◽  
Hans Juergen Krueger ◽  
...  
Keyword(s):  
Radiation Therapy ◽  
Metastatic Spread ◽  
Flow Cytometric ◽  
Fractionated Radiation Therapy ◽  
Rat Rhabdomyosarcoma R1h ◽  
Fractionated Radiation

scholarly journals Flow Cytometric Determination of Genome Size in the Taxodiaceae, Cupressaceae sensu stricto and Sciadopityaceae.

CYTOLOGIA ◽  
2001 ◽  
Vol 66 (3) ◽  
pp. 307-311 ◽  
Author(s):  
Masahiro Hizume ◽  
Teiji Kondo ◽  
Fukashi Shibata ◽  
Ryoko Ishizuka
Keyword(s):  
Genome Size ◽  
Sensu Stricto ◽  
Flow Cytometric

scholarly journals Flow cytometric determination of atypical antigen expression in acute leukemia for the study of minimal residual disease

Cytometry ◽  
1992 ◽  
Vol 13 (8) ◽  
pp. 893-901 ◽  
Author(s):  
Johannes Drach ◽  
Doris Drach ◽  
Herta Glassl ◽  
Claus Gattringer ◽  
Heinz Huber
Keyword(s):  
Acute Leukemia ◽  
Minimal Residual Disease ◽  
Residual Disease ◽  
Antigen Expression ◽  
Flow Cytometric ◽  
Minimal Residual

scholarly journals Flow cytometric determination of glutathione in clinical samples

Cytometry ◽  
1995 ◽  
Vol 21 (1) ◽  
pp. 68-71 ◽  
Author(s):  
Sue Chow ◽  
David Hedley
Keyword(s):  
Clinical Samples ◽  
Flow Cytometric

Flow Cytometric Determination of Percentage of Red Blood Vesicles in β-Thalassemia

2008 ◽  
Vol 8 (2) ◽  
pp. 182-187 ◽  
Author(s):  
Laila Hegazy . ◽  
Sahar Kamal . ◽  
Azza Ahmed Aly . ◽  
Nevine E. Saad . ◽  
Nermine El Desouki . ◽  
...  
Keyword(s):  
Flow Cytometric

scholarly journals Flow cytometric analysis of herpes simplex virus type 1 susceptibility to acyclovir, ganciclovir, and foscarnet.

1997 ◽  
Vol 41 (12) ◽  
pp. 2686-2692 ◽  
Author(s):  
I Pavić ◽  
A Hartmann ◽  
A Zimmermann ◽  
D Michel ◽  
W Hampl ◽  
...  
Keyword(s):  
Flow Cytometry ◽  
Herpes Simplex Virus ◽  
Herpes Simplex ◽  
Cytopathic Effect ◽  
Flow Cytometric Analysis ◽  
Flow Cytometric ◽  
Resistant Strains ◽  
Simplex Virus

We established a quantitative flow cytometric method for determination of herpes simplex virus type 1 (HSV-1) susceptibility to acyclovir (ACV), ganciclovir, and foscarnet in vitro. Susceptibility was defined in terms of the drug concentration which reduced the number of cells expressing HSV-1 glycoprotein C (gpC) with a fluorescence intensity of > or =10(2) by 50% (IC50). Flow cytometry allowed us to use a high (1.0) as well as a low (0.005) multiplicity of infection, and determination of the IC50 was possible after one or more viral replicative cycles. IC50s were dependent on virus input and on time postinfection. In mixture experiments, 1 to 2% resistant viruses added to a sensitive strain could be detected. The results obtained by flow cytometry showed a good qualitative correlation with those achieved by cytopathic effect inhibitory assay. However, flow cytometry might detect more quantitative differences in drug susceptibility, especially among resistant strains, as confirmed also by determination of intracellular drug phosphorylation. The mean IC50s for ACV-sensitive strains were 0.45 to 1.47 microM, and those for ACV-resistant strains were between 140 and 3,134 microM. Flow cytometric analysis was fast and accurate, automatizable, and highly reproducible. Flow cytometry may be a more powerful tool than standard cytopathic effect-based assays and could have advantages for the detection of low levels of drug resistance or mixtures of sensitive and resistant virus strains.

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