Detection of dead cells and measurement of cell killing by flow cytometry.
暂无分享,去创建一个
[1] J. Dangl,et al. Rapid isolation of cloned isotype switch variants using fluorescence activated cell sorting. , 2005, Cytometry.
[2] C. Reutelingsperger,et al. Flow cytometry of apoptotic cell death. , 2000, Journal of immunological methods.
[3] M. King,et al. Flow cytometric analysis of cell killing by the jumper ant venom peptide pilosulin 1. , 1998, Cytometry.
[4] R. Braylan,et al. Measurement of absolute concentration and viability of CD34+ cells in cord blood and cord blood products using fluorescent beads and cyanine nucleic acid dyes. , 1998, Cytometry.
[5] D. Sutherland,et al. Single platform flow cytometric absolute CD34+ cell counts based on the ISHAGE guidelines. International Society of Hematotherapy and Graft Engineering. , 1998, Cytometry.
[6] M. Poot,et al. Bacterial viability and antibiotic susceptibility testing with SYTOX green nucleic acid stain , 1997, Applied and environmental microbiology.
[7] Simon C Watkins,et al. Current Protocols In Cytometry , 1997 .
[8] M. King,et al. Use of four-colour flow cytometry to evaluate conjugate formation between human peripheral blood mononuclear cells and tumour target cells. , 1996, Cytometry.
[9] B. Jonsson,et al. Cytotoxic activity of calcein acetoxymethyl ester (Calcein/AM) on primary cultures of human haematological and solid tumours. , 1996, European journal of cancer.
[10] B. Sarkadi,et al. Transport properties of the multidrug resistance‐associated protein (MRP) in human tumour cells , 1996, FEBS letters.
[11] A. Yamauchi,et al. Target-induced death by apoptosis in human lymphokine-activated natural killer cells. , 1996, Blood.
[12] B. Bonavida,et al. Target-induced inactivation and cell death by apoptosis in a subset of human NK cells. , 1996, Journal of immunology.
[13] K. Nilsson,et al. Cytotoxic effect of calcein acetoxymethyl ester on human tumor cell lines: drug delivery by intracellular trapping. , 1995, Anti-cancer drugs.
[14] M. Pagé,et al. Measurement of tumor necrosis factor activity by flow cytometry. , 1995, Cytometry.
[15] K. Pantel,et al. A novel non-radioactive cellular cytotoxicity test based on the differential assessment of living and killed target and effector cells. , 1995, Journal of immunological methods.
[16] W. Bolton,et al. Comparison of cell viability probes compatible with fixation and permeabilization for combined surface and intracellular staining in flow cytometry. , 1995, Cytometry.
[17] N. Papadopoulos,et al. An improved fluorescence assay for the determination of lymphocyte-mediated cytotoxicity using flow cytometry. , 1994, Journal of immunological methods.
[18] S. Cook,et al. A cytotoxicity assay utilizing a fluorescent dye that determines accurate surviving fractions of cells. , 1994, Journal of immunological methods.
[19] C. Bridts,et al. Use of fluorescent dyes in the determination of adherence of human leucocytes to endothelial cells and the effect of fluorochromes on cellular function. , 1994, Journal of immunological methods.
[20] S. Schuval,et al. Flow cytometric analysis of natural killer cell function as a clinical assay. , 1994, Cytometry.
[21] R. Raison,et al. Cell membrane changes induced by the cytolytic peptide, melittin, are detectable by 90° laser scatter , 1994 .
[22] L. Lebeck,et al. Rapid flow cytometric assay for the assessment of natural killer cell activity. , 1993, Journal of immunological methods.
[23] M. Vitale,et al. Subtraction of autofluorescent dead cells from the lymphocyte flow cytometric binding assay. , 1993, Cytometry.
[24] I. Pastan,et al. Fluorescent cellular indicators are extruded by the multidrug resistance protein. , 1993, The Journal of biological chemistry.
[25] G. Radcliff,et al. Quantification of effector/target conjugation involving natural killer (NK) or lymphokine activated killer (LAK) cells by two-color flow cytometry. , 1991, Journal of immunological methods.
[26] B. D. de Grooth,et al. A simple and sensitive flow cytometric assay for the determination of the cytotoxic activity of human natural killer cells. , 1990, Journal of immunological methods.
[27] C. Parish,et al. New fluorescent dyes for lymphocyte migration studies. Analysis by flow cytometry and fluorescence microscopy. , 1990, Journal of immunological methods.
[28] M. Hallett,et al. Reversible cell damage by T-cell perforins. Calcium influx and propidium iodide uptake into K562 cells in the absence of lysis. , 1990, The Biochemical journal.
[29] J. Watson,et al. An improved method for the detection of cell surface antigens in samples of low viability using flow cytometry. , 1990, Journal of immunological methods.
[30] K. Bair,et al. Limitations of the fluorescent probe viability assay. , 1989, Molecular toxicology.
[31] J. Ordonez,et al. Estimation of cell survival by flow cytometric quantification of fluorescein diacetate/propidium iodide viable cell number. , 1989, Cancer research.
[32] M. Vitale,et al. Natural killer function in flow cytometry. II. Evaluation of NK lytic activity by means of target cell morphological changes detected by right angle light scatter. , 1989, Journal of immunological methods.
[33] P. Horan,et al. Cell-mediated cytotoxicity. A highly sensitive and informative flow cytometric assay. , 1989, Journal of immunological methods.
[34] J. Ellwart,et al. Drug testing in established cell lines by flow cytometric vitality measurements versus clonogenic assay. , 1988, Cancer research.
[35] P. Workman,et al. Polar fluorescein derivatives as improved substrate probes for flow cytoenzymological assay of cellular esterases. , 1988, Molecular and cellular probes.
[36] M. Vitale,et al. Natural killer function in flow cytometry. I. Evaluation of NK lytic activity on K562 cell line. , 1988, Journal of immunological methods.
[37] M. Tong,et al. The application of flow cytometry in the study of natural killer cell cytotoxicity. , 1987, Clinical immunology and immunopathology.
[38] E. Engleman,et al. Discrimination of viable and non-viable cells using propidium iodide in two color immunofluorescence. , 1987, Cytometry.
[39] R. Penny,et al. A fluorescence NK assay using flow cytometry. , 1986, Journal of immunological methods.
[40] Lippman Me,et al. Clonogenic and nonclonogenic in vitro chemosensitivity assays , 1985 .
[41] R. Higashikubo,et al. Comparison of the cell kill measured by the Hoechst-propidium iodide flow cytometric assay and the colony formation assay. , 1983, Cell and tissue kinetics.
[42] H. Shapiro,et al. Monitoring the effect of anti‐cancer drugs on L1210 cells by a mitochondrial probe, rhodamine‐123 , 1982, International journal of cancer.
[43] M. Loken,et al. Flow cytometry as an analytical and preparative tool in immunology. , 1982, Journal of immunological methods.
[44] M. Melamed,et al. Interaction of rhodamine 123 with living cells studied by flow cytometry. , 1982, Cancer research.
[45] E. Hamori,et al. Selection of viable cells with known DNA content. , 1980, Cytometry.
[46] B. Bohn. High-sensitivity cytofluorometric quantitation of lectin and hormone binding to surfaces of living cells. , 1976, Experimental cell research.
[47] B. Drewinko,et al. Comparison of in vitro methods to determine drug-induced cell lethality. , 1976, Cancer research.
[48] T. J. Fraser,et al. Comparison of different methods of determining cell viability after exposure to cytotoxic compounds. , 1976, Experimental cell research.
[49] A Krishan,et al. Rapid flow cytofluorometric analysis of mammalian cell cycle by propidium iodide staining , 1975, The Journal of cell biology.
[50] J. Yuhas,et al. Neuraminidase and cell viability: failure to detect cytotoxic effects with dye-exclusion techniques. , 1974, Journal of the National Cancer Institute.
[51] B. Chapuis,et al. Quantitative assay of the lytic action of immune lymphoid cells on 51-Cr-labelled allogeneic target cells in vitro; inhibition by isoantibody and by drugs. , 1968, Immunology.
[52] J. Giorgi,et al. Flow cytometric analysis of live cell proliferation and phenotype in populations with low viability. , 1999, Cytometry.
[53] T. Idziorek,et al. YOPRO-1 permits cytofluorometric analysis of programmed cell death (apoptosis) without interfering with cell viability. , 1995, Journal of immunological methods.
[54] R. Förster,et al. A versatile flow cytometry-based assay for the determination of short- and long-term natural killer cell activity. , 1995, Journal of immunological methods.
[55] K. Bauer,et al. Clinical flow cytometry : principles and application , 1993 .
[56] I Schmid,et al. Dead cell discrimination with 7-amino-actinomycin D in combination with dual color immunofluorescence in single laser flow cytometry. , 1992, Cytometry.
[57] C. Stewart,et al. Use of a photolabeling technique to identify nonviable cells in fixed homologous or heterologous cell populations. , 1991, Cytometry.
[58] P. Workman,et al. Multiparametric analysis of cell membrane permeability by two colour flow cytometry with complementary fluorescent probes. , 1990, Cytometry.
[59] Howard M. Shapiro,et al. Practical Flow Cytometry , 1985 .
[60] L. Weisenthal,et al. Comparison of dye exclusion assays with a clonogenic assay in the determination of drug-induced cytotoxicity. , 1983, Cancer research.
[61] C. Pipho,et al. Use of propidium iodide staining and flow cytometry to measure anti-mediated cytotoxicity: resolution of complement-sensitive and resistant target cells. , 1983, Journal of immunological methods.
[62] B. Rotman,et al. Membrane properties of living mammalian cells as studied by enzymatic hydrolysis of fluorogenic esters. , 1966, Proceedings of the National Academy of Sciences of the United States of America.