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Mol. and Cell. Diff. 3(1), 91-109. In vitro neutralization of vascular endothelial growth factor activation of Flk-1 by a monoclonal antibody. 1995

Rockwell, P., Neufeld, G., Glassman, A., Caron, D. and Goldstein, N. I

Notes: The CellTiter 96® Non-Radioactive Cell Proliferation Assay was used to measure the inhibitory effects of a monoclonal antibody (DC 101) on VEGF-induced growth of human vascular endothelial cells (HUVEC). (2069)

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J. Biol. Chem. 270(36), 20922-20929. Increased cytotoxicity of 3-morpholinosydnonimine to HepG2 cells in the presence of superoxide dismutase. 1995

Gergel, D., Misik, V., Ondrias, K. and Cederbaum, A.I.

Notes: The CellTiter 96® Non-Radioactive Cell Proliferation Assay (MTT) was used to measure the cytotoxicity of SIN-1 on HepG2 cells. SIN-1 is the chemical named in the title that is widely used to generate nitric oxide and superoxide radicles. (2114)

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J. Biol. Chem. 270(36), 20922-20929. Increased cytotoxicity of 3-morpholinosydnonimine to HepG2 cells in the presence of superoxide dismutase. Role of hydrogen peroxide and iron. 1995

Gergel, D., Misik, V., Ondrias, K., Cederbaum, AI.

Notes: The CellTiter 96® Assay (MTT) was used to measure the cytotoxicity of SIN-1 (a chemical which generates nitric oxide and superoxide radicles) on HepG2 cells. (2907)

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Asian Pac. J. Allergy Immunol. 13(1), 43-45. Radioactive and non-radioactive lymphocyte proliferation assays for measuring rabies-specific cellular immunity. 1995

Kasempimolporn, S., Chomchey, P. and Sitprija, V.

Notes: This paper compares 3H-thymidine incorporation with the CellTiter 96® Non-Radioactive Cell Proliferation Assay for measuring lymphocyte proliferation in an assay to detect rabies-specific cell-mediated immunity. The results of both tests were in good agreement; however, the degree of positivity was different and the sensitivity was reported to be greater with the 3H-thymidine incorporation method. (2096)

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Gynecol. Oncol. 59(1), 67-74. Secreted ovarian stromal substance inhibits ovarian epithelial cell proliferation. 1995

Karlan, B.Y., Baldwin, R.L., Cirisano, F.D., Mamula, P.W., Jones, J. and Lagasse, L.D.

Notes: The CellTiter 96® Non-Radioactive Cell Proliferation Assay was used to measure proliferation of human ovarian carcinoma cell line Caov-3. The amount of formazan generated was shown to be directly proportional to the number of living cells by cell counting of trypan blue excluding cells. (2094)

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Am. J. Obstet. Gynecol. 173(1), 97-104. Steroid hormone effects on the proliferation of human ovarian surface epithelium. 1995

Karlan, B.Y., Jones, J., Greenwald, M. and Lagasse, L.D.

Notes: The CellTiter 96® Non-Radioactive Cell Proliferation Assay was used to generate growth curves to compare the effects of various steroids on proliferation of primary epithelial cells scraped from human ovaries and subcultured for assay. (2095)

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J. Exp. Med. 179(6), 1945-1956. Amino acid residues that flank core peptide epitopes and the extracellular domains of CD4 modulate differential signaling through the T cell receptor. 1994

Vignali, D.A.A. and Strominger, J.L.

Notes: The authors used the CellTiter 96® Non-Radioactive Cell Proliferation Assay (MTT) to measure IL-2 stimulated proliferation of CTLL-2 cells. The IL-2 was collected from tissue culture supernatants of cells. (1716)

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J. Cell. Biochem. 54(3), 299-308. Apolipoprotein E: A potent inhibitor of endothelial and tumor cell proliferation. 1994

Vogel, T., Guo, N-H., Guy, R., Drezlich, N., Krutzsch, H.C., Blake, D.A., Panet, A., and Roberts, D.D.

Notes: The CellTiter 96® Non-Radioactive Cell Proliferation Assay was used to measure the inhibitory effects of apolipoprotein E or apolipoprotein E dimeric peptide on bovine aortic endothelial (BAE) cells. (1717)

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Pharm. Res. 11(8), 1127-1131. Comparison of cell proliferation and toxicity assays using two cationic liposomes. 1994

Lappalainen, K., Jaaskelainen, I., Syrjanen, K., Urtti, A., Syrjanen, S.

Notes: The CellTiter 96® AQ Assay (MTS) and CytoTox 96® Assays were compared for measuring toxic effects of cationic liposomes on CaSki (human cervical cancer) cells (2882)

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J. Immunol. 152, 1751-1755. Fas antigen and p55 TNF receptor signal apoptosis through distinct pathways 1994

Wong, G. H. W. , Goeddel, D. V.

Notes: The CellTiter 96® Non-Radioactive Cell Proliferation Assay was used to measure viability/cytotoxicity of HuT-78, Jurkat, and Su-4 cells in a study of apoptosis. (0150)

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Mol. Cell. Biol. 14(1), 181-188. Fibroblast growth factor receptors have different signaling and mitogenic potentials. 1994

Wang, J-K., Gao, G., and Goldfarb, M.

Notes: The CellTiter 96® Non-Radioactive Cell Proliferation Assay was used to measure proliferation of BaF3 murine lymphoid (pro-B) cells that were engineered to express FGFR-1, FGFR-4 and chimeric receptor containing extracelular domain of FGFR-4 and intracellular domain of FGFR-1. (1719)

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J. Cell Biol. 127(3), 859-866. Receptor tyrosine kinase signaling required for integrin alpha v beta 5-directed cell motility but not adhesion on vitronectin. 1994

Klemke, R.L., Yebra, M., Bayna, E.M., Cheresh, DA.

Notes: The CellTiter 96® Assay (MTT) was used to assay cell adhesion on vitronectin or collagen coated plates. (2899)

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J. Cell Biol. 127(3), 859-866. Receptor tyrosine kinase signalling required for integrin alpha/v/beta 5-directed cell motility but not adhesion on vitronectin. 1994

Klemke, R.L., Yebra, M., Bayna, E.M., and Cheresh, D.A.

Notes: The CellTiter 96® Non-Radioactive Cell Proliferation Assay (MTT) was used to assay cell adhesion on vitronectin or collagen coated plates. (2100)

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J. Immunol. 153(11), 5026-5037. Tepoxalin, a novel immunosuppressive agent with a different mechanism of action from cyclosporin A. 1994

Zhou, L., Ritchie, D., Wang, E.Y., Barbone, A.G., Argentieri, D., and Lau, C.Y

Notes: The CellTiter 96® Non-Radioactive Cell Proliferation Assay (MTT) was used to measure cell proliferation. (1732)

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Hum. Reprod. 8(10), 1564-1569. Human follicular fluid maturity and endothelial cell mitogenesis. 1993

McClure, N., Macpherson, A.M., Abberton, K.M., Healy, D.L. and Rogers, P.A.

Notes: The CellTiter 96® Non-Radioactive Cell Proliferation Assay (MTT) was used to measure the proliferative effect of follicular fluid (collected from Graafian folicules of 22 ovulatory patients using laparoscopic surgery) on bovine aortic endothelial cells. Intra- and inter-plate coefficients of variation were <9%. (2075)

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J. Biomed. Biotechnol. 53, 74-84. Modulation of endothelial cell proliferation, adhesion, and motility by recombinant heparin-binding domain and synthetic peptides from the type I repeats of thrombospondin 1993

Vogel, T., Guo, N.H., Krutzsch, H.C., Blake, D.A., Hartman, J., Mendelovitz, S., Panet, A., Roberts, D.D.

Notes: CellTiter 96® Non-Radioactive Cell Proliferation Assay was used to study modulation of endothelial cell proliferation by synthetic peptides. (0227)

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J. Cell. Biochem. 53(1), 74-84. Modulation of endothelial cell proliferation, adhesion, and motility by recombinant heparin-binding domain and synthetic peptides from the type I repeats of thrombospondin. 1993

Vogel, T., Guo, N.-H.,Krutzsch, H.C., Blake, D.A., Hartman, J., Mendelovitz, S., Panet, A., and Roberts, D.D.

Notes: The CellTiter 96® Non-Radioactive Cell Proliferation Assay (MTT) was used to measure thrombospondin inhibition of bovine aortic endothelial cell proliferation. (1718)

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Proc. Natl. Acad. Sci. USA 90(21), 10154-10158. Multiple integrins mediate cell attachment to cytotactin/tenascin. 1993

Prieto, A.L., Edelman, G.M. and Crossin, K.L.

Notes: This CellTiter 96® Non-Radioactive Cell Proliferation Assay (MTT) was used to assay cell adhesion. A poster with the same title and authors was presented at the 1993 ASCB meeting in New Orleans. (2083)

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Oncol. Res. 5(10/11), 433-439. Suppression of C-1300 murine neuroblastoma cell proliferation in tissue culture and tumor growth in vivo by (Z)5'-fluoro-4',-5'-didehydro-5'-deoxyadenosine (MDL 28,842), an irreversible inhibitor of S-adenyosyl-L-homocysteine hydrolase. 1993

Zhang, C., Bowlin, T., and Mirkin, B.L.

Notes: The CellTiter 96® Non-Radioactive Cell Proliferation Assay (MTT) was used to measure inhibition of C-1300 murine neuroblastoma cells. (1730)

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Oncol. Res. 5, 433-439. Suppression of C-1300 murine neuroblastoma cell proliferation in tissue culture and tumor growth in vivo by (Z)5'-fluoro-4',5'-didehydro-5'-deoxyadenosine (MDL 28,842), an irreversible inhibitor of S-adenosyl-L-homocysteine hydrolase. 1993

Zhang, C. , Bowlin, T. , Mirkin, B. L.

Notes: MNB (murine neuroblastoma) cells, containing heat inactivated FBS, were used with the CellTiter 96® Non-Radioactive Cell Proliferation System. (0087)

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Biochem. Biophys. Res. Commun. 186, 944-950. Vitamin E protects nerve cells from amyloid beta protein toxicity. 1992

Behl, C., Davis, J., Cole, G.M. and Schubert, D.

Notes: These authors used the CellTiter 96® Non-Radioactive Cell Proliferation Assay (MTT) to measure toxicity of various agents (including peptides from amyloid beta protein, which accumulate in Alzheimer's disease plaques) on PC12 cells. (1541)

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J. Cell Biol. 115(3 Pt. 2), 446a. Differentiation and proliferation in a cloned bovine mammary epithelial cell line: Effects of extracellular matrix and growth factors. 1991

Gibson, C.A. and Baumrucker, C.R.

Notes: The CellTiter 96® Non-Radioactive Cell Proliferation Assay was used to measure proliferation of bovine mammary epithelial cells cultured on plastic or on Matrigel. (2115)

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