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Subsequently, four of the ex vivo derived lines were analysed for corresponding miRNA expression.
Twelve EGFR mutant and one ERBB2 mutant cell lines were analysed for LKB1 genotype.
Virus preparations from each of the infected cell lines were analysed for genetic modifications.
Two different GIST cell lines were analysed for hK1 expression using RT PCR and ELISA.
Thyroid cancer cell lines were analysed for CD133 expression, radiosensitivity and gene expression.
Therefore, 64 CRC cell lines were analysed for the occurrence of proteolytically processed, active Notch.
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Finally, a small panel of human breast cancer cell lines was analysed for PRL mRNA expression by the ISH technique.
The T2 progeny of at least three independent transgenic lines was analysed for each transgene, and in each case the three lines with the strongest phenotypic suppression were chosen for the graphic representations and statistical analyses.
Four well-characterised cell lines are analysed for their responsiveness to exogenous EGF and transforming growth factor alpha (TGF-alpha) as well as for coexpression of EGFR and EGF/TGF-alpha.
17-DMAG IC50 values for a range of cell lines were extrapolated from Lehmann et al. Using the publically available data sets used within this paper (GSE10890 and E-TABM-157), microarray data from cell lines was analysed for S100A2 expression using R (www.r-project.org).org
The trachea of infected and control birds from each line were analysed for viral load using Taqman real-time quantitative RT-PCR assays.
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