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In vitro data from HBV/precore hepatocyte cell lines demonstrated effective intrabody regulation of precore/HBeAg.
Testing of the analogs in ovarian cancer cell lines demonstrated 100 1000-fold decreased antiproliferative activity.
While all cell lines demonstrated hOT7T175 mRNA expressions, only Caki-1 had KiSS-1 transcripts.
Connected lines demonstrated in the phase diagram represent that metal catalyst possess two or more than two levels.
All BM-hMSC donor lines demonstrated conformity to the ISCT criteria but showed a difference in cell morphology.
Cell lines demonstrated that proliferation levels of DLD1, DLD1/SV-rLuc Cells and DLD1/SV-FLuc cells were significantly same relative to non-tumorigenic cell lines [34, 35].
Both mutant tumor cell lines demonstrated metabolic sensitivity to the drug, confirming their feasibility for [18 F]FDG-PET imaging of RO5126766 efficacy.
I V characteristic of a 50-nm SWCNT model (dotted lines) demonstrated in comparison to L ≈ 50 nm semiconducting CNT experimental data (filled diamond).
Transfection experiments in HEK293 and A549 cell lines demonstrated that UOC/pAdTLRGD polyplexes were able to deliver the plasmid and transfect both cell lines.
Polymerase chain reaction and reverse transcriptase polymerase chain reaction analysis performed on individual transgenic lines demonstrated that the MB-1Trp gene was correctly integrated and transcribed into mRNA.
Both OsHsp17.0-OE and OsHsp23.7-OE transgenic lines demonstrated higher germination ability compared to wild-type (WT) plants when subjected to mannitol and NaCl.
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