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Expression of various hepatic markers was studied by RT-qPCR in HepaRG cells exposed or not to FSK and expressed as percentage of those found in freshly isolated human hepatocytes (Table 1).
The association between SSTR2 status and molecular markers was studied with Pearson chi-square analysis by cross-tabulations, and difference in Ki67 with independent samples t test.
In a final step the involvement of the type IV DNA secretion systems encoded in the GGI and the conjugative plasmid in the spread of chromosomal markers was studied.
Chromosome 17 with 1672 markers was studied.
However, only a minority of these markers was studied thoroughly both in vitro and in vivo.
The polymorphism of these markers was studied in four French populations.
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Cell markers were studied at 25 days of culture.
These markers were studied in the whole T1E population and in the 31 new T×E individuals.
Gene expression and the immunostaining of myogenic and neurogenic markers were studied.
The performance of these markers is studied based on the following two aspects: the spatial accuracy of the local heat release rate and the trend in the total heat release rate with equivalence ratio.
The segregation data of the remaining markers were studied with the program MultiPoint ([95] [97]; http://www.multiqtl.com).
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