1 nds have shown to be toxic and mutagenic for procaryotic and eucaryotic cells.

2  Due to the prominent sequence variations of procaryotic and eucaryotic DnaK molecules in the multihe

3 ed in promoters for normal responses of many procaryotic and eucaryotic genes to iron or oxygen stres

4  been reported in RNA viruses, as well as in procaryotic and eucaryotic genes.

5                   DNA polymerases (pol) from procaryotic and eucaryotic organisms incorporate nucleot

6 schemes have been developed for a variety of procaryotic and eucaryotic pathogens and the data genera

7  cloning and expression of a gene encoding a procaryotic bile acid transporter.

8 equence showed an unusual pattern, with this procaryotic enzyme clustering within the animal clade.

9  phosphoproteins, heretofore not possible in procaryotic expression systems.

10 acids having extensive homologies with other procaryotic GGTs.

11 odified in a manner similar to that of other procaryotic lipoproteins.

12                                  So far, all procaryotic NATs resemble the human enzyme which acetyla

13                         The sigma subunit of procaryotic RNA polymerases is responsible for specific

14 own to be correctly expressed in recombinant procaryotic systems are excluded, suggest that the corre

15 e exploration and integration in the area of procaryotic transcriptional gene regulation.

16 onstrate that a chimeric receptor containing procaryotic transmembrane sequences is expressed by a eu

17 with conserved signature residues typical of procaryotic two-component histidine kinases.