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In this work we performed assays for the genetic improvement of the oleaginous yeast Lipomyces starkeyi DSM 70296 focusing on its utilization for lipid biosynthesis from renewable sources.
These samples were distributed in a blinded fashion to nine laboratories which performed assays designed to detect XMRV/MLV nucleic acid, virus replication, and antibody.
To better ascertain this requirement, we performed assays with single-stranded substrates.
We also performed assays to screen for phenotypes related to DNA replication and repair.
To assay whether T1410 influences kinase activity we performed assays with LRRKtide as the substrate (Figure 7A).
SLN performed assays and assembled the data.
JO organized and performed assays and coordindated study participants.
YL designed experiments, performed assays, analyzed data, and wrote the manuscript; DR and LW performed assays; CC designed assays and edited the manuscript.
SE validated and performed assays, and provided input into the manuscript.
To confirm the expression of miR- 207 in vivo, we performed assays on irradiated and control cochleas.
We performed assays for antibodies directed to lytic antigens of HHV-8 in plasma samples, according to a previously well-described method (7 ).
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