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For each protein example, data were screened against each homologue search model (including self), searching all alternative SGs belonging to the reported point group (Table 2).
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Sixteen methanolic extracts obtained from thirteen plant species, selected either from ethnobotanical or chemotaxonomical data, were screened for their antileishmanial activity against Leishmania amazonensis.
Measured data were screened for errors.
The data obtained were screened against human databases downloaded from the Swiss-Prot/TrEMBL homepage (http://www.expasy.ch/sprot).
Initially, all proteins were screened against Swiss-Prot data and publicly available protein sequences from other related organisms.
These genes were screened against a recent proteomics study, where expression data of yeast grown in aerobic and anaerobic carbon-limited chemostats was measured [ 24].
Data was screened for disengaged and missing responses.
Data was screened and cleaned.
The variants were screened against blast disease.
They were screened against three cancer cell-lines (NCIH460; HCT116; U251).
All of the eight proteins were screened against ~60,000 ligand binding sites from the PDB.
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