Exact(1)
During the period from 2000 to 2005 (64% of the included patients) genetic mutation screening were conducted using a setup consisting of denaturing high-performance liquid chromatography (DHPLC), protein truncation test (PTT) and Sanger sequencing analysis in addition to Multiplex Ligation-dependent Probe Amplification (MLPA) for detection of larger copy number abnormalities.
Similar(59)
To identify genes that have synthetic lethality to IDF-11774, RNA interference screening was conducted, using pooled lentiviruses expressing a short hairpin RNA library.
To allow the investigation of different factors, a screening was conducted using the BioLector® microfermentation system (m2p-labs, Germany).
Virtual screening was conducted using the three X-ray crystals 3VRI, 3VRJ, and 3UPR in the presence and absence of peptide.
HIV screening was conducted using Determine® HIV-1/2 (Abbott Laboratories, United Kingdom).
Participant screening was conducted using a telephone questionnaire.
Cognitive screening was conducted using the validated IDEA cognitive screen (11).
On-site couple verification screening was conducted using a somewhat different protocol.
From September 2000 to January 2001, a total of 9665 specimens were collected and initial screening was conducted using the AutoPap system.
Virtual screening was conducted using the 'fast flexible search' method and 1860 compounds out of 247,041 entries (0.8%).
Further screening was conducted using the related drought-tolerance indices of relative water content (RWC) and relative electrical conductivity (REC).
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