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To facilitate genetic cascade screening for familial hypercholesterolemia (FH) in Europe, two versions (7 and 9) of a DNA microarray were developed to detect the most frequent point mutations in the low-density lipoprotein receptor (LDLR), apolipoprotein B (APOB), and proprotein convertase subtilisin/kexin 9 (PCSK9) genes.
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For this application a hapten microarray was developed.
To exploit this new resource the microarray was developed from its predecessor the dot blot.
A microarray was developed to simultaneously screen Escherichia coli and Salmonella enterica for multiple genetic traits.
In this study, a pathogen detection microarray was developed using various 70-mer oligonucleotides specifically targeting the above pathogens.
In this study, a prototype of a 16S rRNA gene-based taxonomic microarray was developed and evaluated for monitoring of planktonic actinobacteria in shrimp ponds.
In this study, a visual DNA microarray was developed for the sensitive and specific detection of hepatitis B virus DNA (HBV-DNA) and its single nucleotide polymorphisms.
The microarray was developed by immobilizing the MBs via the epoxy group on the surface of the slide and the 5′end of the terminal thiol group on the MB.
To investigate the large-scale gene expression in different tea plant clones, a custom oligonucleotide microarray was developed using sequences from the RNA-seq study to design the probes because a commercial array is unavailable for the tea plant.
For this reason, a flow-based chemiluminescence (CL) DNA microarray was developed that is able to quantify viable and non-viable Legionella spp. as well as Legionella pneumophila in one hour.
To effectively monitor microbial populations in acidic environments and bioleaching systems, a comprehensive 50-mer-based oligonucleotide microarray was developed based on most of the known genes associated with the acidophiles.
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