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We review some recent conceptual advances enabling such studies, and corresponding computational models and tools designed to facilitate the concerted experimental and computational investigation of protein-membrane interactions.
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In this study, we review the major efforts that enable such studies.
To enable such studies, here we present the karyotypes and chromosomal C-banding for L. hesperus and L. geometricus.
Array-based techniques also enable such studies to be undertaken by laboratories without prior cytogenetics experience.
He et al. now report a fluorescence-based C. elegans model that will enable such studies.
To enable such studies, genotypic characterization of C. burnetii strains circulating in the different reservoirs is needed.
Use of commercially available antibodies against cell surface antigens will enable such studies in a wide range of genetic backgrounds.
Microarrays probing for 500,000 or 1,000,000 SNP markers equally distributed in a single human genome now enable such studies.
The recently developed ligands, in combination with the availability of M1R knock-out (M1R KO) mice, now enable such studies to be performed.
We anticipate that our new methods will further enable such studies by making analysis of large data sets and development of phylogenetic methods more practical.
CRISPR/Cas9 technology would enable such studies by altering single SNPs in the genome of a model organism while maintaining the native genomic context of the variant.
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