タイトル（掲載誌）Methods in Molecular Biology
DOI10.1007/978-1-4939-2230-7_9
著作権情報https://www.springernature.com/gp/researchers/text-and-data-mining
参照Micro‐scale and rapid expression screening of highly expressed and/or stable membrane protein variants in <i>Saccharomyces cerevisiae</i>
参照Platform for the rapid construction and evaluation of GPCRs for crystallography in Saccharomyces cerevisiae
GPCR Engineering Yields High-Resolution Structural Insights into β
<sub>2</sub>
-Adrenergic Receptor Function
Conformational thermostabilization of the β1-adrenergic receptor in a detergent-resistant form
Structure of the human histamine H1 receptor complex with doxepin
Fusion Partner Toolchest for the Stabilization and Crystallization of G Protein-Coupled Receptors
The G-Protein-Coupled Receptors in the Human Genome Form Five Main Families. Phylogenetic Analysis, Paralogon Groups, and Fingerprints
Stabilization of the Human β2-Adrenergic Receptor TM4–TM3–TM5 Helix Interface by Mutagenesis of Glu1223.41, A Critical Residue in GPCR Structure
Fluorescence-Detection Size-Exclusion Chromatography for Precrystallization Screening of Integral Membrane Proteins
Advanced method for high-throughput expression of mutated eukaryotic membrane proteins in Saccharomyces cerevisiae
High-throughput fluorescent-based optimization of eukaryotic membrane protein overexpression and purification in
<i>Saccharomyces cerevisiae</i>
Membrane chaperone Shr3 assists in folding amino acid permeases preventing precocious ERAD
GFP-based optimization scheme for the overexpression and purification of eukaryotic membrane proteins in Saccharomyces cerevisiae
How many drug targets are there?
連携機関・データベース国立情報学研究所 : CiNii Research