2010 - Fellow of the American Association for the Advancement of Science (AAAS)
Chris A. Kaiser mainly investigates Biochemistry, Endoplasmic reticulum, ER oxidoreductin, Protein disulfide-isomerase and Cell biology. Biochemistry is a component of his Conserved sequence, Saccharomyces cerevisiae and Yeast studies. In his work, Amino acid permease and Regulation of gene expression is strongly intertwined with Amino acid, which is a subfield of Saccharomyces cerevisiae.
The Endoplasmic reticulum study combines topics in areas such as Electron transport chain, Glutathione, Thiol and Dithiol. His ER oxidoreductin research includes elements of RoGFP, Glutaredoxin and Mutant. His research in Protein disulfide-isomerase intersects with topics in Periplasmic space and Protein folding.
Chris A. Kaiser focuses on Biochemistry, Endoplasmic reticulum, Cell biology, Saccharomyces cerevisiae and Protein disulfide-isomerase. His work on Biochemistry deals in particular with Amino acid, Amino acid permease, Yeast, Transport protein and Mutant. Chris A. Kaiser is involved in the study of Endoplasmic reticulum that focuses on ER oxidoreductin in particular.
The study incorporates disciplines such as Vesicle and Secretion in addition to Cell biology. His Saccharomyces cerevisiae research incorporates themes from Invertase and Peptide sequence. His Protein disulfide-isomerase research is multidisciplinary, relying on both Oxidoreductase, Cysteine, Thiol and Stereochemistry.
Chris A. Kaiser mostly deals with Cell biology, Genetics, Endoplasmic reticulum, Biochemistry and Small molecule. His Gene, Synthetic lethality, Karyotype and Gene duplication study, which is part of a larger body of work in Genetics, is frequently linked to Genome instability, bridging the gap between disciplines. Biophysics, Glutathione, Protein disulfide-isomerase, Thiol and Glutathione disulfide is closely connected to Oxidative phosphorylation in his research, which is encompassed under the umbrella topic of Endoplasmic reticulum.
His Yeast, Saccharomyces cerevisiae and Transport protein study in the realm of Biochemistry connects with subjects such as Vacuole. The various areas that Chris A. Kaiser examines in his Saccharomyces cerevisiae study include Amino acid, Protein catabolism, Amino acid permease, Mutant and Cell membrane. Chris A. Kaiser works mostly in the field of Small molecule, limiting it down to concerns involving Computational biology and, occasionally, In vivo and Small Molecule Libraries.
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The genetic landscape of a cell.
Michael Costanzo;Anastasia Baryshnikova;Jeremy Bellay;Yungil Kim.
Science (2010)
Distinct sets of SEC genes govern transport vesicle formation and fusion early in the secretory pathway
Chris A. Kaiser;Randy Schekman.
Cell (1990)
Formation and transfer of disulphide bonds in living cells.
Carolyn S. Sevier;Chris A. Kaiser.
Nature Reviews Molecular Cell Biology (2002)
Nitrogen regulation in Saccharomyces cerevisiae.
Boris Magasanik;Chris A Kaiser.
Gene (2002)
The ERO1 gene of yeast is required for oxidation of protein dithiols in the endoplasmic reticulum
Alison R Frand;Chris A Kaiser.
Molecular Cell (1998)
Exploration of essential gene functions via titratable promoter alleles
Sanie Mnaimneh;Armaity P Davierwala;Jennifer Haynes;Jason Moffat.
Cell (2004)
Ero1p oxidizes protein disulfide isomerase in a pathway for disulfide bond formation in the endoplasmic reticulum.
Alison R Frand;Chris A Kaiser.
Molecular Cell (1999)
Many random sequences functionally replace the secretion signal sequence of yeast invertase.
Chris A. Kaiser;Daphne Preuss;Paula Grisafi;David Botstein.
Science (1987)
Pathways for protein disulphide bond formation.
Alison R Frand;John W Cuozzo;Chris A Kaiser.
Trends in Cell Biology (2000)
Competition between glutathione and protein thiols for disulphide-bond formation.
John W. Cuozzo;Chris A. Kaiser.
Nature Cell Biology (1999)
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