3 results match your criteria: "Physical and Chemical Research Institute (RIKEN)[Affiliation]"
Autoimmun Rev
April 2005
Laboratory for Rheumatic Diseases, SNP Research Center, The Physical and Chemical Research Institute (RIKEN), 1-7-22 Suehirocho, Tsurumiku, Yokohama, Kanagawa 230-0045, Japan.
Anticitrullinated peptide antibodies seem to be one of the most clinically reliable serologic markers for rheumatoid arthritis (RA). A genetic approach revealed that one of the citrullinating enzymes has a RA-susceptible variant. Peptidyl citrullination alters the chemical character of peptides and, subsequently, their antigenicity as well.
View Article and Find Full Text PDFBiochem Biophys Res Commun
December 1994
Animal and Cellular Systems Laboratory, Physical and Chemical Research Institute (RIKEN), Saitama, Japan.
Destruxin B, a peptide antibiotic, inhibits vacuolar-type ATPase (V-ATPase) specifically and dose-dependently among ATPases examined. Acidification of intracellular organelles is also blocked by destruxin B at comparable concentrations when assessed by accumulation of acridine orange. The inhibitory activity of destruxin B is weaker than that of bafilomycin A1 and folimycin, well known macrolide inhibitors of V-ATPase, when compared at the same molar concentration.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
December 1990
Laboratory of Molecular Oncology, Tsukuba Life Science Center, Physical and Chemical Research Institute (RIKEN), Ibaraki, Japan.
In attempting to produce a mutant mouse with embryonic stem cells, the critical step is the efficient isolation of homologous recombinants; the frequency of the homologous recombination is usually low and the potency of the cells to differentiate into germ cells is unstable in culture. Here, we report an efficacious method for such isolation in which the diphtheria toxin A-fragment gene is used to negatively select nonhomologous recombinants. In contrast to the use of the herpes simplex virus thymidine kinase gene, the selection can be made singly by the neomycin analog G418 without using a drug such as ganciclovir, a nucleoside analog.
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