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1 ortho-oxygen-stabilized iodonium derivative (OID).
2 inds OGT, termed the OGT-interacting domain (OID).
4 /demulsification and interconversion between OID and Pickering emulsions together with control of the
6 cancer by PET, which demonstrates that this OID approach is a convenient and highly efficient way of
8 hion, along with considerations of diradical(oid) design, provides a rational understanding of this i
9 gely is controlled by aluminum-oxide mineral(oid) electrostatic sorption, whereas long-chain PFAS mob
12 hibit enhanced growth when transplanted into OID females compared to CO mammary glands transplanted i
13 rom F1 CO female offspring transplanted into OID females has a higher proliferation/apoptosis rate.
14 r, we show that granddaughters (F2) from the OID grand-paternal germline have accelerated tumor growt
15 nal consumption of an obesity-inducing diet (OID) increased breast cancer susceptibility in the offsp
17 is established, leading to the tetraradical(oid) molecule, which has been predicted to have narrow l
21 competitively inhibited glycosylation of the OID protein, but did not inhibit glycosylation of a 12-a
22 update of the heteroatom-centered diradical(oid)s and tetraradical(oid)s published in the last 10 ye
23 mpass the precipitation of U-bearing mineral(oid)s and the complexation of U by a vast range of (in)o
24 his work, we explore the series of diradical(oid)s based on 2,2'-(5,11-dihydroindolo[3,2-b]carbazole-
27 ical considerations, the design of diradical(oid)s in terms of ligand choice, steric, symmetry, elect
29 ted details of the spectroscopy of diradical(oid)s, followed by an update of the heteroatom-centered
33 all peptide substrates, glycosylation of the OID was dependent upon its interaction with the first 6
34 characterizing ocular inflammatory disease (OID) within the IRIS((R)) Registry (Intelligent Research