戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ortho-oxygen-stabilized iodonium derivative (OID).
2 inds OGT, termed the OGT-interacting domain (OID).
3 d 176 peer-reviewed papers to evaluate metal(oid) accumulation in Ulva.
4 /demulsification and interconversion between OID and Pickering emulsions together with control of the
5 ND), patients with other autoimmune disease (OID), and normal controls.
6  cancer by PET, which demonstrates that this OID approach is a convenient and highly efficient way of
7 elopment and likely cancer predisposition in OID daughters.
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
10  bonding, resulting in the transformation of OID emulsions into Pickering emulsions.
11                    Stable oil-in-dispersion (OID) emulsions in strong acidity (pH=2) can be co-stabil
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
16 ated with changes in sperm tRNA fragments in OID males.
17  is established, leading to the tetraradical(oid) molecule, which has been predicted to have narrow l
18                       Additionally, both the OID of OIP106 and nucleoporin p62 competed with each oth
19               The apparent Km of OGT for the OID of OIP106 is 3.35 microm.
20 cated that TPRs 2-6 of OGT interact with the OID of OIP106.
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-
25  shifted to the rational design of diradical(oid)s for specific applications.
26                Heteroatom-centered diradical(oid)s have been in the focus of molecular main group che
27 ical considerations, the design of diradical(oid)s in terms of ligand choice, steric, symmetry, elect
28 om-centered diradical(oid)s and tetraradical(oid)s published in the last 10 years since 2013.
29 ted details of the spectroscopy of diradical(oid)s, followed by an update of the heteroatom-centered
30                 The application of diradical(oid)s, for example in small molecule activation or as mo
31                       Semi-quantitative thyr oid stimulating hormone (TSH) lateral flow immunochromat
32                                         This OID strategy addresses an unmet need for a reliable azid
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