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1 lly modified oligonucleotides to introduce a hydrolysis-resistant 3'-S-phosphorothiolate linkage at t
2 trations of these four agonists and with the hydrolysis-resistant adenine nucleoside triphosphate ade
3                                    Also, the hydrolysis-resistant analogue, guanosine 5'-O-(3-thiotri
4                                          The hydrolysis-resistant aryl silicon fragment is promising
5 ted by coincubation of the receptor with the hydrolysis-resistant ATP analog AMP-PNP.
6 sicles with AMP imidodiphosphate (AMPPNP), a hydrolysis-resistant ATP analog, prior to treatment with
7 ncubation of the EGF receptor with AMPPNP, a hydrolysis-resistant ATP analog.
8  than adenylyl imidodiphosphate (AMP-PNP), a hydrolysis-resistant ATP analog; however, this study mai
9                              Addition of the hydrolysis-resistant ATP analogue, adenosine 5'-O-(3-thi
10          Phosphorylation of the channel with hydrolysis-resistant ATPgammaS prevented the suppressant
11 s are more potent than the cAMP analogs, and hydrolysis-resistant cAMP analogs are not antiproliferat
12 de (SNP), a nitric oxide (NO) donor, and the hydrolysis-resistant cGMP analogue 8-(4-chlorophenylthio
13 ed apical PepT1 levels and absorption of the hydrolysis-resistant dipeptide L-Phe(PsiS)-L-Ala (1 mM),
14 take of 1.9 microm glycylsarcosine (a model, hydrolysis-resistant dipeptide) in isolated choroid plex
15 ation in response to saturating doses of the hydrolysis-resistant enkephalin [D-Ala2,N-MePhe4,Gly5-ol
16                              We found, using hydrolysis-resistant GTP analogs and a mutant Ran unable
17 ase activity of T alpha and the binding of a hydrolysis-resistant GTP analogue to T alpha, while P ga
18                             Inclusion of the hydrolysis-resistant guanine nucleotide GDP-beta-S in th
19   This finding prompted us to synthesize its hydrolysis-resistant methylenebis(phosphonate) and diflu
20  By contrast, expression of Arf6 Q67L, a GTP hydrolysis-resistant mutant, induced the formation of PI
21 t intradermal administration of ATPgammaS, a hydrolysis-resistant P2 agonist, results in an enhanced
22                  Synthesis of stereospecific hydrolysis resistant phosphorothioate 2AP-labeled DNA al

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