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1 ed levels of the pleiotropic metabolite beta-aminoisobutyric acid.
2 s = 100-700 nm) the binding of (125)I-[alpha-aminoisobutyric acid(1,3),M]PTH(1-15) and were severely
3 -15) inhibited the agonist actions of [alpha-aminoisobutyric acid(1,3)]PTH(1-34) and [M]PTH(1-14) (IC
4           Two fluorinated analogues of alpha-aminoisobutyric acid, 2-amino-3-fluoro-2-methylpropanoic
5 se in the basal uptake of glucose and methyl-aminoisobutyric acid (a substrate for the system A amino
6 ived from the achiral monomers such as alpha-aminoisobutyric acid (Aib) and meso-cyclohexane-1,2-diam
7                           Oligomers of alpha-aminoisobutyric acid (Aib) are achiral peptides that typ
8 osition 18 with a second substitution, alpha-aminoisobutyric acid (Aib) at position 16, abrogates end
9  conformationally favoured cyclisation of an aminoisobutyric acid (Aib) derivative.
10  receptors (R)-1 and (S)-1 are helical alpha-aminoisobutyric acid (Aib) foldamers that replicate key
11 oton of an alanine residue to generate alpha-aminoisobutyric acid (Aib) in alanine-based oligopeptide
12 indered and helix-promoting amino acid alpha-aminoisobutyric acid (Aib) in N-terminal PTH oligopeptid
13 t this need, an iterative synthesis of alpha-aminoisobutyric acid (Aib) oligomers was used to create
14 ormationally constrained residues like alpha-aminoisobutyric acid (Aib) or DPro that nucleate helical
15 (ACPC) and alpha-residues derived from alpha-aminoisobutyric acid (Aib) or l-alanine (Ala).
16                                 Either alpha-aminoisobutyric acid (Aib) or N-methylalanine (MeAla) we
17 the Ala series with the helix promoter alpha-aminoisobutyric acid (Aib) produced similar results, exc
18                  The achiral symmetric alpha-aminoisobutyric acid (Aib) replaced the critical N-termi
19 e modified at the amino terminal by an alpha-aminoisobutyric acid (Aib) residue.
20 no acids Trp, His, and Lys or the analogue 2-aminoisobutyric acid (AIB) was observed during infection
21 t of (125)I-PTH-(1-34) binding by rat [alpha-aminoisobutyric acid (Aib)(1,3),Nle(8),Gln(10),Har(11),A
22                                 Notably, a 2-aminoisobutyric acid (AIB)-utilizing NRPS module has bee
23 ncreased the transport of radiolabeled alpha-aminoisobutyric acid and dextran into brain tumors.
24    Uptake measurements using (3)H-FDG, (14)C-aminoisobutyric acid, and Na(125)iodide were performed t
25 which includes metabotropic glutamate, gamma-aminoisobutyric acid, and pheromone receptors.
26 partic acid, serine, glycine, alanine, alpha-aminoisobutyric acid, and valine were optimized by varyi
27 ic levels of ADMA and SDMA, and also of beta-aminoisobutyric acid (BAIB)-a modulator of lipid metabol
28                                         beta-Aminoisobutyric acid (BAIBA) belongs to natural beta-ami
29 eine and to a lesser extent by L-alanine and aminoisobutyric acid, but was not inhibited by alpha-(me
30 ss of antibiotics known for their high alpha-aminoisobutyric acid content and their synthesis as a mi
31 tion, and -alkynylation of isobutyric acid/2-aminoisobutyric acid derivatives, which may serve as a p
32 reased N-methylnicotinamide and reduced beta-aminoisobutyric acid excretion.
33  a screw-sense preference in a helical oligo(aminoisobutyric acid) foldamer, which is relayed to a re
34 lpha-dependent myokine FNDC5/irisin and beta-aminoisobutyric acid from myotubes and muscle in rats an
35                    Here we report that the 2-aminoisobutyric acid hydroxylase from Rhodococcus wratis
36  of tracer glucose was maintained and methyl-aminoisobutyric acid increased 166% (P < 0.005) per gram
37 of the fully conserved Pro residues by alpha-aminoisobutyric acid leads to a large increase in beta-t
38 lacental transfer of glucose, but not methyl-aminoisobutyric acid (MeAIB), was greater in C18 and C9
39 the expression of genes associated with beta-aminoisobutyric acid metabolism in I. scapularis, result
40 t, Ki, for [14C]dextran (Mr 70,000) and [14C]aminoisobutyric acid (Mr 103,000), with or without inhib
41 Aib-D-Val15 -Leu-Phe-Val-Val-OMe (Aib, alpha-aminoisobutyric acid; OMe, methyl ester) was intended to
42 motility, Na(+)-dependent transport of alpha-aminoisobutyric acid, or H(+)-dependent synthesis of ATP
43 Hence, urinary N-methylnicotinamide and beta-aminoisobutyric acid represent promising biomarkers for
44 exibility of the peptides, helix-promoting 2-aminoisobutyric acid residues and helix-inducing tethers
45 n protein structures, and incorporates alpha-aminoisobutyric acid residues.
46  by replacing alanine with glycine and alpha-aminoisobutyric acid resulted in analogues with activiti
47         Moreover, the glucose metabolism and aminoisobutyric acid uptake significantly decreased in v
48             In the 3rd group, 14C-AIB (alpha-aminoisobutyric acid) was used to evaluate BBB transport
49 , dipeptides 6a and 6c (D-penicillamyl-alpha-aminoisobutyric acid) were able to reduce this AcH level