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1 [0.90] para 1; 0.32 [1.1] para 2; 0.21 [1.1] para > or = 3; p<0.0001) and placental weight (mean 655
4 itochondrial DNA (mtDNA) introgression among para- and sympatric species in the T. quadrivittatus gro
5 Me, Et, iPr, and tBu) and position (meta and para) of the alkyl groups were varied in a molecular bal
6 pyridinium nitrogen, ipso, ortho, meta, and para, we found a variation in the interaction energy of
8 ortho-xylene exceeding 25 were observed and para- and ortho- liquid mixtures were efficiently separa
11 ependent and independent, act through auto-, para- or intracrine mechanisms and can be modified by ho
12 ious mono- and disubstituted tolanes bearing para- and ortho-substituents demonstrated that the regio
13 tro and demonstrate that virtually all, both para- and transcellular, diapedesis occurs in the contex
14 rivative, o-LHBDI, and H2BDI possessing both para- and ortho-hydroxyl groups such that the inherent r
17 rbazole-5,7(6H)-dione (NB506), camptothecin-(para)-4beta-amino-4'-O-demethyl Epipodophyllotoxin (W1),
18 bidopsis cytochrome P450s (P450s) catalyzing para- and meta-hydroxylations of the phenolic ring of mo
19 stant was found in the case of penta-charged para (Mn(III)TM-4-PyP(5+)) and meta isomers (Mn(III)TM-3
20 of the substituent and the solvent on delta(para), particularly the contact contribution, are demons
21 erature-independent) and paramagnetic (delta(para), temperature-dependent) contributions to the total
23 differentially expressed (P < 0.005) during para- to endo-dormant and endo- to eco-dormant transitio
24 hylene activities were also increased during para- to endodormancy transition, which may play some ro
25 he nitroxide and imide nitrogen atoms either para (1) or meta (3) to one another, as well as through
26 eir carboxylic acid recognition site: either para (M(p)) or meta (M(m)) relative to the maleimide rin
29 r binding of a series of radical anions from para- and ortho-substituted nitrobenzenes with 1,3-dieth
32 mutations in the Na+ channel structural gene para, but enhanced by loss-of-function mutations in a se
33 0T) into the Drosophila sodium channel gene, para, causes a semidominant temperature-induced seizure
34 Knockdown studies of three candidate genes (para, Rab2, and Rim) in sensory neurons innervating the
35 ransfer (HT) between redox sites attached in para- or in meta-positions to a central benzene bridge,
36 by a single pattern showing inferotemporal, (para-)hippocampal, and cerebellar loadings for patients
37 ecules of the form X-m-X (X-p-X), with meta (para) connections in the central ring, were predominantl
38 tic substitution pattern (i.e., ortho, meta, para) of the parent phenylacetylene monomer undergo modi
39 Finally, we show coupling between I(Na) (para) and I(K) (Shal) such that Pum-mediated change in p
40 of dormancy under natural conditions, namely para-, endo-, and ecodormancy in summer, fall, and winte
41 oarene (G(o)ortho - G(o)H or G(o)ortho - G(o)para) by inflicting molecular strain and consequently we
42 ra Br-C6H5-CF3, allowing for introduction of para -C6H5CF3 groups while maintaining the desirable che
43 date the mechanisms regulating expression of para, which encodes the major class of sodium channels i
45 ltra-selective performance for separation of para- from ortho-xylene (separation factor >10 000).
46 much less polar than either the meta (1m) or para (1p) because 1o (but not 1m and 1p) can adopt a fol
47 lcohol derivatives, in which remote (meta or para) substituents are used to systematically perturb th
51 t to accomplish selective ortho-ortho, ortho-para, or para-para homo-couplings of phenols are describ
52 of the ratio of the two spin isomers (ortho/para) of molecular hydrogen, H2, which decreases monoton
53 n, as well as cacophony (cac) and paralytic (para), voltage-gated ion channels central to neuronal ex
56 ic interactions characteristic of paralytic (para) and maleless (mle) mutations that cause reduced ex
57 nknown function homologous to the paralytic (para) sodium channel, which mediates neuronal excitabili
59 y required functionalization of the position para (or ortho) to a fluorine atom on the aromatic ring
66 le metal-organic framework selectively sorbs para- (pX) over meta-xylene (mX) by synergic restructuri
70 (H(2)NCTPPs) with substituents on either the para- or the 3,5-positions of the meso phenyl rings were
71 d electron-withdrawing substituents in their para, ortho, and meta positions in THF at room temperatu
72 tribromide promoted deprotection, ortho- to para- naphthoquinone spiroketal rearrangement, and a tau
73 spectrum myxovirus inhibitors in parallel to para- and orthomyxovirus-specific hit candidates in a si
75 thogenicity improves our understanding of V. para. infections and more generally, host-pathogen inter
76 Y-X, where X represents pyridyl anchors with para (p), meta (m) or ortho (o) connectivities and Y rep
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