ライフサイエンスコーパス: para-

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

2 The 1,4 (para) point on the conical intersection is higher in ene

3 iod (16-8 h) over a 3-month period induced a para- to endo-dormant transition in crown buds.

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

7 Water exists in two spin isomers, ortho and para, that have different nuclear spin states.

8 ortho-xylene exceeding 25 were observed and para- and ortho- liquid mixtures were efficiently separa

9 ed to a benzene bridge via alkyne spacers at para- and meta-positions.

10 We also provide evidence of auto-, para-, and feedback regulation among these factors at th

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

15 at similar molecular mechanisms promote both para- and transcellular migration.

16 Hepatoprotection by ISO is mediated by para- and autocrine effects of Wnt signaling.

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

22 dergo three well-defined phases of dormancy, para-, endo-, and ecodormancy.

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

27 ture-Aroclor 1260-mainly by removing flanked para- and doubly flanked meta-chlorines.

28 Ratios of single-component fluxes for para- and ortho-xylene exceeding 25 were observed and pa

29 r binding of a series of radical anions from para- and ortho-substituted nitrobenzenes with 1,3-dieth

30 ght) is required to induce a transition from para- to endo-dormancy in UABs of leafy spurge.

31 When UABs transitioned from para- to endodormancy, ABA and PA levels decreased, wher

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

44 The rate constants of para-/orthohydrogen (p-/o-H2) nuclear spin isomerization

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

48 the position of the carboxyl moiety (meta or para).

49 f the position of the group (ortho, meta, or para).

50 partition into membranes followed the order para > meta > ortho.

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

54 CG9947, CG4420, eIF2a, Rbp2, and paralytic (para).

55 hila voltage-gated sodium channel paralytic (para).

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

58 ke behaviors, as an allele of the paralytic (para) voltage-gated Na(+) (Na(V)) channel gene.

59 y required functionalization of the position para (or ortho) to a fluorine atom on the aromatic ring

60 rings: pseudo-ortho, pseudo-meta, and pseudo-para, in equal amounts.

61 Electron-rich para- and meta-substituted aryl halides (including unpro

62 while the 1,3,4-trisubstituted systems show para, meta (instead of ortho, meta) selectivity.

63 ed using the Hammett equation, between sigma(para) and the rate of the IEDDA reaction.

64 When the Hammett sigma(para) constants for the functional groups para to the an

65 ivity factors and initial rates to the sigma(para) Hammett parameters.

66 le metal-organic framework selectively sorbs para- (pX) over meta-xylene (mX) by synergic restructuri

67 and therefore results in selectivity for the para, meta product.

68 The para- and ortho-isomers desilylate directly from such st

69 The plants separately reduced both the para- and ortho-nitro groups and produced glycosylated p

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

74 Vibrio parahaemolyticus (V. para) is a Gram-negative bacterium that causes gastroent

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

77 Aryl iodides with para- and meta-substituents are tolerated.