ライフサイエンスコーパス: hetero-

1 By 28 DAP labeling of hetero-(1-->4)-beta-D-mannan is observed in the walls of

2 resulting EtZn(Ar(Hetero)) intermediates (Ar(Hetero) = 2- and 3-thiophenyl, 2-benzothiophenyl, 3-fury

3 This rapid synthesis utilized a novel hetero-[2 + 2]-cycloaddition reaction between two aryl y

4 concurrent reactions via O-imidoylation and hetero-[3 + 2] pathways.

5 first time, the power of the intramolecular hetero [4+2] cycloaddition reaction in the total synthes

6 of a stereoselective inverse electron demand hetero-[4 + 2] cycloaddition of chiral allenamides in na

7 Finally, the hetero-[4]pseudorotaxane was constructed, and the order

8 A hetero-[4]pseudorotaxane was designed to perform a molec

9 ium ion chain to effect the synthesis of the hetero-[4]pseudorotaxane.

10 Tracking of lacZ activities in hetero- (Agtr1a +/-) and homozygous (Agtr1a -/-) deletio

11 isorders, obsessive-compulsive behaviors and hetero- and autoaggression.

12 otected (alpha-aminoacyl)benzotriazoles with hetero- and benzenoid- aromatics give alpha-amino ketone

13 es are readily cyclized to the corresponding hetero- and carbocycles with 5 mol % iron and 4 atm H(2)

14 The reduction of a series of hetero- and carbocyclic aromatic compounds under ammonia

15 used heterocycle, in coupling reactions with hetero- and carbon nucleophiles to give C(3)-quaternary-

16 concentration and movement and formation of hetero- and homo-oligomeric complexes.

17 s a protein association domain that mediates hetero- and homo-protein associations with SCAN box cont

18 In the bsAb samples, hetero- and homodimer species, along with partial molecu

19 maps of DNA binding of the proteins in their hetero- and homodimeric forms.

20 ization (LAD) to artificially induce protein hetero- and homodimerization in live cells using light.

21 In the intracellular death program, hetero- and homodimerization of different anti- and pro-

22 should help to elucidate the mechanism(s) of hetero- and homodimerization of the c-erbB receptors.

23 e DNA-binding domain and motifs that mediate hetero- and homodimerization.

24 on X-100 and Triton X-114 readily enable Bax hetero- and homodimerization.

25 sodium cholate allow varying degrees of Bax hetero- and homodimerization.

26 They have potential to both hetero- and homodimerize through their bHLHLZ domains, s

27 utative transmembrane domain, that the ESyts hetero- and homodimerize, and that ESyt2 homodimerizatio

28 100 proteins exist in cells as anti-parallel hetero- and homodimers and upon calcium binding interact

29 was composed of predominately c-Jun and JunD hetero- and homodimers as determined by electrophoretic

30 S100a8 and S100a9 genes results in S100A8/A9 hetero- and homodimers, which stimulate the release of c

31 K pathway stimulates activation of NF-kappaB hetero- and homodimers, which, in turn, drive iNOS expre

32 wn assays, MORF proteins can connect to form hetero- and homodimers.

33 regulator composed of HNF1alpha and HNF1beta hetero- and homodimers.

34 P hydrolysis is stimulated 2-5-fold by short hetero- and homoduplex DNAs.

35 rence between the hybridization rates of the hetero- and homoduplex were observed with varying concen

36 Isolated motifs demonstrate hetero- and homomeric interactions, suggesting a propens

37 DEG/ENaC subunits associate as hetero- and homomultimers to generate channels; however

38 ure of the a-DNA-AuNPs allows regioselective hetero- and homonuclear assembly with high monodispersit

39 ermined directly by one- and two-dimensional hetero- and homonuclear NMR techniques.

40 The NMR data comprise an extensive set of hetero- and homonuclear residual dipolar coupling and 31

41 rotein interaction domain that mediates both hetero- and homoprotein associations.

42 ne/dialkyl ether mixtures forms ensembles of hetero- and homosolvated dimers.

43 ng pathway provides a cellular mechanism for hetero- and homosynaptic control of interneuronal activi

44 ynaptic LTD maintenance mechanism, such that hetero- and homosynaptic induction produce similar alter

45 n structural and mechanical behavior between hetero- and homotrimers.

46 d established the SCAN domain as a selective hetero- and homotypic oligomerization domain.

47 The corresponding HR for hetero- and homozygote carriers of the CYP2C19*17 allele

48 5 (CI 0.78-1.42) and 0.79 (CI 0.32-1.94) for hetero- and homozygote carriers, respectively.

49 higher (P = 0.04), respectively, among women hetero- and homozygous for the CYP17 A2 allele compared

50 each of two lines, we detected plants null, hetero- and homozygous for the two genes in one line, an

51 n cortex and cerebellum from 3- and 24 m old hetero- and homozygous male mutant mice resulted in lowe

52 Both hetero- and homozygous mutants demonstrate an altered be

53 myofibers and myofibrils isolated from young hetero- and homozygous R349P desmin knock-in mice, which

54 ety of sterically and electronically diverse hetero- and nonheteroaryl-containing triarylmethanes, a

55 rates maximized, discrimination between the hetero- and the homoduplex can be obtained at lower, les

56 to changes in the sensitivity of presynaptic hetero- and/or autoreceptors on the dopaminergic axons.

57 and have been shown to be non-toxic, can be hetero- and/or polyfunctionalized and thus represent pro

58 despite their similarity and ability to form hetero (and homo) dimers, DDX5 and DDX17 are used by HIV

59 nt efficiencies for heteroaggregation, alpha hetero, are required as input parameters in environmenta

60 st for dicarboxylic acids and the least for (hetero-) aromatic compounds.

61 Furthermore, hetero- but not homosynaptic alterations are blocked by

62 The dimer (both homo and hetero) can survive the introduction into the gas phase,

63 for the cross-coupling between electron-rich hetero-/carbocyclic arenes and electron-poor arenes bear

64 egans PKD, DKF-2A, are exclusively (homo- or hetero-) dimers in cell extracts and intact cells.

65 In studies of the hetero (eight subunit)-dimeric 220,000 molecular weight

66 eaction, unnatural N-to-N and C-to-C linked (hetero) fusion proteins are established.

67 s found to be equally accurate in detecting (hetero-)glycopeptide-intermediate S. aureus compared to

68 The resulting EtZn(Ar(Hetero)) intermediates (Ar(Hetero) = 2- and 3-thiophenyl

69 fonic acid (Chaps) and Brij 35 allow neither hetero- nor homodimer formation.

70 f action of FHR1, wherein homodimeration and hetero- oligomerization with FHR2 and FHR5 generates mor

71 Survival statistics compared hetero- (+/-) or homozygotic (-/-) carriers with noncarr

72 ositions in the debate are that it is either hetero- or autotrophic, which suggests either substantia

73 U2OS cells, was used to induce ROS damage in hetero- or euchromatin, respectively.

74 Nup58 cognate segments form crystallographic hetero- or homo-oligomers, we proposed that these oligom

75 Patients were hetero- or homoallelic for nine different FECH mutations

76 on of the PDGF B-chain in the context of the hetero- or homodimer.

77 The STAT1 SH2 domain is critical for STAT1 hetero- or homodimerization.

78 Upon ligand binding, TLR/IL-1Rs hetero- or homodimerize and recruit MyD88 through their

79 ore was rhodamine or fluorescein; or whether hetero- or homotransfer was measured.

80 thnicities, this allele was found deleted in hetero- or homozygosity in all groups at ~50% frequency.

81 t greater in schizophrenia subjects who were hetero- or homozygous for the Met66 allele.

82 significance for human individuals carrying hetero- or homozygous NQO1P187S mutation and are deficie

83 ructural comparison reveals a more favorable hetero- than homodimerization interface, thereby suggest

84 cer cell line to CDDP is associated with the hetero- to homoplasmic shift of a nonsynonymous mutation