ライフサイエンスコーパス: permissiveness

1 e plasticity that may underlie its substrate permissiveness.

2 xhibits a reduction in macrophage Legionella permissiveness.

3 correlate with differences in L. pneumophila permissiveness.

4 hord involvement in dorsal myotome change of permissiveness.

5 vels by a subset of animals, suggesting poor permissiveness.

6 as been suggested as a step that blocks B19V permissiveness.

7 nvolved in the Huh7.5 phenotype of increased permissiveness.

8 pany corneal transition to nerve growth cone permissiveness.

9 reported to be a limiting step in B19 virus permissiveness.

10 ges in its product were predicted to control permissiveness.

11 4.5) were screened for C. burnetii metabolic permissiveness.

12 e cells as inhibition of HDACs induces viral permissiveness and increases MIEP activity.

13 ously identified the transition stage of HCV permissiveness and now investigate whether a host protei

14 pTfh cells) and non-pTfh cells to assess HIV permissiveness and persistence.

15 dening susceptibility, as the specificity of permissiveness and resistance to other scrapie isolates

16 The reduced permissiveness appeared to be due to the near absence of

17 trength of punishment and degree of latitude/permissiveness) at the state level in the United States,

18 increase in acetylation, or transcriptional permissiveness, at the ICP0 promoter.

19 KSHV target cell permissiveness correlated closely with endogenous expres

20 xpression implicates Naip5 in the Legionella permissiveness differences among mouse strains.

21 t polymorphisms in Naip5 are involved in the permissiveness differences of mouse macrophages for intr

22 tin signature in the host cells predicts the permissiveness for Ascl1 pioneering activity among diffe

23 vacuole and is associated with differential permissiveness for association of the IRG proteins Irga6

24 s and NMDA receptors (NMDARs) and increasing permissiveness for burst firing.

25 persistence, host tissue carcinogenesis, and permissiveness for cancer progression.

26 ls in all tested cell lines, indicating that permissiveness for EBOV at cell and organism levels do n

27 These determine permissiveness for expression, with subsequent induction

28 ing that the lipid environment may influence permissiveness for fusion.

29 his response is absent in cells selected for permissiveness for HCV RNA replication.

30 -alpha/beta immune defenses that impact cell permissiveness for hepatitis C virus (HCV).

31 particular PD1(+) pTfh cells, showed greater permissiveness for HIV infection than non-pTfh cells.

32 Permissiveness for human cytomegalovirus (HCMV) infectio

33 ort HBV transcriptional activity and initial permissiveness for infection are marked by distinct stag

34 ous inbred mice exhibit large differences in permissiveness for intracellular replication of Legionel

35 ary infection was associated with macrophage permissiveness for intracellular replication, and (iii)

36 eport that LPS triggers a monocyte phenotype permissiveness for lytic infection directly correlating

37 ings in Drosophila and shows that the unique permissiveness for microRNA innovation at this stage is

38 eated with NeoB showed decreased replicative permissiveness for poliovirus, which also replicates in

39 lion (TG) neurons were assessed for relative permissiveness for productive infection.

40 er these defenses and their effect upon host permissiveness for specific viral pathogens are not well

41 ed Lgn1 determines differences in macrophage permissiveness for the intracellular replication of Legi

42 rmore, the differential regulation of fusion permissiveness for the two classes of Envs is consistent

43 Although this permissiveness in binding is unanticipated, based on the

44 n messenger RNA levels correlated with HIV-1 permissiveness in diverse human cell types.

45 athogenic only for European rabbits, but its permissiveness in human cancer cells gives it potential

46 he overarching theme of increased ecological permissiveness in PID skin was counterbalanced by the ma

47 may play a critical role in determining HCMV permissiveness in some cell types and perhaps also in th

48 ory have described a significant increase in permissiveness in the absence of interleukin-4 (IL-4), t

49 We show that permissiveness in the different populations of macrophag

50 studies indicate that there is a structural permissiveness in the quaternary relationships between t

51 MYXV permissiveness in these human cancer cells is dependent

52 luding genetic complementation revealed that permissiveness is due to mutational inactivation of RIG-

53 noculated; some of the spin-induced cellular permissiveness may be beyond the natural capacity of an

54 Greater permissiveness may be warranted in older black candidate

55 If this is true, permissiveness may partially explain the pronounced chem

56 The wMel strain of Wolbachia can reduce the permissiveness of Aedes aegypti mosquitoes to disseminat

57 nmental milieu is critical in regulating the permissiveness of astrocytes to HIV infection.

58 regulation of DC function contributes to the permissiveness of both gastric and intestinal mucosa to

59 We sought to analyze the permissiveness of CD4+ T cells to RSV infection.

60 The level of permissiveness of cell lines harboring neo replicons can

61 The enhanced permissiveness of CytD-preincubated monocytes was found

62 offers a molecular mechanism to explain the permissiveness of DC for both M- and T-tropic viruses.

63 , there is a notochord-dependent decrease in permissiveness of dorsal myotome for CaP axonal outgrowt

64 l myotomes were non-permissive, showing that permissiveness of dorsal myotome for normal CaP pathfind

65 suggesting that the mechanisms governing the permissiveness of enhanced cells are independent from vi

66 ed reduction of CypA expression enhanced the permissiveness of HeLa cells to infection by the T54A mu

67 iciency may be responsible for the increased permissiveness of IgE(-/-) mice as hosts following infec

68 Impaired permissiveness of intestinal macrophages to HIV-1 may pl

69 This marked reduction in the permissiveness of intestinal macrophages to HIV-1 was no

70 ommon to other herpesviruses, is the partial permissiveness of latently infected cells to lytic-cycle

71 f Naip5 causes an increase in the Legionella permissiveness of macrophages.

72 tumor tropism is generally dependent on the permissiveness of malignant cells to viral replication r

73 The increased permissiveness of one of the cured cell lines allowed us

74 for pocket 9 of DRB1*0901, causing complete permissiveness of pocket 9 when a small polar residue is

75 , is considered a primary determinant of the permissiveness of porcine alveolar macrophages for infec

76 To test the permissiveness of pulmonary endothelial cells to virus i

77 g reports on the maturation state and growth permissiveness of PV harboring virulent phase I or aviru

78 The relative permissiveness of TG neurons to viral gene expression ne

79 o in vitro SIV infection correlated with the permissiveness of the animals for early in vivo viral re

80 nd, along with the hyperplasia, increase the permissiveness of the cellular microenvironment for neop

81 moiety may account for the substrate binding permissiveness of the enzyme.

82 The permissiveness of the insertion after I368 in TM IX lead

83 Although reduced permissiveness of the neuronal environment is widely acc

84 e used during selection do not influence the permissiveness of the resulting enhanced-cell population

85 HIV-1 infections, which are dependent on the permissiveness of the target cell.

86 es relative to CD4(+) T cells in ES, despite permissiveness of these cells to HIV-1 viral entry ex vi

87 e CCR5 ligands, are associated with enhanced permissiveness of these cells to HIV.

88 ted histone deacetylation contributes to the permissiveness of U2OS cells for DeltaICP0 mutants.

89 of human CTR1 was sufficient to confer CERV2 permissiveness on otherwise resistant hamster cells, and

90 ophages display distinct phenotype and HIV-1 permissiveness profiles.

91 eplicon removal is responsible for increased permissiveness, since this effect could be reproduced ei

92 a, Aspergillus) supported increased PID skin permissiveness, suggesting that skin may serve as a rese

93 Heightened permissiveness, the presence of highly infectious virion

94 Expression of MX2 reduces permissiveness to a variety of lentiviruses, whereas dep

95 HSCs and assessed the CD36(+) EPCs for their permissiveness to B19V infection.

96 and mesenchymal cell lines was examined for permissiveness to C. parvum and the ability to bind CSL.

97 side of the valve, suggesting side-specific permissiveness to calcification.

98 Although increased permissiveness to FIV infection of CD4+ CD25- cells foll

99 ent of proteoglycan-deficient cells restores permissiveness to GDVII virus, indicating that sialic ac

100 Here we show that poor permissiveness to gene transfer and limited proficiency

101 ere is significant variation in the cellular permissiveness to H1N1pdm09 infection among different do

102 rent human donors vary dramatically in their permissiveness to HBV infection, suggesting that factors

103 cell line, contain cell clones with diverse permissiveness to HBV replication.

104 a pathogen receptor that regulates cellular permissiveness to HCV replication and, as an interferon-

105 e prevented signaling and increased cellular permissiveness to HCV.

106 evels of HIV-1, probably because of impaired permissiveness to HIV-1 entry associated with the near a

107 The permissiveness to HMPV infection was also abolished when

108 s in response to IFNs, resulted in a reduced permissiveness to infection and subsequent natural kille

109 e activity, preferentially enhances cellular permissiveness to infection by Nef-defective versus wild

110 The mechanism(s) underlying this increased permissiveness to infection is not known.

111 urrence, composition, activation status, and permissiveness to infection of peritoneal leukocytes (PL

112 (+) T cells vary in their susceptibility and permissiveness to infection.

113 which probably contribute to their relative permissiveness to infection.

114 imits HCV production and constrains cellular permissiveness to infection.

115 on during infection, and alveolar macrophage permissiveness to intracellular replication in vitro.

116 t PI3-K activity is critical to host barrier permissiveness to microbes, and that pathogens exploit b

117 Few surviving pre-B cell clones had acquired permissiveness to oncogenic signaling by strong activati

118 n increased the levels of Ras activation and permissiveness to oncolytic herpes.

119 therapy success is largely due to bacterial permissiveness to phage killing.

120 t on the development, microbiota content and permissiveness to Plasmodium of Anopheles coluzzii.

121 show that Th17 cells also exhibit heightened permissiveness to productive HIV infection.

122 D4 T cells that is associated with increased permissiveness to SIV infection.

123 Endothelial cell permissiveness to the deposition of circulating immune c

124 nother carnivore family, the Mustelidae, for permissiveness to the HIV-1 life cycle.

125 p-2 and U2OS cells, regardless of the cell's permissiveness to the ICP0-null virus.

126 wo alleles of the TAP2 chain differ in their permissiveness to the transport of peptides with small h

127 n of the molecular determinants of host-cell permissiveness to this virus an important objective.

128 Cellular permissiveness to viral infection is modulated by innate

129 Four cell lines that varied in their permissiveness to VSV-DeltaM51 and CRAd dl1520 were test

130 lthy HIV-negative donors were tested for HIV permissiveness using green fluorescent protein (GFP)-exp

131 The increase in permissiveness was blocked either by transfection of HEK

132 This permissiveness was caused by the viral glycoprotein usag

133 The HBV permissiveness was impaired upon treatment with microtub

134 There is also evidence of increasing permissiveness with age of normal tissues in vivo for so

135 PID skin displayed increased ecological permissiveness with altered population structures, decre

136 ine trimming rates, thus combining substrate permissiveness with sequence bias.