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1 IFITM proteins are important effectors in interferon-med
2 IFITM proteins are located in the plasma membrane and en
3 IFITM proteins deter HIV-1 entry when expressed in targe
4 IFITM proteins impede viral entry, and ZMPSTE24 expressi
5 IFITM-2 and -3 restricted RVFV infection mostly by preve
6 interferon-induced transmembrane protein 1 (IFITM-1), IFITM-2, and IFITM-3 exhibit a broad spectrum
7 n-induced transmembrane protein 1 (IFITM-1), IFITM-2, and IFITM-3 exhibit a broad spectrum of antivir
8 nducible transmembrane proteins 1, 2, and 3 (IFITM 1,2, and 3) are viral restriction factors that med
9 t low doses of alpha interferon (IFN-alpha), IFITM-2 and -3 mediated more than half of the antiviral
11 We found that large fractions of IFITM-2 and IFITM-3 occupy vesicular compartments that are distinct
12 nsmembrane protein 1 (IFITM-1), IFITM-2, and IFITM-3 exhibit a broad spectrum of antiviral activity a
13 the viral envelope glycoproteins as well as IFITM subcellular localization within the target cell.
14 also mediate a physical association between IFITM proteins, and the loss of this interaction decreas
16 was restricted by IFITM-2 and -3 but not by IFITM-1, whereas the remaining viruses were equally rest
18 e data suggest that higher prefrontal cortex IFITM mRNA levels in schizophrenia may be attributable t
21 ion film analysis revealed markedly elevated IFITM mRNA levels (+114% and +117%, respectively) in pre
23 mRNA levels were also markedly elevated for IFITM (+304%), multiple cytokines including IL-6 (+493%)
25 ouse models of neuroinflammation have higher IFITM levels and deficits in gamma-aminobutyric acid (GA
26 The authors sought to clarify whether higher IFITM mRNA levels and other immune-related disturbances
27 re unknown, and it is unclear whether higher IFITM mRNA levels are associated with lower GABA-related
28 ding that schizophrenia subjects with higher IFITM mRNA levels in cortical blood vessels have greater
33 9%) and interferon-beta (+29%), which induce IFITM expression; lower mRNA levels for Schnurri-2 (-10%
36 0%), a transcriptional inhibitor that lowers IFITM expression; and higher mRNA levels for nuclear fac
39 er, few reports have evaluated the impact of IFITM genes on viral pathogenesis in vivo In this study,
40 However, the cell types that overexpress IFITM messenger RNA (mRNA) in schizophrenia are unknown,
41 interferon-inducible transmembrane protein (IFITM) family inhibits a growing number of pathogenic vi
42 he interferon-induced transmembrane protein (IFITM) family of proteins inhibit infection of several d
45 ng interferon-induced transmembrane protein (IFITM) have been reported to inhibit multiple families o
47 or interferon-induced transmembrane protein (IFITM), which inhibits viral entry and replication-have
48 film and grain counting analyses to quantify IFITM mRNA levels in prefrontal cortex area 9 of 57 schi
49 lators, including those reported to regulate IFITM expression, in the prefrontal cortex from 62 schiz
50 proteins of several different viruses resist IFITM inhibition, the detailed mechanisms are not fully
52 hizophrenia and comparison subjects revealed IFITM mRNA expression in pia mater and blood vessels.
53 chemical and membrane fusion studies suggest IFITM proteins have the ability to inhibit viral entry,
54 to infect different host species, suggesting IFITM proteins may provide a crucial barrier for zoonoti
63 that the structural motifs critical for the IFITM proteins' enhancement of HCoV-OC43 infection are d
64 terferon-stimulated proteins, members of the IFITM (interferon-induced transmembrane) family are uniq
65 tion and demonstrate that the actions of the IFITM proteins are indeed virus and cell-type specific.
67 ew the discovery and characterization of the IFITM proteins, describe the spectrum of their antiviral
68 ent developments in our understanding of the IFITM's molecular determinants, potential mechanisms of
71 Further characterization revealed that the IFITM proteins inhibit the early replication of flavivir
75 onstrated that S-palmitoylation of all three IFITM proteins is essential for anti-HCV activity, where
78 s have shown that IFN-induced transmembrane (IFITM) proteins, including IFITM1, IFITM2, and IFITM3, r
79 restricted interferon-induced transmembrane (IFITM)-like protein (BRIL) and pigment epithelium-derive
80 that the interferon-inducible transmembrane (IFITM) protein family members potently restrict the repl
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