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1 to the skin induced a robust time-dependent protection of mice from a lethal Klebsiella pneumoniae p
3 s have been confirmed to be potent in actual protection of mice from acute toxicity (convulsion and l
5 these studied surfactant systems, suggesting protection of citral from an acidic environment once it
9 ated by this pathway plays a key role in the protection of cells from apoptosis and the mediation of
10 ogical function for the CDK inhibitor p27 is protection of cells from apoptosis by constraining CDK2
11 of the PKB/Akt activation is sufficient for protection of cells from apoptosis induced by the deplet
12 gen-regulated protein kinase involved in the protection of cells from apoptosis, the promotion of cel
20 g that pigments are essential not simply for protection of spores from biotic and abiotic stresses bu
23 lts point to a unique function for desmin in protection of mitochondria from calcium exposure that ca
24 ct evidence that perinatal IgG transport and protection of IgG from catabolism are mediated by FcRn,
26 timulation of cell survival is mainly due to protection of cells from cell death rather than by stimu
27 pensable for B7-DC cross-linking Ab-mediated protection of DC from cell death caused by cytokine with
30 e, in agreement with preliminary data on the protection of lymphocytes from chemotoxicity in fasting
31 1 in hyperglycemia appeared to be due to the protection of IAP from cleavage that occurred during exp
32 times with cDNA encoding VP2 led to partial protection of mice from CNS demyelinating disease as det
33 may represent an important mechanism for the protection of EC from complement-mediated injury during
34 lectrochemical water oxidation and effective protection of Si from corrosion at high pH (pH 13.6).
36 Our data reveal a mechanism of efficient protection of telomeres from damage through Nek7-depende
37 nhibitor, survivin, in endothelial cells and protection of endothelium from death-inducing stimuli.
38 tramuscular (i.m.) vaccination provided full protection of hamsters from death and diarrhea while the
39 -3511 (26) displayed concentration-dependent protection of neurons from degeneration in vitro and dem
40 LK in retina results in robust and sustained protection of RGCs from degeneration after optic nerve i
41 TTP-14-3-3 complex formation appeared to be protection of TTP from dephosphorylation by inhibition o
42 howed that HBsu altered alpha/beta-type SASP protection of pUC19 from DNase digestion, induced negati
43 preservation of mitochondrial networking and protection of cardiomyocytes from doxorubicin-mediated c
44 o of 20:1 (N/P approximately 27.3), complete protection of siRNA from early enzymatic degradation was
45 findings may have potential applications in protection of buildings from earthquakes and isolating s
46 ine and human cell lines and induces in vivo protection of mice from encephalomyocarditis virus infec
47 ng prokaryotic mRNA decay theories: ribosome protection of mRNA from endonucleases, 5' binding and sl
48 e placement, usually measured by quantifying protection of DNA from enzymatic digestion, can regulate
49 he maintenance of immunological homeostasis, protection of lymphocytes from excessive cell death is e
52 on of their proliferation cannot account for protection of spermatogenesis from exposure to cytotoxic
58 questered in separate sites by PgDps provide protection of DNA from H(2)O(2)-mediated free radical da
59 ly high levels of H(2)O(2), resulting in the protection of PTPs from H(2)O(2)-mediated oxidation.
60 ponsiveness of macrophages that leads to the protection of mice from hepatic injury and death caused
61 A single dose of vaccine conferred complete protection of ferrets from homologous wt A/Anhui/1/2013
62 ted T cells do not play an important role in protection of mice from HSV, an important role for these
65 that may explain the experimentally observed protection of amides from hydrogen exchange and the exis
69 a definite role for FLIP in the SCF-induced protection of ECFCs from IFNgamma-initiated apoptosis.
70 balamin indicates that MeaB is necessary for protection of mutase from inactivation during catalysis.
72 ur study reveals a mechanism of DNA-mediated protection of p53 from interactions with partners involv
73 erase micro gene in 32Dcl3 cells resulted in protection of cells from interleukin-3 withdrawal-induce
74 ed exocytosis plays an important role in the protection of kidneys from ischemia-reperfusion injury.
75 rc tyrosine kinase family/ERK signaling, and protection of neurons from ischemic injury and cell deat
76 in human umbilical cord blood cell-mediated protection of oligodendrocytes from ischemic conditions.
77 cine and both provided complete, single-dose protection of macaques from lethal challenge with the Ma
78 indicate that while IL-6 plays a role in the protection of mice from lethal HSV infection, it does no
79 g the classical pathway of complement in the protection of mice from lethal infection with virulent S
81 A primary role for chaperones appears to be protection of effectors from Lon-associated degradation
85 tious conditions, which may be important for protection of insects from microbial infection during mo
86 evant in vivo target of miR-21 and show that protection of pdcd4b from miR-21 binding results in fail
87 enervation also prevented ultrasound-induced protection of kidneys from moderate (26-minute ischemia)
88 hod determines Cu binding sites based on the protection of His from modification by diethyl pyrocarbo
89 -specific B-cell responses are essential for protection of macaques from monkeypox virus, a variola v
90 Several studies have implicated TRF2 in the protection of telomeres from NHEJ, but the underlying me
91 ammals, thus providing passive immunity, and protection of IgG from normal serum protein catabolism.
93 ns of drug transporters may involve both the protection of bacteria from outside toxins and the trans
94 ormation through mechanisms that may include protection of LDL from oxidation and suppression of vasc
98 e1 is a multifunctional protein operating in protection of cells from oxidative stress via its DNA re
102 stained PI3K inhibition leads to significant protection of neurons from oxidative stress-induced neur
103 substituted by respiratory O2 uptake in the protection of nitrogenase from oxidative damage and, thu
105 ons but they are unable to provide wild-type protection of nitrogenase from oxygen, so they cannot by
106 Although immune responses may provide good protection of plants from pathogen attack, excessive imm
112 ation of mice is likely due to CD47-mediated protection of exosomes from phagocytosis by monocytes an
113 cofilin action appears to be a result of the protection of phosphocofilin from phosphatase-mediated d
114 teolysis and whether p26 is required for the protection of eIF2alpha from phosphorylation, we have an
116 vides a molecular mechanism for the observed protection of Tibetans from polycythemia at high altitud
117 eterminants are required for Alpha4-mediated protection of PP2Ac from polyubiquitination and degradat
118 einylglycine, GSH) is essential for adequate protection of pneumocytes from potential toxicity mediat
119 ent intracellular delivery of siRNAs and the protection of siRNAs from premature degradation before r
121 and pentapeptide binding of CheB fragments, protection of CheB from proteolysis by pentapeptide, and
123 on, up-regulation of p21(CIP1), and complete protection of cells from rapamycin-induced apoptosis.
124 ancy of exosite 1 partially accounts for the protection of thrombin from rapid inactivation by PAI-1
125 the scavenging of the toxic heavy metals and protection of cells from reactive oxygen intermediates.
127 of these particles resulted in the complete protection of mice from RSV replication in the lungs.
129 effective as the CSF1R/IR in mediating CSF-1 protection of cells from staurosporine-induced apoptosis
134 expense of host-cell growth rate; and (iii) protection of cells from the toxic effects of overexpres
137 nhibition of host gene expression and to the protection of EEEV from the antiviral effects of IFNs.
138 tivity, alphaA-crystallin may be involved in protection of hepatocytes from the toxic effects of high
140 ency), determining the efficacy in practical protection of mice from the acute cocaine toxicity and f
141 al role that trypomastigote CRP plays in the protection of parasites from the deleterious effects of
143 t the telomeric overhang is required for the protection of telomeres from the DNA damage response.
144 cytokines and plays an important role in the protection of tissues from the damaging consequences of
145 some provides significant, but not complete, protection of trypanosomes from the dangerous design of
146 Protein aggregation is irreversible, and protection of proteins from thermal aggregation is a str
148 s are essential for NF-kappaB activation and protection of cells from TNF-alpha-induced apoptosis.
149 ings provide a mechanistic rationale for the protection of hepatocytes from TNF-induced cell death by
150 ssion resulted in a consistent, but partial, protection of cells from undergoing IR-induced apoptosis
151 tion of Nrf2 is a promising strategy for the protection of tissues from various types of insults and
152 tions of today's understanding of CPs in the protection of crops from viral infection and use in the
153 , induction of strong adaptive immunity, and protection of mice from wild-type (WT) WNV infection.
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