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1  trivalent inactivated influenza vaccine for protection of infants against a first episode of laborat
2 ished ATPase activity in vitro and abrogated protection of Mtb against acidified nitrite.
3          This first report of rIL-12-induced protection of primates against an infectious agent suppo
4 nd showed that the Ab titers correlated with protection of macrophages against anthrax lethal toxin (
5 ding protein that has been implicated in the protection of cells against apoptosis.
6 h receptor function is impaired for the self-protection of tumors against apoptosis.
7 th in the promotion of cell death and in the protection of cells against apoptotic insults.
8 f the alternative respiratory pathway in the protection of plants against biotic stress was examined
9 omplete Freund's adjuvant showed evidence of protection of protection against blood-stage challenge w
10                                              Protection of cattle against bovine tuberculosis by vacc
11 T cell- and interferon (IFN)-gamma-dependent protection of mice against challenge with Py sporozoites
12 nd induction of CTL that are able to provide protection of mice against challenge with tumor cells.
13 iveness to a nonmutated tumor Ag and provide protection of mice against challenge with tumor cells.
14 r pathogenesis, immunogenicity, and level of protection of mice against challenge with wild-type VSV.
15 enic antigens may play critical roles in the protection of mice against challenge.
16 49 cells, but did not confer any significant protection of telomeres against chemotherapy-induced deg
17                 These data indicate that the protection of Arabidopsis against CMV by strain 90-166 f
18 nia vaccine provided significantly increased protection of macaques against cutaneous Leishmania infe
19 ATA-4 mutant (S105A) suppresses HGF-mediated protection of cells against daunorubicin-induced apoptos
20 es, zein/CMCS nanoparticles exhibited better protection of I3C against degradation and better inhibit
21 way plays an important role in mediating the protection of erythropoietin against diabetic neuropathy
22    (3) Estrogen treatment also prevented the protection of caffeine against dopamine loss in young ma
23 icate that AKT3 signaling contributes to the protection of mice against EAE.
24 y replicon particles (VRPs) can induce rapid protection of mice against either homologous or, in some
25 bling the storage of Fe which contributes to protection of plants against Fe-induced oxidative stress
26 immunomodulatory and antiviral activities in protection of swine against FMDV.
27 ystemic chiral fungicide used in postharvest protection of citruses against fungi development for dur
28 t htt in cultured astrocytes decreased their protection of neurons against glutamate excitotoxicity.
29                  These studies indicate that protection of mice against H. pylori infection by immuni
30  cells, but not CD8+ T cells, were vital for protection of mice against heterosubtypic challenge.
31 nation of core plus NmerA shows an increased protection of cells against Hg(2+) in the media when Nme
32 ons of Mugwanya and colleagues' findings for protection of women against HIV infection during breastf
33 hermore, time-course study suggests that the protection of chaperones against huntingtin toxicity is
34   Trapping of NO with hemoglobin resulted in protection of ADH against inactivation by NO.
35                                          The protection of calcineurin against inactivation by supero
36 lpha-mannosyl glycolipids contributed to the protection of mice against infection with S. pneumoniae
37 ineteen variables related to vaccine-induced protection of mice against infection with virulent bruce
38 ody assays with this specificity may predict protection of vaccinees against infection.
39  of PTX3, which actively participates in the protection of neonates against infections.
40 antimicrobial peptides are essential for the protection of skin against invasive bacterial infection.
41 xygenase-1 (H(mox-1)) has been implicated in protection of cells against ischemia/reperfusion injury.
42                                              Protection of heart against ischemia-reperfusion injury
43 important role in learning and memory and in protection of neurons against ischemic injury.
44 rse array of physiologic functions including protection of tissue against ischemic insult, regulation
45                     UL141 mediated efficient protection of cells against killing by a wide range of h
46                              Vaccine-induced protection of chimpanzees against laboratory-adapted and
47 temperature-sensitive H1N1 virus resulted in protection of mice against lethal challenge with the PR8
48 superior capacity to wild-type DCs in innate protection of mice against lethal infection by Listeria
49                                      To test protection of mice against lethal P. yoelii challenge, t
50 on CRP is necessary for CRP-mediated initial protection of mice against lethal pneumococcal infection
51 at the level of transcription, the cell, and protection of mice against lethal viral infection.
52                                              Protection of mice against lethality due to S. aureus st
53 phagy as a potential therapeutic strategy in protection of cells against lipotoxicity and lipid-relat
54 nnate immune system activity, leading to the protection of animals against LPS-induced pro-inflammato
55 nism of action, and this absorption leads to protection of ice against melting as well as freezing.
56   The collagen-like region of SP-A conferred protection of SLPI against MMP mediated cleavage.
57 of consumption of antioxidants important for protection of DNA against naturally produced reactive ox
58                  There was also no substrate protection of Cys71 against Nbs2, which, however, caused
59 restricted T cells play an important role in protection of mice against neuroinvasive HSV infection a
60 r II, and leupeptin all provided significant protection of SGNs against neurotrophin-withdrawal and h
61              Telomeres are essential for the protection of chromosomes against nucleases and recombin
62 MTF against proteolytic cleavage by tRNA and protection of tRNA against nucleolytic cleavage by MTF.
63 ial rich sources of natural antioxidants for protection of foods against oxidation.
64 n E:cholesterol attributed to milk increased protection of LDL against oxidation.
65 an additional role of these compounds in the protection of cells against oxidative damage.
66 -initiating factor XPC are implicated in the protection of cells against oxidative DNA damages.
67      To elucidate mechanisms involved in the protection of cells against oxidative stress, immortal m
68 hat these kinases contribute to GPx-mediated protection of cells against oxidative stress.
69 B10 is essential for erythropoiesis, and for protection of mitochondria against oxidative stress.
70 servations suggest a novel mechanism for the protection of mtDNA against oxidative insults whereby a
71                                              Protection of sGC against oxidative inactivation may con
72 in the detoxification of xenobiotics and the protection of tissues against oxidative damage.
73 nsfer and proton motive force is crucial for protection of PSI against photodamage, which occurred pa
74 nts have emerged as a potential resource for protection of plants against phytopathogens.
75 ted decrease in bacteremia and the resulting protection of mice against pneumococcal infection.
76 mophilia A via restoration of TAFIa-mediated protection of clots against premature lysis.
77 is likely to be mediated by RASSF2-dependent protection of MST2 against proteolytic degradation.
78 ng two complementary protection experiments: protection of MTF against proteolytic cleavage by tRNA a
79 LR2-deficient mice, but TLR2 is required for protection of mice against PSM-producing S. aureus.
80  vitro and may have a biological role in the protection of telomeres against rapid degradation in res
81 (MT-I) and MT-II have been implicated in the protection of cells against reactive oxygen species (ROS
82 suppression of JNK signaling, contributes to protection of cells against reactive oxygen species-medi
83 of quinones and their derivatives leading to protection of cells against redox cycling and oxidative
84 -throughput screening and reported for their protection of cells against RIPs.
85 nucleotides, and thicker PEG layer increased protection of DNA against serum degradation.
86 itochondria may be a viable approach for the protection of cells against some of the deleterious effe
87 d interleukin-12 (IL-12) led to long-lasting protection of mice against subcutaneous (sc) challenge w
88      The notion that SiR plays a role in the protection of plants against sulfite is supported by the
89 nstrate a novel role of TRPC channels in the protection of neurons against Tat through the CCL2/CCR2
90 g agents, suggesting a role of pol lambda in protection of cells against the cytotoxic effects of oxi
91 onuclease activity, and is essential for the protection of cells against the toxic effects of several
92 rative pest management (IPM) program for the protection of corn against the South American corn rootw
93 signaling the survival of mature T cells and protection of thymocytes against TNF-induced apoptosis.
94 ration (EC(50)) of 0.1 nM, and provided 100% protection of rats against toxin challenge with a 0.5 su
95 al enzyme-substrate complex is necessary for protection of MTF against trypsin cleavage.
96                        The need for improved protection of HCWs against tuberculosis disease is clear
97 ata suggest that they may be involved in the protection of bacteria against various forms of environm
98 termine if these peptides play a part in the protection of skin against wound infections, the anti-mi

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