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3 CRISPR functions as a long-term memory-based defense against a diverse landscape of viral species, we
7 a therefore implicate CIITA and CD74 in host defense against a range of viruses, and they identify an
9 tigated the IL-1 family member IL-33 in lung defense against A. fumigatus IL-33 was detected in the n
12 nfer inceptin-induced responses and enhanced defense against armyworms (Spodoptera exigua) in tobacco
13 iew, we first discuss novel concepts in host defense against Aspergillus infections and emphasize new
17 Amphibians have complex and varied immune defenses against B. dendrobatidis, but the fungus also h
18 hat human NK cells also contribute to immune defense against bacteria through recognition of a conser
21 ivity, but the participation of PTEN in host defense against bacterial infection is less well underst
23 whether IL-17D has a role in mediating host defense against bacterial infections, we studied i.p. in
26 ic multiprotein complexes that initiate host defense against bacterial pathogens by activating caspas
29 lymphoid cells (ILC3s) are critical for lung defense against bacterial pneumonia in the neonatal peri
30 inase-I.9), was shown to contribute to plant defense against bacterial, oomycete, and fungal pathogen
32 ible bacteria by acting as the first line of defense against beta-lactam antibiotics, and antibiotic
37 red the role of platelets in antifungal host defense against C. albicans PBMCs were stimulated with h
40 obial peptides that are the ultimate line of defense against carbapenem-resistant pathogens in clinic
42 Yet, T cell-mediated inflammation and host defense against Citrobacter rodentium were not impaired
44 n many recent advances in understanding host defenses against common fungi, this work illuminates not
46 e of Gram-negative bacteria functions in the defense against cytotoxic substances, such as antibiotic
52 id cells are, beside as the first barrier of defense against diseases, an excellent model system to i
53 ol of lysosome function broadly impacts host defense against diverse viral and microbial pathogens.
55 -the enabling of gas exchange, and the first defense against drought-this trade-off constrains the ra
57 e results suggest the importance of CH25H in defense against education of normal cells by TEV and arg
58 epithelium plays fundamental roles in immune defenses against enteric viral infections by integrating
60 innate and adaptive immunity leading to host defense against enteropathogenic bacterial infection.
68 unctions to induce a broad range of cellular defenses against exogenous and endogenous stresses, incl
69 ation by commensal C. albicans improves host defense against extracellular pathogens, but with potent
71 umoral immunity may provide vital first-line defense against fatal outcomes in case of an A(H7N9) pan
73 -3-ols (catechin and proanthocyanidins) as a defense against foliar rust fungi, but the regulation of
74 tion of plant growth and modulation of plant defenses against foliar pathogens Botrytis cinerea and P
79 fibrin degradation, thwarts T cell-mediated defense against fully virulent Y. pestis Introducing a s
87 e to infer the molecular mechanisms of plant defense against GB, little is known about the effect of
91 A well-known trade-off exists between plant defenses against herbivores and defenses against pathoge
92 her they also function as generalized direct defenses against herbivores and pathogens remains unknow
93 ecific metabolites that function as indirect defenses against herbivores of the wild tobacco Nicotian
97 nisms of antibiotic resistance and bacterial defense against host immunity; however, there is little
98 The vaginal epithelium is the first line of defense against HSV-2 and coordinates the immune respons
100 blood glucose concentrations compromises the defense against hypoglycemia, a common complication in d
106 roducing gammadelta T cells in neonatal host defense against infection and provide a mechanistic expl
107 Neutrophils act as the body's first line of defense against infection and respond to diverse inflamm
109 ler (NK) cells, which are implicated in host defense against infection with herpesviruses, including
110 lular traps (NETs) are important in the host defense against infection, but they also promote intrava
116 f immune cells is a vital cornerstone of our defense against infections and a key challenge of immuno
118 lving MyD88 or STING constitute a first-line defense against infections mainly through production of
121 ovel role for GPER activation in skin innate defense against infectious disease suggests that G-1 may
122 n-coupled estrogen receptor (GPER) to innate defense against infectious disease, particularly with re
123 onocytes and macrophages, is a first line of defense against infectious diseases and plays a key role
126 dicate that exposure to dry air impairs host defense against influenza infection, reduces tissue repa
127 dings demonstrate that the initial intrinsic defense against influenza is mediated by platelet-neutro
128 significant insight into this first line of defense against influenza virus infection and provide a
130 ins unknown whether plants can amplify their defenses against insect eggs by responding to cues indic
131 the hypothesis that a plant strengthens its defenses against insect eggs by responding to insect sex
133 ascertain whether IL-26 contributes to host defense against intracellular bacteria, we studied lepro
136 rophils represent the first line of cellular defense against invading microorganism by rapidly moving
140 ages (Mphi) are critical for the coordinated defense against invading S. aureus, yet they have a limi
142 nal epithelial autophagy is crucial for host defense against invasive pathogens, and defects in this
143 ing, suggesting that Toll mediates antiviral defense against Kallithea virus infection but that it is
144 ism by which L-selectin participates in host defense against Klebsiella pneumoniae-induced pulmonary
146 , cell types known to be important for early defenses against L. monocytogenes in the spleen, as well
149 PFKP), pentose phosphate pathway (G6PD), and defense against lipid peroxidation (GPX4) scored high as
150 ally prevent cells from mounting an adequate defense against lipid peroxidation and thereby promote f
151 -MLKL pathway in nonimmune cell-derived host defense against Listeria invasion, which is mediated thr
152 esponse to IL-12 and for an efficient immune defense against Listeria monocytogenes Deletion of TYK2
156 NK) cells are important players in the early defense against many viral infections, the NK cell respo
158 l and pathological processes, including host defense against microbial infections, anti-tumor immunit
159 spase-11 (caspase-1/-4/-5/-11)) mediate host defense against microbial infections, processing pro-inf
164 ssity of l-citrulline metabolism for myeloid defense against mycobacterial infection and highlight th
168 g cassette (ABC) transporter plays a role in defense against numerous pathogens and is recruited to s
171 spond to these VOC cues by priming their own defenses against oncoming herbivory, thereby reducing fu
172 bility to store H2S in vivo and as a line of defense against oxidative stress, from which it is clear
176 play between the nuclear lamina and cellular defenses against oxidative DNA damage, with implications
177 idant enzymes, gut cell renewal as potential defenses against oxidative injuries and the profile of m
178 33c's activity was consistent with a role in defenses against oxidative stress generated during host
179 age-FABP4 has a novel role in pulmonary host defense against P. aeruginosa infection by facilitating
180 ffects of the propolis envelope as a natural defense against Paenibacillus larvae, the causative agen
182 Anthelmintic drugs are the major line of defense against parasitic nematode infections, but the a
183 stinal mucous layer provides a critical host defense against pathogen exposure and epithelial injury,
189 icrobial activity, presumed to contribute in defense against pathogenic microorganisms as plants with
190 ptive immunity genes that contribute to host defense against pathogenic viruses such as herpes viruse
193 n the control of cell-signaling pathways and defense against pathogens and whose imbalance leads to p
194 AIM2 plays essential roles not only in host defense against pathogens but also in inflammatory disea
195 cells (LCs) in the skin are a first line of defense against pathogens but also play an essential rol
196 al killer (NK) cells are critical for innate defense against pathogens through direct cytotoxicity of
197 gammat for development and contribute to the defense against pathogens through IL-22 and IL-17 secret
198 een shown to be involved in the constitutive defense against pathogens through the secretion of toxic
199 repertoire development, to provide lifelong defense against pathogens while maintaining self-toleran
200 luding tissue development and repair, innate defense against pathogens, and generation of adaptive im
201 h as the regulation of endogenous processes, defense against pathogens, and response to abiotic stres
202 masome activation is critical for the host's defense against pathogens, but dysregulation of inflamma
203 nate immune system acts as the first line of defense against pathogens, including coronaviruses (CoVs
204 nce of peptidoglycan N-deacetylation on host defense against pathogens, we investigated the virulence
216 mmatory response is necessary for the host's defense against pathogens; however, uncontrolled or unre
218 development and provides insights into host defenses against pathogens and the immunological mechani
220 optosis is a form of cell death important in defenses against pathogens that can also result in a pot
221 etween plant defenses against herbivores and defenses against pathogens, but few studies incorporate
223 ilized effector molecule that can operate in defense against persistent infection at times when other
227 tial roles for fibrin during T cell-mediated defense against Pla-mutant Y. pestis Moreover, the effic
229 ucan and signal at Fcgamma receptors enhance defense against Pneumocystis f. sp. murina, though it is
235 tissue-resident memory T cells (TRM) in the defense against recurring pathogens and malignant neopla
237 primed innate immune system is an effective defense against retroviral pathogenesis, resulting in re
238 estriction factors provide the first line of defense against retrovirus infection by posing several b
242 ypothesis that platelets participate in host defense against S. aureus both through direct killing of
243 ty of mouse platelets to participate in host defense against S. aureus infection was determined by as
244 y pathway consisting of human monocyte-based defense against S. aureus suggests that targeting the NK
252 vement of Jonah66Ci in the Drosophila immune defense against Steinernema carpocapsae nematode infecti
255 f a single allele of A20 results in enhanced defense against systemic Candida albicans infection and
257 t nociceptor neurons critically mediate host defense against the bacterial pathogen Salmonella enteri
258 ay protective and regulatory roles in immune defense against the opportunistic mold Aspergillus fumig
259 ybean) Sec4 functions in the root during its defense against the parasitic nematode Heterodera glycin
262 these cells upon infection are critical for defense against the virus, and therefore, it is importan
263 nfection sites is a fundamental step in host defenses against the frequent human pathogen group B Str
269 matory monocytes (iMO) are critical for host defense against toxoplasmosis and malaria but their role
272 iller (NK) cells are important in the immune defense against tumor cells and pathogens, and they regu
274 Nase 7 has a role in kidney and bladder host defense against UPEC and establish a foundation for inve
275 odulation, augmentation of the Cu-based host defense against UTI represents a novel approach to limit
276 nd topically applied DHA potentiate cellular defense against UVB-induced skin inflammation and photoc
277 RTANCE Innate immune signaling is a critical defense against viral infection and represents a central
278 necroptosis, has been implicated in the host defense against viral infection primary in immune cells.
287 ng the p53 and pRB pathways, or disrupt host defenses against viral infections, including interferon
289 te immune system, contributing to first-line defenses against viral, bacterial, and fungal pathogens.
294 tive immune systems provide prokaryotes with defense against viruses by degradation of specific invad
295 its prokaryotic host with an adaptive immune defense against viruses that have been previously encoun
296 ntrinsic immunity is known to be a frontline defense against viruses through host anti-viral restrict
300 s on the horizon, we risk losing our primary defense against widespread morbidity and mortality from