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1 where it is hyperendemic, provide a model of natural resistance.
2 tomato and can potently suppress the host's natural resistance.
4 hat structural motifs that evolved to confer natural resistance against conspecific long-chain alpha-
5 sion may have been advantageous by providing natural resistance against viral pathogens that exploite
9 blem, and there is still much to learn about natural resistance and cellular immunity to pneumococcus
10 tists to consider the best approaches to map natural resistance and foster ecosystem resilience in th
11 alidity of the inference that differences in natural resistance are relevant in explaining what diffe
18 2+) transporter Pmr1 and which depend on the natural resistance-associated macrophage protein (NRAMP)
21 valent ion transporter formerly known as the natural resistance-associated macrophage protein (NRAMP1
22 mphocyte--associated protein 4 (CTLA-4), and natural resistance-associated macrophage protein (NRAMP1
23 ine if these patients have a defect in their natural resistance-associated macrophage protein (NRAMP1
24 d INO expression increases the expression of NATURAL RESISTANCE-ASSOCIATED MACROPHAGE PROTEIN 1 (NRAM
25 equired for virulence in mice expressing the natural resistance-associated macrophage protein 1 (Nram
26 ratios were compared based on expression of natural resistance-associated macrophage protein 1 (Nram
27 a functional host-resistant regulator, i.e. natural resistance-associated macrophage protein 1 (Nram
28 ntH is a bacterial homolog of the eukaryotic natural resistance-associated macrophage protein 1 (Nram
29 (FPN1), divalent metal transporter 1 (DMT1), natural resistance-associated macrophage protein 1 (Nram
31 MntH, a bacterial homolog of the mammalian natural resistance-associated macrophage protein 1 (Nram
33 typhoid fever is critically dependent on the natural resistance-associated macrophage protein 1 (Nram
38 tNramp1 (Medtr3g088460) is the M. truncatula Natural Resistance-Associated Macrophage Protein family
39 rine macrophages transfected with either the natural resistance-associated macrophage protein gene 1
43 acuolar Fe transporters, yellow stripe-like, natural resistance-associated macrophage protein, and ol
44 he transition metal-chelating S100 proteins, natural resistance-associated macrophage protein-1 (NRAM
45 nels, cation diffusion facilitator proteins, natural resistance-associated macrophage proteins (NRAMP
46 g Arabidopsis thaliana seedlings require the natural resistance-associated macrophage proteins (NRAMP
50 2 or 3 (DMT1/DCT1/SLC11A2), a member of the natural-resistance-associated macrophage protein (Nramp)
51 129sv mice with a functional deletion of the natural-resistance-associated macrophage protein 1 gene
56 he synthetic drug linezolid which involves a natural resistance gene with the capability of dissemina
59 enesis of HIV-1 (immunosuppression) and SIV (natural resistance) in humans and non-human primates, re
63 1 (HO-1) after 3 hours, a 2-fold increase in natural resistance macrophage-associated protein 1 (Nram
67 c UV exposure or natural ageing overcame the natural resistance of back-skin basal cells to undergoin
71 ural killer (NK) cells are essential for the natural resistance of nonimmune C57BL/6 (B6) to mousepox
73 tic hydrolysis - the steps that overcome the natural resistance of plants to biological breakdown - o
80 es one mechanism that may contribute to this natural resistance: some elite controllers have CD4(+) T
82 formerly called NRAMP1) gene is important in natural resistance to a variety of intracellular infecti
86 laber) are long-lived mammals that possess a natural resistance to cancer and other age-related patho
91 vation of complement represents one means of natural resistance to infection from a wide variety of p
92 Vgamma2Vdelta2 cell responses and impair the natural resistance to infectious diseases or the respons
93 nclude that nonhemopoietic cells mediate the natural resistance to intestinal amoebiasis of B6 mice,
94 eria are of special consideration due to the natural resistance to many common antibiotics due to the
95 ssible, is difficult to process owing to its natural resistance to mechanical shearing and high level
101 ur findings provide a new target for seeking natural resistance to potyviruses and new opportunities
102 in astrocytes, we reported that part of this natural resistance to productive replication of HIV in a
103 testing of biochemical parameters, including natural resistance to pyrazinamide and defective pyrazin
106 a number of novel phenotypes that mimic the natural resistance to stress characteristic of C. albica
107 flavone that, when present in silks, confers natural resistance to the maize earworm (Helicoverpa zea
111 ntly shown that C57BL/6 (B6) mice lose their natural resistance to wild-type (WT) ectromelia virus (E
113 For aptamers carrying family 1 pseudoknots, natural resistance was essentially all-or-none and corre
114 ected to be a response to the development of natural resistance, which often mechanistically mimics c