戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 reatment murine model for acute infection by L. infantum.
2 us immunity mediated by prior infection with L. infantum.
3  promastigotes as well as L. amazonensis and L. infantum amastigotes.
4                           Vector-transmitted L. infantum and L. donovani caused >/=5-fold increase in
5                      These data suggest that L. infantum and L. major differentially activate keratin
6 essful development of an SPR sensor for anti-L. infantum antibodies detection in short time, showing
7 nosensor shows good specificity against anti-L. infantum antibodies.
8 agasi-containing dermal leukocytes and total L. infantum chagasi parasites in draining lymph nodes we
9 e inoculation site, we introduced metacyclic L. infantum chagasi promastigotes intradermally into BAL
10  the dermis even late after inoculation, and L. infantum chagasi trafficked through neutrophils in bo
11                    From 3 days onward, total L. infantum chagasi-containing dermal leukocytes and tot
12                Nonetheless, a second wave of L. infantum chagasi-containing neutrophils occurred 7 da
13 ere tracked with fluorescent mCherry-labeled L. infantum chagasi.
14                                        Thus, L. infantum CYP51 is the first example of a plant-like s
15                                     Although L. infantum CYP51 prefers C4-monomethylated sterol subst
16 microM semipermeable membrane suggested that L. infantum-exposed keratinocytes release soluble factor
17                              By screening an L. infantum expression library with sera from human VL p
18         Therefore, our results indicate that L. infantum induces IL-17A production, which promotes th
19                            The prevalence of L. infantum infection in the females fell from 85 to 45%
20 PL-SE induced significant protection against L. infantum infection, with reductions in parasite loads
21                        Only vector-initiated L. infantum infections caused cutaneous lesions at trans
22 was more sensitive than an IFA for detecting L. infantum infections in patients with AIDS.
23 rn Brazilian State of Minas Gerais where L. (L.) infantum is also endemic.
24 rates datasets from Leishmania braziliensis, L. infantum, L. major, L. tarentolae, Trypanosoma brucei
25  rK39 in HIV-negative patients infected with L. infantum or L. chagasi declined during treatment with
26 d by confocal microscopy analysis applied to L. infantum promastigotes.
27 sults suggest that TR regions from the novel L. infantum proteins identified in this study are immuno
28 at enhance monocyte control of intracellular L. infantum replication (P < 0.01).
29                 Keratinocytes incubated with L. infantum significantly increased expression of proinf
30  (Trypanosoma brucei, Trypanosoma cruzi, and L. infantum) suggests that substrate preferences of plan
31 ochondrial chaperone reservoir, which allows L. infantum to deal successfully with protein unfolding
32                      The soluble antigens of L. infantum were securely immobilized on an SPR gold dis
33  fly gut populations of both L. mexicana and L. infantum were significantly reduced in caspar-deplete

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。