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1 n to harbor highly encapsulated, replicating cryptococci.
2 Ab to facilitate attachment and ingestion of cryptococci.
3 anner that is characteristic of encapsulated cryptococci.
4 driven by aberrant T-cell responses against cryptococci.
5 elial cells that facilitate the migration of cryptococci across the BBB and ultimately induce endothe
7 hages had increased numbers of intracellular cryptococci and YM1 crystals, indicative of alternativel
9 y early interactions between macrophages and cryptococci are critical in the outcome of cryptococcosi
12 yptococcal culture filtrate Ag + heat-killed cryptococci-CFA), or controls, stimulated significant in
13 to the nonprotective immunogen (heat-killed cryptococci-CFA), the nonprotective immunogen mixed with
14 fter suddenly stopping in brain capillaries, cryptococci cross into the central nervous system in a p
15 ature and a "Trojan horse" mechanism whereby cryptococci enter the central nervous system after macro
16 week-old immunized and infected mice cleared cryptococci from brain, spleen, and liver in a manner si
17 levels were elevated in cultures containing cryptococci grown in RPMI 1640 at 37 degrees C in an atm
18 MAbs facilitate phagocytosis of encapsulated cryptococci, (ii) some anti-GXM antibodies are opsonic i
23 and subpleural granulomas that harbor viable cryptococci inside macrophages and epithelioid cells.
27 crophages are able to suppress the growth of cryptococci seen in mammalian cells despite C. neoforman
28 lthy individuals can maintain low numbers of cryptococci that can become a nidus for re-activation di
29 elial cells associate with, and internalize, cryptococci, they upregulate the expression of several p
32 onment associated with impaired clearance of cryptococci while high IL-7 levels may reflect IL-7/IL-7
33 that macrophages preferentially phagocytose cryptococci with smaller polysaccharide capsules and tha
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