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1 ine sand flies of the genera Phlebotomus and Lutzomyia.
3 sand flies (Psathyromyia abonnenci, formerly Lutzomyia abonnenci) that are unique to the New World.
4 Morphological similarities between female Lutzomyia cruzi and Lutzomyia longipalpis present a sign
5 to characterize the human immune response to Lutzomyia intermedia saliva in 264 individuals, from an
6 expressed recombinant salivary proteins from Lutzomyia intermedia, a vector of Leishmania braziliensi
7 itivity to rLinB-13, a salivary protein from Lutzomyia intermedia, predicted sand fly exposure and wa
8 tructed from midgut tissue from the sand fly Lutzomyia longipalpis and analyzed the transcripts prese
9 idence that salivary gland extracts (SGE) of Lutzomyia longipalpis enhances L. amazonensis infection.
10 on salivary gland extracts from the sandfly Lutzomyia longipalpis identified SALO (salivary anticomp
12 e well-characterized salivary component from Lutzomyia longipalpis is maxadilan (MAX), a vasodilator
13 ivary gland lysate of the New World sand fly Lutzomyia longipalpis markedly enhanced L. major infecti
15 fected hamsters underwent xenodiagnoses with Lutzomyia longipalpis on the same or different sites on
16 ilarities between female Lutzomyia cruzi and Lutzomyia longipalpis present a significant challenge fo
18 d hematophagous insect vectors, the sand fly Lutzomyia longipalpis s.l., the mosquitoes Anopheles dar
20 ishmania major is enhanced when the sand fly Lutzomyia longipalpis salivary peptide maxadilan (MAX) i
28 tivity of a cDNA from the salivary glands of Lutzomyia longipalpis, a blood-sucking insect, with subs
31 abundant salivary protein from the sand fly Lutzomyia longipalpis, belongs to the insect "yellow" fa
32 vary recombinant protein LJM11 (rLJM11) from Lutzomyia longipalpis, in the absence of adjuvant, induc
35 N-glycans from the salivary glycoproteins of Lutzomyia longipalpis, vector of visceral leishmaniasis