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1 enic break points between E. histolytica and E. dispar and hence, could work as recombination hot spo
2 IgA antibody response to E. histolytica and E. dispar infection and revealed that ALA subjects exhib
4 ransposase-coding gene in E. histolytica and E. dispar related to the mariner transposon Hydargos fro
6 PCR (capable of detecting E. histolytica and E. dispar), our tetraplex real-time PCR assay demonstrat
8 E. gallinarum, E. casseliflavus/flavescens, E. dispar, E. pseudoavium, E. sulfureus, E. malodoratus,
9 to correctly distinguish E. histolytica from E. dispar was evaluated with DNA extracted from patients
11 these, four species (Entamoeba histolytica, E. dispar, E. moshkovskii, and E. bangladeshi) are morph
12 and 97.4%, respectively; for E. histolytica/E. dispar, 99, 96.0%, and 99.1%, respectively; and for C
13 the detection of G. lamblia, E. histolytica/E. dispar, and C. parvum in fresh or fresh-frozen fecal
16 on of Giardia lamblia, Entamoeba histolytica/E. dispar, and Cryptosporidium parvum in fresh or fresh,
17 four were positive for Entamoeba histolytica/E. dispar, and three were positive for Cryptosporidium p
18 found 415 genes expressed at lower levels in E. dispar and 32 genes with lower expression in E. histo
19 amilies of LINE and SINE retrotransposons in E. dispar and provide evidence for how the different LIN
20 changing with recent reports of detection of E. dispar deoxyribonucleic acid sequences, previously co
21 intestinalis or Entamoeba histolytica and/or E. dispar in 89 adults and adolescents, 22 of whom were
22 intestinalis, 53 with E. histolytica and/or E. dispar, and 14 with both G. intestinalis and E. histo
24 ains the genomes of three Entamoeba species (E. dispar, E. invadens and E. histolityca) and microarra
25 owing a E. histolytica infection compared to E. dispar (P = 0.01) and, for either, were of greater he