Cell culture-Taqman PCR assay for evaluation of Cryptosporidium parvum disinfection.
about
Oxidative stress control by apicomplexan parasitesCritical processes affecting Cryptosporidium oocyst survival in the environment.Use of DNA melting simulation software for in silico diagnostic assay design: targeting regions with complex melting curves and confirmation by real-time PCR using intercalating dyes.Solar radiation induces non-nuclear perturbations and a false start to regulated exocytosis in Cryptosporidium parvum.Inactivation of single-celled Ascaris suum eggs by low-pressure UV radiation.Quantification of in vitro and in vivo Cryptosporidium parvum infection by using real-time PCR.Determining fungi rRNA copy number by PCR.Cryptosporidium.The pulsed light inactivation of veterinary relevant microbial biofilms and the use of a RTPCR assay to detect parasite species within biofilm structures.Inactivation of protozoan parasites in food, water, and environmental systems.Efficacy of using harmless Bacillus endospores to estimate the inactivation of Cryptosporidium parvum oocysts in water.Dissection of the hierarchy and synergism of the bile derived signal on Cryptosporidium parvum excystation and infectivity.Comparison of assays for sensitive and reproducible detection of cell culture-infectious Cryptosporidium parvum and Cryptosporidium hominis in drinking waterCryptosporidium cell culture infectivity assay design.Stress-induced Hsp70 gene expression and inactivation of Cryptosporidium parvum oocysts by chlorine-based oxidants.Aged HCT-8 cell monolayers support Cryptosporidium parvum infection.Quantitative-PCR assessment of Cryptosporidium parvum cell culture infection.Environmental temperature controls Cryptosporidium oocyst metabolic rate and associated retention of infectivityPCR slippage across the ML-2 microsatellite of the Cryptosporidium MIC1 locus enables development of a PCR assay capable of distinguishing the zoonotic Cryptosporidium parvum from other human infectious Cryptosporidium species.Solar UV reduces Cryptosporidium parvum oocyst infectivity in environmental waters.Flow cytometric assessment of distinct physiological stages within Cryptosporidium parvum sporozoites post-excystation.Three-dimensional (3D) culture of adult murine colon as an in vitro model of cryptosporidiosis: Proof of concept.Assessing viability and infectivity of foodborne and waterborne stages (cysts/oocysts) of Giardia duodenalis, Cryptosporidium spp., and Toxoplasma gondii: a review of methods.
P2860
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P2860
Cell culture-Taqman PCR assay for evaluation of Cryptosporidium parvum disinfection.
description
2003 nî lūn-bûn
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2003年の論文
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2003年学术文章
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2003年学术文章
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2003年学术文章
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name
Cell culture-Taqman PCR assay for evaluation of Cryptosporidium parvum disinfection.
@en
Cell culture-Taqman PCR assay for evaluation of Cryptosporidium parvum disinfection.
@nl
type
label
Cell culture-Taqman PCR assay for evaluation of Cryptosporidium parvum disinfection.
@en
Cell culture-Taqman PCR assay for evaluation of Cryptosporidium parvum disinfection.
@nl
prefLabel
Cell culture-Taqman PCR assay for evaluation of Cryptosporidium parvum disinfection.
@en
Cell culture-Taqman PCR assay for evaluation of Cryptosporidium parvum disinfection.
@nl
P2860
P1476
Cell culture-Taqman PCR assay for evaluation of Cryptosporidium parvum disinfection.
@en
P2093
Alexandra R Keegan
Stella Fanok
P2860
P304
P356
10.1128/AEM.69.5.2505-2511.2003
P407
P577
2003-05-01T00:00:00Z