Detection of a single viable Cryptosporidium parvum oocyst in environmental water concentrates by reverse transcription-PCR.
about
Development of a PCR-enzyme immunoassay oligoprobe detection method for Toxoplasma gondii oocysts, incorporating PCR controlsA randomized, blinded, controlled trial investigating the gastrointestinal health effects of drinking water quality.Development of procedures for direct extraction of Cryptosporidium DNA from water concentrates and for relief of PCR inhibitorsPhylogenetic relationships of Cryptosporidium parasites based on the 70-kilodalton heat shock protein (HSP70) gene.beta-tubulin mRNA as a marker of Cryptosporidium parvum oocyst viability.Detection of infectious Cryptosporidium parvum oocysts in surface and filter backwash water samples by immunomagnetic separation and integrated cell culture-PCR.Comparison of animal infectivity and nucleic acid staining for assessment of Cryptosporidium parvum viability in water.Molecular characterization of cryptosporidium oocysts in samples of raw surface water and wastewaterPCR-restriction fragment length polymorphism analysis of a diagnostic 452-base-pair DNA fragment discriminates between Cryptosporidium parvum and C. meleagridis and between C. parvum isolates of human and animal originAn assay combining cell culture with reverse transcriptase PCR to detect and determine the infectivity of waterborne Cryptosporidium parvumDetection of viable Cryptosporidium parvum in soil by reverse transcription-real-time PCR targeting hsp70 mRNAInteraction of Cryptosporidium parvum with mouse dendritic cells leads to their activation and parasite transportation to mesenteric lymph nodesTowards a rational strategy for monitoring of microbiological quality of ambient waters.Identification of Mycobacterium ulcerans in the environment from regions in Southeast Australia in which it is endemic with sequence capture-PCR.Determination of pyrimidine dimers in Escherichia coli and Cryptosporidium parvum during UV light inactivation, photoreactivation, and dark repairSensitive and rapid detection of viable Giardia cysts and Cryptosporidium parvum oocysts in large-volume water samples with wound fiberglass cartridge filters and reverse transcription-PCRStress-induced Hsp70 gene expression and inactivation of Cryptosporidium parvum oocysts by chlorine-based oxidants.Quantitative-PCR assessment of Cryptosporidium parvum cell culture infection.Development of sensitive detection of cryptosporidium and giardia from surface water in iran.Oligonucleotide-gold nanoparticle networks for detection of Cryptosporidium parvum heat shock protein 70 mRNA.
P2860
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P2860
Detection of a single viable Cryptosporidium parvum oocyst in environmental water concentrates by reverse transcription-PCR.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年学术文章
@wuu
1996年学术文章
@zh-cn
1996年学术文章
@zh-hans
1996年学术文章
@zh-my
1996年学术文章
@zh-sg
1996年學術文章
@yue
1996年學術文章
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1996年學術文章
@zh-hant
name
Detection of a single viable C ...... by reverse transcription-PCR.
@en
Detection of a single viable C ...... by reverse transcription-PCR.
@nl
type
label
Detection of a single viable C ...... by reverse transcription-PCR.
@en
Detection of a single viable C ...... by reverse transcription-PCR.
@nl
prefLabel
Detection of a single viable C ...... by reverse transcription-PCR.
@en
Detection of a single viable C ...... by reverse transcription-PCR.
@nl
P2093
P2860
P1476
Detection of a single viable C ...... by reverse transcription-PCR.
@en
P2093
P2860
P304
P407
P577
1996-09-01T00:00:00Z