Titlebook: Diagnosis of Human Viruses by Polymerase Chain Reaction Technology; Yechiel Becker,Gholamreza Darai Book 1992 Springer-Verlag Berlin Heide

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書目名稱Diagnosis of Human Viruses by Polymerase Chain Reaction Technology被引頻次




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書目名稱Diagnosis of Human Viruses by Polymerase Chain Reaction Technology讀者反饋




書目名稱Diagnosis of Human Viruses by Polymerase Chain Reaction Technology讀者反饋學(xué)科排名

MAZE

Detection of Human Spumaviruses by Polymerase Chain Reactionhniques. The only serious problem encountered is the oversensitivity of this method that can lead to false-positive results due to laboratory contaminations. Controls and the complete physical separation of all reagents and equipment are required to avoid any contaminations.

吸氣

ONYM

Ilaria Tarricone,Anita Riecher-R?sslerhniques. The only serious problem encountered is the oversensitivity of this method that can lead to false-positive results due to laboratory contaminations. Controls and the complete physical separation of all reagents and equipment are required to avoid any contaminations.

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悄悄移動

Human Immunodeficiency Virus Type 1 (HIV-1) Detection by Polymerase Chain Reaction in Children of Ine second and third testing. I conclude that, in most cases, PCR will not detect the presence of HIV-1 proviral DNA at birth, but it is a powerful technique that can be used for the diagnosis of perinatal HIV-1 infection from the second month of life.

悄悄移動

領(lǐng)帶

Alexandra Boccarossa,Sébastien Fleurettivation of HCV. PCR based diagnostics, the rapid accumulation of HCV sequence information and the availability of cDNA/PCR generated cDNA clones for the expression of putative viral antigens has contributed greatly to our understanding of the structure and biology of HCV.

MELD

Case Study: Cynthia’s Story: The Netherlandsg the earliest stages of central nervous system infection. The assay has also been used for the detection of HSV DNA in CSF samples from patients with HSE. The results are discussed and compared with those published elsewhere.

Contort

Paul Bowie,Simon Paterson-Brownngement known to disrupt viral latency. Technical details of amplification, oligonucleotide hybridization, and semiquantitative EBV DNA analysis are described. A sensitive detection system of the Bam W/Bam Z rearrangement is also presented.