نتایج جستجو برای: pcr 3

تعداد نتایج: 1948300  

Journal: :Journal of clinical microbiology 2011
Liang Chen José R Mediavilla Andrea Endimiani Marnie E Rosenthal Yanan Zhao Robert A Bonomo Barry N Kreiswirth

Carbapenem resistance mediated by plasmid-borne Klebsiella pneumoniae carbapenemases (KPC) is an emerging problem of significant clinical importance in Gram-negative bacteria. Multiple KPC gene variants (bla(KPC)) have been reported, with KPC-2 (bla(KPC-2)) and KPC-3 (bla(KPC-3)) associated with epidemic outbreaks in New York City and various international settings. Here, we describe the develo...

2017
Yong Yan Jian-Yong Luo Yin Chen Heng-Hui Wang Guo-Ying Zhu Pei-Yan He Jin-Lei Guo Yong-Liang Lei Zhong-Wen Chen

We utilized one-step multiplex reverse transcription-PCR (RT-PCR) and Luminex xMAP technology to develop a respiratory multiplex liquid-chip assay (rMLA) for simultaneous detection of 6 common respiratory viruses, including influenza virus type A (FluA) and type B (FluB), para-influenza virus type 3 (PIV-3), respiratory syncytial virus (RSV), human metapneumovirus (MPV) and a threatening virus ...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2012
Rui Wang Yunjian Pan Chenguang Li Haichuan Hu Yang Zhang Hang Li Xiaoyang Luo Jie Zhang Zhaoyuan Fang Yuan Li Lei Shen Hongbin Ji David Garfield Yihua Sun Haiquan Chen

PURPOSE Approximately 3% to 7% of non-small cell lung cancers (NSCLC) harbor an ALK fusion gene, thus defining a tumor group that may be responsive to targeted therapy. The breakpoint in ALK consistently occurs at exon 20 and EML4 or other fusion partners, thus driving a strong expression of ALK kinase domain and resulting in an unbalanced expression in 5' and 3' portions of ALK transcripts. We...

2010
Neil I. Bower Ian A. Johnston

Amplification of the 5' ends of cDNA, although simple in theory, can often be difficult to achieve. We describe a novel method for the specific amplification of cDNA ends. An oligo-dT adapter incorporating a dUTP-containing PCR primer primes first-strand cDNA synthesis incorporating dUTP. Using the Cap finder approach, another distinct dUTP containing adapter is added to the 3' end of the newly...

2003
V Thakur SK Sarin

Objective Third generation anti-HCV ELISA is currently recommended for the diagnosis of HCV infection. We determined its specificity in voluntary blood donors (VBDs) and patients with chronic liver disease (CLD) in relation to confirmatory line immunoassay (LIA) and reverse transcription polymerase chain reaction (RT-PCR). Material and Methods: 1926 serum samples of VBDs and 16 HCV related CLD ...

Journal: :British Journal of Haematology 2021

Neonatal alloimmune neutropenia (NAIN) is caused by maternal alloimmunisation to fetal human neutrophil antigens (HNAs). This study investigated HNA/HLA alloantibodies involved with NAIN and identified the frequency of in Brazilian neonates. (neutrophil count < 1.5 × 109/L) was samples from 10,000 unselected neonates, resulting 88 neutropenic newborns (NBs) their 83 mothers. Genotyping performe...

Journal: :BioTechniques 1996
A Chenchik L Diachenko F Moqadam V Tarabykin S Lukyanov P D Siebert

An efficient cDNA amplification procedure is described for determining of the 5' and 3' ends of mRNAs and cloning full-length cDNAs. In this approach, a double-stranded (ds) adaptor is ligated to both ends of a library of ds cDNA by T4 DNA ligase. This adaptor-ligated ds cDNA is then used to selectively amplify 5'- or 3'-cDNA fragments by PCR with a combination of gene-specific and adaptor-spec...

2003
V Thakur

Objective Third generation anti-HCV ELISA is currently recommended for the diagnosis of HCV infection. We determined its specificity in voluntary blood donors (VBDs) and patients with chronic liver disease (CLD) in relation to confirmatory line immunoassay (LIA) and reverse transcription polymerase chain reaction (RT-PCR). Material and Methods: 1926 serum samples of VBDs and 16 HCV related CLD ...

2002
P. L. Winokur

1. Abstract 2. Introduction 3. Phenotypic techniques 3.1. Serotype analysis 3.2. Biotype and phage type analysis 3.3. Antibiotic susceptibility patterns 4. Genotypic techniques 4.1. Plasmid analysis 4.2. Chromosomal restriction fragment analysis and pulsed-field gel electrophoresis (PFGE) 4.3. Chromosomal restriction-hybridization techniques 4.3.1. Ribotype analysis 4.3.2. IS200 4.4. Locus-spec...

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