نتایج جستجو برای: qrt pcr

تعداد نتایج: 175149  

2008
Bela Molnar Lajos Floro Ferenc Sipos Bernadett Toth Lydia Sreter Zsolt Tulassay

AIMS Cytokeratin(CK) based real-time RT-PCR assays (QRT-PCR) are now available for peripheral blood circulating tumor cell (CTC) evaluations in colorectal cancer(CRC) patients. Results are non-existent for the application of these techniques to the determination of progression and therapy response in Dukes stage D CRC patients. PATIENTS AND METHODS Each month 30 ml peripheral blood of 30 Duke...

Journal: :iranian journal of basic medical sciences 0
zhixiong fang department of infectious disease, xiangtan city central hospital, xiangtan, people's republic of china langqiu he department of infectious disease, xiangtan city central hospital, xiangtan, people's republic of china hui jia department of infectious disease, xiangtan city central hospital, xiangtan, people's republic of china qiusheng huang department of infectious disease, xiangtan city central hospital, xiangtan, people's republic of china dan chen edong healthcare city hospital of traditional chinese medicine, inefections disease hospital, huangshi, people's republic of china zhiwei zhang cancer research institute, university of south china, key laboratory of cancer cellular and molecular pathology of hunan provincial university, hengyang, people's republic of china

objective(s): to explore the correlation between expression patterns and functions of mir-383 and ldha in hepatocellular cancer (hcc). materials and methods: we detected the expression of mir-383 and ldha in 30 hcc tissues and their matched adjacent normal tissues using qrt-pcr. then we performed mtt assay, foci formation assay, transwell migration assay, glucose uptake assay and lactate produc...

Journal: :Nature Communications 2021

Abstract Coronavirus disease 2019 (COVID-19) is a highly contagious caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Diagnosis of COVID-19 depends on quantitative reverse transcription PCR (qRT-PCR), which time-consuming and requires expensive instrumentation. Here, we report an ultrasensitive electrochemical biosensor based isothermal rolling circle amplification (RCA) f...

2017
Huey-Ling You Shun-Jen Chang Hong-Ren Yu Chia-Chin Li Chang-Han Chen Wei-Ting Liao

BACKGROUND Both respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) are important viral pathogens causing respiratory tract infection (RTI) in the pediatric population. However, the clinical manifestations of RSV and hMPV infections are similar. Therefore, a reliable and rapid diagnostic tool is needed for diagnostic performance. METHODS In order to optimize diagnosis efficienc...

Journal: :Journal of clinical microbiology 2011
Edwin Kamau Ladonna S Tolbert Luke Kortepeter Michael Pratt Nancy Nyakoe Linda Muringo Bernard Ogutu John N Waitumbi Christian F Ockenhouse

A highly sensitive genus-specific quantitative reverse transcriptase real-time PCR (qRT-PCR) assay for detection of Plasmodium has been developed. The assay amplifies total nucleic acids (RNA and DNA) of the 18S rRNA genes with a limit of detection of 0.002 parasite/μl using cultured synchronized ring stage 3D7 parasites. Parasite densities as low as 0.000362 parasite/μl were detected when anal...

Journal: :BMC Veterinary Research 2006
Honghe Cao Leah C Kabaroff Qiumei You Alexander Rodriguez Herman J Boermans Niel A Karrow

BACKGROUND During systemic gram-negative bacterial infections, lipopolysaccharide (LPS) ligation to the hepatic Toll-like receptor-4 complex induces the production of hepatic acute phase proteins that are involved in the host response to infection and limit the associated inflammatory process. Identifying the genes that regulate this hepatic response to LPS in ruminants may provide insight into...

Journal: :Applied and environmental microbiology 2008
Elisabetta Lambertini Susan K Spencer Phillip D Bertz Frank J Loge Burney A Kieke Mark A Borchardt

Available filtration methods to concentrate waterborne viruses are either too costly for studies requiring large numbers of samples, limited to small sample volumes, or not very portable for routine field applications. Sodocalcic glass wool filtration is a cost-effective and easy-to-use method to retain viruses, but its efficiency and reliability are not adequately understood. This study evalua...

Journal: :The International journal of developmental biology 2006
Erik Willems Ileana Mateizel Caroline Kemp Greet Cauffman Karen Sermon Luc Leyns

Embryonic Stem (ES) cells have the potential to form every cell of the body and thus are of great promise for tissue transplantation. One of the rising techniques that allows studying the differentiation state of ES cells is quantitative RT-PCR (qRT-PCR). When relative quantification by qRT-PCR is applied, accurate normalization is necessary, since differentiated embryonic stem cells and develo...

2006
Michael W. Pfaffl

Reverse transcription (RT) followed by a polymerase chain reaction (PCR) represents the most powerful technology to amplify and detect trace amounts of mRNA (Heid et al., 1996; Lockey, 1998). To quantify these low abundant expressed genes in any biological matrix the real-time quantitative RT-PCR (qRT-PCR) is the method of choice. Real-time qRT-PCR has advantages compared with conventionally pe...

2013
Wei Jiang Hai-tao Yu Ke Zhao Ye Zhang Hong Du Ping-zhong Wang Xue-fan Bai

Hantaan virus (HTNV) is a major zoonotic pathogen that causes hemorrhagic fever with renal syndrome (HFRS) in Asia, especially in China. Shaanxi province, which is located in northwest of China, is one of the areas in China most severely afflicted with HFRS epidemics annually. This study aims to establish a quantitative RT-PCR (qRT-PCR) assay to detect HTNV both in cell culture and clinical ser...

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