نتایج جستجو برای: pcr technology

تعداد نتایج: 638949  

2007
Cinzia Bonanno Erlet Shehi Daniel Adlerstein Mike Makrigiorgos

Background: Aberrant promoter methylation is a major mechanism for silencing tumor suppressor genes in cancer. Detection of hypermethylation is used as a molecular marker for early cancer diagnosis, as a prognostic index, or to define therapeutic targets for reversion of aberrant methylation. We report on a novel signal generation technology for real-time PCR to detect gene promoter methylation...

Journal: :Clinical chemistry 2010
Stela Filipovic-Sadic Sachin Sah Liangjing Chen Julie Krosting Edward Sekinger Wenting Zhang Paul J Hagerman Timothy T Stenzel Andrew G Hadd Gary J Latham Flora Tassone

BACKGROUND Fragile X syndrome (FXS) is a trinucleotide-repeat disease caused by the expansion of CGG sequences in the 5' untranslated region of the FMR1 (fragile X mental retardation 1) gene. Molecular diagnoses of FXS and other emerging FMR1 disorders typically rely on 2 tests, PCR and Southern blotting; however, performance or throughput limitations of these methods currently constrain routin...

2000
P. O. PETRUCCI G. HENRI G. PELLETIER

We investigate the effect of pair creation on a shock structure. Actually, particles accelerated by a shock can be sufficiently energetic to boost, via Inverse Compton (IC) process for example, surrounding soft photons above the rest mass electron energy and thus to trigger the pair creation process. The increase of the associated pair pressure is thus able to disrupt the plasma flow and possib...

2010
Igor V. Kutyavin

The article describes a new technology for real-time polymerase chain reaction (PCR) detection of nucleic acids. Similar to Taqman, this new method, named Snake, utilizes the 50-nuclease activity of Thermus aquaticus (Taq) DNA polymerase that cleaves dual-labeled Förster resonance energy transfer (FRET) probes and generates a fluorescent signal during PCR. However, the mechanism of the probe cl...

Journal: :Journal of clinical periodontology 2004
Laura Lau Mariano Sanz David Herrera Juan Manuel Morillo Conchita Martín Augusto Silva

OBJECTIVE The purpose of this investigation was to validate a real-time quantitative polymerase chain reaction (PCR) assay in identifying and quantifying Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis and Tannerella forsythensis from subgingival plaque samples taken from subjects with different periodontal conditions, when compared with conventional cultural procedures. PATIEN...

Journal: : 2021

Identification systems that use biometric characteristics to solve the problem of access information are becoming more common. The article proposes a new method identification computer users, based on determination integral Volterra model human oculo-motor system (OMS) according experimental research "input-output" using innovative eye tracking technology. With help Tobii Pro TX300 tracker, dat...

Journal: :Asian Pacific journal of cancer prevention : APJCP 2007
Arkom Chaiwongkot Chamsai Pientong Tipaya Ekalaksananan Bunkerd Kongyingyoes Jadsada Thinkhamrop Pissamai Yuenyao Supannee Sriamporn

High risk human papillomaviruses (HR-HPVs) are associated with increased risk of normal cervical cells developing to dysplasia and cervical carcinoma. Therefore, HR-HPV DNA testing can predict an endpoint of cervical carcinogenesis that is earlier than the development of cervical abnormalities. Not only the sensitivity of methods but also the amount of HPV DNA are very important and might be pa...

Journal: :Asian Pacific journal of cancer prevention : APJCP 2010
P P Chong N Asyikin M Rusinahayati S Halimatun R Rozita C K Ng W H Wan Hamilton B C Tan N Noraihan A Rohani H Faezah L Latiffah A Maha A R Sabariah

Persistent high-risk human papillomavirus (HPV) infection is known to play an important role in the genesis of cervical cancer. Since new screening and prevention strategies, namely improved HPV testing and HPV vaccination have been aggressively promoted recently, it is crucial to investigate the HPV distribution in Malaysia in order to maximize their cost-effectiveness. This study was therefor...

Journal: :Revue scientifique et technique 1993
M Rodríguez A A Schudel

The authors describe and summarise the use of nucleic acid hybridisation and polymerase chain reaction (PCR) technologies in the diagnosis of animal diseases. PCR is a powerful biological tool which enables exponential enzymatic amplification in vitro of a given deoxyribonucleic acid sequence. This technique is currently used to study the molecular pathogenesis of many infectious diseases and a...

2011
Hidenori Nagai Yusuke Fuchiwaki Keiichiro Yamanaka Masato Saito Eiichi Tamiya

To detect the biological agents, the DNA detection is most usable due to the sensitivity and the selectivity. Although the key technology of DNA detection is real-time polymerase chain reaction (PCR), which uses exponential amplification of PCR and real-time detection of the amplified DNA fragments, the long thermal cycling time has been the problem to apply the rapid detection of pathogenic or...

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