نتایج جستجو برای: pcr sequencing

تعداد نتایج: 283892  

Journal: :Forensic Science International: Genetics Supplement Series 2019

2009
Vassiliki Kotoula Elpida Charalambous Bart Biesmans Andigoni Malousi Eleni Vrettou George Fountzilas George Karkavelas

BACKGROUND Testing for tumor specific mutations on routine formalin-fixed paraffin-embedded (FFPE) tissues may predict response to treatment in Medical Oncology and has already entered diagnostics, with KRAS mutation assessment as a paradigm. The highly sensitive real time PCR (Q-PCR) methods developed for this purpose are usually standardized under optimal template conditions. In routine diagn...

Journal: :Journal of clinical microbiology 2009
Fei Zhou Fanrong Kong Kenneth McPhie Mala Ratnamohan Linda Donovan Frank Zeng Gwendolyn L Gilbert Dominic E Dwyer

The more than 100 human enterovirus (HEV) serotypes can also be classified into four species, HEV-A to -D, based on phylogenetic analysis of multiple gene regions. Current molecular typing methods depend largely on reverse transcription-PCR (RT-PCR) amplification and nucleotide sequencing of the entire or 3' half of the VP1 gene. An RT-PCR-based reverse line blot (RLB) hybridization assay was d...

2015
Liesbet Vliegen Christophe Dooms Wim De Kelver Eric Verbeken Johan Vansteenkiste Peter Vandenberghe

BACKGROUND Treatment decisions in advanced non-small cell lung cancer rely on accurate analysis of the EGFR mutation status in small tissue samples. Sanger sequencing of PCR products is unbiased and cheap, but its detection threshold requiring 20 % infiltration by malignant cells is not optimal. Commercial kits, based on quantitative real-time PCR have better detection limits and can detect a w...

Journal: :Biotechnology 1988
M A Innis K B Myambo D H Gelfand M A Brow

The highly thermostable DNA polymerase from Thermus aquaticus (Taq) is ideal for both manual and automated DNA sequencing because it is fast, highly processive, has little or no 3'-exonuclease activity, and is active over a broad range of temperatures. Sequencing protocols are presented that produce readable extension products greater than 1000 bases having uniform band intensities. A combinati...

Journal: :BioTechniques 2001
P Bugert S Decker H Klüter

Gene polymorphisms and mutations have been correlated to different diseases and clinical syndromes. Therefore, screening for gene mutations is an appropriate approach to researching disease. The location of mutation hot spots is not known in new or rarely analyzed genes. To locate such hot spots, the screening of a complete gene sequence in a representative number of individuals is required. Se...

2014
Susana Benlloch Maria Luisa Botero Jordi Beltran-Alamillo Clara Mayo Ana Gimenez-Capitán Itziar de Aguirre Cristina Queralt Jose Luis Ramirez Santiago Ramón y. Cajal Barbara Klughammer Mariette Schlegel Walter Bordogna David Chen Guili Zhang Barbara Kovach Felice Shieh John F. Palma Lin Wu H. Jeffrey Lawrence Miquel Taron

The EURTAC trial demonstrated that the tyrosine kinase inhibitor (TKI) erlotinib was superior to chemotherapy as first-line therapy for advanced non-small cell lung cancers (NSCLC) that harbor EGFR activating mutations in a predominantly Caucasian population. Based on EURTAC and several Asian trials, anti-EGFR TKIs are standard of care for EGFR mutation-positive NSCLC. We sought to validate a r...

2012
Bárbara Angulo Esther Conde Ana Suárez-Gauthier Carlos Plaza Rebeca Martínez Pilar Redondo Elisa Izquierdo Belén Rubio-Viqueira Luis Paz-Ares Manuel Hidalgo Fernando López-Ríos

The objective of this study is to compare two EGFR testing methodologies (a commercial real-time PCR kit and a specific EGFR mutant immunohistochemistry), with direct sequencing and to investigate the limit of detection (LOD) of both PCR-based methods. We identified EGFR mutations in 21 (16%) of the 136 tumours analyzed by direct sequencing. Interestingly, the Therascreen EGFR Mutation Test kit...

Journal: :BioTechniques 1998
M Ronaghi B Pettersson M Uhlén P Nyrén

The need for a primer hybridization step before sequencing has been eliminated using a stem-loop structure generated by PCR. The loop structure is obtained by careful design of the PCR primer or by cloning the target DNA into a dedicated vector (pRIT 28HP). After solid-phase capture of the PCR product, the loop is formed by elution of the non-bound strand. Here, we show that both the immobilize...

اکیا, علیشا, حمزوی, یزدان,

Background and purpose: Iran is one of the endemic focuses of cutaneous leishmaniasis (CL) in the world. The disease is commonly seen in some tropical regions of Kermanshah province (West of Iran). In this study, patients with CL were diagnosed and identified using RFLP-PCR and DNA sequencing. Materials and methods: In this descriptive study all suspected cases of CL attended a clinic affili...

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