نتایج جستجو برای: fusion pcr

تعداد نتایج: 291966  

2012
Jamshid Faghri Delavar Shahbazzadeh Kamran Pooshang Bagheri Sharareh Moghim Hajieh Ghasemian Safaei Bahram Nasr Esfahani Hossein Fazeli Rahmatolah Yazdani Hamid Mirmohammad Sadeghi

OBJECTIVES Staphylococcus aureus is a foremost source of numerous nosocomial and community acquired infections. Antibiotic therapy for vancomycin resistant S. aureus (VRSA) can not promise the eradication of infections. Since adhesion is the major route of infections, adhesin based vaccine could suppress S. aureus infections. Fibronectin binding protein A (FnBPA) and clumping factor A (ClfA) ar...

Journal: :Journal of pediatric hematology/oncology 2010
Yung-Li Yang Shu-Rung Lin Jiann-Shiuh Chen Chih-Cheng Hsiao Kai-Hsin Lin Jiunn-Ming Sheen Chao-Neng Cheng Kang-Hsi Wu Shu-Wha Lin Sung-Liang Yu Hsuan-Yu Chen Meng-Yao Lu Hsiu-Hao Chang Ching-Tzu Yen Jing-Fang Lin Ying-Hui Su Ya-Ping Li Chien-Yu Lin Shiann-Tarng Jou Dong-Tsamn Lin

BACKGROUND The classification of B-lineage acute lymphoblastic leukemia (ALL) by specific chromosomal translocations has prognostic implications for risk-directed therapy. Reverse transcription-polymerase chain reaction (RT-PCR) assay is a useful tool for detecting fusion transcripts from common chromosomal translocations of ALL cells. METHODS Multiplex RT-PCR and nested-PCR assays were used ...

Journal: :International journal of clinical and experimental pathology 2013
Takashi Kobayashi Motoshi Ichikawa Yasuhiko Kamikubo Mineo Kurokawa

A 77 year-old female was found with FAB M4Eo acute myeloid leukemia. Although CBFB-MYH11 mRNA was detected in RT-PCR, the conventional cytogenetic analysis failed to reveal inv(16). Fluorescence in situ hybridization (FISH) and the sequence analysis revealed a fusion between the exon 5 of CBFB and the exon 8 of MYH11, resulting in a minor variant fusion product previously reported as type D. In...

Background & Aim: Bacterial superantigens, stimulate polyclonal T cells irrespective of their antigen specificity, resulting in a massive release of cytokines from T cells and monocytes, and suggest that that they could be candidates of new antitumor agents. Recent attempts have been done to specifically target superantigens towards tumors. Here, we evaluate TGFαL3-SEB fusion protein as a new a...

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2002
W I Lee H Kantarjian A Glassman M Talpaz M S Lee

BACKGROUND Quantitative real-time polymerase chain reaction (Q-Rt-PCR) is a new tool in the detection and quantification of the BCR/abl fusion transcripts in chronic myelogenous leukemia (CML). This study investigates its specificity, sensitivity and potential clinical usefulness. PATIENTS AND METHODS Parallel analysis of Q-Rt-PCR and the conventional reverse transcription-mediated PCR (RT-PC...

Journal: :hepatitis monthly 0
seyed younes hosseini department of virology, vaswmu} oodmwe{cuniwg{wow}s, tarbiat modares university, p. o. box: 14115-331, ir iran +98-2182883880, [email protected]; gastroentero -hepatology research center, shiraz university of medical sciences, ir iran farzaneh sabahi department of virology, vaswmu} oodmwe{cuniwg{wow}s, tarbiat modares university, p. o. box: 14115-331, ir iran +98-2182883880, [email protected]; department of virology, vaswmu} oodmwe{cuniwg{wow}s, tarbiat modares university, p. o. box: 14115-331, ir iran +98-2182883880, [email protected] seyed mohammad moazzeni department of immunology, tarbiat modares university, ir iran mohammad hossein modarressi department of medical genetic, tehran university of medical sciences, ir iran mehdi saberi firoozi digestive disease research center, tehran university of medical sciences, ir iran mehrdad ravanshad department of virology, vaswmu} oodmwe{cuniwg{wow}s, tarbiat modares university, p. o. box: 14115-331, ir iran +98-2182883880, [email protected]

background in spite of dozens of clinical trials to establish effective therapeutic and/or preventive vaccine to resolve hcv infection, no real vaccine has been proved to date. genetic vaccines based on replication-defective adenoviruses have proved to elicit strong and long lasting t-cell responses against a number of viral antigens and are even currently being used for vaccine trials in human...

2000
Heiko Wittor Hermann Leying Andreas Hochhaus Rob van Miltenburg

Literature indicates that in 95 % of all subjects with chronic myeloid leukemia (CML) and in 25-30 % of subjects with acute lymphoblastic leukemia (ALL) a reciprocal translocation between the long arms of chromosome 9 and chromosome 22 [t(9;22)] can be found. This translocation or the resulting fusion product can be detected by a number of techniques, including fluorescent in situ hybridization...

2001
Sabine Strehl Margit König Georg Mann Oskar A. Haas

To determine the incidence of leukemiaspecific rearrangements, 60 cases of childhood acute myeloblastic leukemia and transient myeloproliferative disorder were screened with a novel multiplex reverse transcriptase–polymerase chain reaction (RT-PCR) assay, and the results were correlated with the cytogenetic findings. The RT-PCR assay detects 28 different fusion genes and more than 80 different ...

Journal: :Methods in molecular biology 2007
Hongxin Fan Ryan S Robetorye

The real-time quantitative reverse transcriptase polymerase chain reaction (RQ-PCR) has become the method of choice for the quantification of specific mRNAs. This method is fast, extremely sensitive, and accurate, requires only very small amounts of input RNA, and is relatively simple to perform. These characteristics have made it the method of choice for minimal residual disease monitoring suc...

Journal: :British journal of haematology 2001
J D Curry M C Glaser M T Smith

A real-time reverse transcription polymerase chain reaction (RT-PCR) method is described that enabled the detection and quantification of E2A-PBX1 fusion gene transcripts associated with t(1;19). The method was highly reproducible and offered exceptional sensitivity at 5 fg of fusion transcript per reaction, without the need for a nested PCR primer design. To illustrate the usefulness of this n...

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