نتایج جستجو برای: amplified refractory mutation system

تعداد نتایج: 2553865  

Journal: :The New England Journal of Medicine 2021

Hairy-cell leukemia (HCL) is a CD20+ indolent B-cell cancer in which BRAF V600E kinase–activating mutation plays pathogenetic role. In clinical trials involving patients with refractory or relapsed HCL, the targeting of oral inhibitor vemurafenib led to response 91% patients; 35% had complete response. However, median relapse-free survival was only 9 months after treatment stopped.

Mohammad Hossein Ahmadi Mohammad Reza Sarookhani, Naser Amirizadeh,

Background: Beta thalassemia is a common inherited disease, resulting from one or more of 200 different mutations in the beta-globin gene. Qazvin province has attracted migrations of several different populations due to industrialization during the past five decades. The aim of this study was to define the molecular spectrum of beta-thalassemia mutations in Qazvin province. Methods: Ethylen dia...

2015
Yaping Xu Yuanda Zheng Xiaojiang Sun Xinmin Yu Jialei Gu Wei Wu Gu Zhang Jinlin Hu Wenyong Sun Weimin Mao

The survival rate associated with esophageal cancer is very poor due to diagnosis at advanced stages of disease and insensitivity to chemotherapy. This study investigated the efficacy of gefitinib combination with radiation in 20 elderly patients with esophageal squamous cell carcinoma (ESCC) who were not eligible for platinum-based chemotherapy. Immunohistochemistry was performed to analyze ep...

Khazaei Koohpar, Zeinab, Ranji, Najmeh, Rezaei, Omid,

Introduction: Mutation in SLC26A4 gene is one of reason of syndromic and non-syndomic hearing loss. Mutation in this gene is reported to be the second most common cause of deafness in the worldwide, after GJB2 gene. The aim of this study was to evaluate mutations in exon 10 of SLC26A4 gene in individuals with hearing loss in Guilan province. Materials and Methods: In this descriptive cross-sect...

Journal: :Clinical chemistry 1997
P Carrera A M Barbieri M Ferrari P G Righetti M Perego C Gelfi

A quick diagnosis of the classic form of 21-hydroxylase deficiency (simple virilizing and salt wasting) is of great importance, especially for prenatal diagnosis and treatment in pregnancies at risk. A method for simultaneous detection of common point mutations in the P450c21 B gene is here proposed by combining a nested PCR amplification refractory mutation system (ARMS) with capillary zone el...

2016
Hiroshi Mizuuchi Kenichi Suda Isao Murakami Kazuko Sakai Katsuaki Sato Yoshihisa Kobayashi Masaki Shimoji Masato Chiba Yuichi Sesumi Kenji Tomizawa Toshiki Takemoto Yoshitaka Sekido Kazuto Nishio Tetsuya Mitsudomi

Mutant selective epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs), such as rociletinib and AZD9291, are effective for tumors with T790M secondary mutation that become refractory to first-generation EGFR-TKI. However, acquired resistance to these prospective drugs is anticipated considering the high adaptability of cancer cells and the mechanisms remain largely obscure. He...

Journal: :Haematologica 2006
Angel F Remacha Josep F Nomdedéu Guiomar Puget Camino Estivill M Pilar Sarda Carme Canals Anna Aventin

The JAK2/V617F mutation has been noted in essential thrombocytemia. We investigated 19 cases with refractory anemia with ringed sideroblasts (RARS), including three RARS with thrombocytosis (RARS-T). Only the RARS-T patients showed this mutation. More cases need to be analyzed to determine the prevalence of the JAK2/V617F mutation in RARS-T.

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2016
Ryan D Morin Sarit Assouline Miguel Alcaide Arezoo Mohajeri Rebecca L Johnston Lauren Chong Jasleen Grewal Stephen Yu Daniel Fornika Kevin Bushell Torsten Holm Nielsen Tina Petrogiannis-Haliotis Michael Crump Axel Tosikyan Bruno M Grande David MacDonald Caroline Rousseau Maryam Bayat Pierre Sesques Remi Froment Marco Albuquerque Yury Monczak Kathleen Klein Oros Celia Greenwood Yasser Riazalhosseini Madeleine Arseneault Errol Camlioglu André Constantin Qiang Pan-Hammarstrom Roujun Peng Koren K Mann Nathalie A Johnson

PURPOSE Relapsed or refractory diffuse large B-cell lymphoma (rrDLBCL) is fatal in 90% of patients, and yet little is known about its biology. EXPERIMENTAL DESIGN Using exome sequencing, we characterized the mutation profiles of 38 rrDLBCL biopsies obtained at the time of progression after immunochemotherapy. To identify genes that may be associated with relapse, we compared the mutation freq...

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