نتایج جستجو برای: mutation igvh status

تعداد نتایج: 694113  

Journal: :Haematologica 2005
Gerard Tobin Ulf Thunberg Anna Laurell Karin Karlsson Anna Aleskog Kerstin Willander Ola Söderberg Mats Merup Juhani Vilpo Magnus Hultdin Christer Sundström Göran Roos Richard Rosenquist

BACKGROUND AND OBJECTIVES The immunoglobulin VH gene mutation status is a strong prognostic indicator in B-cell chronic lymphocytic leukemia (CLL), since unmutated VH genes are correlated with short survival. However, the traditional cut-off level dividing mutated and unmutated cases, i.e. more or less than 2% mutations, has been questioned and other cut-offs have been suggested. We investigate...

Journal: :Journal of the National Cancer Institute 2013
Shuji Ogino Xiaoyun Liao Yu Imamura Mai Yamauchi Nadine J McCleary Kimmie Ng Donna Niedzwiecki Leonard B Saltz Robert J Mayer Renaud Whittom Alexander Hantel Al B Benson Rex B Mowat Donna Spiegelman Richard M Goldberg Monica M Bertagnolli Jeffrey A Meyerhardt Charles S Fuchs

BACKGROUND Somatic mutations in PIK3CA (phosphatidylinositol-4,5-bisphosphonate 3-kinase [PI3K], catalytic subunit alpha gene) activate the PI3K-AKT signaling pathway and contribute to pathogenesis of various malignancies, including colorectal cancer. METHODS We examined associations of PIK3CA oncogene mutation with relapse, survival, and treatment efficacy in 627 stage III colon carcinoma ca...

Journal: :Cukurova Medical Journal 2021

Purpose: Ischemic stroke is a serious health condition in patients with young adults. This study aims to determine thrombophilia polymorphisms ischemic and associations other risk factors.
 Materials Methods: We evaluated 64 under 50 years old. Computerized Tomography Angiography, Holter Electrocardiography, Transthoracic Echocardiography, status, Modifying Rankin Scale (MRS) baseline firs...

Journal: :Blood 2010
Claire L Green Catherine M Evans Robert K Hills Alan K Burnett David C Linch Rosemary E Gale

Mutations in the isocitrate dehydrogenase gene (IDH1) were recently described in patients with acute myeloid leukemia (AML). To investigate their prognostic significance we determined IDH1 status in 1333 young adult patients, excluding acute promyelocytic leukemia, treated in the United Kingdom MRC AML10 and 12 trials. A mutation was detected in 107 patients (8%). Most IDH1(+) patients (91%) ha...

2017
Ziwei Guo Fumei Yi Wencheng Yin Yu Zhang Qian Li Yangchun Gu Yu Xiao Baoshan Cao Liwen Ma Li Liang

BACKGROUND We explored correlations between the new International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society classification, epidermal growth factor receptor (EGFR) mutation status, and prognosis. METHODS Data from 293 patients with lung adenocarcinoma were classified according to the new classification. Fisher's exact, χ2 , and log-rank te...

2016
Kun-Ming Rau Han-Ku Chen Li-Yen Shiu Tsai-Ling Chao Yi-Ping Lo Chin-Chou Wang Meng-Chih Lin Chao-Cheng Huang

Mutations on epidermal growth factor receptor (EGFR) of adenocarcinomas of lung have been found to be associated with increased sensitivity to EGFR tyrosine kinase inhibitors and K-ras mutations may correlate with primary resistance. We aimed to explore the discordant mutation statuses of EGFR and K-ras between primary tumors and matched brain metastases in adenocarcinomas of lung. We used a se...

Journal: :Asian Pacific journal of cancer prevention : APJCP 2015
Xing Kang Rong Chen Jie Zhang Gang Li Peng-Gao Dai Chao Chen Hui-Juan Wang

BACKGROUND Zinc transporters have been considered as essential regulators in many cancers; however, their mechanisms remain unknown, especially in gliomas. Isocitrate dehydrogenase 1(IDH1) mutation is crucial to glioma. This study aimed to investigate whether zinc transporters are correlated with glioma grade and IDH1 mutation status. MATERIALS AND METHODS IDH1 mutation status and mRNA expres...

Journal: :hepatitis monthly 0
rym ayari laboratory of immunology research center, kidney transplantation and immunopathology (lr03sp01), charles nicolle hospital, university of tunis el manar, tunisia +216-25462623, [email protected]; laboratory of immunology research center, kidney transplantation and immunopathology (lr03sp01), charles nicolle hospital, university of tunis el manar, tunisia +216-25462623, [email protected] yousr lakhoua-gorgi laboratory of immunology research center, kidney transplantation and immunopathology (lr03sp01), charles nicolle hospital, university of tunis el manar, tunisia +216-25462623, [email protected] lamjed bouslama borj cedria center for biotechnology, hammam lif, tunisia imen safar laboratory of immunology research center, kidney transplantation and immunopathology (lr03sp01), charles nicolle hospital, university of tunis el manar, tunisia +216-25462623, [email protected] fatma houissa kchouk laboratory of immunology research center, kidney transplantation and immunopathology (lr03sp01), charles nicolle hospital, university of tunis el manar, tunisia +216-25462623, [email protected] houda aouadi laboratory of immunology research center, kidney transplantation and immunopathology (lr03sp01), charles nicolle hospital, university of tunis el manar, tunisia +216-25462623, [email protected]

background in this study, we evaluated the prevalence of the most common mutations occurring in enhancer ii (enhii), basal core promoter (bcp), precore (pc), and core (c) regions of hepatitis b virus (hbv) genome. objectives we also investigated the correlation between hbv variants, their genotypes, and patients’ hbe antigen (hbeag: soluble shape of the capsid antigen) status patients and metho...

2016
Ian A. Cree

RAS mutation analysis is an important companion diagnostic test. Treatment of colorectal cancer with anti-Epidermal Growth Factor Receptor (EGFR) therapy requires demonstration of RAS mutation status (both KRAS and NRAS), and it is good practice to include BRAF. In Non-Small Cell Lung Cancer (NSCLC) and melanoma, assessment of RAS mutation status can be helpful in triaging patient samples for m...

2015
Ruza Arsenic Denise Treue Annika Lehmann Michael Hummel Manfred Dietel Carsten Denkert Jan Budczies

BACKGROUND Phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha, PIK3CA, is one of the most frequently mutated genes in breast cancer, and the mutation status of PIK3CA has clinical relevance related to response to therapy. The aim of our study was to investigate the mutation status of PIK3CA gene and to evaluate the concordance between NGS and SGS for the most important hots...

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