نتایج جستجو برای: mutation igvh status

تعداد نتایج: 694113  

2015
Lin Yang Chuanhao Tang Bin Xu Weixia Wang Jianjie Li Xiaoyan Li Haifeng Qin Hongjun Gao Kun He Santai Song Xiaoqing Liu Ramon Andrade de Mello

OBJECTIVES Epidermal growth factor receptor (EGFR) gene mutations in tumors predict tumor response to EGFR tyrosine kinase inhibitors (EGFR-TKIs) in non-small-cell lung cancer (NSCLC). However, obtaining tumor tissue for mutation analysis is challenging. Here, we aimed to detect serum peptides/proteins associated with EGFR gene mutation status, and test whether a classification algorithm based ...

2004
William D. Foulkes Kelly Metcalfe Ping Sun Wedad M. Hanna Henry T. Lynch Parviz Ghadirian Nadine Tung Olufunmilayo I. Olopade Barbara L. Weber Jane McLennan Ivo A. Olivotto Louis R. Bégin Steven A. Narod

Purpose: BRCA1-related breast cancers are more frequently estrogen receptor (ER) negative than are either BRCA2-related or nonhereditary breast cancers. The relationship between ER status and other clinical features of hereditary breast cancers has not been well studied. Experimental Design: ER status, grade, and histological tumor type were evaluated in 1131 women with invasive breast cancer, ...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2004
William D Foulkes Kelly Metcalfe Ping Sun Wedad M Hanna Henry T Lynch Parviz Ghadirian Nadine Tung Olufunmilayo I Olopade Barbara L Weber Jane McLennan Ivo A Olivotto Louis R Bégin Steven A Narod

PURPOSE BRCA1-related breast cancers are more frequently estrogen receptor (ER) negative than are either BRCA2-related or nonhereditary breast cancers. The relationship between ER status and other clinical features of hereditary breast cancers has not been well studied. EXPERIMENTAL DESIGN ER status, grade, and histological tumor type were evaluated in 1131 women with invasive breast cancer, ...

Journal: :Journal of neurology, neurosurgery, and psychiatry 2004
J M Ringman C Diaz-Olavarrieta Y Rodriguez M Chavez F Paz J Murrell M Angel Macias M Hill C Kawas

OBJECTIVES To study depressive symptoms in preclinical presenilin-1 (PS1) related Alzheimer's disease. METHODS Participants were 33 Mexican women at risk for inheriting PS1 mutations who were not demented. They were interviewed, underwent cognitive testing, and completed the Beck depression inventory (BDI). PS1 mutation status was determined. Mean BDI scores were compared between PS1 mutation...

Journal: :Blood 2009
Susanne Schnittger Wolfgang Kern Claudia Tschulik Tamara Weiss Frank Dicker Brunangelo Falini Claudia Haferlach Torsten Haferlach

Nucleophosmin (NPM1)-mutated acute myeloid leukemia (AML), which is recognized as a provisional entity in the World Health Organization 2008 classification of myeloid neoplasms, accounts for 30% of AML. We analyzed 1227 diagnostic and follow-up samples in 252 NPM1-mutated AML patients with 17 different NPM1 mutation-specific real-time quantitative polymerase chain reaction (RQ-PCR) assays. Pair...

اکرمی پور, رضا, خالقی, سمیه, علی بخشی, رضا, بیدکی, سید کاظم ,

  Background: Alpha thalassemia is a single gene disorder, inherited in an autosomal recessive manner. The thalassemia occurs mostly in peoples from the Mediterranean to Southeast Asia. The present study was aimed to identify the prevalence of nondeletional Alpha thalassemia mutations in our samples in the Kermanshah province.   Methods : This study included Alpha thalassemia individuals who ha...

Journal: :International journal of clinical and experimental pathology 2015
Huanli Duan Junliang Lu Tao Lu Jie Gao Jing Zhang Yan Xu Mengzhao Wang Huanwen Wu Zhiyong Liang Tonghua Liu

BACKGROUND The aims were to compare the consistency of epidermal growth factor receptor (EGFR) mutations in the plasma and tumor tissue of NSCLC patients, and to explore the prognostic significance of plasma EGFR mutation status in tyrosine kinase inhibitors (TKIs)-treated patients with tumor EGFR mutation. METHODS We evaluated EGFR gene (exons 18, 19, 20 and 21) mutation status in paired pla...

2016
Krzysztof Roszkowski Jacek Furtak Bogdan Zurawski Tadeusz Szylberg Marzena A. Lewandowska

The IDH1/2 gene mutations, ATRX loss/mutation, 1p/19q status, and MGMT promoter methylation are increasingly used as prognostic or predictive biomarkers of gliomas. However, the effect of their combination on radiation therapy outcome is discussable. Previously, we demonstrated that the IDH1 c.G395A; p.R132H mutation was associated with longer survival in grade II astrocytoma and GBM (Glioblast...

Journal: :Blood 2008
Fu Jun Li Shouluan Ding Jicun Pan Mikhail A Shakhmatov Elena Kashentseva Jiongru Wu Yufeng Li Seng-jaw Soong Nicholas Chiorazzi Randall S Davis

CD38 and ZAP-70 are both useful prognostic markers for B-cell chronic lymphocytic leukemia (CLL), but are variably discordant with IGHV mutation status. A total of 5 human Fc receptor-like molecules (FCRL1-5) have tyrosine-based immunoregulatory potential and are expressed by B-lineage subpopulations. To determine their prognostic potential in CLL, FCRL expression was compared with IGHV mutatio...

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