نتایج جستجو برای: itd mutation

تعداد نتایج: 292736  

Journal: :Acta medica Okayama 2017
Yuka Iwasaki Rituo Nishiuchi Michinori Aoe Takahide Takahashi Hirokazu Watanabe Chiho Tokorotani Kiyoshi Kikkawa Akira Shimada

Acute myeloid leukemia (AML) patients with fms-related tyrosine kinase 3 (FLT3)-internal tandem duplication (ITD) often have a poor prognosis, even after hematopoietic stem cell transplantation (HSCT). We report a case of AML with FLT3-ITD identified upon initial diagnosis, who received HSCT at complete remission after 3 consecutive chemotherapies. However, the patient relapsed when the same FL...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2011
Brian J Fischer Louisa J Steinberg Bertrand Fontaine Romain Brette Jose L Peña

Detecting interaural time difference (ITD) is crucial for sound localization. The temporal accuracy required to detect ITD, and how ITD is initially encoded, continue to puzzle scientists. A fundamental question is whether the monaural inputs to the binaural ITD detectors differ only in their timing, when temporal and spectral tunings are largely inseparable in the auditory pathway. Here, we in...

Journal: :Blood 2005
Roel G W Verhaak Chantal S Goudswaard Wim van Putten Maarten A Bijl Mathijs A Sanders Wendy Hugens André G Uitterlinden Claudia A J Erpelinck Ruud Delwel Bob Löwenberg Peter J M Valk

Mutations in nucleophosmin NPM1 are the most frequent acquired molecular abnormalities in acute myeloid leukemia (AML). We determined the NPM1 mutation status in a clinically and molecularly well-characterized patient cohort of 275 patients with newly diagnosed AML by denaturing high-performance liquid chromatography (dHPLC). We show that NPM1 mutations are significantly underrepresented in pat...

2012
Ender Coşkunpınar Sema Anak Leyla Ağaoğlu Ayşegül Ünüvar Ömer Devecioğlu Gönül Aydoğan Çetin Timur Ahmet Faik Öner Yıldız Yıldırmak Tiraje Celkan İnci Yıldız Nazan Sarper Uğur Özbek

OBJECTIVE To identify the well-known common translocations and FLT3 mutations in childhood acute myelogenousleukemia (AML) patients in Turkey. MATERIAL AND METHODS The study included 50 newly diagnosed patients in which t(15;17), t(8;21), and inv(16)chromosomal translocations were identified using real-time PCR and FLT3 gene mutations were identified via direct PCR amplification PCR-RE analys...

Journal: :The hematology journal : the official journal of the European Haematology Association 2002
Birgit Kainz Daniel Heintel Rodrig Marculescu Ilse Schwarzinger Wolfgang Sperr Trang Le Ansgar Weltermann Christa Fonatsch Oskar A Haas Christine Mannhalter Klaus Lechner Ulrich Jaeger

INTRODUCTION Internal tandem duplication of the FLT3 gene (FLT3/ITD) has been linked to poor outcome in acute myeloid leukemia (AML). However, the prognostic value of FLT3/ITD in various cytogenetic risk groups is still a matter of debate. The aim of this study was to evaluate the prognostic significance in patients with de novo AML and a normal karyotype or a t(15;17), t(8;21) or inv(16) (good...

Journal: :Blood 2002
Christian Thiede Christine Steudel Brigitte Mohr Markus Schaich Ulrike Schäkel Uwe Platzbecker Martin Wermke Martin Bornhäuser Markus Ritter Andreas Neubauer Gerhard Ehninger Thomas Illmer

Constitutive activation of the FLT3 receptor tyrosine kinase, either by internal tandem duplication (ITD) of the juxtamembrane region or by point mutations in the second tyrosine kinase domain (TKD), has been described in patients with acute myelogenous leukemia (AML). We analyzed the prevalence and the potential prognostic impact of FLT3 mutations in 979 AML patients. Results were correlated w...

Journal: :Blood 2002
Kevin W H Yee Anne Marie O'Farrell Beverly D Smolich Julie M Cherrington Gerald McMahon Cecily L Wait Laura S McGreevey Diana J Griffith Michael C Heinrich

Internal tandem duplication (ITD) in the juxtamembrane portion of Fms-like tyrosine kinase 3 (FLT3), a type III receptor tyrosine kinase (RTK), is the most common molecular defect associated with acute myeloid leukemia (AML). The high prevalence of this activating mutation makes it a potential target for molecularly based therapy. Indolinone tyrosine kinase inhibitors have known activity agains...

Objective(s): Mutant forms FMS-like tyrosine kinase-3 (FLT3), are reported in 25% of childhood acute lymphoid leukemia (ALL) and 30% of acute myeloid leukemia (AML) patients. In this study, drug response, growth promoting, and protein trafficking of FLT3 wild-type was compared with two active mutants (Internal Tandem Duplication (ITD)) and D835Y. Materials and Methods:FLT3 was expressed on fact...

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