نتایج جستجو برای: ژن npm1

تعداد نتایج: 16927  

2007
Brunangelo Falini Ildo Nicoletti Massimo F. Martelli Cristina Mecucci

The nucleophosmin (NPM1) gene encodes for a multifunctional nucleocytoplasmic shuttling protein that is localized mainly in the nucleolus. NPM1 mutations occur in 50% to 60% of adult acute myeloid leukemia with normal karyotype (AML-NK) and generate NPM mutants that localize aberrantly in the leukemic-cell cytoplasm, hence the term NPM-cytoplasmic positive (NPMc AML). Cytoplasmic NPM accumulati...

Journal: :Blood 2005
Giovanni Cazzaniga Maria Grazia Dell'Oro Cristina Mecucci Emanuela Giarin Riccardo Masetti Vincenzo Rossi Franco Locatelli Massimo F Martelli Giuseppe Basso Andrea Pession Andrea Biondi Brunangelo Falini

Nucleophosmin (NPM) is a nucleocytoplasmic shuttling protein involved in leukemia-associated chromosomal translocations, and it regulates the alternate reading frame (ARF)-p53 tumor-suppressor pathway. Recently, it has been demonstrated that mutations of the NPM1 gene alter the protein at its C-terminal, causing its cytoplasmic localization. Cytoplasmic NPM was detected in 35% of adult patients...

Journal: :Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2010
Claire L Green Kenneth K Koo Robert K Hills Alan K Burnett David C Linch Rosemary E Gale

PURPOSE To determine the clinical relevance of mutations in the CCAAT/enhancer binding protein alpha (CEBPA) gene in acute myeloid leukemia (AML) and to examine factors that might modify prognostic impact. PATIENTS AND METHODS The entire CEBPA coding sequence was screened in 1,427 young adult patients with AML, excluding acute promyelocytic leukemia, using denaturing high-performance liquid c...

Journal: :Haematologica 2008
Brunangelo Falini Cristina Mecucci Giuseppe Saglio Francesco Lo Coco Daniela Diverio Patrick Brown Fabrizio Pane Marco Mancini Maria Paola Martelli Stefano Pileri Torsten Haferlach Claudia Haferlach Susanne Schnittger

Acute myeloid leukemia carrying NPM1 mutations and cytoplasmic nucleophosmin (NPMc(+) acute myeloid leukemia) represents one-third of adult AML (50-60% of all acute myeloid leukemia with normal karyotype) and shows distinct biological, pathological and clinical features. We confirm in 2562 patients with acute myeloid leukemia our previous observation that NPM1 mutations and cytoplasmic nucleoph...

2015
Lawrence WC Chan Xihong Lin Godwin Yung Thomas Lui Ya Ming Chiu Fengfeng Wang Nancy BY Tsui William CS Cho SP Yip Parco M. Siu SC Cesar Wong Benjamin YM Yung

Co-expression analysis reveals useful dysregulation patterns of gene cooperativeness for understanding cancer biology and identifying new targets for treatment. We developed a structural strategy to identify co-expressed gene networks that are important for chronic myelogenous leukemia (CML). This strategy compared the distributions of expressional correlations between CML and normal states, an...

Journal: :Journal of the Egyptian National Cancer Institute 2011
Neemat Kassem Alaa Abel Hamid Tarek Attia Sherif Baathallah Somaya Mahmoud Eman Moemen Ezzat Safwat Mohamed Khalaf Olfat Shaker

UNLABELLED Mutations of the nucleophosmin (NPM-1) gene have been reported in 50-60% of acute myeloid leukemia (AML) patients with normal karyotype. This work was designed to study the prevalence and nature of NPM1 gene mutations in a group of Egyptian patients with AML to get an idea about the profile of NPM1 gene mutations in our society. In 45 previously untreated patients with de novo AML, p...

Journal: :The New England journal of medicine 2012
Jay P Patel Mithat Gönen Maria E Figueroa Hugo Fernandez Zhuoxin Sun Janis Racevskis Pieter Van Vlierberghe Igor Dolgalev Sabrena Thomas Olga Aminova Kety Huberman Janice Cheng Agnes Viale Nicholas D Socci Adriana Heguy Athena Cherry Gail Vance Rodney R Higgins Rhett P Ketterling Robert E Gallagher Mark Litzow Marcel R M van den Brink Hillard M Lazarus Jacob M Rowe Selina Luger Adolfo Ferrando Elisabeth Paietta Martin S Tallman Ari Melnick Omar Abdel-Wahab Ross L Levine

BACKGROUND Acute myeloid leukemia (AML) is a heterogeneous disease with respect to presentation and clinical outcome. The prognostic value of recently identified somatic mutations has not been systematically evaluated in a phase 3 trial of treatment for AML. METHODS We performed a mutational analysis of 18 genes in 398 patients younger than 60 years of age who had AML and who were randomly as...

Journal: :The New England journal of medicine 2008
Richard F Schlenk Konstanze Döhner Jürgen Krauter Stefan Fröhling Andrea Corbacioglu Lars Bullinger Marianne Habdank Daniela Späth Michael Morgan Axel Benner Brigitte Schlegelberger Gerhard Heil Arnold Ganser Hartmut Döhner

BACKGROUND Mutations occur in several genes in cytogenetically normal acute myeloid leukemia (AML) cells: the nucleophosmin gene (NPM1), the fms-related tyrosine kinase 3 gene (FLT3), the CCAAT/enhancer binding protein alpha gene (CEPBA), the myeloid-lymphoid or mixed-lineage leukemia gene (MLL), and the neuroblastoma RAS viral oncogene homolog (NRAS). We evaluated the associations of these mut...

2012
Mikael S. Lindström

Biogenesis of eukaryotic ribosomes occurs mainly in a specific subnuclear compartment, the nucleolus, and involves the coordinated assembly of ribosomal RNA and ribosomal proteins. Identification of amino acid sequences mediating nucleolar localization of ribosomal proteins may provide important clues to understand the early steps in ribosome biogenesis. Human ribosomal protein S9 (RPS9), known...

Journal: :Haematologica 2011
Annika C Russ Sandrine Sander Sonja C Lück Katharina M Lang Marion Bauer Frank G Rücker Hans A Kestler Richard F Schlenk Hartmut Döhner Karlheinz Holzmann Konstanze Döhner Lars Bullinger

BACKGROUND MicroRNAs are regulators of gene expression, which act mainly by decreasing mRNA levels of their multiple targets. Deregulated microRNA expression has been shown for acute myeloid leukemia, a disease also characterized by altered gene expression associated with distinct genomic aberrations such as nucleophosmin (NPM1) mutations. To shed further light on the role of deregulated microR...

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