نتایج جستجو برای: ژن npm1

تعداد نتایج: 16927  

Journal: :Blood 2011
Wen-Chien Chou Sheng-Chieh Chou Chieh-Yu Liu Chien-Yuan Chen Hsin-An Hou Yuan-Yeh Kuo Ming-Cheng Lee Bor-Sheng Ko Jih-Luh Tang Ming Yao Woei Tsay Shang-Ju Wu Shang-Yi Huang Szu-Chun Hsu Yao-Chang Chen Yi-Chang Chang Yi-Yi Kuo Kuan-Ting Kuo Fen-Yu Lee Ming-Chi Liu Chia-Wen Liu Mei-Hsuan Tseng Chi-Fei Huang Hwei-Fang Tien

The studies concerning clinical implications of TET2 mutation in patients with primary acute myeloid leukemia (AML) are scarce. We analyzed TET2 mutation in 486 adult patients with primary AML. TET2 mutation occurred in 13.2% of our patients and was closely associated with older age, higher white blood cell and blast counts, lower platelet numbers, normal karyotype, intermediate-risk cytogeneti...

Journal: :The Biochemical journal 2013
Mattia Poletto Carlo Vascotto Pasqualina L Scognamiglio Lisa Lirussi Daniela Marasco Gianluca Tell

The hAPE1 (human apurinic/apyrimidinic endonuclease 1) is an essential enzyme, being the main abasic endonuclease in higher eukaryotes. However, there is strong evidence to show that hAPE1 can directly bind specific gene promoters, thus modulating their transcriptional activity, even in the absence of specific DNA damage. Recent findings, moreover, suggest a role for hAPE1 in RNA processing, wh...

2016
Diana M Mitrea Jaclyn A Cika Clifford S Guy David Ban Priya R Banerjee Christopher B Stanley Amanda Nourse Ashok A Deniz Richard W Kriwacki

The nucleolus is a membrane-less organelle formed through liquid-liquid phase separation of its components from the surrounding nucleoplasm. Here, we show that nucleophosmin (NPM1) integrates within the nucleolus via a multi-modal mechanism involving multivalent interactions with proteins containing arginine-rich linear motifs (R-motifs) and ribosomal RNA (rRNA). Importantly, these R-motifs are...

2014
Min Wang Na He Tian Tian Lu Liu Shuang Yu Daoxin Ma

Since the discovery of JAK2V617F tyrosine kinase-activating mutation, several genes have been found mutated in myeloproliferative neoplasms (MPNs). FLT3-ITD, NPM1, and DNMT3A mutations frequently occurred in AML patients and have been found conferred with myeloproliferative neoplasms in mouse model. Therefore, we sought to search for mutations in JAK2V617F, FLT3-ITD, NPM1, and DNMT3A in 129 cas...

Journal: :The New England journal of medicine 2016
Adam Ivey Robert K Hills Michael A Simpson Jelena V Jovanovic Amanda Gilkes Angela Grech Yashma Patel Neesa Bhudia Hassan Farah Joanne Mason Kerry Wall Susanna Akiki Michael Griffiths Ellen Solomon Frank McCaughan David C Linch Rosemary E Gale Paresh Vyas Sylvie D Freeman Nigel Russell Alan K Burnett David Grimwade

BACKGROUND Despite the molecular heterogeneity of standard-risk acute myeloid leukemia (AML), treatment decisions are based on a limited number of molecular genetic markers and morphology-based assessment of remission. Sensitive detection of a leukemia-specific marker (e.g., a mutation in the gene encoding nucleophosmin [NPM1]) could improve prognostication by identifying submicroscopic disease...

2010
Helena Johansson Stina Simonsson

Embryonic stem (ES) cells have therapeutic potential in regenerative medicine, although the molecular mechanism controlling their pluripotency is not completely understood. Depending on interaction partners most proteins can be involved in several different cellular mechanisms. We screened for novel protein-protein interactions using in situ proximity ligation assays together with specific anti...

Journal: :Blood 2010
Niccolò Bolli Elspeth M Payne Clemens Grabher Jeong-Soo Lee Adam B Johnston Brunangelo Falini John P Kanki A Thomas Look

Mutations in the human nucleophosmin (NPM1) gene are the most frequent genetic alteration in adult acute myeloid leukemias (AMLs) and result in aberrant cytoplasmic translocation of this nucleolar phosphoprotein (NPMc+). However, underlying mechanisms leading to leukemogenesis remain unknown. To address this issue, we took advantage of the zebrafish model organism, which expresses 2 genes ortho...

2015
Srivasavi Dukka David T. Bowen

We present a short case series of elderly patients with NK-AML and isolated NPM1 mutation who were treated with intensive chemotherapy, achieving significant CRs multiple times on reinduction, even with a single course.We hope to highlight the NPM1 as a molecular marker in elderly for consideration of aggressive treatment, even if abridged, as this subset may achieve a durable, good quality res...

2016
Elisa Barbieri Gianluca Deflorian Federica Pezzimenti Debora Valli Marco Saia Natalia Meani Alicja M. Gruszka Myriam Alcalay

Nucleophosmin (NPM1) is a ubiquitous multifunctional phosphoprotein with both oncogenic and tumor suppressor functions. Mutations of the NPM1 gene are the most frequent genetic alterations in acute myeloid leukemia (AML) and result in the expression of a mutant protein with aberrant cytoplasmic localization, NPMc+. Although NPMc+ causes myeloproliferation and AML in animal models, its mechanism...

Journal: :Biomedicines 2023

The current classification of acute myeloid leukemia (AML) relies largely on genomic alterations. AML with mutated nucleophosmin 1 (NPM1-mut) is the largest genetically defined groups, involving about 30% adult AMLs and currently recognized as a distinct entity in actual classifications. NPM1-mut usually occurs de novo associated predominantly normal karyotype relatively favorable prognosis. Ho...

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