Accès ouvert
2014
article
OpenAlex
Marie José Kersten, Willem Kraan, Jeanette K. Doorduijn, Jacoline E. C. Bromberg et autres
Pasqualucci L . The genetic basis of diffuse large B-cell lymphoma. Curr Opin Hematol 2013; 20 : 336–344. Article CAS Google Scholar Ziepert M, Hasenclever D, Kuhnt E, Glass B, Schmitz N, Pfreundschuh M et al . Standard international prognostic index remains …
nl
(code pays fourni par la source)
Accès ouvert
2013
article
OpenAlex
Willem Kraan, Hugo M. Horlings, Martine van Keimpema, Esther J.M. Schilder-Tol et autres
Activating mutations in CD79 and MYD88 have recently been found in a subset of diffuse large B-cell lymphoma (DLBCL), identifying B-cell receptor and MYD88 signalling as potential therapeutic targets for personalized treatment. Here, we report the prevalence of CD79B and MYD88 mutations …
nl
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Accès ouvert
2013
article
OpenAlex
Carolien M. Woolthuis, André B. Mulder, Rikst Nynke Verkaik‐Schakel, S. Rosati et autres
Mutations of nucleophosmin 1 are frequently found in acute myeloid leukemia and lead to aberrant cytoplasmic accumulation of nucleophosmin protein. Immunohistochemical staining is therefore recommended as the technique of choice in front-line screening. In this study, we assessed the sensitivity and specificity …
nl
(code pays fourni par la source)
2013
article
OpenAlex
Wouter J. Pattje, Lieuwe J. Melchers, Lorian Slagter‐Menkema, M F Mastik et autres
AIMS: The Fas-associated death domain gene (FADD) is often overexpressed in squamous cell carcinoma of the head and neck (HNSCC), and is considered to be a driver gene in amplification of the chromosomal 11q13.3 region. Amplification of 11q13.3 is associated with increased …
nl
(code pays fourni par la source)
Accès ouvert
2012
article
OpenAlex
Iván Álvarez‐Twöse, Almudena Matito, Laura Sánchez‐Muñoz, José Mário Morgado et autres
es, nl
(code pays fourni par la source)
Accès ouvert
2012
article
OpenAlex
Jaap J. van Doormaal, Eveline van der Veer, Pieter C. van Voorst Vader, P.M. Kluin et autres
BACKGROUND: Risk indicators of indolent systemic mastocytosis (ISM) in adults with clinical suspicion of ISM without accompanying skin lesions [urticaria pigmentosa (UP)] are lacking. This study aimed at creating a decision tree using clinical characteristics, serum tryptase, and the urinary histamine metabolites …
nl
(code pays fourni par la source)
2011
article
OpenAlex
Carolien M. Woolthuis, Rikst Nynke Verkaik‐Schakel, Djoke van Gosliga, P.M. Kluin et autres
nl, cn
(code pays fourni par la source)
2011
article
OpenAlex
Hendrik J.M. de Jonge, Carolien M. Woolthuis, AnneMarie Vos, André B. Mulder et autres
nl
(code pays fourni par la source)
2010
article
OpenAlex
Carolien M. Woolthuis, Hendrik J.M. de Jonge, Annet Z Vos, André B. Mulder et autres
Abstract Abstract 952 Acute myeloid leukemia (AML) is clinically, cytogenetically and molecularly a heterogeneous disease which makes it challenging to classify it properly. In recent years major advances have been achieved in predicting outcome. However, there is still need for more powerful …
nl
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Accès ouvert
2009
conference-paper
OpenAlex
Huib de Ridder, Johanna G. de Ridder-Sluiter, P.M. Kluin, Henri Christiaans
Ubiquitous computing (or Ambient Intelligence) is an upcoming technology that is usually associated with futuristic smart environments in which information is available anytime anywhere and with which humans can interact in a natural, multimodal way. However spectacular the corresponding scenarios may be, …
2008
article
OpenAlex
Michiel L. Schrijvers, Bernard F. A. M. van der Laan, Geertruida H. de Bock, Wouter J. Pattje et autres
nl
(code pays fourni par la source)
2008
article
OpenAlex
Robert E. Kibbelaar, Harmen Van Kamp, EJ Dreef, J.W. Wessels et autres
An alphoid repetitive DNA (D8Z2) probe specific for the pericentromeric region of chromosome 8 was used to detect extra copies of chromosome 8 in bone marrow cells obtained from 10 patients with hematological disorders and five controls. Numerical aberrations of chromosome 8 …
nl
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