Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Jana Lentes"'
Autor:
Ming Tang, Željko Antić, Pedram Fardzadeh, Stefan Pietzsch, Charlotte Schröder, Adrian Eberhardt, Alena van Bömmel, Gabriele Escherich, Winfried Hofmann, Martin A. Horstmann, Thomas Illig, J. Matt McCrary, Jana Lentes, Markus Metzler, Wolfgang Nejdl, Brigitte Schlegelberger, Martin Schrappe, Martin Zimmermann, Karolina Miarka-Walczyk, Agata Patsorczak, Gunnar Cario, Bernhard Y. Renard, Martin Stanulla, Anke Katharina Bergmann
Publikováno v:
EBioMedicine, Vol 104, Iss , Pp 105171- (2024)
Summary: Background: The increasing volume and intricacy of sequencing data, along with other clinical and diagnostic data, like drug responses and measurable residual disease, creates challenges for efficient clinical comprehension and interpretatio
Externí odkaz:
https://doaj.org/article/73ab5d4f744341ce91b017ca5e0c00a9
Autor:
Gunnar Cario, Veronica Leoni, Valentino Conter, Andishe Attarbaschi, Marketa Zaliova, Lucie Sramkova, Gianni Cazzaniga, Grazia Fazio, Rosemary Sutton, Sarah Elitzur, Shai Izraeli, Melchior Lauten, Franco Locatelli, Giuseppe Basso, Barbara Buldini, Anke K. Bergmann, Jana Lentes, Doris Steinemann, Gudrun Göhring, Brigitte Schlegelberger, Oskar A. Haas, Denis Schewe, Swantje Buchmann, Anja Moericke, Deborah White, Tamas Revesz, Martin Stanulla, Georg Mann, Nicole Bodmer, Nira Arad-Cohen, Jan Zuna, Maria Grazia Valsecchi, Martin Zimmermann, Martin Schrappe, Andrea Biondi
Publikováno v:
Haematologica, Vol 105, Iss 7 (2020)
ABL-class fusions other than BCR-ABL1 characterize around 2–3% of precursor B-cell acute lymphoblastic leukemia. Case series indicated that patients suffering from these subtypes have a dismal outcome and may benefit from the introduction of tyrosi
Externí odkaz:
https://doaj.org/article/7a041ae8297947418cbaf90c99555cfb
Autor:
Georgios Sogkas, Natalia Dubrowinskaja, Anke K. Bergmann, Jana Lentes, Tim Ripperger, Mykola Fedchenko, Diana Ernst, Alexandra Jablonka, Robert Geffers, Ulrich Baumann, Reinhold E. Schmidt, Faranaz Atschekzei
Publikováno v:
Diseases, Vol 7, Iss 2, p 34 (2019)
Immunodeficiency, centromeric instability and facial anomalies syndrome 2 (ICF2) is a rare autosomal recessive primary immunodeficiency disorder. So far, 27 patients have been reported. Here, we present three siblings with ICF2 due to a homozygous ZB
Externí odkaz:
https://doaj.org/article/a72a40d7dffc448e9ddd0a156553ee78
Autor:
Katharina Debowski, Rita Warthemann, Jana Lentes, Gabriela Salinas-Riester, Ralf Dressel, Daniel Langenstroth, Jörg Gromoll, Erika Sasaki, Rüdiger Behr
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0118424 (2015)
Groundbreaking studies showed that differentiated somatic cells of mouse and human origin could be reverted to a stable pluripotent state by the ectopic expression of only four proteins. The resulting pluripotent cells, called induced pluripotent ste
Externí odkaz:
https://doaj.org/article/1c64459cbf0748a2a49bd7ac1c87b915
Autor:
Francesco Ceppi, Giacomo Gotti, Anja Möricke, Daniela Silvestri, Fiona Poyer, Jana Lentes, Anke Bergmann, Jan Trka, Julia Alten, Sara Elitzur, Draga Barbaric, Barbara Buldini, Fabiola Dell'Acqua, Fabian Schumacher, Gabriella Casazza, Joelle Tchinda, Karin Nebral, Valentino Conter, Andishe Attarbaschi, Martin Schrappe
Publikováno v:
European Journal of Cancer. 175:120-124
Near-tetraploidy-defined by DNA index 1.79-2.28 or 81-103 chromosomes-is a rare cytogenetic abnormality observed both in children and adults with T-cell acute lymphoblastic leukaemia (T-ALL) and its prognostic value is not yet determined.We report a
Autor:
Martin Schrappe, Beate Kaune, Gudrun Göhring, Claudia Davenport, Maximilian Schieck, Mustafa Salim, Frederik Heldt, Kathrin Thomay, Winfried Hofmann, Yvonne Lisa Behrens, Brigitte Schlegelberger, Jana Lentes, Anja Möricke, Doris Steinemann, Gunnar Cario
Publikováno v:
Genes, Chromosomes and Cancer. 61:22-26
Acute lymphoblastic leukemia (ALL) is the most frequent malignancy in childhood and adolescence. In more than 60% of cases of this heterogeneous disease, a genetic marker is identified via cytogenetic or molecular analyses. TCF3 gene fusions occur in
Autor:
Željko Antić, Alena van Bömmel, Konstantin Riege, Jana Lentes, Charlotte Schröder, Julia Alten, Lara Fuhrmann, Martin Zimmermann, Cornelia Eckert, Gunnar Cario, Martin Schrappe, Brigitte Schlegelberger, Steve Hoffmann, Anke K. Bergmann
Publikováno v:
Blood. 140:9185-9186
Autor:
Martin Stanulla, Martin Schrappe, Brigitte Schlegelberger, Marie Wolter, Jana Lentes, Marie Stelter, Markéta Žaliová, Maximilian Schieck, Doris Steinemann, Anke K. Bergmann, Gunnar Cario, Jonathan Lukas Lühmann, Anja Möricke, Josephine Kater, Gudrun Göhring
Publikováno v:
Cancers, Vol 13, Iss 4388, p 4388 (2021)
Cancers
Volume 13
Issue 17
Cancers
Volume 13
Issue 17
Acute lymphoblastic leukemia (ALL) is the most prevalent type of cancer occurring in children. ALL is characterized by structural and numeric genomic aberrations that strongly correlate with prognosis and clinical outcome. Usually, a combination of c
Autor:
Claudia Davenport, Brigitte Schlegelberger, Andrea Schienke, Gudrun Göhring, Yvonne Lisa Behrens, Marcel Tauscher, Stefanie Joachim, Stephanie Knirsch, Mareike Rasche, Jana Lentes, Doris Steinemann, Dirk Reinhardt
Publikováno v:
Cancer genetics.
The co-occurrence of an inversion inv(3)(q21q26)/GATA2-MECOM and a Philadelphia translocation t(9;22)(q34;q11)/BCR-ABL1 in the context of chronic myeloid leukemia (CML) in blast crisis or acute myeloid leukemia (AML) has only rarely been described. T
Autor:
Marie Stelter, Martin Zimmermann, Marcel Tauscher, Mareike Jung, Brigitte Schlegelberger, Gunnar Cario, Martin Schrappe, Anke K. Bergmann, Winfried Hofmann, Julia Alten, Maximilian Schieck, Martin Stanulla, Anja Möricke, Doris Steinemann, Jana Lentes
Publikováno v:
Genes, Chromosomes & Cancer
PAX5 is a member of the paired box (PAX) family of transcription factors involved in B‐cell development. PAX5 P80R has recently been described as a distinct genetic B‐cell precursor (BCP) acute lymphoblastic leukemia (ALL) subtype with a favorabl