Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Joelle Tchinda"'
Autor:
Gabriele Manzella, Leonie D. Schreck, Willemijn B. Breunis, Jan Molenaar, Hans Merks, Frederic G. Barr, Wenyue Sun, Michaela Römmele, Luduo Zhang, Joelle Tchinda, Quy A. Ngo, Peter Bode, Olivier Delattre, Didier Surdez, Bharat Rekhi, Felix K. Niggli, Beat W. Schäfer, Marco Wachtel
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-15 (2020)
Patient-specific precision medicine approaches are important for future cancer therapies. Here, the authors show that functional drug profiling with Rhabdomyosarcoma cells isolated from PDX and primary patient tumors uncovers patient-specific vulnera
Externí odkaz:
https://doaj.org/article/e1a776112ff34407a13275f886ecd3a9
Intragenic amplification of PAX5: a novel subgroup in B-cell precursor acute lymphoblastic leukemia?
Autor:
Claire Schwab, Karin Nebral, Lucy Chilton, Cristina Leschi, Esmé Waanders, Judith M. Boer, Markéta Žaliová, Rosemary Sutton, Ingegerd Ivanov Öfverholm, Kentaro Ohki, Yuka Yamashita, Stefanie Groeneveld-Krentz, Eva Froňková, Marleen Bakkus, Joelle Tchinda, Thayana da Conceição Barbosa, Grazia Fazio, Wojciech Mlynarski, Agata Pastorczak, Giovanni Cazzaniga, Maria S. Pombo-de-Oliveira, Jan Trka, Renate Kirschner-Schwabe, Toshihiko Imamura, Gisela Barbany, Martin Stanulla, Andishe Attarbaschi, Renate Panzer-Grümayer, Roland P. Kuiper, Monique L. den Boer, Hélène Cavé, Anthony V. Moorman, Christine J. Harrison, Sabine Strehl
Publikováno v:
Blood Advances, Vol 1, Iss 19, Pp 1473-1477 (2017)
Externí odkaz:
https://doaj.org/article/64841652a85648169d0a262aedd8c662
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:
Mark A. Rubin, Arul M. Chinnaiyan, William R. Sellers, Charles Lee, Matthew Meyerson, Xiao-Wei Sun, Robert Vessella, Rainer Kuefer, Kenneth G. Pienta, Matthias D. Hofer, Scott A. Tomlins, Joelle Tchinda, Sunita Setlur, Juan-Miguel Mosquera, Folke H. Schmidt, Rameen Beroukhim, Francesca Demichelis, Sven Perner
Supplementary Figure 1 from TMPRSS2:ERG Fusion-Associated Deletions Provide Insight into the Heterogeneity of Prostate Cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::965503ec78ac456891c8965c797c17df
https://doi.org/10.1158/0008-5472.22364954
https://doi.org/10.1158/0008-5472.22364954
Autor:
Mark A. Rubin, Arul M. Chinnaiyan, William R. Sellers, Charles Lee, Matthew Meyerson, Xiao-Wei Sun, Robert Vessella, Rainer Kuefer, Kenneth G. Pienta, Matthias D. Hofer, Scott A. Tomlins, Joelle Tchinda, Sunita Setlur, Juan-Miguel Mosquera, Folke H. Schmidt, Rameen Beroukhim, Francesca Demichelis, Sven Perner
Supplementary Figure 3 from TMPRSS2:ERG Fusion-Associated Deletions Provide Insight into the Heterogeneity of Prostate Cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b069ad875f954be2fa773c2341fbe9c
https://doi.org/10.1158/0008-5472.22364948
https://doi.org/10.1158/0008-5472.22364948
Autor:
Mark A. Rubin, Arul M. Chinnaiyan, William R. Sellers, Charles Lee, Matthew Meyerson, Xiao-Wei Sun, Robert Vessella, Rainer Kuefer, Kenneth G. Pienta, Matthias D. Hofer, Scott A. Tomlins, Joelle Tchinda, Sunita Setlur, Juan-Miguel Mosquera, Folke H. Schmidt, Rameen Beroukhim, Francesca Demichelis, Sven Perner
Prostate cancer is a common and clinically heterogeneous disease with marked variability in progression. The recent identification of gene fusions of the 5′-untranslated region of TMPRSS2 (21q22.3) with the ETS transcription factor family members,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13ae7107bc4a75f20ba8311532d31579
https://doi.org/10.1158/0008-5472.c.6494447
https://doi.org/10.1158/0008-5472.c.6494447
Autor:
Mark A. Rubin, Arul M. Chinnaiyan, William R. Sellers, Charles Lee, Matthew Meyerson, Xiao-Wei Sun, Robert Vessella, Rainer Kuefer, Kenneth G. Pienta, Matthias D. Hofer, Scott A. Tomlins, Joelle Tchinda, Sunita Setlur, Juan-Miguel Mosquera, Folke H. Schmidt, Rameen Beroukhim, Francesca Demichelis, Sven Perner
Supplementary Figure 2 from TMPRSS2:ERG Fusion-Associated Deletions Provide Insight into the Heterogeneity of Prostate Cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86595b44d98762d54c31465c1ce6e239
https://doi.org/10.1158/0008-5472.22364951
https://doi.org/10.1158/0008-5472.22364951
Autor:
Federica Raimondi, Ulrich Siler, Oleksandr Pastukhov, Robert S. Pritchard, Joelle Tchinda, Martin Jinek, Janine Reichenbach, Dominik Wrona
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 17, Iss, Pp 936-943 (2020)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy. Methods & Clinical Development
Resurrection of non-processed pseudogenes may increase the efficacy of therapeutic gene editing, upon simultaneous targeting of a mutated gene and its highly homologous pseudogenes. To investigate the potency of this approach for clinical gene therap
Autor:
Nadine Van Roy, Kirsi Jahnukainen, Danielle E. Arnold, Sioban Keel, Katherine R. Calvo, Gudrun Göhring, Cristina Mecucci, Charlotte M. Niemeyer, Joelle Tchinda, Alison A. Bertuch, Jochen Buechner, Dennis D. Hickstein, Olga Haus, Peter Nöllke, Shlomit Barzilai-Birenboim, Courtney D. DiNardo, Martin Čermák, Helena Alaiz, Ayami Yoshimi, Hiroto Inaba, Sara Lewis, Steven M. Holland, Shinsuke Hirabayashi, Brigitte Schlegelberger, Victor B Pastor, Dominik Turkiewicz, Emilia J Kozyra, Hajnalka Andrikovics, Amy P. Hsu, Mark D. Fleming, David R. Betts, Henrik Hasle, Karin Nebral, Masahiro Onozawa, Valerie de Haas, Jan Stary, José Cervera, Francesco Pasquali, Akiko Shimamura, Kalliopi N. Manola, Michael Dworzak, Kiran Tawana, Zuzana Zemanova, Marcin W. Wlodarski, Shaohua Lei, H. Berna Beverloo, Brigitte Strahm
Publikováno v:
Kozyra, E J, Göhring, G, Hickstein, D D, Calvo, K R, DiNardo, C D, Dworzak, M, de Haas, V, Starý, J, Hasle, H, Shimamura, A, Fleming, M D, Inaba, H, Lewis, S, Hsu, A P, Holland, S M, Arnold, D E, Mecucci, C, Keel, S B, Bertuch, A A, Tawana, K, Barzilai, S, Hirabayashi, S, Onozawa, M, Lei, S, Alaiz, H, Andrikovics, H, Betts, D, Beverloo, B H, Buechner, J, Čermák, M, Cervera, J, Haus, O, Jahnukainen, K, Manola, K N, Nebral, K, Pasquali, F, Tchinda, J, Turkiewicz, D, Van Roy, N, Zemanova, Z, Pastor, V B, Strahm, B, Noellke, P, Niemeyer, C M, Schlegelberger, B, Yoshimi, A & Wlodarski, M W 2021, ' Association of unbalanced translocation der(1;7) with germline GATA2 mutations ', Blood, vol. 138, no. 23, pp. 2441-2445 . https://doi.org/10.1182/blood.2021012781
Blood, 138(23), 2441-2445. American Society of Hematology
Blood
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Blood, 138(23), 2441-2445. American Society of Hematology
Blood
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac915d144b3e5e29067d37c55b8eaea0
https://pure.au.dk/ws/files/274410748/Primary_cytotoxic_T_cell_lymphomas_harbor_recurrent_targetable_alterations_in_the_JAK_STAT_pathway.pdf
https://pure.au.dk/ws/files/274410748/Primary_cytotoxic_T_cell_lymphomas_harbor_recurrent_targetable_alterations_in_the_JAK_STAT_pathway.pdf
Autor:
Michèle Hoffmann, Yara Banz, Jörg Halter, Jacqueline Schoumans, Joëlle Tchinda, Ulrike Bacher, Thomas Pabst
Publikováno v:
Current Oncology, Vol 31, Iss 4, Pp 2067-2075 (2024)
Donor cell leukemia (DCL) is a rare complication after allogeneic hematopoietic stem cell transplantation (HSCT) accounting for 0.1% of relapses and presenting as secondary leukemia of donor origin. Distinct in phenotype and cytogenetics from the ori
Externí odkaz:
https://doaj.org/article/b7cce01b312e4f65b8657380b2efa76d