Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Tamara C Pereboom"'
Autor:
Ana T Antunes, Yvonne J Goos, Tamara C Pereboom, Dorien Hermkens, Marcin W Wlodarski, Lydie Da Costa, Alyson W MacInnes
Publikováno v:
PLoS Genetics, Vol 11, Iss 7, p e1005326 (2015)
Mutations in ribosomal protein (RP) genes can result in the loss of erythrocyte progenitor cells and cause severe anemia. This is seen in patients with Diamond-Blackfan anemia (DBA), a pure red cell aplasia and bone marrow failure syndrome that is al
Externí odkaz:
https://doaj.org/article/8d54beec57654e45a3121edf3afcc78a
Autor:
Harry F Heijnen, Richard van Wijk, Tamara C Pereboom, Yvonne J Goos, Cor W Seinen, Brigitte A van Oirschot, Rowie van Dooren, Marc Gastou, Rachel H Giles, Wouter van Solinge, Taco W Kuijpers, Hanna T Gazda, Marc B Bierings, Lydie Da Costa, Alyson W MacInnes
Publikováno v:
PLoS Genetics, Vol 10, Iss 5, p e1004371 (2014)
Mutations affecting the ribosome lead to several diseases known as ribosomopathies, with phenotypes that include growth defects, cytopenia, and bone marrow failure. Diamond-Blackfan anemia (DBA), for example, is a pure red cell aplasia linked to the
Externí odkaz:
https://doaj.org/article/25556d82d8954cb899e0a1e170a1ff3c
Autor:
Justin J. Taylor, Tamara C. Pereboom, Timm Maier, Christoph Hess, Ludivine C. Litzler, David Schreiner, Yusuf I. Ertuna, Nivedya Swarnalekha, Julien Roux, Carolyn G. King, Jonas Lötscher, Florian Geier, Roman P. Jakob, Marco Künzli
CD4; +; memory T cells play an important role in protective immunity and are a key target in vaccine development. Many studies have focused on T central memory (T; cm; ) cells, whereas the existence and functional significance of long-lived T follicu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13b50f08d99b866bbd83994dae4f9554
https://edoc.unibas.ch/78829/
https://edoc.unibas.ch/78829/
Autor:
Florian Geier, Nivedya Swarnalekha, J. T. Taylor, Carolyn G. King, Marco Künzli, Jonas Lötscher, David Schreiner, Tamara C. Pereboom, Julien Roux, Yusuf I. Ertuna, Christoph Hess
SUMMARYCD4 memory T cells play an important role in protective immunity and are a key target in vaccine development. Many studies have focused on T central memory (TCM) cells, while the existence and functional significance of T follicular helper (TF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b998ce2aac9daa0bdce8f5147a38d55c
https://doi.org/10.1101/677559
https://doi.org/10.1101/677559
Publikováno v:
Blood, 118(20), 5458-5465. American Society of Hematology
Dyskeratosis congenita (DC) is a bone marrow failure disorder characterized by shortened telomeres, defective stem cell maintenance, and highly heterogeneous phenotypes affecting predominantly tissues that require high rates of turnover. Here we pres
Autor:
Oliver Rothfuss, Thorsten Schaefer, Martina Konantz, Claudia Lengerke, Tamara C. Pereboom, Anna M. Paczulla, Lothar Kanz, Britta Merz, Hui Wang, Klaus Schulze-Osthoff, Perihan Mir, Tanja Fehm, Sven Perner
Publikováno v:
Oncotarget
The transcription factor SOX2 is a key regulator of pluripotency in embryonic stem cells and plays important roles in early organogenesis. Recently, SOX2 expression was documented in various cancers and suggested as a cancer stem cell (CSC) marker. H
Autor:
Alyson W. MacInnes, Tamara C. Pereboom, Paul B. Essers, M Nicastro, Rachel H. Giles, Karsten Boldt, Timothy D. Klasson, Dorus A. Mans
Publikováno v:
Oncogene, 34(6), 771-9. Nature Publishing Group
Oncogene, 34(6), 771. Nature Publishing Group
Oncogene, 34(6), 771. Nature Publishing Group
Functional loss of the von Hippel-Lindau (VHL) tumor suppressor protein (pVHL), which is part of an E3-ubiquitin ligase complex, initiates most inherited and sporadic clear-cell renal cell carcinomas (ccRCC). Genetic inactivation of the TP53 gene in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8772c7df2b930ddb7593fbd3460a84f8
https://pure.knaw.nl/portal/en/publications/e66241dc-adf0-4432-a048-a980ee19e2d8
https://pure.knaw.nl/portal/en/publications/e66241dc-adf0-4432-a048-a980ee19e2d8
Autor:
Lydie Da Costa, Tamara C. Pereboom, Wouter W. van Solinge, Marc Gastou, Taco W. Kuijpers, Rachel H. Giles, Brigitte A. van Oirschot, Hanna T. Gazda, Rowie van Dooren, Alyson W. MacInnes, Richard van Wijk, Harry F. G. Heijnen, Yvonne J. Goos, Cor W. Seinen, Marc Bierings
Publikováno v:
PLoS Genetics
PLoS genetics, 10(5). Public Library of Science
PLoS Genetics, 10(5). Public Library of Science
PLoS Genetics, Vol 10, Iss 5, p e1004371 (2014)
PLoS genetics, 10(5). Public Library of Science
PLoS Genetics, 10(5). Public Library of Science
PLoS Genetics, Vol 10, Iss 5, p e1004371 (2014)
Mutations affecting the ribosome lead to several diseases known as ribosomopathies, with phenotypes that include growth defects, cytopenia, and bone marrow failure. Diamond-Blackfan anemia (DBA), for example, is a pure red cell aplasia linked to the
Autor:
Tamara C. Pereboom, Martina Konantz, Oliver K. Rothfuss, Tanja Fehm, Britta Merz, Thorsten Schaefer, Hui Wang, Sven Perner, Klaus Schulze-Osthoff, Claudia Lengerke, Perihan Mir, Lothar Kanz
Publikováno v:
Cancer Research. 76:PR06-PR06
The pluripotency-associated transcription factor SOX2 (Sex determining region Y - Box 2) is a key regulator of early organogenesis and embryonic stem cell fate. Supporting the notion that embryonic pathways may reactivate during oncogenesis, SOX2 exp
Autor:
Sebastiaan eWesseling, Paul B. Essers, Maarten P. Koeners, Tamara C. Pereboom, Branko eBraam, Ernst E. van Faassen, Alyson W. MacInnes, Jaap A. Joles
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, 2:52. Frontiers Media SA
Frontiers in Genetics, Vol 2 (2011)
Frontiers in Genetics, 2:52. Frontiers Media SA
Frontiers in Genetics, Vol 2 (2011)
Nitric oxide (NO) is known to depress ribosome biogenesis in vitro. In this study we analyzed the influence of exogenous NO on ribosome biogenesis in vivo using a proven antihypertensive model of perinatal NO administration in genetically hypertensiv