Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sam, de Blank"'
Autor:
Bernadette Jeremiasse, Ravian L van Ineveld, Veerle Bok, Michiel Kleinnijenhuis, Sam de Blank, Maria Alieva, Hannah R Johnson, Esmée J van Vliet, Amber L Zeeman, Lianne M Wellens, Gerard Llibre-Palomar, Mario Barrera Román, Alessia Di Maggio, Johanna F Dekkers, Sabrina Oliveira, Alexander L Vahrmeijer, Jan J Molenaar, Marc HWA Wijnen, Alida FW van der Steeg, Ellen J Wehrens, Anne C Rios
Publikováno v:
EMBO Molecular Medicine, Vol 16, Iss 7, Pp 1495-1514 (2024)
Abstract Achieving complete tumor resection is challenging and can be improved by real-time fluorescence-guided surgery with molecular-targeted probes. However, pre-clinical identification and validation of probes presents a lengthy process that is t
Externí odkaz:
https://doaj.org/article/59beb6ac34b24791970db0bb11a508eb
Autor:
Jose Espejo Valle-Inclan, Christina Stangl, Anouk C. de Jong, Lisanne F. van Dessel, Markus J. van Roosmalen, Jean C. A. Helmijr, Ivo Renkens, Roel Janssen, Sam de Blank, Chris J. de Witte, John W. M. Martens, Maurice P. H. M. Jansen, Martijn P. Lolkema, Wigard P. Kloosterman
Publikováno v:
Genome Medicine, Vol 13, Iss 1, Pp 1-14 (2021)
Abstract Here, we describe a novel approach for rapid discovery of a set of tumor-specific genomic structural variants (SVs), based on a combination of low coverage cancer genome sequencing using Oxford Nanopore with an SV calling and filtering pipel
Externí odkaz:
https://doaj.org/article/dc2d84df5339442da6944319858a489d
Autor:
Christina Stangl, Sam de Blank, Ivo Renkens, Liset Westera, Tamara Verbeek, Jose Espejo Valle-Inclan, Rocio Chamorro González, Anton G. Henssen, Markus J. van Roosmalen, Ronald W. Stam, Emile E. Voest, Wigard P. Kloosterman, Gijs van Haaften, Glen R. Monroe
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-14 (2020)
Fusion genes are a hallmarks of cancer, though breakpoint-position promiscuity restricts diagnostic detection. Here, the authors present FUDGE, a CRISPR-Cas9-based enrichment strategy for nanopore sequencing to identify target fusions irrespective of
Externí odkaz:
https://doaj.org/article/e33d69e505f647c4a248cf888947cfbb
Autor:
Maria Alieva, Frank L. Bos, Anne C. Rios, Ellen J. Wehrens, Johanna F. Dekkers, Michiel Kleinnijenhuis, Hannah Johnson, Jarno Drost, Clara Martínez Mir, Raimond Heukers, Mario Barrera Roman, Sam de Blank, Esmée J. van Vliet, Ravian L. van Ineveld, Susana M. Chuva de Sousa Lopes
Publikováno v:
Nature Biotechnology
Nature Biotechnology, 39(10), 1239-1245. NATURE RESEARCH
Nature Biotechnology, 39(10), 1239-1245. NATURE RESEARCH
Despite advances in three-dimensional (3D) imaging, it remains challenging to profile all the cells within a large 3D tissue, including the morphology and organization of the many cell types present. Here, we introduce eight-color, multispectral, lar
Autor:
Johanna F. Dekkers, Maria Alieva, Astrid Cleven, Farid Keramati, Amber K. L. Wezenaar, Esmée J. van Vliet, Jens Puschhof, Peter Brazda, Inez Johanna, Angelo D. Meringa, Heggert G. Rebel, Maj-Britt Buchholz, Mario Barrera Román, Amber L. Zeeman, Sam de Blank, Domenico Fasci, Maarten H. Geurts, Annelisa M. Cornel, Else Driehuis, Rosemary Millen, Trudy Straetemans, Mara J. T. Nicolasen, Tineke Aarts-Riemens, Hendrikus C. R. Ariese, Hannah R. Johnson, Ravian L. van Ineveld, Froso Karaiskaki, Oded Kopper, Yotam E. Bar-Ephraim, Kai Kretzschmar, Alexander M. M. Eggermont, Stefan Nierkens, Ellen J. Wehrens, Henk G. Stunnenberg, Hans Clevers, Jürgen Kuball, Zsolt Sebestyen, Anne C. Rios
Publikováno v:
Nature Biotechnology. Nature Publishing Group
Extending the success of cellular immunotherapies against blood cancers to the realm of solid tumors will require improved in vitro models that reveal therapeutic modes of action at the molecular level. Here we describe a system, called BEHAV3D, deve
Autor:
Chris J. de Witte, Roel Janssen, Wigard P. Kloosterman, Martijn P. Lolkema, Christina Stangl, Markus J. van Roosmalen, Jose Espejo Valle-Inclan, Anouk C. de Jong, Jean C. A. Helmijr, Sam de Blank, Maurice P.H.M. Jansen, Ivo Renkens, John W.M. Martens, Lisanne F. van Dessel
Publikováno v:
Genome Medicine, Vol 13, Iss 1, Pp 1-14 (2021)
Genome Medicine
Genome Medicine, 13(1):86. BioMed Central Ltd.
Genome Medicine
Genome Medicine, 13(1):86. BioMed Central Ltd.
Here, we describe a novel approach for rapid discovery of a set of tumor-specific genomic structural variants (SVs), based on a combination of low coverage cancer genome sequencing using Oxford Nanopore with an SV calling and filtering pipeline. We a
Autor:
Ravian L, van Ineveld, Michiel, Kleinnijenhuis, Maria, Alieva, Sam, de Blank, Mario, Barrera Roman, Esmée J, van Vliet, Clara, Martínez Mir, Hannah R, Johnson, Frank L, Bos, Raimond, Heukers, Susana M, Chuva de Sousa Lopes, Jarno, Drost, Johanna F, Dekkers, Ellen J, Wehrens, Anne C, Rios
Publikováno v:
Nature biotechnology. 39(10)
Despite advances in three-dimensional (3D) imaging, it remains challenging to profile all the cells within a large 3D tissue, including the morphology and organization of the many cell types present. Here, we introduce eight-color, multispectral, lar
Autor:
Martijn P. Lolkema, Maurice P.H.M. Jansen, Christina Stangl, Wigard P. Kloosterman, Jean C. A. Helmijr, Ivo Renkens, Markus J. van Roosmalen, Lisanne F. van Dessel, Anouk C. de Jong, John W.M. Martens, Sam de Blank, Jose Espejo Valle-Inclan, Chris J. de Witte
Somatic genomic structural variations (SVs) are promising personalized biomarkers for sensitive and specific detection of circulating tumor DNA (ctDNA) in liquid biopsies. However, affordable and fast identification of such SV biomarkers is challengi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d2d249cec9ba1c04d210754386d6638
https://doi.org/10.1101/19011932
https://doi.org/10.1101/19011932
Autor:
Tamara Verbeek, Gijs van Haaften, Ivo Renkens, Markus J. van Roosmalen, Emile E. Voest, Jose Espejo Valle-Inclan, Wigard P. Kloosterman, Christina Stangl, Anton G. Henssen, Sam de Blank, Ronald W. Stam, Rocío Chamorro González, Glen R. Monroe
Fusion genes are hallmarks of various cancer types and important determinants for diagnosis, prognosis and treatment possibilities. The promiscuity of fusion genes with respect to partner choice and exact breakpoint-positions restricts their detectio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cbf643ba2910e04f3ed8a36fe8cf98f
https://doi.org/10.1101/807545
https://doi.org/10.1101/807545