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Tom van Wezel

Showing results (191-200 of 212) with videos related to

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Nature Genetics|November 8, 2011
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndromeTwinkal C Pansuriya, Ronald van Eijk, Pio d'Adamo, et al.
Human Molecular Genetics|November 15, 2011
Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13Sarah L Spain, Luis G Carvajal-Carmona, Kimberley M Howarth, et al.
Plos One|September 17, 2013
Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibilitySimone Picelli, Justo Lorenzo Bermejo, Jenny Chang-Claude, et al.
Nature Communications|June 8, 2021
Robust detection of translocations in lymphoma FFPE samples using targeted locus capture-based sequencingAmin Allahyar, Mark Pieterse, Joost Swennenhuis, et al.
The Lancet. Gastroenterology & Hepatology|April 14, 2017
Somatic POLE proofreading domain mutation, immune response, and prognosis in colorectal cancer: a retrospective, pooled biomarker studyEnric Domingo, Luke Freeman-Mills, Emily Rayner, et al.
Frontiers in Immunology|January 31, 2020
Apparent Lack of <i>BRAF</i><sup></sup> Derived HLA Class I Presented Neoantigens Hampers Neoplastic Cell Targeting by CD8<sup>+</sup> T Cells in Langerhans Cell HistiocytosisPaul G Kemps, Timo C Zondag, Eline C Steenwijk, et al.
Virchows Archiv : an International Journal of Pathology|March 20, 2019
Recommendations for the clinical interpretation and reporting of copy number gains using gene panel NGS analysis in routine diagnosticsAstrid Eijkelenboom, Bastiaan B J Tops, Anke van den Berg, et al.
Blood Advances|September 3, 2021
Frequent mutated B2M, EZH2, IRF8, and TNFRSF14 in primary bone diffuse large B-cell lymphoma reflect a GCB phenotypeRuben A L de Groen, Ronald van Eijk, Stefan Böhringer, et al.
Leukemia|March 5, 2020
Comprehensive diagnostics of acute myeloid leukemia by whole transcriptome RNA sequencingWibowo Arindrarto, Daniel M Borràs, Ruben A L de Groen, et al.
Blood|September 24, 2024
Recurrent CLTC::SYK fusions and CSF1R mutations in juvenile xanthogranuloma of soft tissuePaul G Kemps, Hans J Baelde, Ruben H P Vorderman, et al.
Pageof 22

Showing results (191-200 of 212) with videos related to

Sort By:
Pageof 22
Nature Genetics|November 8, 2011
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndromeTwinkal C Pansuriya, Ronald van Eijk, Pio d'Adamo, et al.
Human Molecular Genetics|November 15, 2011
Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13Sarah L Spain, Luis G Carvajal-Carmona, Kimberley M Howarth, et al.
Plos One|September 17, 2013
Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibilitySimone Picelli, Justo Lorenzo Bermejo, Jenny Chang-Claude, et al.
Nature Communications|June 8, 2021
Robust detection of translocations in lymphoma FFPE samples using targeted locus capture-based sequencingAmin Allahyar, Mark Pieterse, Joost Swennenhuis, et al.
The Lancet. Gastroenterology & Hepatology|April 14, 2017
Somatic POLE proofreading domain mutation, immune response, and prognosis in colorectal cancer: a retrospective, pooled biomarker studyEnric Domingo, Luke Freeman-Mills, Emily Rayner, et al.
Frontiers in Immunology|January 31, 2020
Apparent Lack of <i>BRAF</i><sup></sup> Derived HLA Class I Presented Neoantigens Hampers Neoplastic Cell Targeting by CD8<sup>+</sup> T Cells in Langerhans Cell HistiocytosisPaul G Kemps, Timo C Zondag, Eline C Steenwijk, et al.
Virchows Archiv : an International Journal of Pathology|March 20, 2019
Recommendations for the clinical interpretation and reporting of copy number gains using gene panel NGS analysis in routine diagnosticsAstrid Eijkelenboom, Bastiaan B J Tops, Anke van den Berg, et al.
Blood Advances|September 3, 2021
Frequent mutated B2M, EZH2, IRF8, and TNFRSF14 in primary bone diffuse large B-cell lymphoma reflect a GCB phenotypeRuben A L de Groen, Ronald van Eijk, Stefan Böhringer, et al.
Leukemia|March 5, 2020
Comprehensive diagnostics of acute myeloid leukemia by whole transcriptome RNA sequencingWibowo Arindrarto, Daniel M Borràs, Ruben A L de Groen, et al.
Blood|September 24, 2024
Recurrent CLTC::SYK fusions and CSF1R mutations in juvenile xanthogranuloma of soft tissuePaul G Kemps, Hans J Baelde, Ruben H P Vorderman, et al.
Pageof 22