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J Meijers

Showing results (81-90 of 126) with videos related to

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Journal of Immunology (Baltimore, Md. : 1950)|December 15, 2019
Overexpression of SH2-Containing Inositol Phosphatase Contributes to Chronic Lymphocytic Leukemia SurvivalSimar Pal Singh, Marjolein J W de Bruijn, Catarina Velaso Gago da Graça, et al.
European Journal of Cancer (Oxford, England : 1990)|April 28, 2004
Ipsilateral breast tumour recurrence in hereditary breast cancer following breast-conserving therapyC Seynaeve, L C Verhoog, L M C van de Bosch, et al.
Molecular Genetics & Genomic Medicine|November 16, 2022
Combined germline pathogenic variants in FLCN and TP53 are associated with early onset renal cell carcinoma and brain tumorsIrma van de Beek, Iris E Glykofridis, Anja Wagner, et al.
American Journal of Human Genetics|February 1, 1996
Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16J Wijnen, P M Khan, H Vasen, et al.
The Journal of Molecular Diagnostics : JMD|July 30, 2023
Formalin-Fixed, Paraffin-Embedded-Targeted Locus Capture: A Next-Generation Sequencing Technology for Accurate DNA-Based Gene Fusion Detection in Bone and Soft Tissue TumorsEllen Stelloo, Ruud W J Meijers, Joost F Swennenhuis, et al.
Leukemia|June 15, 2019
Next-generation sequencing of immunoglobulin gene rearrangements for clonality assessment: a technical feasibility study by EuroClonality-NGSBlanca Scheijen, Ruud W J Meijers, Jos Rijntjes, et al.
Human Molecular Genetics|November 28, 2022
PRDM10 directs FLCN expression in a novel disorder overlapping with Birt-Hogg-Dubé syndrome and familial lipomatosisIrma van de Beek, Iris E Glykofridis, Jan C Oosterwijk, et al.
Journal of Medical Genetics|May 23, 2001
Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigreeA Wagner, Y Hendriks, E J Meijers-Heijboer, et al.
International Journal of Cancer|June 21, 2014
Improved overall survival after contralateral risk-reducing mastectomy in BRCA1/2 mutation carriers with a history of unilateral breast cancer: a prospective analysisBernadette A M Heemskerk-Gerritsen, Matti A Rookus, Cora M Aalfs, et al.
Acta Neuropathologica|November 4, 2022
NTRK rearrangements in a subset of NF1-related malignant peripheral nerve sheath tumors as novel actionable targetL S Hiemcke-Jiwa, M T Meister, E Martin, et al.
Pageof 13

Showing results (81-90 of 126) with videos related to

Sort By:
Pageof 13
Journal of Immunology (Baltimore, Md. : 1950)|December 15, 2019
Overexpression of SH2-Containing Inositol Phosphatase Contributes to Chronic Lymphocytic Leukemia SurvivalSimar Pal Singh, Marjolein J W de Bruijn, Catarina Velaso Gago da Graça, et al.
European Journal of Cancer (Oxford, England : 1990)|April 28, 2004
Ipsilateral breast tumour recurrence in hereditary breast cancer following breast-conserving therapyC Seynaeve, L C Verhoog, L M C van de Bosch, et al.
Molecular Genetics & Genomic Medicine|November 16, 2022
Combined germline pathogenic variants in FLCN and TP53 are associated with early onset renal cell carcinoma and brain tumorsIrma van de Beek, Iris E Glykofridis, Anja Wagner, et al.
American Journal of Human Genetics|February 1, 1996
Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16J Wijnen, P M Khan, H Vasen, et al.
The Journal of Molecular Diagnostics : JMD|July 30, 2023
Formalin-Fixed, Paraffin-Embedded-Targeted Locus Capture: A Next-Generation Sequencing Technology for Accurate DNA-Based Gene Fusion Detection in Bone and Soft Tissue TumorsEllen Stelloo, Ruud W J Meijers, Joost F Swennenhuis, et al.
Leukemia|June 15, 2019
Next-generation sequencing of immunoglobulin gene rearrangements for clonality assessment: a technical feasibility study by EuroClonality-NGSBlanca Scheijen, Ruud W J Meijers, Jos Rijntjes, et al.
Human Molecular Genetics|November 28, 2022
PRDM10 directs FLCN expression in a novel disorder overlapping with Birt-Hogg-Dubé syndrome and familial lipomatosisIrma van de Beek, Iris E Glykofridis, Jan C Oosterwijk, et al.
Journal of Medical Genetics|May 23, 2001
Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigreeA Wagner, Y Hendriks, E J Meijers-Heijboer, et al.
International Journal of Cancer|June 21, 2014
Improved overall survival after contralateral risk-reducing mastectomy in BRCA1/2 mutation carriers with a history of unilateral breast cancer: a prospective analysisBernadette A M Heemskerk-Gerritsen, Matti A Rookus, Cora M Aalfs, et al.
Acta Neuropathologica|November 4, 2022
NTRK rearrangements in a subset of NF1-related malignant peripheral nerve sheath tumors as novel actionable targetL S Hiemcke-Jiwa, M T Meister, E Martin, et al.
Pageof 13