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David Creytens

Showing results (111-120 of 118) with videos related to

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Clinical and Translational Medicine|June 23, 2026
A living biobank of sarcoma patient-derived cell cultures reveals multi-omic and functional insights that capture disease heterogeneityStefanie Gijsels, Suzanne Fischer, David Creytens, et al.
Skeletal Radiology|July 18, 2023
Evaluation of response to neoadjuvant chemotherapy in osteosarcoma using dynamic contrast-enhanced MRI: development and external validation of a modelGijsbert M Kalisvaart, Thomas Van Den Berghe, Willem Grootjans, 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.
Acta Neuropathologica|December 17, 2020
Atypical teratoid/rhabdoid tumors (ATRTs) with SMARCA4 mutation are molecularly distinct from SMARCB1-deficient casesDörthe Holdhof, Pascal D Johann, Michael Spohn, et al.
Frontiers in Cell and Developmental Biology|May 10, 2021
Long-Read Sequencing to Unravel Complex Structural Variants of <i>CEP78</i> Leading to Cone-Rod Dystrophy and Hearing LossGiulia Ascari, Nanna D Rendtorff, Marieke De Bruyne, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 6, 2019
Homozygous <i>NLRP1</i> gain-of-function mutation in siblings with a syndromic form of recurrent respiratory papillomatosisScott B Drutman, Filomeen Haerynck, Franklin L Zhong, et al.
Human Mutation|January 31, 2020
Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertilityGiulia Ascari, Frank Peelman, Pietro Farinelli, et al.
Nature Communications|March 7, 2023
SOX11 regulates SWI/SNF complex components as member of the adrenergic neuroblastoma core regulatory circuitryBieke Decaesteker, Amber Louwagie, Siebe Loontiens, et al.
Pageof 12

Showing results (111-120 of 118) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 118 results.
Clinical and Translational Medicine|June 23, 2026
A living biobank of sarcoma patient-derived cell cultures reveals multi-omic and functional insights that capture disease heterogeneityStefanie Gijsels, Suzanne Fischer, David Creytens, et al.
Skeletal Radiology|July 18, 2023
Evaluation of response to neoadjuvant chemotherapy in osteosarcoma using dynamic contrast-enhanced MRI: development and external validation of a modelGijsbert M Kalisvaart, Thomas Van Den Berghe, Willem Grootjans, 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.
Acta Neuropathologica|December 17, 2020
Atypical teratoid/rhabdoid tumors (ATRTs) with SMARCA4 mutation are molecularly distinct from SMARCB1-deficient casesDörthe Holdhof, Pascal D Johann, Michael Spohn, et al.
Frontiers in Cell and Developmental Biology|May 10, 2021
Long-Read Sequencing to Unravel Complex Structural Variants of <i>CEP78</i> Leading to Cone-Rod Dystrophy and Hearing LossGiulia Ascari, Nanna D Rendtorff, Marieke De Bruyne, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 6, 2019
Homozygous <i>NLRP1</i> gain-of-function mutation in siblings with a syndromic form of recurrent respiratory papillomatosisScott B Drutman, Filomeen Haerynck, Franklin L Zhong, et al.
Human Mutation|January 31, 2020
Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertilityGiulia Ascari, Frank Peelman, Pietro Farinelli, et al.
Nature Communications|March 7, 2023
SOX11 regulates SWI/SNF complex components as member of the adrenergic neuroblastoma core regulatory circuitryBieke Decaesteker, Amber Louwagie, Siebe Loontiens, et al.
Pageof 12