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Gerben van der Vries

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Lung Cancer (Amsterdam, Netherlands)|March 28, 2009
Genomic aberrations in squamous cell lung carcinoma related to lymph node or distant metastasisMirjam C Boelens, Klaas Kok, Pieter van der Vlies, et al.
Lung Cancer (Amsterdam, Netherlands)|September 14, 2010
A chronic obstructive pulmonary disease related signature in squamous cell lung cancerMirjam C Boelens, Adam M Gustafson, Dirkje S Postma, et al.
Journal of Personalized Medicine|December 29, 2020
Practical Barriers and Facilitators Experienced by Patients, Pharmacists and Physicians to the Implementation of Pharmacogenomic Screening in Dutch Outpatient Hospital Care-An Explorative Pilot StudyPauline Lanting, Evelien Drenth, Ludolf Boven, et al.
Scientific Reports|October 12, 2019
Transcriptome analysis suggests a compensatory role of the cofactors coenzyme A and NAD<sup>+</sup> in medium-chain acyl-CoA dehydrogenase knockout miceAnne-Claire M F Martines, Albert Gerding, Sarah Stolle, et al.
European Journal of Human Genetics : EJHG|September 22, 2011
Practical guidelines for interpreting copy number gains detected by high-resolution array in routine diagnosticsNicolien M Hanemaaijer, Birgit Sikkema-Raddatz, Gerben van der Vries, et al.
International Journal of Molecular Sciences|April 17, 2025
Nanopore Long-Read Sequencing as a First-Tier Diagnostic Test to Detect Repeat Expansions in Neurological DisordersEddy N de Boer, Arjen J Scheper, Dennis Hendriksen, et al.
Aging Cell|November 10, 2017
Running-wheel activity delays mitochondrial respiratory flux decline in aging mouse muscle via a post-transcriptional mechanismSarah Stolle, Jolita Ciapaite, Aaffien C Reijne, et al.
Frontiers in Immunology|June 12, 2026
A multidisciplinary RNA-guided approach to complement genomic analysis of unsolved patients with an inborn error of immunityWillem T K Maassen, Lotte C E T Pape, Tim Niemeijer, et al.
Brain : a Journal of Neurology|October 21, 2017
Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxiaEsther A R Nibbeling, Anna Duarri, Corien C Verschuuren-Bemelmans, et al.
Gigascience|September 20, 2024
An interconnected data infrastructure to support large-scale rare disease researchLennart F Johansson, Steve Laurie, Dylan Spalding, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Lung Cancer (Amsterdam, Netherlands)|March 28, 2009
Genomic aberrations in squamous cell lung carcinoma related to lymph node or distant metastasisMirjam C Boelens, Klaas Kok, Pieter van der Vlies, et al.
Lung Cancer (Amsterdam, Netherlands)|September 14, 2010
A chronic obstructive pulmonary disease related signature in squamous cell lung cancerMirjam C Boelens, Adam M Gustafson, Dirkje S Postma, et al.
Journal of Personalized Medicine|December 29, 2020
Practical Barriers and Facilitators Experienced by Patients, Pharmacists and Physicians to the Implementation of Pharmacogenomic Screening in Dutch Outpatient Hospital Care-An Explorative Pilot StudyPauline Lanting, Evelien Drenth, Ludolf Boven, et al.
Scientific Reports|October 12, 2019
Transcriptome analysis suggests a compensatory role of the cofactors coenzyme A and NAD<sup>+</sup> in medium-chain acyl-CoA dehydrogenase knockout miceAnne-Claire M F Martines, Albert Gerding, Sarah Stolle, et al.
European Journal of Human Genetics : EJHG|September 22, 2011
Practical guidelines for interpreting copy number gains detected by high-resolution array in routine diagnosticsNicolien M Hanemaaijer, Birgit Sikkema-Raddatz, Gerben van der Vries, et al.
International Journal of Molecular Sciences|April 17, 2025
Nanopore Long-Read Sequencing as a First-Tier Diagnostic Test to Detect Repeat Expansions in Neurological DisordersEddy N de Boer, Arjen J Scheper, Dennis Hendriksen, et al.
Aging Cell|November 10, 2017
Running-wheel activity delays mitochondrial respiratory flux decline in aging mouse muscle via a post-transcriptional mechanismSarah Stolle, Jolita Ciapaite, Aaffien C Reijne, et al.
Frontiers in Immunology|June 12, 2026
A multidisciplinary RNA-guided approach to complement genomic analysis of unsolved patients with an inborn error of immunityWillem T K Maassen, Lotte C E T Pape, Tim Niemeijer, et al.
Brain : a Journal of Neurology|October 21, 2017
Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxiaEsther A R Nibbeling, Anna Duarri, Corien C Verschuuren-Bemelmans, et al.
Gigascience|September 20, 2024
An interconnected data infrastructure to support large-scale rare disease researchLennart F Johansson, Steve Laurie, Dylan Spalding, et al.
Pageof 2