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Filip Pattyn

Showing results (21-30 of 33) with videos related to

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Genome Biology|October 15, 2008
Distinct transcriptional MYCN/c-MYC activities are associated with spontaneous regression or malignant progression in neuroblastomasFrank Westermann, Daniel Muth, Axel Benner, et al.
BMC Bioinformatics|May 22, 2010
Analysing 454 amplicon resequencing experiments using the modular and database oriented Variant Identification PipelineJoachim M De Schrijver, Kim De Leeneer, Steve Lefever, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2012
Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosisFrauke Coppieters, Bram De Wilde, Steve Lefever, et al.
Plos One|August 27, 2013
Effective Alu repeat based RT-Qpcr normalization in cancer cell perturbation experimentsAli Rihani, Tom Van Maerken, Filip Pattyn, et al.
BMC Bioinformatics|May 25, 2005
arrayCGHbase: an analysis platform for comparative genomic hybridization microarraysBjörn Menten, Filip Pattyn, Katleen De Preter, et al.
Biotechnology and Bioengineering|October 16, 2019
Unraveling and resolving inefficient glucolipid biosurfactants production through quantitative multiomics analyses of Starmerella bombicola strainsSofie Lodens, Sophie L K W Roelants, Katarzyna Ciesielska, et al.
Plos One|October 8, 2011
Practical tools to implement massive parallel pyrosequencing of PCR products in next generation molecular diagnosticsKim De Leeneer, Joachim De Schrijver, Lieven Clement, et al.
Nucleic Acids Research|April 30, 2013
MYCN and HDAC2 cooperate to repress miR-183 signaling in neuroblastomaMarco Lodrini, Ina Oehme, Christina Schroeder, et al.
BMC Medical Genomics|May 22, 2012
Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platformSarah De Keulenaer, Jan Hellemans, Steve Lefever, et al.
International Journal of Cancer|July 29, 2011
Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomasAnnelies Fieuw, Candy Kumps, Alexander Schramm, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Genome Biology|October 15, 2008
Distinct transcriptional MYCN/c-MYC activities are associated with spontaneous regression or malignant progression in neuroblastomasFrank Westermann, Daniel Muth, Axel Benner, et al.
BMC Bioinformatics|May 22, 2010
Analysing 454 amplicon resequencing experiments using the modular and database oriented Variant Identification PipelineJoachim M De Schrijver, Kim De Leeneer, Steve Lefever, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2012
Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosisFrauke Coppieters, Bram De Wilde, Steve Lefever, et al.
Plos One|August 27, 2013
Effective Alu repeat based RT-Qpcr normalization in cancer cell perturbation experimentsAli Rihani, Tom Van Maerken, Filip Pattyn, et al.
BMC Bioinformatics|May 25, 2005
arrayCGHbase: an analysis platform for comparative genomic hybridization microarraysBjörn Menten, Filip Pattyn, Katleen De Preter, et al.
Biotechnology and Bioengineering|October 16, 2019
Unraveling and resolving inefficient glucolipid biosurfactants production through quantitative multiomics analyses of Starmerella bombicola strainsSofie Lodens, Sophie L K W Roelants, Katarzyna Ciesielska, et al.
Plos One|October 8, 2011
Practical tools to implement massive parallel pyrosequencing of PCR products in next generation molecular diagnosticsKim De Leeneer, Joachim De Schrijver, Lieven Clement, et al.
Nucleic Acids Research|April 30, 2013
MYCN and HDAC2 cooperate to repress miR-183 signaling in neuroblastomaMarco Lodrini, Ina Oehme, Christina Schroeder, et al.
BMC Medical Genomics|May 22, 2012
Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platformSarah De Keulenaer, Jan Hellemans, Steve Lefever, et al.
International Journal of Cancer|July 29, 2011
Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomasAnnelies Fieuw, Candy Kumps, Alexander Schramm, et al.
Pageof 4