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Frauke Coppieters

Showing results (1-10 of 53) with videos related to

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Human Mutation|August 7, 2010
CEP290, a gene with many faces: mutation overview and presentation of CEP290baseFrauke Coppieters, Steve Lefever, Bart P Leroy, et al.
Genes|May 15, 2019
Antisense Oligonucleotide-Based Downregulation of the G56R Pathogenic Variant Causing <i>NR2E3</i>-Associated Autosomal Dominant Retinitis PigmentosaSarah Naessens, Laurien Ruysschaert, Steve Lefever, et al.
Biomolecular Detection and Quantification|April 15, 2016
Targeted resequencing and variant validation using pxlence PCR assaysFrauke Coppieters, Kimberly Verniers, Kim De Leeneer, et al.
The Laryngoscope|July 3, 2009
Local complement activation in nasal polyposisThibaut Van Zele, Frauke Coppieters, Philippe Gevaert, et al.
Molecular Vision|July 21, 2012
TMEM126A mutation in a Moroccan family with autosomal recessive optic atrophyJulie Désir, Frauke Coppieters, Nicole Van Regemorter, et al.
Scientific Reports|July 4, 2019
The development of a novel SNP genotyping assay to differentiate cacao clonesJocelyn De Wever, Helena Everaert, Frauke Coppieters, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 20, 2012
Enhanced S-cone syndrome with preserved macular structure and severely depressed retinal functionIvan Cima, Jelka Brecelj, Maja Sustar, et al.
BMC Bioinformatics|September 8, 2017
High-throughput PCR assay design for targeted resequencing using primerXLSteve Lefever, Filip Pattyn, Bram De Wilde, et al.
Nature Communications|May 10, 2024
Author Correction: Multi-omics analysis in human retina uncovers ultraconserved cis-regulatory elements at rare eye disease lociVictor Lopez Soriano, Alfredo Dueñas Rey, Rajarshi Mukherjee, et al.
Scientific Reports|January 6, 2026
A rare 5'UTR variant in SEC24D reveals translational dysfunction in osteogenesis imperfecta: a roadmap for RNA therapeutic rescueOsama Essawi, Tamara Jarayseh, Piyanoot Tapaneeyaphan, et al.
Pageof 6

Showing results (1-10 of 53) with videos related to

Sort By:
Pageof 6
Human Mutation|August 7, 2010
CEP290, a gene with many faces: mutation overview and presentation of CEP290baseFrauke Coppieters, Steve Lefever, Bart P Leroy, et al.
Genes|May 15, 2019
Antisense Oligonucleotide-Based Downregulation of the G56R Pathogenic Variant Causing <i>NR2E3</i>-Associated Autosomal Dominant Retinitis PigmentosaSarah Naessens, Laurien Ruysschaert, Steve Lefever, et al.
Biomolecular Detection and Quantification|April 15, 2016
Targeted resequencing and variant validation using pxlence PCR assaysFrauke Coppieters, Kimberly Verniers, Kim De Leeneer, et al.
The Laryngoscope|July 3, 2009
Local complement activation in nasal polyposisThibaut Van Zele, Frauke Coppieters, Philippe Gevaert, et al.
Molecular Vision|July 21, 2012
TMEM126A mutation in a Moroccan family with autosomal recessive optic atrophyJulie Désir, Frauke Coppieters, Nicole Van Regemorter, et al.
Scientific Reports|July 4, 2019
The development of a novel SNP genotyping assay to differentiate cacao clonesJocelyn De Wever, Helena Everaert, Frauke Coppieters, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 20, 2012
Enhanced S-cone syndrome with preserved macular structure and severely depressed retinal functionIvan Cima, Jelka Brecelj, Maja Sustar, et al.
BMC Bioinformatics|September 8, 2017
High-throughput PCR assay design for targeted resequencing using primerXLSteve Lefever, Filip Pattyn, Bram De Wilde, et al.
Nature Communications|May 10, 2024
Author Correction: Multi-omics analysis in human retina uncovers ultraconserved cis-regulatory elements at rare eye disease lociVictor Lopez Soriano, Alfredo Dueñas Rey, Rajarshi Mukherjee, et al.
Scientific Reports|January 6, 2026
A rare 5'UTR variant in SEC24D reveals translational dysfunction in osteogenesis imperfecta: a roadmap for RNA therapeutic rescueOsama Essawi, Tamara Jarayseh, Piyanoot Tapaneeyaphan, et al.
Pageof 6