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Willy Lissens

Showing results (21-30 of 68) with videos related to

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Neuromuscular Disorders : NMD|June 14, 2011
Late onset painful cold-aggravated myotonia: three families with SCN4A L1436P mutationVéronique Bissay, Kathelijn Keymolen, Willy Lissens, et al.
Human Reproduction (Oxford, England)|March 11, 2008
Do we need to search for gr/gr deletions in infertile men in a clinical setting?Katrien Stouffs, Herman Tournaye, Josiane Van der Elst, et al.
Analytica Chimica Acta|August 29, 2007
Gas chromatographic-mass spectrometric analysis of N-acetylated amino acids: the first case of aminoacylase I deficiencyErik Gerlo, Rudy Van Coster, Willy Lissens, et al.
Journal of Tropical Pediatrics|July 10, 2007
Molecular analysis in two siblings African patients with severe form of Hunter Syndrome: identification of a novel (p.Y54X) nonsense mutationLéon Mutesa, Narcisse Muganga, Willy Lissens, et al.
Bioinformatics (Oxford, England)|October 11, 2015
I-PV: a CIRCOS module for interactive protein sequence visualizationIbrahim Tanyalcin, Carla Al Assaf, Alexander Gheldof, et al.
Biomed Research International|March 1, 2016
Sertoli Cell-Only Syndrome: Behind the Genetic ScenesKatrien Stouffs, Alexander Gheldof, Herman Tournaye, et al.
Human Mutation|August 10, 2005
De novo Alu element insertions targeted to a sequence common to the BRCA1 and BRCA2 genesErik Teugels, Sylvia De Brakeleer, Guido Goelen, et al.
BMC Bioinformatics|October 21, 2016
Convert your favorite protein modeling program into a mutation predictor: "MODICT"Ibrahim Tanyalcin, Katrien Stouffs, Dorien Daneels, et al.
Acta Neurologica Belgica|December 13, 2007
The aerobic forearm exercise test, a non-invasive tool to screen for mitochondrial disordersAnn Meulemans, Erik Gerlo, Sara Seneca, et al.
Human Mutation|June 21, 2007
A single mutation in the GALC gene is responsible for the majority of late onset Krabbe disease patients in the Catania (Sicily, Italy) regionWilly Lissens, Alessia Arena, Sara Seneca, et al.
Pageof 7

Showing results (21-30 of 68) with videos related to

Sort By:
Pageof 7
Neuromuscular Disorders : NMD|June 14, 2011
Late onset painful cold-aggravated myotonia: three families with SCN4A L1436P mutationVéronique Bissay, Kathelijn Keymolen, Willy Lissens, et al.
Human Reproduction (Oxford, England)|March 11, 2008
Do we need to search for gr/gr deletions in infertile men in a clinical setting?Katrien Stouffs, Herman Tournaye, Josiane Van der Elst, et al.
Analytica Chimica Acta|August 29, 2007
Gas chromatographic-mass spectrometric analysis of N-acetylated amino acids: the first case of aminoacylase I deficiencyErik Gerlo, Rudy Van Coster, Willy Lissens, et al.
Journal of Tropical Pediatrics|July 10, 2007
Molecular analysis in two siblings African patients with severe form of Hunter Syndrome: identification of a novel (p.Y54X) nonsense mutationLéon Mutesa, Narcisse Muganga, Willy Lissens, et al.
Bioinformatics (Oxford, England)|October 11, 2015
I-PV: a CIRCOS module for interactive protein sequence visualizationIbrahim Tanyalcin, Carla Al Assaf, Alexander Gheldof, et al.
Biomed Research International|March 1, 2016
Sertoli Cell-Only Syndrome: Behind the Genetic ScenesKatrien Stouffs, Alexander Gheldof, Herman Tournaye, et al.
Human Mutation|August 10, 2005
De novo Alu element insertions targeted to a sequence common to the BRCA1 and BRCA2 genesErik Teugels, Sylvia De Brakeleer, Guido Goelen, et al.
BMC Bioinformatics|October 21, 2016
Convert your favorite protein modeling program into a mutation predictor: "MODICT"Ibrahim Tanyalcin, Katrien Stouffs, Dorien Daneels, et al.
Acta Neurologica Belgica|December 13, 2007
The aerobic forearm exercise test, a non-invasive tool to screen for mitochondrial disordersAnn Meulemans, Erik Gerlo, Sara Seneca, et al.
Human Mutation|June 21, 2007
A single mutation in the GALC gene is responsible for the majority of late onset Krabbe disease patients in the Catania (Sicily, Italy) regionWilly Lissens, Alessia Arena, Sara Seneca, et al.
Pageof 7