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Jan Hellemans

Showing results (21-30 of 55) with videos related to

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Scientific Reports|February 17, 2019
Cost-effective and robust genotyping using double-mismatch allele-specific quantitative PCRSteve Lefever, Ali Rihani, Joni Van der Meulen, et al.
BMC Bioinformatics|June 20, 2015
RDML-Ninja and RDMLdb for standardized exchange of qPCR dataJan M Ruijter, Steve Lefever, Jasper Anckaert, et al.
Journal of Alzheimer'S Disease : JAD|October 9, 2010
BACE1 mRNA expression in Alzheimer's disease postmortem brain tissueDavid T R Coulson, Nancy Beyer, Joe G Quinn, et al.
Human Genetics|April 29, 2010
The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2)Delfien Syx, Fransiska Malfait, Lut Van Laer, et al.
Nucleic Acids Research|September 8, 2009
External oligonucleotide standards enable cross laboratory comparison and exchange of real-time quantitative PCR dataJoëlle Vermeulen, Filip Pattyn, Katleen De Preter, et al.
Brain Research|May 8, 2012
α-Synuclein mRNA and soluble α-synuclein protein levels in post-mortem brain from patients with Parkinson's disease, dementia with Lewy bodies, and Alzheimer's diseaseJoseph G Quinn, David T R Coulson, Simon Brockbank, et al.
Human Mutation|February 10, 2011
Massive parallel amplicon sequencing of the breast cancer genes BRCA1 and BRCA2: opportunities, challenges, and limitationsKim De Leeneer, Jan Hellemans, Joachim De Schrijver, et al.
American Journal of Human Genetics|June 15, 2007
Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosaFrauke Coppieters, Bart P Leroy, Diane Beysen, et al.
American Journal of Human Genetics|December 17, 2009
Homozygous inactivating mutations in the NKX3-2 gene result in spondylo-megaepiphyseal-metaphyseal dysplasiaJan Hellemans, Marleen Simon, Annelies Dheedene, et al.
Molecular Therapy. Methods & Clinical Development|February 4, 2022
Consensus guidelines for the validation of qRT-PCR assays in clinical research by the CardioRNA consortiumDavid de Gonzalo-Calvo, Monica Marchese, Jan Hellemans, et al.
Pageof 6

Showing results (21-30 of 55) with videos related to

Sort By:
Pageof 6
Scientific Reports|February 17, 2019
Cost-effective and robust genotyping using double-mismatch allele-specific quantitative PCRSteve Lefever, Ali Rihani, Joni Van der Meulen, et al.
BMC Bioinformatics|June 20, 2015
RDML-Ninja and RDMLdb for standardized exchange of qPCR dataJan M Ruijter, Steve Lefever, Jasper Anckaert, et al.
Journal of Alzheimer'S Disease : JAD|October 9, 2010
BACE1 mRNA expression in Alzheimer's disease postmortem brain tissueDavid T R Coulson, Nancy Beyer, Joe G Quinn, et al.
Human Genetics|April 29, 2010
The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2)Delfien Syx, Fransiska Malfait, Lut Van Laer, et al.
Nucleic Acids Research|September 8, 2009
External oligonucleotide standards enable cross laboratory comparison and exchange of real-time quantitative PCR dataJoëlle Vermeulen, Filip Pattyn, Katleen De Preter, et al.
Brain Research|May 8, 2012
α-Synuclein mRNA and soluble α-synuclein protein levels in post-mortem brain from patients with Parkinson's disease, dementia with Lewy bodies, and Alzheimer's diseaseJoseph G Quinn, David T R Coulson, Simon Brockbank, et al.
Human Mutation|February 10, 2011
Massive parallel amplicon sequencing of the breast cancer genes BRCA1 and BRCA2: opportunities, challenges, and limitationsKim De Leeneer, Jan Hellemans, Joachim De Schrijver, et al.
American Journal of Human Genetics|June 15, 2007
Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosaFrauke Coppieters, Bart P Leroy, Diane Beysen, et al.
American Journal of Human Genetics|December 17, 2009
Homozygous inactivating mutations in the NKX3-2 gene result in spondylo-megaepiphyseal-metaphyseal dysplasiaJan Hellemans, Marleen Simon, Annelies Dheedene, et al.
Molecular Therapy. Methods & Clinical Development|February 4, 2022
Consensus guidelines for the validation of qRT-PCR assays in clinical research by the CardioRNA consortiumDavid de Gonzalo-Calvo, Monica Marchese, Jan Hellemans, et al.
Pageof 6