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M Mannens

Showing results (121-130 of 172) with videos related to

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Plos One|December 28, 2018
A distinct epigenetic profile distinguishes stenotic from non-inflamed fibroblasts in the ileal mucosa of Crohn's disease patientsAndrew Y F Li Yim, Jessica R de Bruyn, Nicolette W Duijvis, et al.
Human Molecular Genetics|April 28, 2017
A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndromeIliana A Chatzispyrou, Marielle Alders, Sergio Guerrero-Castillo, et al.
Circulation|September 19, 2007
Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic featuresZahurul A Bhuiyan, Maarten P van den Berg, J Peter van Tintelen, et al.
European Journal of Human Genetics : EJHG|January 25, 2018
Genetic variant in CACNA1C is associated with PTSD in traumatized police officersIzabela M Krzyzewska, Judith B M Ensink, Laura Nawijn, et al.
The Lancet. Healthy Longevity|February 11, 2022
Epigenetic age acceleration in the emerging burden of cardiometabolic diseases among migrant and non-migrant African populations: the population based cross-sectional RODAM studyFelix P Chilunga, Peter Henneman, Hannah R Elliott, et al.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|May 8, 2021
Differential DNA Methylation Is Associated With Hippocampal Abnormalities in Pediatric Posttraumatic Stress DisorderJudith B M Ensink, Taylor J Keding, Peter Henneman, et al.
Circulation Research|December 11, 1999
A single Na(+) channel mutation causing both long-QT and Brugada syndromesC Bezzina, M W Veldkamp, M P van Den Berg, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|May 28, 2010
Founder mutations in hypertrophic cardiomyopathy patients in the NetherlandsI Christiaans, E A Nannenberg, D Dooijes, et al.
European Journal of Human Genetics : EJHG|March 10, 2011
A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9qJudith B A van de Meerakker, Klaartje van Engelen, Inge B Mathijssen, et al.
Journal of Medical Genetics|November 21, 2013
Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canalA V Postma, M Alders, M Sylva, et al.
Pageof 18

Showing results (121-130 of 172) with videos related to

Sort By:
Pageof 18
Plos One|December 28, 2018
A distinct epigenetic profile distinguishes stenotic from non-inflamed fibroblasts in the ileal mucosa of Crohn's disease patientsAndrew Y F Li Yim, Jessica R de Bruyn, Nicolette W Duijvis, et al.
Human Molecular Genetics|April 28, 2017
A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndromeIliana A Chatzispyrou, Marielle Alders, Sergio Guerrero-Castillo, et al.
Circulation|September 19, 2007
Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic featuresZahurul A Bhuiyan, Maarten P van den Berg, J Peter van Tintelen, et al.
European Journal of Human Genetics : EJHG|January 25, 2018
Genetic variant in CACNA1C is associated with PTSD in traumatized police officersIzabela M Krzyzewska, Judith B M Ensink, Laura Nawijn, et al.
The Lancet. Healthy Longevity|February 11, 2022
Epigenetic age acceleration in the emerging burden of cardiometabolic diseases among migrant and non-migrant African populations: the population based cross-sectional RODAM studyFelix P Chilunga, Peter Henneman, Hannah R Elliott, et al.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|May 8, 2021
Differential DNA Methylation Is Associated With Hippocampal Abnormalities in Pediatric Posttraumatic Stress DisorderJudith B M Ensink, Taylor J Keding, Peter Henneman, et al.
Circulation Research|December 11, 1999
A single Na(+) channel mutation causing both long-QT and Brugada syndromesC Bezzina, M W Veldkamp, M P van Den Berg, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|May 28, 2010
Founder mutations in hypertrophic cardiomyopathy patients in the NetherlandsI Christiaans, E A Nannenberg, D Dooijes, et al.
European Journal of Human Genetics : EJHG|March 10, 2011
A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9qJudith B A van de Meerakker, Klaartje van Engelen, Inge B Mathijssen, et al.
Journal of Medical Genetics|November 21, 2013
Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canalA V Postma, M Alders, M Sylva, et al.
Pageof 18