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Stephan Rust

Showing results (41-50 of 53) with videos related to

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Human Brain Mapping|May 28, 2014
Serotonin transporter gene methylation is associated with hippocampal gray matter volumeUdo Dannlowski, Harald Kugel, Ronny Redlich, et al.
Journal of Inherited Metabolic Disease|August 28, 2020
N-glycome analysis detects dysglycosylation missed by conventional methods in SLC39A8 deficiencyJulien H Park, Robert G Mealer, Abdallah F Elias, et al.
Molecular Genetics and Metabolism Reports|August 11, 2017
Limitations of galactose therapy in phosphoglucomutase 1 deficiencyKristine Nolting, Julien H Park, Laura C Tegtmeyer, et al.
Plos Genetics|May 20, 2006
Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17Martin Farrall, Fiona R Green, John F Peden, et al.
Plos Genetics|April 5, 2014
CNNM2 mutations cause impaired brain development and seizures in patients with hypomagnesemiaFrancisco J Arjona, Jeroen H F de Baaij, Karl P Schlingmann, et al.
The Journal of Biological Chemistry|April 7, 2004
Apolipoprotein A-I-stimulated apolipoprotein E secretion from human macrophages is independent of cholesterol effluxMaaike Kockx, Kerry-Anne Rye, Katharina Gaus, et al.
Acta Neuropathologica Communications|July 27, 2023
Mitochondrial DNA mutations in MedulloblastomaViktoria L E Funke, Sarah Sandmann, Viktoria Melcher, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|November 9, 2017
Association of Serotonin Transporter Gene AluJb Methylation with Major Depression, Amygdala Responsiveness, 5-HTTLPR/rs25531 Polymorphism, and StressIlona Schneider, Harald Kugel, Ronny Redlich, et al.
The New England Journal of Medicine|December 25, 2009
Genetic variants associated with Lp(a) lipoprotein level and coronary diseaseRobert Clarke, John F Peden, Jemma C Hopewell, et al.
American Journal of Human Genetics|December 7, 2015
SLC39A8 Deficiency: A Disorder of Manganese Transport and GlycosylationJulien H Park, Max Hogrebe, Marianne Grüneberg, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Human Brain Mapping|May 28, 2014
Serotonin transporter gene methylation is associated with hippocampal gray matter volumeUdo Dannlowski, Harald Kugel, Ronny Redlich, et al.
Journal of Inherited Metabolic Disease|August 28, 2020
N-glycome analysis detects dysglycosylation missed by conventional methods in SLC39A8 deficiencyJulien H Park, Robert G Mealer, Abdallah F Elias, et al.
Molecular Genetics and Metabolism Reports|August 11, 2017
Limitations of galactose therapy in phosphoglucomutase 1 deficiencyKristine Nolting, Julien H Park, Laura C Tegtmeyer, et al.
Plos Genetics|May 20, 2006
Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17Martin Farrall, Fiona R Green, John F Peden, et al.
Plos Genetics|April 5, 2014
CNNM2 mutations cause impaired brain development and seizures in patients with hypomagnesemiaFrancisco J Arjona, Jeroen H F de Baaij, Karl P Schlingmann, et al.
The Journal of Biological Chemistry|April 7, 2004
Apolipoprotein A-I-stimulated apolipoprotein E secretion from human macrophages is independent of cholesterol effluxMaaike Kockx, Kerry-Anne Rye, Katharina Gaus, et al.
Acta Neuropathologica Communications|July 27, 2023
Mitochondrial DNA mutations in MedulloblastomaViktoria L E Funke, Sarah Sandmann, Viktoria Melcher, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|November 9, 2017
Association of Serotonin Transporter Gene AluJb Methylation with Major Depression, Amygdala Responsiveness, 5-HTTLPR/rs25531 Polymorphism, and StressIlona Schneider, Harald Kugel, Ronny Redlich, et al.
The New England Journal of Medicine|December 25, 2009
Genetic variants associated with Lp(a) lipoprotein level and coronary diseaseRobert Clarke, John F Peden, Jemma C Hopewell, et al.
American Journal of Human Genetics|December 7, 2015
SLC39A8 Deficiency: A Disorder of Manganese Transport and GlycosylationJulien H Park, Max Hogrebe, Marianne Grüneberg, et al.
Pageof 6