User profiles for A. M. van den Maagdenberg

Arn van den Maagdenberg

Professor of Molecular and Functional Neurogenetics, Leiden University Medical Center
Verified email at lumc.nl
Cited by 28822

Diet-induced hyperlipoproteinemia and atherosclerosis in apolipoprotein E3-Leiden transgenic mice.

…, AM Van den Maagdenberg… - The Journal of …, 1994 - Am Soc Clin Investig
Apolipoprotein E3-Leiden (APOE*3-Leiden) transgenic mice have been used to study the
effect of different cholesterol-containing diets on the remnant lipoprotein levels and …

Transgenic mice carrying the apolipoprotein E3-Leiden gene exhibit hyperlipoproteinemia

AM Van den Maagdenberg, MH Hofker… - Journal of Biological …, 1993 - ASBMB
Apolipoprotein (apo) E3-Leiden, described in a large Dutch family, is associated with a
dominantly inherited form of familial dysbetalipoproteinemia. To study the effect of the APOE*3-…

[HTML][HTML] Meta-analysis of genome-wide association for migraine in six population-based European cohorts

…, CM Van Duijn, AM Van Den Maagdenberg… - European Journal of …, 2011 - nature.com
Migraine is a common neurological disorder with a genetically complex background. This
paper describes a meta-analysis of genome-wide association (GWA) studies on migraine, …

Metabolic Age Based on the BBMRI-NL 1H-NMR Metabolomics Repository as Biomarker of Age-related Disease

…, LM 't Hart, AM Van Den Maagdenberg… - Circulation: Genomic …, 2020 - Am Heart Assoc
Background: The blood metabolome incorporates cues from the environment and the host’s
genetic background, potentially offering a holistic view of an individual’s health status. …

Familial dysbetalipoproteinemia associated with apolipoprotein E3-Leiden in an extended multigeneration pedigree.

P De Knijff, AM Van den Maagdenberg… - The Journal of …, 1991 - Am Soc Clin Investig
By the careful screening of familial dysbetalipoproteinemic (FD) patients, five probands showing
heterozygosity for the APOE*3-Leiden allele were found. Genealogical studies revealed …

Noradrenergic and cholinergic modulation of belief updating

…, B de Vries, AM van den Maagdenberg… - Journal of cognitive …, 2018 - direct.mit.edu
… During each session, participants received a capsule of clonidine or placebo at 09:35 am
and a capsule of scopolamine or placebo at 10:35 am The different kinetic profiles of clonidine …

Genetic heterogeneity in familial dysbetalipoproteinemia. The E2 (lys146—-gln) variant results in a dominant mode of inheritance.

…, C Groenendijk, AM van den Maagdenberg… - Journal of Lipid …, 1990 - Elsevier
As determined by isoelectric focusing, most patients with familial dysbetalipoproteinemia (FD)
exhibit the homozygous apolipoprotein (apo) E2E2 phenotype. Only rarely does FD …

Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering α1A Ca2+ channel mutation

JJ Plomp, MN Vergouwe, AM Van den Maagdenberg… - Brain, 2000 - academic.oup.com
… The authors wish to thank Mr JA van der Zwet for breeding the tg mice and Drs AR
Wintzen, JJGM Verschuuren, RJ van den Berg and DL Ypey for valuable discussions. …

Mutant P/Q-type calcium channel electrophysiology and migraine.

JJ Plomp, AM Van den Maagdenberg… - Current Opinion in …, 2001 - europepmc.org
The pathophysiological mechanisms of migraine are not yet very well understood. The gene
CACNA1A, coding for the alpha 1A subunit of neuronal P/Q-type Ca2+ channels is mutated …

[PDF][PDF] Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation

…, J Haan, AM van den Maagdenberg… - …, 2009 - scholarlypublications …
Febrile seizures are the most common form of convulsions between the age of 6 months and
5 years1, but genetic factors have not been identified. Here we investigated the molecular …