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Monique N. Vergouwe

Researcher at Maastricht University

Publications -  20
Citations -  3645

Monique N. Vergouwe is an academic researcher from Maastricht University. The author has contributed to research in topics: Inflammation & Familial hemiplegic migraine. The author has an hindex of 16, co-authored 20 publications receiving 3516 citations. Previous affiliations of Monique N. Vergouwe include Leiden University.

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Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

TL;DR: A brain-specific P/Q-type Ca2+ channel alpha1-subunit gene, CACNL1A4, covering 300 kb with 47 exons is characterized, revealing polymorphic variations, including a (CA)n-repeat (D19S1150), a (CAG) n-repeat in the 3'-UTR, and different types of deleterious mutations in FHM and EA-2.
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Inhibition of NF-kappaB activation in macrophages increases atherosclerosis in LDL receptor-deficient mice.

TL;DR: The data show that inhibition of the NF-kappaB pathway in macrophages leads to more severe atherosclerosis in mice, possibly by affecting the pro- and anti-inflammatory balance that controls the development of Atherosclerosis.
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Myeloid Type I Interferon Signaling Promotes Atherosclerosis by Stimulating Macrophage Recruitment to Lesions

TL;DR: It is demonstrated that IFNbeta enhances macrophage-endothelial cell adhesion and promotes leukocyte attraction to atherosclerosis-prone sites in mice in a chemokine-dependent manner and it is shown that type I IFN signaling is upregulated in ruptured human atherosclerotic plaques.
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Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura.

TL;DR: The increased allele sharing in the CACNA1A gene region on 19p13 is consistent with an important involvement of this region in migraine, especially migraine with aura.
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Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine

TL;DR: It is concluded that the I1811L mutation causes both FHM and cerebellar ataxia independent of the number of CAG repeats, supporting the hypothesis that FHM is part of the migraine spectrum.