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Annelies Janssens

Researcher at Katholieke Universiteit Leuven

Publications -  116
Citations -  6832

Annelies Janssens is an academic researcher from Katholieke Universiteit Leuven. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 31, co-authored 84 publications receiving 5945 citations. Previous affiliations of Annelies Janssens include The Catholic University of America & Catholic University of Leuven.

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The principle of temperature-dependent gating in cold- and heat-sensitive TRP channels

TL;DR: Kinetic analysis of gating at different temperatures indicates that temperature sensitivity in TRPM8 and TRPV1 arises from a tenfold difference in the activation energies associated with voltage-dependent opening and closing.
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Cell swelling, heat, and chemical agonists use distinct pathways for the activation of the cation channel TRPV4.

TL;DR: It is demonstrated that blockers of phospholipase A2 (PLA2) and cytochrome P450 epoxygenase inhibit activation of TRPV4 by osmotic cell swelling but not by heat and 4α-phorbol 12,13-didecanoate, and it is concluded that TRpV4-activating stimuli promote channel opening by means of distinct pathways.
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TRPA1 acts as a cold sensor in vitro and in vivo

TL;DR: It is concluded that TRPA1 acts as a major sensor for noxious cold, and a specific subset of cold-sensitive trigeminal ganglion neurons that is absent inTRPA1-deficient mice are identified.
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TRPM3 Is a Nociceptor Channel Involved in the Detection of Noxious Heat

TL;DR: Evidence is provided that TRPM3 functions as a chemo- and thermosensor in the somatosensory system and an unanticipated role for TR PM3 as a thermosensitive nociceptor channel implicated in the detection of noxious heat is revealed.
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Modulation of the Ca2 Permeable Cation Channel TRPV4 by Cytochrome P450 Epoxygenases in Vascular Endothelium

TL;DR: It is established that CYP-derived EETs modulate the activity of TRPV4 channels in endothelial cells and shows the unraveling of novel modulatory pathways via CYP2C modulation and sEH inhibition.