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Johannes C. Lodder

Researcher at VU University Amsterdam

Publications -  46
Citations -  1784

Johannes C. Lodder is an academic researcher from VU University Amsterdam. The author has contributed to research in topics: Lymnaea stagnalis & Inhibitory postsynaptic potential. The author has an hindex of 25, co-authored 46 publications receiving 1615 citations. Previous affiliations of Johannes C. Lodder include University of California, San Francisco.

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Label-free live brain imaging and targeted patching with third-harmonic generation microscopy

TL;DR: It is found that THG brain imaging allows rapid, noninvasive label-free imaging of neurons, white-matter structures, and blood vessels simultaneously, and opens up possibilities for the development of laser-guided microsurgery techniques in the living brain.
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Unique membrane properties and enhanced signal processing in human neocortical neurons

TL;DR: It is shown that layer 2/3 pyramidal neurons from human temporal cortex (HL2/3 PCs) have a specific membrane capacitance (Cm) of ~0.5 µF/cm2, half of the commonly accepted 'universal' value for biological membranes.
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Induction of egg-laying in the pond snail Lymnaea stagnalis by environmental stimulation of the release of ovulation hormone from the Caudo—Dorsal Cells

TL;DR: Elevated O2-content of the water, a clear jar and clean water all have a positive effect on egg-laying, and the size of the egg capsule depends on the number of ripe eggs in the ovotestis and the packaging capacity of the female accessory sex organs.
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Cholinergic modulation of nucleus accumbens medium spiny neurons

TL;DR: Electrophysiological recordings in rat nucleus accumbens showed that γ‐aminobutyric acid‐mediated inhibition of the output neurons might be facilitated by activation of nicotinic acetylcholine receptors, in addition to being suppressed via activation of muscarinic acetylCholine receptors.
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Progesterone-metabolite prevents protein kinase C-dependent modulation of γ-aminobutyric acid type A receptors in oxytocin neurons

TL;DR: A form of nongenomic progesterone signaling is described by showing that 3α-OH-DHP not only potentiates GABAA receptor-channel activity but also prevents its modulation by protein kinase C (PKC).