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D

D.R. Gardner

Researcher at Carleton University

Publications -  25
Citations -  382

D.R. Gardner is an academic researcher from Carleton University. The author has contributed to research in topics: Lymnaea stagnalis & Membrane potential. The author has an hindex of 9, co-authored 25 publications receiving 378 citations.

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Journal ArticleDOI

Stretch Activation of a K+ Channel in Molluscan Heart Cells

TL;DR: It is concluded that the stretch-sensitive kinetic component of theHeart ventricle cells of Lymnaea stagnalis contain a stretch-activated K + channel which exhibits two open states and three closed states.
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A Potassium-Selective Channel in Isolated Lymnaea Stagnalis Heart Muscle Cells

TL;DR: The relationship between the membrane potential, the external potassium concentration and the channel currents, when compared with results obtained from whole cell recording, suggests that this channel could mediate a large part of the cell's resting conductance.
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The peptide FMRFamide activates a divalent cation-conducting channel in heart muscle cells of the snail Lymnaea stagnalis.

TL;DR: Both sodium and barium currents were initiated when the peptides were applied to the cell outside of the patch pipette indicating that a secondary messenger is likely to be involved in the FMRFamide response.
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The Ionic Basis of the Resting Potential in a Cross-Striated Muscle of the Aquatic Snail Lymnaea Stagnalis

TL;DR: The membrane of the heart ventricle muscle cells appears to be permeable to both potassium and chloride, as changes in the extracellular concentration of either of these ions resulted in a change in the membrane potential.
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FMRFamide-activated Ca2+ channels in Lymnaea heart cells are modulated by "SEEPLY," a neuropeptide encoded on the same gene.

TL;DR: The cell-attached, patch-clamp technique was used to investigate the modulatory role of the neuropeptide SEQPDVDDYLRDVVLQSEEPLY on FMRFamide-activated Ca2+ channels in isolated Lymnaea heart ventricular cells and suggested that corelease of the two peptides might act together to regulate the level of Ca2-activated channel activity within a defined range.