Below are the most recent publications written about "Calcium Channels, L-Type" by people in Profiles.
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Hohman TJ, Bush WS, Jiang L, Brown-Gentry KD, Torstenson ES, Dudek SM, Mukherjee S, Naj A, Kunkle BW, Ritchie MD, Martin ER, Schellenberg GD, Mayeux R, Farrer LA, Pericak-Vance MA, Haines JL, Thornton-Wells TA. Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium. Neurobiol Aging. 2016 Feb; 38:141-150.
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Genewsky A, Jost I, Busch C, Huber C, Stindl J, Skerka C, Zipfel PF, Rohrer B, Strauß O. Activation of endogenously expressed ion channels by active complement in the retinal pigment epithelium. Pflugers Arch. 2015 Oct; 467(10):2179-91.
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Spencer S, Brown RM, Quintero GC, Kupchik YM, Thomas CA, Reissner KJ, Kalivas PW. a2d-1 signaling in nucleus accumbens is necessary for cocaine-induced relapse. J Neurosci. 2014 Jun 18; 34(25):8605-11.
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Rohrer B, Kunchithapautham K, Genewsky A, Strauß O. Prolonged SRC kinase activation, a mechanism to turn transient, sublytic complement activation into a sustained pathological condition in retinal pigment epithelium cells. Adv Exp Med Biol. 2014; 801:221-7.
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Scaringi JA, Rosa AO, Morad M, Cleemann L. A new method to detect rapid oxygen changes around cells: how quickly do calcium channels sense oxygen in cardiomyocytes? J Appl Physiol (1985). 2013 Dec; 115(12):1855-61.
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Rosa AO, Movafagh S, Cleemann L, Morad M. Hypoxic regulation of cardiac Ca2+ channel: possible role of haem oxygenase. J Physiol. 2012 Sep 01; 590(17):4223-37.
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Movafagh S, Cleemann L, Morad M. Regulation of cardiac Ca(2+) channel by extracellular Na(+). Cell Calcium. 2011 Mar; 49(3):162-73.
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Das A, Smith JA, Gibson C, Varma AK, Ray SK, Banik NL. Estrogen receptor agonists and estrogen attenuate TNF-a-induced apoptosis in VSC4.1 motoneurons. J Endocrinol. 2011 Feb; 208(2):171-82.
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Movafagh S, Morad M. L-type calcium channel as a cardiac oxygen sensor. Ann N Y Acad Sci. 2010 Feb; 1188:153-8.
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Zhou H, Lillis S, Loy RE, Ghassemi F, Rose MR, Norwood F, Mills K, Al-Sarraj S, Lane RJ, Feng L, Matthews E, Sewry CA, Abbs S, Buk S, Hanna M, Treves S, Dirksen RT, Meissner G, Muntoni F, Jungbluth H. Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene. Neuromuscul Disord. 2010 Mar; 20(3):166-73.