Anamika Dayal
Affiliations: | Innsbruck Medical University, Innsbruck, Tirol, Austria |
Area:
Calcium channelsGoogle:
"Anamika Dayal"Mean distance: 16.5 (cluster 46) | S | N | B | C | P |
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Publications
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McClenaghan C, Mukadam MA, Roeglin J, et al. (2023) Skeletal muscle delimited myopathy and verapamil toxicity in SUR2 mutant mouse models of AIMS. Embo Molecular Medicine. e16883 |
Dayal A, Perni S, Franzini-Armstrong C, et al. (2022) The distal C terminus of the dihydropyridine receptor β subunit is essential for tetrad formation in skeletal muscle. Proceedings of the National Academy of Sciences of the United States of America. 119: e2201136119 |
Dayal A, Fernández-Quintero ML, Liedl KR, et al. (2021) Pore mutation N617D in the skeletal muscle DHPR blocks Ca influx due to atypical high-affinity Ca binding. Elife. 10 |
Myers JH, Denman K, DuPont C, et al. (2021) The mechanism underlying transient weakness in myotonia congenita. Elife. 10 |
Idoux R, Fuster C, Jacquemond V, et al. (2020) Divalent cations permeation in a Ca non-conducting skeletal muscle dihydropyridine receptor mouse model. Cell Calcium. 91: 102256 |
Dayal A, Ng SFJ, Grabner M. (2019) Ca-activated Cl channel TMEM16A/ANO1 identified in zebrafish skeletal muscle is crucial for action potential acceleration. Nature Communications. 10: 115 |
Kaplan MM, Sultana N, Benedetti A, et al. (2018) Calcium Influx and Release Cooperatively Regulate AChR Patterning and Motor Axon Outgrowth during Neuromuscular Junction Formation. Cell Reports. 23: 3891-3904 |
Dayal A, Schrötter K, Pan Y, et al. (2017) The Ca(2+) influx through the mammalian skeletal muscle dihydropyridine receptor is irrelevant for muscle performance. Nature Communications. 8: 475 |
Schrötter K, Dayal A, Grabner M. (2016) The mammalian skeletal muscle DHPR has larger Ca(2+) conductance and is phylogenetically ancient to the early ray-finned fish sterlet (Acipenser ruthenus). Cell Calcium |
Josephine Ng SF, Dayal A, Grabner M. (2015) The Calcium-Activated Chloride Channel in Zebrafish Skeletal Muscle is Activated during Excitation-Contraction Coupling Biophysical Journal. 108: 420a |