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5541.
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5542.
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5543.
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Dantrolene rescues arrhythmogenic RYR2 defect in a patient-specific stem cell model of catecholaminergic polymorphic ventricular tachycardia. [electronic resource] by
- Jung, Christian B
- Moretti, Alessandra
- Mederos y Schnitzler, Michael
- Iop, Laura
- Storch, Ursula
- Bellin, Milena
- Dorn, Tatjana
- Ruppenthal, Sandra
- Pfeiffer, Sarah
- Goedel, Alexander
- Dirschinger, Ralf J
- Seyfarth, Melchior
- Lam, Jason T
- Sinnecker, Daniel
- Gudermann, Thomas
- Lipp, Peter
- Laugwitz, Karl-Ludwig
Producer: 20120716
In:
EMBO molecular medicine vol. 4
Availability: No items available.
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5544.
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5545.
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RyR1 deficiency in congenital myopathies disrupts excitation-contraction coupling. [electronic resource] by
- Zhou, Haiyan
- Rokach, Ori
- Feng, Lucy
- Munteanu, Iulia
- Mamchaoui, Kamel
- Wilmshurst, Jo M
- Sewry, Caroline
- Manzur, Adnan Y
- Pillay, Komala
- Mouly, Vincent
- Duchen, Michael
- Jungbluth, Heinz
- Treves, Susan
- Muntoni, Francesco
Producer: 20140127
In:
Human mutation vol. 34
Availability: No items available.
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5546.
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5547.
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5548.
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5549.
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Simvastatin activates single skeletal RyR1 channels but exerts more complex regulation of the cardiac RyR2 isoform. [electronic resource] by
- Venturi, Elisa
- Lindsay, Chris
- Lotteau, Sabine
- Yang, Zhaokang
- Steer, Emma
- Witschas, Katja
- Wilson, Abigail D
- Wickens, James R
- Russell, Angela J
- Steele, Derek
- Calaghan, Sarah
- Sitsapesan, Rebecca
Producer: 20190603
In:
British journal of pharmacology vol. 175
Availability: No items available.
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5550.
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Congenital myopathy results from misregulation of a muscle Ca2+ channel by mutant Stac3. [electronic resource] by
- Linsley, Jeremy W
- Hsu, I-Uen
- Groom, Linda
- Yarotskyy, Viktor
- Lavorato, Manuela
- Horstick, Eric J
- Linsley, Drew
- Wang, Wenjia
- Franzini-Armstrong, Clara
- Dirksen, Robert T
- Kuwada, John Y
Producer: 20180409
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 114
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5551.
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5552.
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Primary structure and expression from complementary DNA of skeletal muscle ryanodine receptor. [electronic resource] by
- Takeshima, H
- Nishimura, S
- Matsumoto, T
- Ishida, H
- Kangawa, K
- Minamino, N
- Matsuo, H
- Ueda, M
- Hanaoka, M
- Hirose, T
Producer: 19890713
In:
Nature vol. 339
Availability: No items available.
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5553.
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5554.
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5555.
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5556.
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5557.
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The G1021A substitution in the RYR1 gene does not cosegregate with malignant hyperthermia susceptibility in a British pedigree. [electronic resource] by
- Adeokun, A M
- West, S P
- Ellis, F R
- Halsall, P J
- Hopkins, P M
- Foroughmand, A M
- Iles, D E
- Robinson, R L
- Stewart, A D
- Curran, J L
Producer: 19970508
In:
American journal of human genetics vol. 60
Availability: No items available.
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5558.
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5559.
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5560.
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