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ZFIN ID:
ZDB-ATB-120223-2
CITATIONS
(22 total)
Antibody Name:
Ab1-ryr
Bennett, A.H., O'Donohue, M.F., Gundry, S.R., Chan, A.T., Widrick, J., Draper, I., Chakraborty, A., Zhou, Y., Zon, L.I., Gleizes, P.E., Beggs, A.H., Gupta, V.A. (2018) RNA helicase, DDX27 regulates skeletal muscle growth and regeneration by modulation of translational processes. PLoS Genetics. 14:e1007226
Bovo, E., Dvornikov, A.V., Mazurek, S.R., de Tombe, P.P., and Zima, A.V. (2013) Mechanisms of Ca2+ handling in zebrafish ventricular myocytes. Pflugers Archiv : European journal of physiology. 465(12):1775-84
Caprara, G.A., Perni, S., Morabito, C., Mariggiò, M.A., Guarnieri, S. (2014) Specific association of growth-associated protein 43 with calcium release units in skeletal muscles of lower vertebrates. European journal of histochemistry : EJH. 58:2453
Chagovetz, A.A., Klatt Shaw, D., Ritchie, E., Hoshijima, K., Grunwald, D.J. (2019) Interactions among Ryanodine Receptor isotypes contribute to muscle fiber type development and function. Disease models & mechanisms. 13(2):
Cheung, C.Y., Webb, S.E., Love, D.R., and Miller, A.L. (2011) Visualization, characterization and modulation of calcium signaling during the development of slow muscle cells in intact zebrafish embryos. The International journal of developmental biology. 55(2):153-74
Endo, Y., Groom, L., Celik, A., Kraeva, N., Lee, C.S., Jung, S.Y., Gardner, L., Shaw, M.A., Hamilton, S.L., Hopkins, P.M., Dirksen, R.T., Riazi, S., Dowling, J.J. (2022) Variants in ASPH cause exertional heat illness and are associated with malignant hyperthermia susceptibility. Nature communications. 13:3403
Espinosa, K.G., Geissah, S., Groom, L., Volpatti, J., Scott, I.C., Dirksen, R.T., Zhao, M., Dowling, J.J. (2022) Characterization of a novel zebrafish model of SPEG-related centronuclear myopathy. Disease models & mechanisms. 15(5):
Fero, K., Bergeron, S.A., Horstick, E.J., Codore, H., Li, G.H., Ono, F., Dowling, J.J., and Burgess, H.A. (2014) Impaired embryonic motility in dusp27 mutants reveals a developmental defect in myofibril structure. Disease models & mechanisms. 7(2):289-98
Furlan, S., Campione, M., Murgia, M., Mosole, S., Argenton, F., Volpe, P., Nori, A. (2020) Calsequestrins New Calcium Store Markers of Adult Zebrafish Cerebellum and Optic Tectum. Frontiers in Neuroanatomy. 14:15
Furlan, S., Mosole, S., Murgia, M., Nagaraj, N., Argenton, F., Volpe, P., Nori, A. (2016) Calsequestrins in skeletal and cardiac muscle from adult Danio rerio. Journal of muscle research and cell motility. 37(1-2):27-39
Gibbs, E.M., Davidson, A.E., Telfer, W.R., Feldman, E.L., and Dowling, J.J. (2014) Defective tubulation associated with the myopathy causing S619L DNM2 mutation. Disease models & mechanisms. 7(1):157-61
Horstick, E.J., Gibbs, E.M., Li, X., Davidson, A.E., and Dowling, J.J. (2013) Analysis of embryonic and larval zebrafish skeletal myofibers from dissociated preparations. Journal of visualized experiments : JoVE. (81):e50259
Horstick, E.J., Linsley, J.W., Dowling, J.J., Hauser, M.A., McDonald, K.K., Ashley-Koch, A., Saint-Amant, L., Satish, A., Cui, W.W., Zhou, W., Sprague, S.M., Stamm, D.S., Powell, C.M., Speer, M.C., Franzini-Armstrong, C., Hirata, H., and Kuwada, J.Y. (2013) Stac3 is a component of the excitation-contraction coupling machinery and mutated in Native American myopathy. Nature communications. 4:1952
Kelu, J.J., Chan, H.L., Webb, S.E., Cheng, A.H., Ruas, M., Parrington, J., Galione, A., Miller, A.L. (2015) Two-Pore Channel 2 activity is required for slow muscle cell-generated Ca
2+
signaling during myogenesis in intact zebrafish. The International journal of developmental biology. 59:313-325
Kelu, J.J., Webb, S.E., Parrington, J., Galione, A., Miller, A.L. (2017) Ca
2+
release via two-pore channel type 2 (TPC2) is required for slow muscle cell myofibrillogenesis and myotomal patterning in intact zebrafish embryos.. Developmental Biology. 425(2):109-129
Linsley, J.W., Hsu, I.U., Groom, L., Yarotskyy, V., Lavorato, M., Horstick, E.J., Linsley, D., Wang, W., Franzini-Armstrong, C., Dirksen, R.T., Kuwada, J.Y. (2017) Congenital myopathy results from misregulation of a muscle Ca2+ channel by mutant Stac3. Proceedings of the National Academy of Sciences of the United States of America. 114(2):E228-E236
Linsley, J.W., Hsu, I.U., Wang, W., Kuwada, J.Y. (2017) Transport of the alpha subunit of the L-type calcium channel through the sarcoplasmic reticulum occurs prior to localization to triads and requires the beta subunit but not Stac3 in skeletal muscles. Traffic (Copenhagen, Denmark). 18(9):622-632
Pistocchi, A., Gaudenzi, G., Foglia, E., Monteverde, S., Moreno-Fortuny, A., Pianca, A., Cossu, G., Cotelli, F., and Messina, G. (2013) Conserved and divergent functions of Nfix in skeletal muscle development during vertebrate evolution. Development (Cambridge, England). 140(7):1528-1536
Wu, H.H., Brennan, C., and Ashworth, R. (2011) Ryanodine receptors, a family of intracellular calcium ion channels, are expressed throughout early vertebrate development. BMC research notes. 4(1):541
Zhao, M., Smith, L., Volpatti, J., Fabian, L., Dowling, J.J. (2019) Insights into wild type dynamin 2 and the consequences of DNM2 mutations from transgenic zebrafish. Human molecular genetics. 28(24):4186-4196
Additional Citations (2):
ZFIN Staff (2002) Scientific Curation. Manually curated data.
ZFIN Staff (2008) Antibody information from supplier. Manually curated data.
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