Cav1.3
From Wikipedia, the free encyclopedia
Cav1.3 also known as the calcium channel, voltage-dependent, L type, alpha 1D subunit (CACNA1D), is a human gene.[1]
See also
References
Further reading
- Williams ME, Feldman DH, McCue AF, et al. (1992). "Structure and functional expression of alpha 1, alpha 2, and beta subunits of a novel human neuronal calcium channel subtype.". Neuron 8 (1): 71–84. doi:10.1016/0896-6273(92)90109-Q. PMID 1309651.
- Seino S, Chen L, Seino M, et al. (1992). "Cloning of the alpha 1 subunit of a voltage-dependent calcium channel expressed in pancreatic beta cells". Proc. Natl. Acad. Sci. U.S.A. 89 (2): 584–8. doi:10.1073/pnas.89.2.584. PMC 48283. PMID 1309948.
- Seino S, Yamada Y, Espinosa R, et al. (1992). "Assignment of the gene encoding the alpha 1 subunit of the neuroendocrine/brain-type calcium channel (CACNL1A2) to human chromosome 3, band p14.3". Genomics 13 (4): 1375–7. doi:10.1016/0888-7543(92)90078-7. PMID 1324226.
- Chin HM, Kozak CA, Kim HL, et al. (1992). "A brain L-type calcium channel alpha 1 subunit gene (CCHL1A2) maps to mouse chromosome 14 and human chromosome 3". Genomics 11 (4): 914–9. doi:10.1016/0888-7543(91)90014-6. PMID 1664412.
- Mori Y, Friedrich T, Kim MS, et al. (1991). "Primary structure and functional expression from complementary DNA of a brain calcium channel". Nature 350 (6317): 398–402. doi:10.1038/350398a0. PMID 1849233.
- Yamada Y, Masuda K, Li Q, et al. (1995). "The structures of the human calcium channel alpha 1 subunit (CACNL1A2) and beta subunit (CACNLB3) genes". Genomics 27 (2): 312–9. doi:10.1006/geno.1995.1048. PMID 7557998.
- Puro DG, Hwang JJ, Kwon OJ, Chin H (1996). "Characterization of an L-type calcium channel expressed by human retinal Müller (glial) cells". Brain Res. Mol. Brain Res. 37 (1–2): 41–8. doi:10.1016/0169-328X(96)80478-5. PMID 8738134.
- Yang SN, Larsson O, Bränström R, et al. (1999). "Syntaxin 1 interacts with the LD subtype of voltage-gated Ca2+ channels in pancreatic β cells". Proc. Natl. Acad. Sci. U.S.A. 96 (18): 10164–9. doi:10.1073/pnas.96.18.10164. PMC 17860. PMID 10468580.
- Bell DC, Butcher AJ, Berrow NS, et al. (2001). "Biophysical properties, pharmacology, and modulation of human, neuronal L-type (alpha(1D), Ca(V)1.3) voltage-dependent calcium currents". J. Neurophysiol. 85 (2): 816–27. PMID 11160515.
- Rosenthal R, Thieme H, Strauss O (2001). "Fibroblast growth factor receptor 2 (FGFR2) in brain neurons and retinal pigment epithelial cells act via stimulation of neuroendocrine L-type channels (Ca(v)1.3)". FASEB J. 15 (6): 970–7. doi:10.1096/fj.00-0188com. PMID 11292657.
- Davare MA, Avdonin V, Hall DD, et al. (2001). "A beta2 adrenergic receptor signaling complex assembled with the Ca2+ channel Cav1.2". Science 293 (5527): 98–101. doi:10.1126/science.293.5527.98. PMID 11441182.
- Namkung Y, Skrypnyk N, Jeong MJ, et al. (2001). "Requirement for the L-type Ca2+ channel α1D subunit in postnatal pancreatic β cell generation". J. Clin. Invest. 108 (7): 1015–22. doi:10.1172/JCI13310. PMC 200955. PMID 11581302.
- Stokes L, Gordon J, Grafton G (2004). "Non-voltage-gated L-type Ca2+ channels in human T cells: pharmacology and molecular characterization of the major alpha pore-forming and auxiliary beta-subunits". J. Biol. Chem. 279 (19): 19566–73. doi:10.1074/jbc.M401481200. PMID 14981074.
- Qu Y, Baroudi G, Yue Y, Boutjdir M (2006). "Novel molecular mechanism involving alpha1D (Cav1.3) L-type calcium channel in autoimmune-associated sinus bradycardia". Circulation 111 (23): 3034–41. doi:10.1161/CIRCULATIONAHA.104.517326. PMID 15939813.
- Baroudi G, Qu Y, Ramadan O, et al. (2006). "Protein kinase C activation inhibits Cav1.3 calcium channel at NH2-terminal serine 81 phosphorylation site". Am. J. Physiol. Heart Circ. Physiol. 291 (4): H1614–22. doi:10.1152/ajpheart.00095.2006. PMID 16973824.
- Olsen JV, Blagoev B, Gnad F, et al. (2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks". Cell 127 (3): 635–48. doi:10.1016/j.cell.2006.09.026. PMID 17081983.
External links
- CACNA1D protein, human at the US National Library of Medicine Medical Subject Headings (MeSH)
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