References
- Burnashev N, Monyer H, Seeburg PH, Sakmann B. Divalent ion permeability of AMPA receptor channels is dominated by the edited form of a single subunit. Neuron 8: 189-198, 1992 https://doi.org/10.1016/0896-6273(92)90120-3
- Engelman HS, Albuquerque C, Lee CJ, Allen TB, MacDermott AB. Calcium permeable AMPA receptors expressed in laminae I and II of the postnatal rat spinal cord. Soc Neurosci Abstr 23: 1754, 1997
- Engelman HS, Allen TB, MacDermott AB. The distribution of neurons expressing calcium-permeable AMPA receptors in the superficial laminae of the spinal cord dorsal horn. J Neuroscience 19(6): 2081-2089, 1999
-
Geiger JR, Melcher T, Koh DS, Sakmann B, Seeburg PH, Jonas P, Monyer H. Relative abundance of subunit mRNAs determines gating and Ca2
$^+$ permeability of AMPA receptors in principal neurons and interneurons in rat CNS. Neuron 15: 193-204, 1995 https://doi.org/10.1016/0896-6273(95)90076-4 -
Gu JG, Albuquerque C, Lee CJ, MacDermott AB. Synaptic streng thening through activation of Ca2
$^+$ -permeable AMPA receptors. Nature 381: 793-796, 1996 https://doi.org/10.1038/381793a0 -
Hollmann M, Hartley M, Heinemann S. Ca2
$^+$ permeability of KAAMPA- gated glutamate receptor channels depends on subunit composition. Science 252: 851-853, 1991 https://doi.org/10.1126/science.1709304 - Hollmann M, Heinemann S. Cloned glutamate receptors. Annu Rev Neurosci 17: 31-108, 1994 https://doi.org/10.1146/annurev.ne.17.030194.000335
- Hume RI, Dingledine R, Heinemann SF. Identification of a site in glutamate receptor subunits that controls calcium permeability. Science 253: 1028-10031, 1991 https://doi.org/10.1126/science.1653450
- Finch EA, Augustine GJ. Local calcium signalling by inositol-1, 4,5-trisphosphate in Purkinje cell dendrites. Nature 396(6713): 753-756, 1998 https://doi.org/10.1038/25541
- Jia Z, Agopyan N, Miu P, Xiong Z, Henderson J, Gerlai R, Taverna FA, Velumian A, MacDonald J, Carlen P, Abramow-Newerly W, Roder J. Enhanced LTP in mice deficient in the AMPA receptor GluR2. Neuron 17: 945-956, 1996 https://doi.org/10.1016/S0896-6273(00)80225-1
- Jonas P, Burnashev N. Molecular mechanisms controlling calcium entry through AMPA-type glutamate receptor channels. Neuron 15(5): 987-990, 1995 https://doi.org/10.1016/0896-6273(95)90087-X
-
Liberman DN, Mody I. Regulation of NMDA channel function by endogenous Ca2
$^+$ -dependent phosphatase. Nature 369(6477): 235-239, 1994 https://doi.org/10.1038/369235a0 - Mahanty NK, Sah P. Calcium-permeable AMPA receptors mediate long-term potentiation in interneurons in the amygdala. Nature 394: 683-687, 1998 https://doi.org/10.1038/29312
- Mayer ML, Westbrook GL, Guthrie PB. Voltage-dependent block by Mg2+ of NMDA receptors in spinal cord neurons. Nature 309: 261-263, 1984 https://doi.org/10.1038/309261a0
- McBain CJ, Mayer ML. N-methyl-D-aspartic acid receptor struc ture and function. Physiol Rev 74: 723-760, 1994 https://doi.org/10.2466/pr0.1994.74.3.723
- Nagy I, Woolf CJ, Dray A, Urban L. Cobalt accumulation in neurons expressing ionotropic excitatory amino acid receptors in young rat spinal cord: morphology and distribution. J Comp Neurol 344: 321-335, 1994 https://doi.org/10.1002/cne.903440302
- Nishiyama M, Hong K, Mikoshiba K, Poo MM, Kato K. Calcium stores regulate the polarity and input specific of synaptic modification. Nature 408(6812): 584-588, 2000 https://doi.org/10.1038/35046067
- Takechi H, Eilers J, Konnerth A. A new class of synaptic response involving calcium release in dendritic spines. Nature 396(6713): 757-760, 1998 https://doi.org/10.1038/25547
- Tempia F, Alojado ME, Strata P, Knopfel T. Characterization of the mGluR(1)-mediated electrical and calcium signaling in Purkinje cells of mouse cerebellar slices. J Neurophysiol 86(3): 1389-1397, 2001
- Washburn MS, Numberger M, Zhang S, Dingledine R. Differential dependence on GluR2 expression of three characteristic features of AMPA receptors. J Neurosci 17: 9393-9406, 1997
- Yoshimura M, Jessell T. Amino acid-mediated EPSPs at primary afferent synapses with substantia gelatinosa neurones in the rat spinal cord. J Physiol (Lond) 430: 315-335, 1990 https://doi.org/10.1113/jphysiol.1990.sp018293