montage resized.png

PUBLICATIONS

2018

Thomas, J.R., Hagen, J., Soh, D., and A. Lee. (2018) Molecular moieties masking Ca2+-dependent facilitation of voltage-gated Cav2.2 Ca2+ channels. J. Gen. Physiol. 150: 83-94.

Yang, T., Choi, J.E., Soh, D., Tobin, K., Joiner, M.L., Hansen, M., and A. Lee. (2018) CaBP1 regulates Cav1 L-type Ca2+ channels and their coupling to neurite growth and gene transcription in mouse spiral ganglion neurons. Mol. Cell. Neurosci. 88:342-352.

Yang, T., Hu, N., Pangrsic, T., Green, S.H., Hansen, M. and A. Lee. (2018) Functions of CaBP1 and CaBP2 in the peripheral auditory system. Hearing Res. 364:48-58.

Yang, T., Britt, J.K., Cintrón-Pérez, C.J., Vázquez-Rosa, E., Tobin, K.V., Stalker, G., Hardie, J., Taugher, R.J., Wemmie, J., Pieper, A.A., and A. Lee. (2018) Ca2+ binding protein 1 regulates hippocampal-dependent memory and synaptic plasticity. Neuroscience 380:90-102.


Nanou, E., Lee, A., and W.A. Catterall. (2018) Control of excitation/inhibition balance in a hippocampal circuit by calcium sensor protein regulation of presynaptic calcium channels. J. Neurosci. 38:4430-4440.


Kerov, V., Laird, J.G., Joiner, M.L., Knecht, S., Soh, D., Hagen, J., Gardner, S.H., Gutierrez, W., Yoshimatsu, T., Bhattarai, S., Puthussery, T., Artemyev, N.O., Drack, A.V., Wong, R.O., Baker, S.A., and A. Lee. (2018) α2δ-4 is required for the molecular and structural organization of rod and cone photoreceptor synapses. J. Neurosci. 38: 6145-6160.


Garza-Lopez, E., Lopez, J., Hagen, J., Sheffield, R., Meiner, V. and A. Lee. (2018) Role of a conserved glutamine in the function of voltage-gated Ca2+ channels revealed by a mutation in human CACNA1D. J. Biol. Chem. 293: 14444-14454.


Williams, B.., Haeeleer, F., and A. Lee. (2018) Splicing of an automodulatory domain in Cav1.4 Ca2+ channels confers distinct regulation by calmodulin. J. Gen. Physiol. 150: 1676-1687

2013

Haeseleer, F., Sokal, I., Gregory, F.D., and A. Lee. (2013) Protein phosphatase 2A dephosphorylates CaBP4 in the retina and regulates CaBP4 function. Invest. Ophthalmol. Vis. Sci. 54:1214-1226.


Oz, S., Benmocha, A., Sasson, Y., Sachyani, D., Almagor, L., Lee, A., Hirsch, J. A., and N.Dascal. (2013) Competitive and non-competitive regulation of calcium-dependent inactivation in CaV1.2 L-type Ca2+ channels by calmodulin and Ca2+-binding protein 1. J Biol. Chem. 288:12680-12691.


Hall, D.D., Dai, S., Tseng P.Y., Malik, Z., Nguyen, M., Matt. L., Schnizler, K., Shepherd, A., Mohapatra, D.P., Tsuruta, F., Dolmetsch, R.E., Christel, C. J., Lee, A., Burette, A., Weinberg, R.J., and J. W. Hell. (2013) Competition between a-actinin and Ca2+/calmodulin controls surface retention of the L-type Ca2+ channel Cav1.2. Neuron 78:483-497.


Inagaki, A., and A. Lee. (2013) Developmental alterations in the biophysical properties of Cav1.3 Ca2+ channels in mouse inner hair cells. Channels 7:171-181.


Gregory, F. D., Pangrsic, T., Calin-Jageman, I. E., Moser, T., and A. Lee. (2013) Harmonin enhances voltage-dependent facilitation of Cav1.3 channels and synchronous exocytosis in mouse inner hair cells. J. Physiol. 591:3252-3269.


Knoflach, D., Kerov, V., Sartori, S. B., Obermair, G. J., Schmuckermair, C., Liu, X., Sothilingam, V., Garrido, M. G., Baker, S., Glösmann, M., Schicker, K., Seeliger, M., Lee. A., and A. Koschak.(2013) Cav1.4 IT mouse as model for vision impairment in human Congenital Stationary Night Blindness Type 2. Channels 7:502-512.


Liu, X., Kerov, V., Haeseleer, F., Majumder, A., Artemyev, N., Baker, S. A., and A. Lee. (2013) Dysregulation of Cav1.4 channels disrupts the maturation of photoreceptor synaptic ribbons in congenital stationary night blindness type 2. Channels 7:513-522.

2012

Christel, C. and A. Lee. (2012) Electrophysiological analysis of Ca2+-dependent modulation of voltage-gated Ca2+ channels. Biochem. Biophys. Acta 1820:1243-1252.

Lee, A.S., Ra, S., Rajadhyaksha, A.M., Britt, J.K., Jesus-Cortes, D. H., Gonzales, K. L., 
Moosmang, S., Lee, A., Hofmann, F., Pieper, A.A., Rajadhyaksha, A.M. (2012) Forebrain elimination of CACNA1C mediates anxiety-like behavior in mice. Mol. Psychiatry. 17:1054-1055.


Lee, A.S., Gonzales, K.L., Lee, A., Moosmang, S., Hofmann, F., Pieper, A.A., Rajadhyaksha, A.M. (2012) Selective genetic deletion of CACNA1C in the mouse prefrontal cortex. Mol. Psychiatry. 17:1051.


Schrauwen, I., Helfmann, S., Inagaki, A., Wolk, F., Tabatabaiefar, M.A., Picher M.M., Sommen, M., ZazoSeco, C., Kremer, H., Dheedene, A., Claes, C., Fransen,E., Reimnitz, F., Diederichsen, U., HashemzadehM., Couke, P., Lee, A., Moser, T., and G. Van Camp. (2012) A mutation in CABP2, expressed in cochlear hair cells, causes autosomal recessive hearing impairment. Am. J. Hum. Genet. 91(4):636-45.


Christel, C.J., Schaer, R., Wang, S., Henzi, T., Kreiner, L., Grabs, D., Schwaller, B., and A. Lee. (2012) Calretinin regulates Ca2+-dependent inactivation and facilitation of Cav2.1 Ca2+ channels through a direct interaction with the α12.1 subunit. J. Biol. Chem. 287:39766-39775.


Christel, C.J., Cardona, N., Mesirca, P., Herrmann, S., Hofmann, F., Striessnig, J., Ludwig, A., Mangoni, M.E.,and A. Lee. (2012) Distinct localization and modulation of Cav1.2 and Cav1.3 L-type Ca2+ channels in mouse sinoatrial node. J. Physiol. 590: 6327-6341.


Zou, J., Lee, A., and J. Yang. (2012) The expression of whirlin and Cav1.3α1 is mutually independent in photoreceptors. Vision Res. 75:53-59