Diane M. Papazian

Affiliations: 
University of California, Los Angeles, Los Angeles, CA 
Area:
K Channels
Website:
http://149.142.237.180/faculty/papazian.htm
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"Diane Papazian"
Mean distance: 15.92 (cluster 11)
 

Children

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William R. Silverman grad student 2002 UCLA
Natali A. Minassian grad student 2010 UCLA
Naomi Nagaya post-doc UCLA
Seema K. Tiwari-Woodruff post-doc 1994-1998 UCLA (Cell Biology Tree)
Michael P. Myers post-doc 1998-2001 UCLA
Fadi A. Issa post-doc 2009-2014 UCLA
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Publications

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Duarri A, Lin MC, Fokkens MR, et al. (2015) Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant manner. Cellular and Molecular Life Sciences : Cmls
Hsieh JY, Ulrich B, Issa FA, et al. (2014) Rapid development of Purkinje cell excitability, functional cerebellar circuit, and afferent sensory input to cerebellum in zebrafish. Frontiers in Neural Circuits. 8: 147
Lee H, Lin MC, Kornblum HI, et al. (2014) Exome sequencing identifies de novo gain of function missense mutation in KCND2 in identical twins with autism and seizures that slows potassium channel inactivation. Human Molecular Genetics. 23: 3481-9
Issa FA, Mock AF, Sagasti A, et al. (2012) Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development. Disease Models & Mechanisms. 5: 921-9
Minassian NA, Lin MC, Papazian DM. (2012) Altered Kv3.3 channel gating in early-onset spinocerebellar ataxia type 13. The Journal of Physiology. 590: 1599-614
Lin MC, Hsieh JY, Mock AF, et al. (2011) R1 in the Shaker S4 occupies the gating charge transfer center in the resting state. The Journal of General Physiology. 138: 155-63
Issa FA, Mazzochi C, Mock AF, et al. (2011) Spinocerebellar ataxia type 13 mutant potassium channel alters neuronal excitability and causes locomotor deficits in zebrafish. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 6831-41
Figueroa KP, Waters MF, Garibyan V, et al. (2011) Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13). Plos One. 6: e17811
Issa FA, O'Brien G, Kettunen P, et al. (2011) Neural circuit activity in freely behaving zebrafish (Danio rerio). The Journal of Experimental Biology. 214: 1028-38
Mock AF, Richardson JL, Hsieh JY, et al. (2010) Functional effects of spinocerebellar ataxia type 13 mutations are conserved in zebrafish Kv3.3 channels. Bmc Neuroscience. 11: 99
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