Altered Kv3.3 channel gating in early‐onset spinocerebellar ataxia type 13
Minassian, Natali A., Lin, Meng‐Chin A., Papazian, Diane M.
Published in The Journal of physiology (01.04.2012)
Published in The Journal of physiology (01.04.2012)
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Neural circuit activity in freely behaving zebrafish (Danio rerio)
Issa, Fadi A, O'Brien, Georgeann, Kettunen, Petronella, Sagasti, Alvaro, Glanzman, David L, Papazian, Diane M
Published in Journal of experimental biology (15.03.2011)
Published in Journal of experimental biology (15.03.2011)
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Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant manner
Duarri, Anna, Lin, Meng-Chin A, Fokkens, Michiel R, Meijer, Michel, Smeets, Cleo J. L. M, Nibbeling, Esther A. R, Boddeke, Erik, Sinke, Richard J, Kampinga, Harm H, Papazian, Diane M, Verbeek, Dineke S
Published in Cellular and molecular life sciences : CMLS (01.09.2015)
Published in Cellular and molecular life sciences : CMLS (01.09.2015)
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Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)
Figueroa, Karla P, Waters, Michael F, Garibyan, Vartan, Bird, Thomas D, Gomez, Christopher M, Ranum, Laura P W, Minassian, Natali A, Papazian, Diane M, Pulst, Stefan M
Published in PloS one (29.03.2011)
Published in PloS one (29.03.2011)
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Structural Basis of Two-Stage Voltage-Dependent Activation in K+Channels
Silverman, William R., Roux, Benoît, Papazian, Diane M.
Published in Proceedings of the National Academy of Sciences - PNAS (04.03.2003)
Published in Proceedings of the National Academy of Sciences - PNAS (04.03.2003)
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Journal Article
Distance Measurements Reveal a Common Topology of Prokaryotic Voltage-Gated Ion Channels in the Lipid Bilayer
Richardson, Jessica, Blunck, Rikard, Ge, Pinghua, Selvin, Paul R., Bezanilla, Francisco, Papazian, Diane M., Correa, Ana M.
Published in Proceedings of the National Academy of Sciences - PNAS (24.10.2006)
Published in Proceedings of the National Academy of Sciences - PNAS (24.10.2006)
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Exome sequencing identifies de novo gain of function missense mutation in KCND2 in identical twins with autism and seizures that slows potassium channel inactivation
Lee, Hane, Lin, Meng-chin A, Kornblum, Harley I, Papazian, Diane M, Nelson, Stanley F
Published in Human molecular genetics (01.07.2014)
Published in Human molecular genetics (01.07.2014)
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Optical detection of rate-determining ion-modulated conformational changes of the ether-à-go-go K+ channel voltage sensor
Bannister, John P A, Chanda, Baron, Bezanilla, Francisco, Papazian, Diane M
Published in Proceedings of the National Academy of Sciences - PNAS (20.12.2005)
Published in Proceedings of the National Academy of Sciences - PNAS (20.12.2005)
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Voltage-dependent structural interactions in the Shaker K(+) channel
Tiwari-Woodruff, S K, Lin, M A, Schulteis, C T, Papazian, D M
Published in The Journal of general physiology (01.02.2000)
Published in The Journal of general physiology (01.02.2000)
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Mg2+ Modulates Voltage-Dependent Activation in Ether-à-Go-Go Potassium Channels by Binding between Transmembrane Segments S2 and S3
Silverman, William R., Tang, Chih-Yung, Mock, Allan F., Huh, Kyung-Bong, Papazian, Diane M.
Published in The Journal of general physiology (01.11.2000)
Published in The Journal of general physiology (01.11.2000)
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Journal Article
Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes
Pulst, Stefan M, Waters, Michael F, Minassian, Natali A, Stevanin, Giovanni, Figueroa, Karla P, Bannister, John P A, Nolte, Dagmar, Mock, Allan F, Evidente, Virgilio Gerald H, Fee, Dominic B, Müller, Ulrich, Dürr, Alexandra, Brice, Alexis, Papazian, Diane M
Published in Nature genetics (01.04.2006)
Published in Nature genetics (01.04.2006)
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KCNC3: phenotype, mutations, channel biophysics--a study of 260 familial ataxia patients
Figueroa, Karla P, Minassian, Natali A, Stevanin, Giovanni, Waters, Michael, Garibyan, Vartan, Forlani, Sylvie, Strzelczyk, Adam, Bürk, Katrin, Brice, Alexis, Dürr, Alexandra, Papazian, Diane M, Pulst, Stefan M
Published in Human mutation (01.02.2010)
Published in Human mutation (01.02.2010)
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