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Select item 98523831.

Jerome Clatot, Natalie Ginn, Gregory Costain, Ethan M. Goldberg

Ann Clin Transl Neurol. 2023 Jan; 10(1): 111–117. Published online 2022 Nov 23. doi: 10.1002/acn3.51707

PMCID:: PMC9852383

Abstract Article PDF–720K

Select item 92874122.

Cryo-EM structure of the human Kv3.1 channel reveals gating control by the cytoplasmic T1 domain

Gamma Chi, Qiansheng Liang, Akshay Sridhar, John B. Cowgill, Kasim Sader, Mazdak Radjainia, Pu Qian, Pablo Castro-Hartmann, Shayla Venkaya, Nanki Kaur Singh, Gavin McKinley, Alejandra Fernandez-Cid, Shubhashish M. M. Mukhopadhyay, Nicola A. Burgess-Brown, Lucie Delemotte, Manuel Covarrubias, Katharina L. Dürr

Nat Commun. 2022; 13: 4087. Published online 2022 Jul 15. doi: 10.1038/s41467-022-29594-w

PMCID:: PMC9287412

Abstract Article PDF–3.1M

Select item 86184073.

Cross Pharmacological, Biochemical and Computational Studies of a Human Kv3.1b Inhibitor from Androctonus australis Venom

Sonia Maatoug, Amani Cheikh, Oussema Khamessi, Hager Tabka, Zied Landoulsi, Jean-Marie Guigonis, Sylvie Diochot, Saïd Bendahhou, Rym Benkhalifa

Int J Mol Sci. 2021 Nov; 22(22): 12290. Published online 2021 Nov 13. doi: 10.3390/ijms222212290

PMCID:: PMC8618407

Abstract Article PDF–3.0M

Select item 84367684.

Progressive myoclonus epilepsy KCNC1 variant causes a developmental dendritopathy

Jenna C. Carpenter, Roope Männikkö, Catherine Heffner, Jana Heneine, Marisol Sampedro‐Castañeda, Gabriele Lignani, Stephanie Schorge

Epilepsia. 2021 May; 62(5): 1256–1267. Published online 2021 Mar 18. doi: 10.1111/epi.16867

PMCID:: PMC8436768

Abstract Article PDF–1.8M

Select item 84099505.

A KCNC1 mutation in epilepsy of infancy with focal migrating seizures produces functional channels that fail to be regulated by PKC phosphorylation

Yalan Zhang, Syed R. Ali, Rima Nabbout, Giulia Barcia, Leonard K. Kaczmarek

J Neurophysiol. 2021 Aug 1; 126(2): 532–539. Published online 2021 Jul 7. doi: 10.1152/jn.00257.2021

PMCID:: PMC8409950

Abstract Article

Select item 80202016.

Methylation gene KCNC1 is associated with overall survival in patients with seminoma

Saipeng Chen, Longfei Xiao, Huahong Peng, Zhen Wang, Jianbing Xie

Oncol Rep. 2021 May; 45(5): 73. Published online 2021 Mar 22. doi: 10.3892/or.2021.8024

PMCID:: PMC8020201

Abstract Article PDF–1.7M

Select item 66496177.

Joohyun Park, Mahmoud Koko, Ulrike B. S. Hedrich, Andreas Hermann, Kirsten Cremer, Edda Haberlandt, Mona Grimmel, Bader Alhaddad, Stefanie Beck‐Woedl, Merle Harrer, Daniela Karall, Lisa Kingelhoefer, Andreas Tzschach, Lars C. Matthies, Tim M. Strom, Erich Bernd Ringelstein, Marc Sturm, Hartmut Engels, Markus Wolff, Holger Lerche, Tobias B. Haack

Ann Clin Transl Neurol. 2019 Jul; 6(7): 1319–1326. Published online 2019 Jun 7. doi: 10.1002/acn3.50799

PMCID:: PMC6649617

Abstract Article PDF–750K

Select item 54379098.

Loss of Function of KCNC1 is associated with intellectual disability without seizures

Karine Poirier, Géraldine Viot, Laura Lombardi, Clémence Jauny, Pierre Billuart, Thierry Bienvenu

Eur J Hum Genet. 2017 May; 25(5): 560–564. Published online 2017 Feb 1. doi: 10.1038/ejhg.2017.3

PMCID:: PMC5437909

Abstract Article PDF–391K

Select item 47038669.

K_v3.1 uses a timely resurgent K⁺ current to secure action potential repolarization

Alain J. Labro, Michael F. Priest, Jérôme J. Lacroix, Dirk J. Snyders, Francisco Bezanilla

Nat Commun. 2015; 6: 10173. Published online 2015 Dec 17. doi: 10.1038/ncomms10173

PMCID:: PMC4703866

Abstract Article PDF–1.5M

Select item 428126010.

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy

Mikko Muona, Samuel F Berkovic, Leanne M Dibbens, Karen L Oliver, Snezana Maljevic, Marta A Bayly, Tarja Joensuu, Laura Canafoglia, Silvana Franceschetti, Roberto Michelucci, Salla Markkinen, Sarah E Heron, Michael S Hildebrand, Eva Andermann, Frederick Andermann, Antonio Gambardella, Paolo Tinuper, Laura Licchetta, Ingrid E Scheffer, Chiara Criscuolo, Alessandro Filla, Edoardo Ferlazzo, Jamil Ahmad, Adeel Ahmad, Betul Baykan, Edith Said, Meral Topcu, Patrizia Riguzzi, Mary D King, Cigdem Ozkara, Danielle M Andrade, Bernt A Engelsen, Arielle Crespel, Matthias Lindenau, Ebba Lohmann, Veronica Saletti, João Massano, Michael Privitera, Alberto J Espay, Birgit Kauffmann, Michael Duchowny, Rikke S Møller, Rachel Straussberg, Zaid Afawi, Bruria Ben-Zeev, Kaitlin E Samocha, Mark J Daly, Steven Petrou, Holger Lerche, Aarno Palotie, Anna-Elina Lehesjoki

Nat Genet. Author manuscript; available in PMC 2015 Jul 1.

Published in final edited form as: Nat Genet. 2015 Jan; 47(1): 39–46. Published online 2014 Nov 17. doi: 10.1038/ng.3144

PMCID:: PMC4281260

Abstract Article PDF–1004K

Select item 758304811.

First Evidence of Kv3.1b Potassium Channel Subtype Expression during Neuronal Serotonergic 1C11 Cell Line Development

Hager Tabka, Amani Cheikh, Sonia Maatoug, Mohamed El Ayeb, Saïd Bendahhou, Rym Benkhalifa

Int J Mol Sci. 2020 Oct; 21(19): 7175. Published online 2020 Sep 29. doi: 10.3390/ijms21197175

PMCID:: PMC7583048

Abstract Article PDF–2.9M

Select item 710896212.

Mechanisms underlying the hyperexcitability of CA3 and dentate gyrus hippocampal neurons derived from bipolar disorder patients.

Shani Stern, Anindita Sarkar, Tchelet Stern, Arianna Mei, Ana P. D. Mendes, Yam Stern, Gabriela Goldberg, Dekel Galor, Thao Nguyen, Lynne Randolph-Moore, Yongsung Kim, Guy Rouleau, Anne Bang, Martin Alda, Renata Santos, Maria C. Marchetto, Fred H. Gage

Biol Psychiatry. Author manuscript; available in PMC 2021 Jul 15.

Published in final edited form as: Biol Psychiatry. 2020 Jul 15; 88(2): 139–149. Published online 2019 Oct 1. doi: 10.1016/j.biopsych.2019.09.018