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Items: 1 to 20 of 191

1.
EMC chaperone–CaV structure reveals an ion channel assembly intermediate
Zhou Chen, Abhisek Mondal, Fayal Abderemane-Ali, Seil Jang, Sangeeta Niranjan, José L. Montaño, Balyn W. Zaro, Daniel L. Minor, Jr
Nature. Author manuscript; available in PMC 2024 Feb 26.
Published in final edited form as: Nature. 2023 Jul; 619(7969): 410–419. Published online 2023 May 17. doi: 10.1038/s41586-023-06175-5
PMCID:
PMC10896479
AbstractArticlePDF–5.5M
2.
Lobe-related concentration- and Ca2+-dependent interactions of calmodulin with C- and N-terminal tails of the CaV1.2 channel
Guilin He, Feng Guo, Tong Zhu, Dongxue Shao, Rui Feng, Dandan Yin, Xuefei Sun, Huiyuan Hu, Ahhyeon Hwang, Etsuko Minobe, Masaki Kameyama, Liying Hao
J Physiol Sci. 2013 Sep; 63(5): 345–353. Published online 2013 Jun 4. doi: 10.1007/s12576-013-0270-y
PMCID:
PMC10717684
AbstractArticlePDF–571K
3.
CACNA1C-related channelopathies
Kevin G. Herold, John W. Hussey, Ivy E. Dick
Handb Exp Pharmacol. Author manuscript; available in PMC 2023 Oct 15.
Published in final edited form as: Handb Exp Pharmacol. 2023; 279: 159–181. doi: 10.1007/164_2022_624
PMCID:
PMC10576998
AbstractArticlePDF–833K
4.
The rs216009 single-nucleotide polymorphism of the CACNA1C gene is associated with phantom tooth pain
Masako Morii, Seii Ohka, Daisuke Nishizawa, Junko Hasegawa, Kyoko Nakayama, Yuko Ebata, Moe Soeda, Ken-ichi Fukuda, Kaori Yoshida, Kyotaro Koshika, Tatsuya Ichinohe, Kazutaka Ikeda
Mol Pain. 2023; 19: 17448069231193383. Published online 2023 Aug 17. doi: 10.1177/17448069231193383
PMCID:
PMC10437699
AbstractArticlePDF–764K
5.
Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia
Yu-Han H. Hsu, Greta Pintacuda, Ruize Liu, Eugeniu Nacu, April Kim, Kalliopi Tsafou, Natalie Petrossian, William Crotty, Jung Min Suh, Jackson Riseman, Jacqueline M. Martin, Julia C. Biagini, Daya Mena, Joshua K.T. Ching, Edyta Malolepsza, Taibo Li, Tarjinder Singh, Tian Ge, Shawn B. Egri, Benjamin Tanenbaum, Caroline R. Stanclift, Annie M. Apffel, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Stanley Global Asia Initiatives, Steven A. Carr, Monica Schenone, Jake Jaffe, Nadine Fornelos, Hailiang Huang, Kevin C. Eggan, Kasper Lage
iScience. 2023 May 19; 26(5): 106701. Published online 2023 Apr 18. doi: 10.1016/j.isci.2023.106701
PMCID:
PMC10189495
AbstractArticlePDF–5.3M
6.
Cross-linking mass spectrometry discovers, evaluates, and corroborates structures and protein–protein interactions in the human cell
Tara K. Bartolec, Xabier Vázquez-Campos, Alexander Norman, Clement Luong, Marcus Johnson, Richard J. Payne, Marc R. Wilkins, Joel P. Mackay, Jason K. K. Low
Proc Natl Acad Sci U S A. 2023 Apr 25; 120(17): e2219418120. Published online 2023 Apr 18. doi: 10.1073/pnas.2219418120
PMCID:
PMC10151615
AbstractArticlePDF–2.9M
7.
FBXO22 promotes leukemogenesis by targeting BACH1 in MLL-rearranged acute myeloid leukemia
Xiao-Na Zhu, Yu-Sheng Wei, Qian Yang, Hao-Ran Liu, Zhe Zhi, Di Zhu, Li Xia, Deng-Li Hong, Yun Yu, Guo-Qiang Chen
J Hematol Oncol. 2023; 16: 9. Published online 2023 Feb 11. doi: 10.1186/s13045-023-01400-0
PMCID:
PMC9922468
AbstractArticlePDF–4.9M
8.
Reviving Cav1.2 as an attractive drug target to treat bladder dysfunction
Weiqun Yu
FASEB J. Author manuscript; available in PMC 2023 Jan 16.
Published in final edited form as: FASEB J. 2022 Jan; 36(1): e22118. doi: 10.1096/fj.202101475R
PMCID:
PMC9841550
AbstractArticlePDF–775K
9.
A CACNA1C variant associated with cardiac arrhythmias provides mechanistic insights in the calmodulation of L-type Ca2+ channels
Juan Zhao, Emilie Segura, Mireille Marsolais, Lucie Parent
J Biol Chem. 2022 Dec; 298(12): 102632. Published online 2022 Oct 21. doi: 10.1016/j.jbc.2022.102632
PMCID:
PMC9691931
AbstractArticlePDF–12M
10.
Analysis of CACNA1C and KCNH2 Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia
Alexander Refisch, Shoko Komatsuzaki, Martin Ungelenk, Andy Schumann, Ha-Yeun Chung, Susann S. Schilling, Wibke Jantzen, Sabine Schröder, Markus M. Nöthen, Thomas W. Mühleisen, Christian A. Hübner, Karl-Jürgen Bär
Genes (Basel) 2022 Nov; 13(11): 2132. Published online 2022 Nov 16. doi: 10.3390/genes13112132
PMCID:
PMC9691174
AbstractArticlePDF–1.2M
11.
Interactome of Aiolos/Ikaros Reveals Combination Rationale of Cereblon Modulators with HDAC Inhibitors in DLBCL
Patrick R. Hagner, Hsiling Chiu, Vivek S. Chopra, Martino Colombo, Nisha Patel, Maria Ortiz Estevez, Michelle F. Waldman, Remco Loos, Fadi Towfic, Anita K. Gandhi
Clin Cancer Res. 2022 Aug 2; 28(15): 3367–3377. Published online 2022 May 18. doi: 10.1158/1078-0432.CCR-21-3347
PMCID:
PMC9662945
AbstractArticlePDF–1.6M
12.
Inhibition of L‐type voltage‐gated calcium channel‐mediated Ca2+ influx suppresses the collective migration and invasion of ameloblastoma
Shujin Li, Hyun‐Yi Kim, Dong‐Joon Lee, Sung‐Ho Park, Keishi Otsu, Hidemitsu Harada, Young‐Soo Jung, Han‐Sung Jung
Cell Prolif. 2022 Nov; 55(11): e13305. Published online 2022 Jul 6. doi: 10.1111/cpr.13305
PMCID:
PMC9628225
AbstractArticlePDF–13M
13.
Genetic Polymorphisms in miR-137 and Its Target Genes, TCF4 and CACNA1C, Contribute to the Risk of Bipolar Disorder: A Preliminary Case-Control Study and Bioinformatics Analysis
Mohammad Ali Mokhtari, Saman Sargazi, Ramin Saravani, Milad Heidari Nia, Shekoufeh Mirinejad, Kinga Hadzsiev, Judit Bene, Mansoor Shakiba
Dis Markers. 2022; 2022: 1886658. Published online 2022 Sep 22. doi: 10.1155/2022/1886658
PMCID:
PMC9526595
AbstractArticlePDF–1.1M
14.
Novel CACNA1C R511Q mutation, located in domain Ⅰ-Ⅱ linker, causes non-syndromic type-8 long QT syndrome
Tadashi Nakajima, Reika Kawabata-Iwakawa, Shuntaro Tamura, Hiroshi Hasegawa, Takashi Kobari, Hideki Itoh, Minoru Horie, Masahiko Nishiyama, Masahiko Kurabayashi, Yoshiaki Kaneko, Hideki Ishii
PLoS One. 2022; 17(7): e0271796. Published online 2022 Jul 21. doi: 10.1371/journal.pone.0271796
PMCID:
PMC9302756
AbstractArticlePDF–1.5M
15.
Increased Ca2+ influx through CaV1.2 drives aortic valve calcification
Maiko Matsui, Rihab Bouchareb, Mara Storto, Yasin Hussain, Andrew Gregg, Steven O. Marx, Geoffrey S. Pitt
JCI Insight. 2022 Mar 8; 7(5): e155569. Published online 2022 Mar 8. doi: 10.1172/jci.insight.155569
PMCID:
PMC8983132
AbstractArticlePDF–15M
16.
Diltiazem inhibits SARS-CoV-2 cell attachment and internalization and decreases the viral infection in mouse lung
Xinxin Wang, Jie Luo, Zhiyuan Wen, Lei Shuai, Chong Wang, Gongxun Zhong, Xijun He, Huizhen Cao, Renqiang Liu, Jinying Ge, Ronghong Hua, Ziruo Sun, Xijun Wang, Jinliang Wang, Zhigao Bu
PLoS Pathog. 2022 Feb; 18(2): e1010343. Published online 2022 Feb 17. doi: 10.1371/journal.ppat.1010343
PMCID:
PMC8890723
AbstractArticlePDF–3.8M
17.
A Selectivity Filter Gate Controls Voltage-Gated Calcium Channel Calcium-Dependent Inactivation
Fayal Abderemane-Ali, Felix Findeisen, Nathan D. Rossen, Daniel L. Minor, Jr.
Neuron. Author manuscript; available in PMC 2022 Feb 25.
Published in final edited form as: Neuron. 2019 Mar 20; 101(6): 1134–1149.e3. Published online 2019 Feb 4. doi: 10.1016/j.neuron.2019.01.011
PMCID:
PMC8878153
AbstractArticlePDF–2.0M
18.
Disrupted Cacna1c gene expression perturbs spontaneous Ca2+ activity causing abnormal brain development and increased anxiety
Erik Smedler, Lauri Louhivuori, Roman A. Romanov, Débora Masini, Ivar Dehnisch Ellström, Chungliang Wang, Martino Caramia, Zoe West, Songbai Zhang, Paola Rebellato, Seth Malmersjö, Irene Brusini, Shigeaki Kanatani, Gilberto Fisone, Tibor Harkany, Per Uhlén
Proc Natl Acad Sci U S A. 2022 Feb 15; 119(7): e2108768119. Published online 2022 Feb 8. doi: 10.1073/pnas.2108768119
PMCID:
PMC8851547
AbstractArticlePDF–6.2M
19.
Co-expression of calcium and hERG potassium channels reduces the incidence of proarrhythmic events
Sara Ballouz, Melissa M Mangala, Matthew D Perry, Stewart Heitmann, Jesse A Gillis, Adam P Hill, Jamie I Vandenberg
Cardiovasc Res. 2021 Sep 1; 117(10): 2216–2227. Published online 2020 Oct 1. doi: 10.1093/cvr/cvaa280
PMCID:
PMC8785951
AbstractArticlePDF–7.7M
20.
Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations
Lance H. Rodan, Rebecca C. Spillmann, Harley T. Kurata, Shawn M. Lamothe, Jasmine Maghera, Rami Abou Jamra, Anna Alkelai, Stylianos E. Antonarakis, Isis Atallah, Omer Bar-Yosef, Frédéric Bilan, Kathrine Bjorgo, Xavier Blanc, Patrick Van Bogaert, Yoav Bolkier, Lindsay C. Burrage, Björn U. Christ, Jorge L. Granadillo, Patricia Dickson, Kirsten A. Donald, Christèle Dubourg, Aviva Eliyahu, Lisa Emrick, Kendra Engleman, Michaela Veronika Gonfiantini, Jean-Marc Good, Judith Kalser, Chiara Kloeckner, Guus Lachmeijer, Marina Macchiaiolo, Francesco Nicita, Sylvie Odent, Emily O’Heir, Xilma Ortiz-Gonzalez, Marta Pacio-Miguez, María Palomares-Bralo, Loren Pena, Konrad Platzer, Mathieu Quinodoz, Emmanuelle Ranza, Jill A. Rosenfeld, Eliane Roulet-Perez, Avni Santani, Fernando Santos-Simarro, Ben Pode-Shakked, Cara Skraban, Rachel Slaugh, Andrea Superti-Furga, Isabelle Thiffault, Richard H. van Jaabrsveld, Marie Vincent, Hong-Gang Wang, Pia Zacher, Undiagnosed Diseases Network, Eric Rush, Geoffrey Pitt, Ping Yee Billie Au, Vandana Shashi
Genet Med. Author manuscript; available in PMC 2022 Apr 1.
Published in final edited form as: Genet Med. 2021 Oct; 23(10): 1922–1932. Published online 2021 Jun 23. doi: 10.1038/s41436-021-01232-8
Correction in:
Genet Med. 2021 Sep 14
PMCID:
PMC8488020
AbstractArticlePDF–1.3M

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