PMC Links for Gene (Select 775) - PMC

Links from Gene

Items: 1 to 20 of 188

<< First< Prev

Page of 10

Select item 107176841.

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

Article PDF–571K

Select item 105769982.

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

Article PDF–833K

Select item 104376993.

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

Article PDF–764K

Select item 98415504.

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

Article PDF–775K

Select item 96919315.

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

Article PDF–12M

Select item 96282256.

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

Article PDF–13M

Select item 93027567.

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

Article PDF–1.5M

Select item 88515478.

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

Article PDF–6.2M

Select item 84880209.

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

Article PDF–1.3M

Select item 825224610.

CACNA1C is a prognostic predictor for patients with ovarian cancer

Xiaohan Chang, Yunxia Dong

J Ovarian Res. 2021; 14: 88. Published online 2021 Jul 1. doi: 10.1186/s13048-021-00830-z

PMCID:: PMC8252246

Article PDF–6.3M

Select item 822283211.

Expanding the phenotype of CACNA1C mutation disorders

Lindsey Gakenheimer‐Smith, Lindsay Meyers, Derek Lundahl, Shaji C. Menon, T. Jared Bunch, Briana L. Sawyer, Martin Tristani‐Firouzi, Susan P. Etheridge

Mol Genet Genomic Med. 2021 Jun; 9(6): e1673. Published online 2021 Apr 1. doi: 10.1002/mgg3.1673

PMCID:: PMC8222832

Article PDF–507K

Select item 816522912.

Update on the Molecular Genetics of Timothy Syndrome

Rosemary Bauer, Katherine W. Timothy, Andy Golden

Front Pediatr. 2021; 9: 668546. Published online 2021 May 17. doi: 10.3389/fped.2021.668546

PMCID:: PMC8165229

Article PDF–1.1M

Select item 790912813.

CACNA1C rs1006737 SNP increases the risk of essential hypertension in both Chinese Han and ethnic Russian people of Northeast Asia

Hao Zhang, Boris Pushkarev, Jiexin Zhou, Yuyuan Mu, Olga Bolshakova, Sandeep Shrestha, Ningning Wang, Baiyu Jian, Ming Jin, Keyong Zhang, Mingyu Cong, Jicheng Liu, Yuri Vitkovsky, Changchun Qiu

Medicine (Baltimore) 2021 Feb 26; 100(8): e24825. Published online 2021 Feb 26. doi: 10.1097/MD.0000000000024825

PMCID:: PMC7909128

Article PDF–483K

Select item 790900514.

Tissue-specific adrenergic regulation of the L-type Ca²⁺ channel Ca_V1.2

Kwun Nok Mimi Man, Peter Bartels, Mary C. Horne, Johannes W. Hell

Sci Signal. Author manuscript; available in PMC 2021 Jun 22.

Published in final edited form as: Sci Signal. 2020 Dec 22; 13(663): eabc6438. Published online 2020 Dec 22. doi: 10.1126/scisignal.abc6438

PMCID:: PMC7909005

Article PDF–683K

Select item 782898215.

CACNA1C polymorphism and brain cortical structure in bipolar disorder

Erik Smedler, Christoph Abé, Erik Pålsson, Martin Ingvar, Mikael Landén

J Psychiatry Neurosci. 2020 May; 45(3): 182–187. Published online 2019 Dec 12. doi: 10.1503/jpn.190029

PMCID:: PMC7828982

Article PDF–476K

Select item 769625116.

New Cav1.2 Channelopathy with High-Functioning Autism, Affective Disorder, Severe Dental Enamel Defects, a Short QT Interval, and a Novel CACNA1C Loss-of-Function Mutation

Dominique Endres, Niels Decher, Isabell Röhr, Kirsty Vowinkel, Katharina Domschke, Katalin Komlosi, Andreas Tzschach, Birgitta Gläser, Miriam A. Schiele, Kimon Runge, Patrick Süß, Florian Schuchardt, Kathrin Nickel, Birgit Stallmeyer, Susanne Rinné, Eric Schulze-Bahr, Ludger Tebartz van Elst

Int J Mol Sci. 2020 Nov; 21(22): 8611. Published online 2020 Nov 15. doi: 10.3390/ijms21228611

PMCID:: PMC7696251

Article PDF–2.2M

Select item 741470817.

The genome-wide supported CACNA1C gene polymorphisms and the risk of schizophrenia: an updated meta-analysis

Yong-ping Liu, Xue Wu, Xi Xia, Jun Yao, Bao-jie Wang

BMC Med Genet. 2020; 21: 159. Published online 2020 Aug 8. doi: 10.1186/s12881-020-01084-0

PMCID:: PMC7414708

Article PDF–1.9M

Select item 687977418.

Highlight article: Dysfunctional Cav1.2 channel in Timothy syndrome, from cell to bedside

Dan Han, Xiaolin Xue, Yang Yan, Guoliang Li

Exp Biol Med (Maywood) 2019 Sep; 244(12): 960–971. Published online 2019 Jul 19. doi: 10.1177/1535370219863149

PMCID:: PMC6879774

Article PDF–843K

Select item 686979619.

Association of rs1006737 in CACNA1C with alterations in prefrontal activation and fronto‐hippocampal connectivity

Frieder M. Paulus, Johannes Bedenbender, Sören Krach, Martin Pyka, Axel Krug, Jens Sommer, Miriam Mette, Markus M. Nöthen, Stephanie H. Witt, Marcella Rietschel, Tilo Kircher, Andreas Jansen

Hum Brain Mapp. 2014 Apr; 35(4): 1190–1200. Published online 2013 Feb 13. doi: 10.1002/hbm.22244

PMCID:: PMC6869796

Article PDF–319K

Select item 661791020.

Identification of a novel mutation in the CACNA1C gene in a Chinese family with autosomal dominant cerebellar ataxia

Jiajun Chen, Yajuan Sun, Xiaoyang Liu, Jia Li

BMC Neurol. 2019; 19: 157. Published online 2019 Jul 10. doi: 10.1186/s12883-019-1381-8

PMCID:: PMC6617910

Article PDF–755K

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 188

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity