Insights on possible interplay between epithelial-mesenchymal transition and T-type voltage gated calcium channels genes in metastatic breast carcinoma by Fawziya A.E. Ragab Ibrahim, Zain Ulabdeen Naser Hussein, Amany I. Yousef, Nadia Ahmed Abd El Moneim, Amr Mahmoud Hussein, Ayman Farouk Mohammad Ahmed, Noha Mohamed Ragab, O. Al-Masry

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L-type calcium channels and neuropsychiatric diseases: Insights into genetic risk variant-associated genomic regulation and impact on brain development by Madelyn R. Baker, Andrew S. Lee, Anjali M. Rajadhyaksha

Subjects: “…CACNA1C…”
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A novel CACNA1A variant in a child with early stroke and intractable epilepsy by Franciska J. Gudenkauf, Mahshid S. Azamian, Jill V. Hunter, Anuranjita Nayak, Seema R. Lalani

Subjects: “…CACNA1A…”
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Generation of induced pluripotent stem cell lines carrying monoallelic (UCSFi001-A-60) or biallelic (UCSFi001-A-61; UCSFi001-A-62) frameshift variants in CACNA1A using CRISPR/Cas9 by Marina P. Hommersom, Chantal Bijnagte-Schoenmaker, Silvia Albert, Bart P.C. van de Warrenburg, Nael Nadif Kasri, Hans van Bokhoven

Subjects: “…CACNA1A…”
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The Drosophila ortholog of the schizophrenia-associated CACNA1A and CACNA1B voltage-gated calcium channels regulate memory, sleep and circadian rhythms by Sergio Hidalgo, Jorge M. Campusano, James J.L. Hodge

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CACNA1C Gene rs1006737 Polymorphism Affects Cognitive Performance in Chinese Han Schizophrenia by Chen M, Jiang Q, Zhang L

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Many Channels Lead to Aldosterone by Holger S. Willenberg

Subjects: “…CACNA1H…”
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Longitudinal MRI brain findings in the R1349Q pathogenic variant of CACNA1A by Chang Y. Ho, MD, Harrison L. Love, MSIV, Deborah K. Sokol, MD, Laurence E. Walsh, MD

Subjects: “…CACNA1A…”
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Epileptic Encephalopathy due to CACNA1A Variant: A Case Report and Diagnostic Challenges from Resource-Limited Settings by Hilary Chipongo, Samina Chaki, Ronald Mclarty

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Mutation analysis of CACNA1A gene in Iranian migrainous and review literatures by Rokhsareh Meamar, Maryam Ostadsharif, Mohammad Saadatnia, Abbas Ghorbani, Nayereh Nouri, Leila Dehghani, Mansoor Salehi

Subjects: “…CACNA1A gene…”
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Further evidence for the genetic association between CACNA1I and schizophrenia by Yijun Xie, Di Huang, Li Wei, Xiong-Jian Luo

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The first-line antihypertensive nitrendipine potentiated the therapeutic effect of oxaliplatin by downregulating CACNA1D in colorectal cancer by Lai Chengzhe, Liu Jinghu, Zhou Jingna, Zhou Haokun

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New CACNA1A deletions are associated to migraine phenotypes by G. S. Grieco, S. Gagliardi, I. Ricca, O. Pansarasa, M. Neri, F. Gualandi, G. Nappi, A. Ferlini, C. Cereda

Subjects: “…CACNA1A…”
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Autophagy is affected in patients with hypokalemic periodic paralysis: an involvement in vacuolar myopathy? by Thomas O. Krag, Sonja Holm-Yildiz, Nanna Witting, John Vissing

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Expanding the Phenotype of the CACNA1C-Associated Neurological Disorders in Children: Systematic Literature Review and Description of a Novel Mutation by Lorenzo Cipriano, Raffaele Piscopo, Chiara Aiello, Antonio Novelli, Achille Iolascon, Carmelo Piscopo

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CACNA1C (rs1006737) may be a susceptibility gene for schizophrenia: An updated meta‐analysis by Dongjian Zhu, Jingwen Yin, Chunmei Liang, Xudong Luo, Dong Lv, Zhun Dai, Susu Xiong, Jiawu Fu, You Li, Juda Lin, Zhixiong Lin, Yajun Wang, Guoda Ma

Subjects: “…CACNA1C…”
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Ocular Manifestation of CACNA1A Pathogenic Variants by Karit Reinson, Katrin Õunap

Subjects: “…cacna1a…”
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The expanding phenotype of hypokalemic periodic paralysis in a Japanese family with p.Val876Glu mutation in CACNA1S by Mari Kurokawa, Michiko Torio, Kazuhiro Ohkubo, Vlad Tocan, Noriko Ohyama, Naoko Toda, Kanako Ishii, Kei Nishiyama, Yuichi Mushimoto, Ryuichi Sakamoto, Maki Nakaza, Riho Horie, Tomoya Kubota, Masanori P. Takahashi, Yasunari Sakai, Masatoshi Nomura, Shouichi Ohga

Subjects: “…CACNA1S…”
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Differential trigeminovascular nociceptive responses in the thalamus in the familial hemiplegic migraine 1 knock-in mouse: A Fos protein study by JungWook Park, HeuiSoo Moon, Simon Akerman, Philip R. Holland, Michele P. Lasalandra, Anna P. Andreou, Michel D. Ferrari, Arn M.J.M. van den Maagdenberg, Peter J. Goadsby

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Familial hypokalemic periodic paralysis: a case induced by concurrent hyperthyroidism by Zein Alabdin Hannouneh, C. Elena Cervantes, C. John Sperati, Mohamad Hanouneh

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