"KCNA1 protein, human"[nm] - Search Results

Year	Number of Results
1994	2
1995	4
1996	5
1998	7
1999	13
2000	7
2001	7
2002	10
2003	6
2004	11
2005	4
2006	2
2007	3
2008	3
2009	6
2010	5
2011	3
2012	3
2013	5
2014	6
2015	1
2016	5
2017	3
2018	7
2019	2
2020	9
2021	3
2022	3
2023	3
2024	0

1

Novel Genetic Variants Expand the Functional, Molecular, and Pathological Diversity of KCNA1 Channelopathy.

Paulhus K, Glasscock E. Paulhus K, et al. Int J Mol Sci. 2023 May 16;24(10):8826. doi: 10.3390/ijms24108826. Int J Mol Sci. 2023. PMID: 37240170 Free PMC article. Review.

2

Clinical Spectrum of KCNA1 Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity.

Paulhus K, Ammerman L, Glasscock E. Paulhus K, et al. Int J Mol Sci. 2020 Apr 17;21(8):2802. doi: 10.3390/ijms21082802. Int J Mol Sci. 2020. PMID: 32316562 Free PMC article. Review.

3

KCNA1 gain-of-function epileptic encephalopathy treated with 4-aminopyridine.

Müller P, Takacs DS, Hedrich UBS, Coorg R, Masters L, Glinton KE, Dai H, Cokley JA, Riviello JJ, Lerche H, Cooper EC. Müller P, et al. Ann Clin Transl Neurol. 2023 Apr;10(4):656-663. doi: 10.1002/acn3.51742. Epub 2023 Feb 15. Ann Clin Transl Neurol. 2023. PMID: 36793218 Free PMC article.

4

Isoform-Selective KCNA1 Potassium Channel Openers Built from Glycine.

Manville RW, Abbott GW. Manville RW, et al. J Pharmacol Exp Ther. 2020 Jun;373(3):391-401. doi: 10.1124/jpet.119.264507. Epub 2020 Mar 26. J Pharmacol Exp Ther. 2020. PMID: 32217768 Free PMC article.

5

[Episodic ataxias].

Herrmann A, Braathen GJ, Russell MB. Herrmann A, et al. Tidsskr Nor Laegeforen. 2005 Aug 11;125(15):2005-7. Tidsskr Nor Laegeforen. 2005. PMID: 16100538 Free article. Review. Norwegian.

6

Adenosine-to-inosine RNA editing in neurological development and disease.

Yang Y, Okada S, Sakurai M. Yang Y, et al. RNA Biol. 2021 Jul;18(7):999-1013. doi: 10.1080/15476286.2020.1867797. Epub 2021 Jan 6. RNA Biol. 2021. PMID: 33393416 Free PMC article. Review.

7

Ion channel shake-down.

Ptácek L. Ptácek L. Nat Genet. 1994 Oct;8(2):111-2. doi: 10.1038/ng1094-111. Nat Genet. 1994. PMID: 7531055 No abstract available.

8

Silencing of KCNA1 suppresses the cervical cancer development via mitochondria damage.

Liu L, Chen Y, Zhang Q, Li C. Liu L, et al. Channels (Austin). 2019 Dec;13(1):321-330. doi: 10.1080/19336950.2019.1648627. Channels (Austin). 2019. PMID: 31354026 Free PMC article.

9

Primary episodic ataxias: diagnosis, pathogenesis and treatment.

Jen JC, Graves TD, Hess EJ, Hanna MG, Griggs RC, Baloh RW; CINCH investigators. Jen JC, et al. Brain. 2007 Oct;130(Pt 10):2484-93. doi: 10.1093/brain/awm126. Epub 2007 Jun 15. Brain. 2007. PMID: 17575281 Review.

10

Complete loss of KCNA1 activity causes neonatal epileptic encephalopathy and dyskinesia.

Verdura E, Fons C, Schlüter A, Ruiz M, Fourcade S, Casasnovas C, Castellano A, Pujol A. Verdura E, et al. J Med Genet. 2020 Feb;57(2):132-137. doi: 10.1136/jmedgenet-2019-106373. Epub 2019 Oct 5. J Med Genet. 2020. PMID: 31586945 Free PMC article.

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