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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 4
1996 4
1997 12
1998 7
1999 10
2000 11
2001 7
2002 11
2003 15
2004 18
2005 18
2006 17
2007 30
2008 36
2009 66
2010 71
2011 42
2012 39
2013 54
2014 44
2015 40
2016 26
2017 32
2018 25
2019 23
2020 26
2021 22
2022 16
2023 7
2024 3

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PubMed (RefSeq) for id: 2241236946

632 results

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Page 1
KCNQ1 p.D446E Variant as a Risk Allele for Arrhythmogenic Phenotypes: Electrophysiological Characterization Reveals a Complex Phenotype Affecting the Slow Delayed Rectifier Potassium Current (IKs) Voltage Dependence by Causing a Hyperpolarizing Shift and a Lack of Response to Protein Kinase A Activation.
González-Garrido A, López-Ramírez O, Cerda-Mireles A, Navarrete-Miranda T, Flores-Arenas AI, Rojo-Domínguez A, Arregui L, Iturralde P, Antúnez-Argüelles E, Domínguez-Pérez M, Jacobo-Albavera L, Carnevale A, Villarreal-Molina T. González-Garrido A, et al. Int J Mol Sci. 2024 Jan 12;25(2):953. doi: 10.3390/ijms25020953. Int J Mol Sci. 2024. PMID: 38256028 Free PMC article.
Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population.
Sieliwonczyk E, Alaerts M, Simons E, Snyders D, Nijak A, Vandendriessche B, Schepers D, Akdeniz D, Van Craenenbroeck E, Knaepen K, Rabaut L, Heidbuchel H, Van Laer L, Saenen J, Labro AJ, Loeys B. Sieliwonczyk E, et al. Orphanet J Rare Dis. 2023 Jan 31;18(1):23. doi: 10.1186/s13023-023-02618-4. Orphanet J Rare Dis. 2023. PMID: 36721196 Free PMC article.
632 results