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Gabapentin Modulates HCN4 Channel Voltage-Dependence.
Tae HS, Smith KM, Phillips AM, Boyle KA, Li M, Forster IC, Hatch RJ, Richardson R, Hughes DI, Graham BA, Petrou S, Reid CA. Tae HS, et al. Among authors: forster ic. Front Pharmacol. 2017 Aug 21;8:554. doi: 10.3389/fphar.2017.00554. eCollection 2017. Front Pharmacol. 2017. PMID: 28871229 Free PMC article.
Functional consequences of the CAPOS mutation E818K of Na+,K+-ATPase.
Roenn CP, Li M, Schack VR, Forster IC, Holm R, Toustrup-Jensen MS, Andersen JP, Petrou S, Vilsen B. Roenn CP, et al. Among authors: forster ic. J Biol Chem. 2019 Jan 4;294(1):269-280. doi: 10.1074/jbc.RA118.004591. Epub 2018 Nov 8. J Biol Chem. 2019. PMID: 30409907 Free PMC article.
Impaired Color Recognition in HCN1 Epilepsy: A Single Case Report.
Mckenzie CE, Ho CJ, Forster IC, Soh MS, Phillips AM, Chang YC, Scheffer IE, Reid CA, Tsai MH. Mckenzie CE, et al. Among authors: forster ic. Front Neurol. 2022 Mar 10;13:834252. doi: 10.3389/fneur.2022.834252. eCollection 2022. Front Neurol. 2022. PMID: 35359652 Free PMC article.
Corrigendum to "Biophysical analysis of an HCN1 epilepsy variant suggests a critical role for S5 helix Met-305 in voltage sensor to pore domain coupling" [Prog. Biophys. Mol. Biol. 166 (2021) 156-172].
Hung A, Forster IC, Mckenzie CE, Berecki G, Petrou S, Kathirvel A, Soh MS, Reid CA. Hung A, et al. Among authors: forster ic. Prog Biophys Mol Biol. 2022 Aug;172:90. doi: 10.1016/j.pbiomolbio.2022.05.003. Epub 2022 May 21. Prog Biophys Mol Biol. 2022. PMID: 35606165 No abstract available.
Mono and biallelic variants in HCN2 cause severe neurodevelopmental disorders.
Houdayer C, Phillips AM, Chabbert M, Bourreau J, Maroofian R, Houlden H, Richards K, Saadi NW, Dad'ová E, Van Bogaert P, Rupin M, Keren B, Charles P, Smol T, Riquet A, Pais L, O'Donnell-Luria A, VanNoy GE, Bayat A, Møller RS, Olofsson K, Abou Jamra R, Syrbe S, Dasouki M, Seaver LH, Sullivan JA, Shashi V, Alkuraya FS, Poss AF, Spence JE, Schnur RE, Forster IC, Mckenzie CE, Simons C, Wang M, Snell P, Kothur K, Buckley M, Roscioli T, Elserafy N, Dauriat B, Procaccio V, Henrion D, Lenaers G, Colin E, Verbeek NE, Van Gassen KL, Legendre C, Bonneau D, Reid CA, Howell KB, Ziegler A, Legros C. Houdayer C, et al. Among authors: forster ic. medRxiv [Preprint]. 2024 Mar 22:2024.03.19.24303984. doi: 10.1101/2024.03.19.24303984. medRxiv. 2024. PMID: 38562733 Free PMC article. Preprint.
Novel GABRA2 variants in epileptic encephalopathy and intellectual disability with seizures.
Maljevic S, Keren B, Aung YH, Forster IC, Mignot C, Buratti J, Lafitte A, Freihuber C, Rodan LH, Bergin A, Hubert L, Poirier K, Munnich A, Besmond C, Hauser N, Miller R, McWalter K, Nabbout R, Héron D, Leguern E, Depienne C, Petrou S, Nava C. Maljevic S, et al. Among authors: forster ic. Brain. 2019 May 1;142(5):e15. doi: 10.1093/brain/awz079. Brain. 2019. PMID: 31032849 No abstract available.
118 results