Schmitt N - Search Results

1

Genetic variation in the two-pore domain potassium channel, TASK-1, may contribute to an atrial substrate for arrhythmogenesis.

Liang B, Soka M, Christensen AH, Olesen MS, Larsen AP, Knop FK, Wang F, Nielsen JB, Andersen MN, Humphreys D, Mann SA, Huttner IG, Vandenberg JI, Svendsen JH, Haunsø S, Preiss T, Seebohm G, Olesen SP, Schmitt N, Fatkin D. Liang B, et al. Among authors: schmitt n. J Mol Cell Cardiol. 2014 Feb;67:69-76. doi: 10.1016/j.yjmcc.2013.12.014. Epub 2013 Dec 27. J Mol Cell Cardiol. 2014. PMID: 24374141

2

Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation.

Olesen MS, Bentzen BH, Nielsen JB, Steffensen AB, David JP, Jabbari J, Jensen HK, Haunsø S, Svendsen JH, Schmitt N. Olesen MS, et al. Among authors: schmitt n. BMC Med Genet. 2012 Apr 3;13:24. doi: 10.1186/1471-2350-13-24. BMC Med Genet. 2012. PMID: 22471742 Free PMC article.

3

Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation.

Christophersen IE, Olesen MS, Liang B, Andersen MN, Larsen AP, Nielsen JB, Haunsø S, Olesen SP, Tveit A, Svendsen JH, Schmitt N. Christophersen IE, et al. Among authors: schmitt n. Eur Heart J. 2013 May;34(20):1517-25. doi: 10.1093/eurheartj/ehs442. Epub 2012 Dec 21. Eur Heart J. 2013. PMID: 23264583

4

A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation.

Olesen MS, Refsgaard L, Holst AG, Larsen AP, Grubb S, Haunsø S, Svendsen JH, Olesen SP, Schmitt N, Calloe K. Olesen MS, et al. Among authors: schmitt n. Cardiovasc Res. 2013 Jun 1;98(3):488-95. doi: 10.1093/cvr/cvt028. Epub 2013 Feb 11. Cardiovasc Res. 2013. PMID: 23400760

5

Genetic modifier of the QTc interval associated with early-onset atrial fibrillation.

Andreasen L, Nielsen JB, Christophersen IE, Holst AG, Sajadieh A, Tveit A, Haunsø S, Svendsen JH, Schmitt N, Olesen MS. Andreasen L, et al. Among authors: schmitt n. Can J Cardiol. 2013 Oct;29(10):1234-40. doi: 10.1016/j.cjca.2013.06.009. Can J Cardiol. 2013. PMID: 24074973

6

Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation.

Olesen MS, Andreasen L, Jabbari J, Refsgaard L, Haunsø S, Olesen SP, Nielsen JB, Schmitt N, Svendsen JH. Olesen MS, et al. Among authors: schmitt n. Heart Rhythm. 2014 Feb;11(2):246-51. doi: 10.1016/j.hrthm.2013.10.034. Epub 2013 Oct 18. Heart Rhythm. 2014. PMID: 24144883

7

Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation.

Nielsen JB, Bentzen BH, Olesen MS, David JP, Olesen SP, Haunsø S, Svendsen JH, Schmitt N. Nielsen JB, et al. Among authors: schmitt n. Biomark Med. 2014;8(4):557-70. doi: 10.2217/bmm.13.137. Biomark Med. 2014. PMID: 24796621

8

The two-pore domain potassium channel, TWIK-1, has a role in the regulation of heart rate and atrial size.

Christensen AH, Chatelain FC, Huttner IG, Olesen MS, Soka M, Feliciangeli S, Horvat C, Santiago CF, Vandenberg JI, Schmitt N, Olesen SP, Lesage F, Fatkin D. Christensen AH, et al. Among authors: schmitt n. J Mol Cell Cardiol. 2016 Aug;97:24-35. doi: 10.1016/j.yjmcc.2016.04.006. Epub 2016 Apr 19. J Mol Cell Cardiol. 2016. PMID: 27103460

9

Functional consequences of genetic variation in sodium channel modifiers in early onset lone atrial fibrillation.

Denti F, Paludan-Müller C, Olesen SP, Haunsø S, Svendsen JH, Olesen MS, Bentzen BH, Schmitt N. Denti F, et al. Among authors: schmitt n. Per Med. 2018 Mar;15(2):93-102. doi: 10.2217/pme-2017-0076. Epub 2018 Jan 31. Per Med. 2018. PMID: 29714131

10

Characterizations of a loss-of-function mutation in the Kir3.4 channel subunit.

Calloe K, Ravn LS, Schmitt N, Sui JL, Duno M, Haunso S, Grunnet M, Svendsen JH, Olesen SP. Calloe K, et al. Among authors: schmitt n. Biochem Biophys Res Commun. 2007 Dec 28;364(4):889-95. doi: 10.1016/j.bbrc.2007.10.106. Epub 2007 Oct 29. Biochem Biophys Res Commun. 2007. PMID: 17967416

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