David JP - Search Results

1

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: david jp. Biomark Med. 2014;8(4):557-70. doi: 10.2217/bmm.13.137. Biomark Med. 2014. PMID: 24796621

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: david jp. 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

Trafficking of the IKs -complex in MDCK cells: site of subunit assembly and determinants of polarized localization.

David JP, Andersen MN, Olesen SP, Rasmussen HB, Schmitt N. David JP, et al. Traffic. 2013 Apr;14(4):399-411. doi: 10.1111/tra.12042. Epub 2013 Feb 13. Traffic. 2013. PMID: 23324056 Free article.

4

Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A.

Calloe K, Schmitt N, Grubb S, Pfeiffer R, David JP, Kanter R, Cordeiro JM, Antzelevitch C. Calloe K, et al. Among authors: david jp. Can J Physiol Pharmacol. 2011 Oct;89(10):723-36. doi: 10.1139/y11-070. Epub 2011 Sep 6. Can J Physiol Pharmacol. 2011. PMID: 21895525 Free PMC article.

5

High incidence of functional ion-channel abnormalities in a consecutive Long QT cohort with novel missense genetic variants of unknown significance.

Steffensen AB, Refaat MM, David JP, Mujezinovic A, Calloe K, Wojciak J, Nussbaum RL, Scheinman MM, Schmitt N. Steffensen AB, et al. Among authors: david jp. Sci Rep. 2015 Jun 12;5:10009. doi: 10.1038/srep10009. Sci Rep. 2015. PMID: 26066609 Free PMC article.

6

Auxiliary KCNE subunits modulate both homotetrameric Kv2.1 and heterotetrameric Kv2.1/Kv6.4 channels.

David JP, Stas JI, Schmitt N, Bocksteins E. David JP, et al. Sci Rep. 2015 Aug 5;5:12813. doi: 10.1038/srep12813. Sci Rep. 2015. PMID: 26242757 Free PMC article.

7

Deletion in mice of X-linked, Brugada syndrome- and atrial fibrillation-associated Kcne5 augments ventricular K_V currents and predisposes to ventricular arrhythmia.

David JP, Lisewski U, Crump SM, Jepps TA, Bocksteins E, Wilck N, Lossie J, Roepke TK, Schmitt N, Abbott GW. David JP, et al. FASEB J. 2019 Feb;33(2):2537-2552. doi: 10.1096/fj.201800502R. Epub 2018 Oct 5. FASEB J. 2019. PMID: 30289750 Free PMC article.

8

Functional phenotype variations of two novel K_V 7.1 mutations identified in patients with Long QT syndrome.

Hammami Bomholtz S, Refaat M, Buur Steffensen A, David JP, Espinosa K, Nussbaum R, Wojciak J, Hjorth Bentzen B, Scheinman M, Schmitt N. Hammami Bomholtz S, et al. Among authors: david jp. Pacing Clin Electrophysiol. 2020 Feb;43(2):210-216. doi: 10.1111/pace.13870. Epub 2020 Jan 11. Pacing Clin Electrophysiol. 2020. PMID: 31899541

9

Engineering of Impact Ionization Characteristics in GaAs/GaAsBi Multiple Quantum Well Avalanche Photodiodes.

Tao X, Jin X, Gao S, Yi X, Liu Y, Rockett TBO, Bailey NJ, Harun F, Adham NA, H Tan C, Richards RD, David JPR. Tao X, et al. Among authors: david jpr. ACS Photonics. 2024 Nov 8;11(11):4846-4853. doi: 10.1021/acsphotonics.4c01343. eCollection 2024 Nov 20. ACS Photonics. 2024. PMID: 39584037 Free PMC article.

10

Frailty in heart failure according to the presence or absence of wild-type transthyretin cardiac amyloidosis.

Broussier A, Paugam M, Liu N, Oghina S, Kharoubi M, Lafont C, Zaroui A, Galat A, Hittinger L, Teiger E, David JP, Bastuji-Garin S, Damy T. Broussier A, et al. Among authors: david jp. ESC Heart Fail. 2024 Sep 16. doi: 10.1002/ehf2.15026. Online ahead of print. ESC Heart Fail. 2024. PMID: 39285643 Free article.

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