Nielsen HN - Search Results

1

ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.

Vetro A, Nielsen HN, Holm R, Hevner RF, Parrini E, Powis Z, Møller RS, Bellan C, Simonati A, Lesca G, Helbig KL, Palmer EE, Mei D, Ballardini E, Van Haeringen A, Syrbe S, Leuzzi V, Cioni G, Curry CJ, Costain G, Santucci M, Chong K, Mancini GMS, Clayton-Smith J, Bigoni S, Scheffer IE, Dobyns WB, Vilsen B, Guerrini R; ATP1A2/A3-collaborators. Vetro A, et al. Among authors: nielsen hn. Brain. 2021 Jun 22;144(5):1435-1450. doi: 10.1093/brain/awab052. Brain. 2021. PMID: 33880529

2

Reaction of phenylhydrazine with erythrocytes. Cross-linking of spectrin by disulfide exchange with oxidized hemoglobin.

Vilsen B, Nielsen H. Vilsen B, et al. Biochem Pharmacol. 1984 Sep 1;33(17):2739-48. doi: 10.1016/0006-2952(84)90690-7. Biochem Pharmacol. 1984. PMID: 6466381

3

Relationship between intracellular Na+ concentration and reduced Na+ affinity in Na+,K+-ATPase mutants causing neurological disease.

Toustrup-Jensen MS, Einholm AP, Schack VR, Nielsen HN, Holm R, Sobrido MJ, Andersen JP, Clausen T, Vilsen B. Toustrup-Jensen MS, et al. Among authors: nielsen hn. J Biol Chem. 2014 Feb 7;289(6):3186-97. doi: 10.1074/jbc.M113.543272. Epub 2013 Dec 19. J Biol Chem. 2014. PMID: 24356962 Free PMC article.

4

Distinct neurological disorders with ATP1A3 mutations.

Heinzen EL, Arzimanoglou A, Brashear A, Clapcote SJ, Gurrieri F, Goldstein DB, Jóhannesson SH, Mikati MA, Neville B, Nicole S, Ozelius LJ, Poulsen H, Schyns T, Sweadner KJ, van den Maagdenberg A, Vilsen B; ATP1A3 Working Group. Heinzen EL, et al. Lancet Neurol. 2014 May;13(5):503-14. doi: 10.1016/S1474-4422(14)70011-0. Lancet Neurol. 2014. PMID: 24739246 Free PMC article. Review.

5

Importance of a Potential Protein Kinase A Phosphorylation Site of Na+,K+-ATPase and Its Interaction Network for Na+ Binding.

Einholm AP, Nielsen HN, Holm R, Toustrup-Jensen MS, Vilsen B. Einholm AP, et al. Among authors: nielsen hn. J Biol Chem. 2016 May 13;291(20):10934-47. doi: 10.1074/jbc.M115.701201. Epub 2016 Mar 24. J Biol Chem. 2016. PMID: 27013656 Free PMC article.

6

Distinct effects of Q925 mutation on intracellular and extracellular Na⁺ and K⁺ binding to the Na⁺, K⁺-ATPase.

Nielsen HN, Spontarelli K, Holm R, Andersen JP, Einholm AP, Artigas P, Vilsen B. Nielsen HN, et al. Sci Rep. 2019 Sep 16;9(1):13344. doi: 10.1038/s41598-019-50009-2. Sci Rep. 2019. PMID: 31527711 Free PMC article.

7

Role of a conserved ion-binding site tyrosine in ion selectivity of the Na+/K+ pump.

Spontarelli K, Infield DT, Nielsen HN, Holm R, Young VC, Galpin JD, Ahern CA, Vilsen B, Artigas P. Spontarelli K, et al. Among authors: nielsen hn. J Gen Physiol. 2022 Jul 4;154(7):e202113039. doi: 10.1085/jgp.202113039. Epub 2022 Jun 3. J Gen Physiol. 2022. PMID: 35657726 Free PMC article.

8

Na⁺,K⁺-ATPase with Disrupted Na⁺ Binding Sites I and III Binds Na⁺ with Increased Affinity at Site II and Undergoes Na⁺-Activated Phosphorylation with ATP.

Nielsen HN, Holm R, Sweazey R, Andersen JP, Artigas P, Vilsen B. Nielsen HN, et al. Biomolecules. 2024 Jan 22;14(1):135. doi: 10.3390/biom14010135. Biomolecules. 2024. PMID: 38275764 Free PMC article.

9

Characterization of detergent-solubilized sarcoplasmic reticulum Ca2+-ATPase by high-performance liquid chromatography.

Andersen JP, Vilsen B, Nielsen H, Møller JV. Andersen JP, et al. Biochemistry. 1986 Oct 21;25(21):6439-47. doi: 10.1021/bi00369a015. Biochemistry. 1986. PMID: 2947626

10

Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension.

Beuschlein F, Boulkroun S, Osswald A, Wieland T, Nielsen HN, Lichtenauer UD, Penton D, Schack VR, Amar L, Fischer E, Walther A, Tauber P, Schwarzmayr T, Diener S, Graf E, Allolio B, Samson-Couterie B, Benecke A, Quinkler M, Fallo F, Plouin PF, Mantero F, Meitinger T, Mulatero P, Jeunemaitre X, Warth R, Vilsen B, Zennaro MC, Strom TM, Reincke M. Beuschlein F, et al. Among authors: nielsen hn. Nat Genet. 2013 Apr;45(4):440-4, 444e1-2. doi: 10.1038/ng.2550. Epub 2013 Feb 17. Nat Genet. 2013. PMID: 23416519

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