Rikke H. Holm

Arhus, 8000, Denmark

Last Updated: 09/26/2026

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Found 20 publications

A Highly Conserved Glycine in a Hotspot for Neurological Disease Mutations in Na+,K+-ATPase Is Critical to Na+ and K+ Occlusion.

A Highly Conserved Glycine in a Hotspot for Neurological Disease Mutations in Na+,K+-ATPase Is Critical to Na+ and K+ Occlusion.

Journal: Biomolecules
Published: March 11, 2026

On the mechanism of hypomagnesemia with treatment-resistant seizures caused by variants of the Na+,K+-ATPase α1 subunit (ATP1A1).

On the mechanism of hypomagnesemia with treatment-resistant seizures caused by variants of the Na+,K+-ATPase α1 subunit (ATP1A1).

Journal: The Journal of general physiology
Published: December 22, 2025

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.

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.

Journal: Biomolecules
Published: December 12, 2023

On the track of the lipid transport pathway of the phospholipid flippase ATP8A2 - Mutation analysis of residues of the transmembrane segments M1, M2, M3 and M4.

On the track of the lipid transport pathway of the phospholipid flippase ATP8A2 - Mutation analysis of residues of the transmembrane segments M1, M2, M3 and M4.

Journal: Biochimica et biophysica acta. Molecular cell research
Published: July 03, 2023

Temperature instability of a mutation at a multidomain junction in Na,K-ATPase isoform ATP1A3 (p.Arg756His) produces a fever-induced neurological syndrome.

Temperature instability of a mutation at a multidomain junction in Na,K-ATPase isoform ATP1A3 (p.Arg756His) produces a fever-induced neurological syndrome.

Journal: The Journal of biological chemistry
Published: July 01, 2022

Electrogenic reaction step and phospholipid translocation pathway of the mammalian P4-ATPase ATP8A2.

Electrogenic reaction step and phospholipid translocation pathway of the mammalian P4-ATPase ATP8A2.

Journal: FEBS letters
Published: June 16, 2022

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

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

Journal: The Journal of general physiology
Published: October 19, 2021

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

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

Journal: Brain : a journal of neurology
Published: August 14, 2020

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

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

Journal: Scientific reports
Published: May 17, 2019

Functional consequences of the CAPOS mutation E818K of Na+,K+-ATPase.

Functional consequences of the CAPOS mutation E818K of Na+,K+-ATPase.

Journal: The Journal of biological chemistry
Published: June 29, 2018

Germline De Novo Mutations in ATP1A1 Cause Renal Hypomagnesemia, Refractory Seizures, and Intellectual Disability.

Germline De Novo Mutations in ATP1A1 Cause Renal Hypomagnesemia, Refractory Seizures, and Intellectual Disability.

Journal: American journal of human genetics
Published: June 13, 2018

The α2β2 isoform combination dominates the astrocytic Na+ /K+ -ATPase activity and is rendered nonfunctional by the α2.G301R familial hemiplegic migraine type 2-associated mutation.

The α2β2 isoform combination dominates the astrocytic Na+ /K+ -ATPase activity and is rendered nonfunctional by the α2.G301R familial hemiplegic migraine type 2-associated mutation.

Journal: Glia
Published: May 24, 2017
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Last Updated: 09/26/2026