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Publications by Bente Vilsen

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

American Journal of Human Genetics
Genetics
2018English

Arginine Substitution of a Cysteine in Transmembrane Helix M8 Converts Na+,K+-ATPase to an Electroneutral Pump Similar to H+,k+-ATPase

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2016English

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

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2016English

Functional Consequences of the CAPOS Mutation E818K of Na+,K+-ATPase

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2018English

Identification and Function of a Cytoplasmic K+Site of the Na+, K+-ATPase

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2008English

Importance of Conserved N-Domain Residues Thr441, Glu442, Lys515, Arg560, and Leu562of Sarcoplasmic Reticulum Ca2+-ATPase for MgATP Binding and Subsequent Catalytic Steps

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2003English

Importance of Leu99in Transmembrane Segment M1 of the Na+,K+-ATPase in the Binding and Occlusion of K+

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2007English

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