M. Toustrup-Jensen

发表

Mutation of Gly-94 in transmembrane segment M1 of Na+,K+-ATPase interferes with Na+ and K+ binding in E2P conformation.

A. P. Einholm, J. Andersen, B. Vilsen, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Functional Consequences of Alterations to Ile279, Ile283, Glu284, His285, Phe286, and His288 in the NH2-terminal Part of Transmembrane Helix M3 of the Na+,K+-ATPase*

B. Vilsen, M. Toustrup-Jensen, Mads S. Toustrup-Jensen, 2003, Journal of Biological Chemistry.

Importance of Glu282 in Transmembrane Segment M3 of the Na+,K+-ATPase for Control of Cation Interaction and Conformational Changes*

B. Vilsen, M. Toustrup-Jensen, 2002, The Journal of Biological Chemistry.

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

S. Petrou, Melody Li, J. Andersen, 2018, The Journal of Biological Chemistry.

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

A. P. Einholm, B. Vilsen, M. Toustrup-Jensen, 2016, The Journal of Biological Chemistry.

Crystal structure of the sodium–potassium pump

P. Nissen, J. P. Morth, B. P. Pedersen, 2007, Nature.

A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism.

Hugo Gutiérrez-de-Terán, Angel Carracedo, H. Gutiérrez‐de‐Terán, 2009, Human molecular genetics.

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

L. Ozelius, A. Brashear, K. Sweadner, 2022, The Journal of biological chemistry.

Neurological disease mutations of α3 Na+,K+-ATPase: Structural and functional perspectives and rescue of compromised function.

A. P. Einholm, J. Andersen, B. Vilsen, 2016, Biochimica et biophysica acta.

The Rapid-onset Dystonia Parkinsonism Mutation D923N of the Na+,K+-ATPase α3 Isoform Disrupts Na+ Interaction at the Third Na+ Site*

A. P. Einholm, J. Andersen, B. Vilsen, 2010, The Journal of Biological Chemistry.

Functional consequences of the CAPOS mutation E818K of Na (cid:2) ,K -ATPase

S. Petrou, Melody Li, J. Andersen, 2018 .

Relationship between Intracellular Na+ Concentration and Reduced Na+ Affinity in Na+,K+-ATPase Mutants Causing Neurological Disease*

M. Sobrido, A. P. Einholm, T. Clausen, 2013, The Journal of Biological Chemistry.

Importance of Conserved Thr214 in Domain A of the Na+,K+-ATPase for Stabilization of the Phosphoryl Transition State Complex in E 2P Dephosphorylation*

B. Vilsen, M. Toustrup-Jensen, Mads S. Toustrup-Jensen, 2003, The Journal of Biological Chemistry.

Mutations Phe785Leu and Thr618Met in Na+,K+-ATPase, Associated with Familial Rapid-onset Dystonia Parkinsonism, Interfere with Na+ Interaction by Distinct Mechanisms*

B. Vilsen, M. Toustrup-Jensen, Vivien Rodacker, 2006, Journal of Biological Chemistry.

The structure of the Na+,K+-ATPase and mapping of isoform differences and disease-related mutations

P. Nissen, J. P. Morth, H. Poulsen, 2009, Philosophical Transactions of the Royal Society B: Biological Sciences.

The C Terminus of Na+,K+-ATPase Controls Na+ Affinity on Both Sides of the Membrane through Arg935*♦

P. Nissen, J. P. Morth, A. P. Einholm, 2009, The Journal of Biological Chemistry.

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

P. Nissen, J. P. Morth, J. Andersen, 2008, Journal of Biological Chemistry.

Interaction between the Catalytic Site and the A-M3 Linker Stabilizes E2/E2P Conformational States of Na+,K+-ATPase*

B. Vilsen, M. Toustrup-Jensen, Mads S. Toustrup-Jensen, 2005, Journal of Biological Chemistry.