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Danny Mollerup Sørensen

Showing results (1-10 of 10) with videos related to

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Plos One|October 20, 2022
ATP hydrolytic activity of purified Spf1p correlate with micellar lipid fluidity and is dependent on conserved residues in transmembrane helix M1Johan Ørskov Ipsen, Danny Mollerup Sørensen
Biochimica Et Biophysica Acta|April 27, 2010
Structural divergence between the two subgroups of P5 ATPasesDanny Mollerup Sørensen, Morten J Buch-Pedersen, Michael Gjedde Palmgren
Physiologia Plantarum|July 4, 2019
Evolution of P2A and P5A ATPases: ancient gene duplications and the red algal connection to green plants revisitedMichael Palmgren, Danny Mollerup Sørensen, Björn M Hallström, et al.
Biochimica Et Biophysica Acta|May 20, 2014
Towards defining the substrate of orphan P5A-ATPasesDanny Mollerup Sørensen, Henrik Waldal Holen, Tine Holemans, et al.
The Journal of Biological Chemistry|June 26, 2012
Ca2+ induces spontaneous dephosphorylation of a novel P5A-type ATPaseDanny Mollerup Sørensen, Annette B Møller, Mia K Jakobsen, et al.
The Biochemical Journal|February 14, 2019
The lipid head group is the key element for substrate recognition by the P4 ATPase ALA2: a phosphatidylserine flippaseLisa Theorin, Kristina Faxén, Danny Mollerup Sørensen, et al.
Plos One|March 6, 2018
Parkinson disease related ATP13A2 evolved early in animal evolutionDanny Mollerup Sørensen, Tine Holemans, Sarah van Veen, et al.
Molecular Biology of the Cell|February 21, 2019
The P5A ATPase Spf1p is stimulated by phosphatidylinositol 4-phosphate and influences cellular sterol homeostasisDanny Mollerup Sørensen, Henrik Waldal Holen, Jesper Torbøl Pedersen, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 3, 2015
A lipid switch unlocks Parkinson's disease-associated ATP13A2Tine Holemans, Danny Mollerup Sørensen, Sarah van Veen, et al.
Brain : a Journal of Neurology|February 1, 2017
Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78)Alejandro Estrada-Cuzcano, Shaun Martin, Teodora Chamova, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Plos One|October 20, 2022
ATP hydrolytic activity of purified Spf1p correlate with micellar lipid fluidity and is dependent on conserved residues in transmembrane helix M1Johan Ørskov Ipsen, Danny Mollerup Sørensen
Biochimica Et Biophysica Acta|April 27, 2010
Structural divergence between the two subgroups of P5 ATPasesDanny Mollerup Sørensen, Morten J Buch-Pedersen, Michael Gjedde Palmgren
Physiologia Plantarum|July 4, 2019
Evolution of P2A and P5A ATPases: ancient gene duplications and the red algal connection to green plants revisitedMichael Palmgren, Danny Mollerup Sørensen, Björn M Hallström, et al.
Biochimica Et Biophysica Acta|May 20, 2014
Towards defining the substrate of orphan P5A-ATPasesDanny Mollerup Sørensen, Henrik Waldal Holen, Tine Holemans, et al.
The Journal of Biological Chemistry|June 26, 2012
Ca2+ induces spontaneous dephosphorylation of a novel P5A-type ATPaseDanny Mollerup Sørensen, Annette B Møller, Mia K Jakobsen, et al.
The Biochemical Journal|February 14, 2019
The lipid head group is the key element for substrate recognition by the P4 ATPase ALA2: a phosphatidylserine flippaseLisa Theorin, Kristina Faxén, Danny Mollerup Sørensen, et al.
Plos One|March 6, 2018
Parkinson disease related ATP13A2 evolved early in animal evolutionDanny Mollerup Sørensen, Tine Holemans, Sarah van Veen, et al.
Molecular Biology of the Cell|February 21, 2019
The P5A ATPase Spf1p is stimulated by phosphatidylinositol 4-phosphate and influences cellular sterol homeostasisDanny Mollerup Sørensen, Henrik Waldal Holen, Jesper Torbøl Pedersen, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 3, 2015
A lipid switch unlocks Parkinson's disease-associated ATP13A2Tine Holemans, Danny Mollerup Sørensen, Sarah van Veen, et al.
Brain : a Journal of Neurology|February 1, 2017
Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78)Alejandro Estrada-Cuzcano, Shaun Martin, Teodora Chamova, et al.
Pageof 1