Elin Larsson

Work Environment Representative

Publications

Author

Title

Year sorteringsordning

Fulltext

Hoernke, Maria
Mohan, Jagan
Larsson, Elin; et al.

EHD2 restrains dynamics of caveolae by an ATP-dependent, membrane-bound, open conformation
Proceedings of the National Academy of Sciences of the United States of America, 114(22): E4360-E4369

2017

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Holst, Mikkel Roland
Vidal-Quadras, Maite
Larsson, Elin; et al.

Clathrin-Independent Endocytosis Suppresses Cancer Cell Blebbing and Invasion
Cell reports, 20(8): 1893-1905

2017

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Vidal-Quadras, Maite
Holst, Mikkel R.
Francis, Monika K.; et al.

Endocytic turnover of Rab8 controls cell polarization
Journal of Cell Science, 130(6): 1147-1157

2017

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Melo, Arthur Alves
Hegde, Balachandra G.
Shah, Claudio; et al.

Structural insights into the activation mechanism of dynamin-like EHD ATPases
Proceedings of the National Academy of Sciences of the United States of America, 114(22): 5629-5634

2017

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Daste, Frederic
Walrant, Astrid
Holst, Mikkel R.; et al.

Control of actin polymerization via the coincidence of phosphoinositides and high membrane curvature
Journal of Cell Biology, 216(11): 3745-3765

2017

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Hoernke, Maria
Larsson, Elin
Mohan, Jagan; et al.

Structural Mechanism in a Membrane Remodelling ATP-ASE
Biophysical Journal, 110(3): 578A-578A

2016

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Mohan, Jagan
Morén, Björn
Larsson, Elin; et al.

Cavin3 interacts with cavin1 and caveolin1 to increase surface dynamics of caveolae
Journal of Cell Science, 128(5): 979-991

2015

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Larsson, Elin

The use of monogenic disease to study basal and disease associated mechanisms with focus on NGF dependent pain insensitivity and ISCU myopathy

2012

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Nordin, Angelica
Larsson, Elin
Holmberg, Monica

The defective splicing caused by the ISCU intron mutation in patients with myopathy with lactic acidosis is repressed by PTBP1 but can be de-repressed by IGF2BP1
Human Mutation, 33(3): 467-470

2012

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Nordin, Angelica
Larsson, Elin
Thornell, Lars-Eric; et al.

Tissue-specific splicing of ISCU results in a skeletal muscle phenotype in myopathy with lactic acidosis, while complete loss of ISCU results in early embryonic death in mice
Human Genetics, 129(4): 371-378

2011

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