Kevin Lüthy

发表

STIM1 mutation associated with a syndrome of immunodeficiency and autoimmunity.

F. Rieux-Laucat, A. Fischer, C. Picard, 2009, The New England journal of medicine.

Investigating rare and ultrarare epilepsy syndromes with Drosophila models

P. Lasko, Kevin Lüthy, 2021, Faculty reviews.

TBC1D24 genotype–phenotype correlation

J. Rosenfeld, I. Scheffer, J. Gécz, 2016, Neurology.

TBC 1 D 24 genotype – phenotype correlation Epilepsies and other neurologic features

J. Rosenfeld, A. Pagnamenta, P. Verstreken, 2022 .

Skywalker-TBC1D24 has a lipid-binding pocket mutated in epilepsy and required for synaptic function

P. Verstreken, W. Versées, Sabine Kuenen, 2016, Nature Structural &Molecular Biology.

Crystal structure of the TLDc domain of Skywalker/TBC1D24 from Drosophila melanogaster

P. Verstreken, P. Aridon, W. Versées, 2019 .

T‐cell‐specific deletion of STIM1 and STIM2 protects mice from EAE by impairing the effector functions of Th1 and Th17 cells

S. Feske, C. Mccarl, S. Khalil, 2010, European journal of immunology.

The irre Cell Recognition Module (IRM) Protein Kirre Is Required to Form the Reciprocal Synaptic Network of L4 Neurons in the Drosophila Lamina

Zhiyuan Lu, I. Meinertzhagen, K. Fischbach, 2014, Journal of neurogenetics.

Functional Study of Mammalian Neph Proteins in Drosophila melanogaster

Ashish, K. Fischbach, S. Rensing, 2012, PloS one.

TBC1D24-TLDc-related epilepsy exercise-induced dystonia: rescue by antioxidants in a disease model.

P. Verstreken, P. Aridon, W. Versées, 2019, Brain : a journal of neurology.