scispace - formally typeset
T

Tobias M. Rasse

Researcher at Heidelberg University

Publications -  6
Citations -  5353

Tobias M. Rasse is an academic researcher from Heidelberg University. The author has contributed to research in topics: Tau protein & Dynein. The author has an hindex of 5, co-authored 5 publications receiving 4895 citations. Previous affiliations of Tobias M. Rasse include German Cancer Research Center.

Papers
More filters
Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
Journal ArticleDOI

Impaired retrograde transport by the Dynein/Dynactin complex contributes to Tau-induced toxicity

TL;DR: The data suggest that Tau-induced detrimental effects most likely originate from axonal rather than synaptic dysfunction and that impaired retrograde transport intensifies detrimental effects of Tau in axons, which contribute to the elucidation of disease mechanisms in tauopathy.
Journal ArticleDOI

Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

Daniel J. Klionsky, +2522 more
- 01 Jan 2016 - 
TL;DR: Author(s): Klionsky, DJ; Abdelmohsen, K; Abe, A; Abedin, MJ; Abeliovich, H; A Frozena, AA; Adachi, H, Adeli, K, Adhihetty, PJ; Adler, SG; Agam, G; Agarwal, R; Aghi, MK; Agnello, M; Agostinis, P; Aguilar, PV; Aguirre-Ghis
Journal ArticleDOI

Cellular and molecular modifier pathways in tauopathies: the big picture from screening invertebrate models.

TL;DR: The utility and application of invertebrate models in elucidating the cellular and molecular functions of novel and uncharacterized disease modifiers identified in large‐scale screens as well as for investigating the function of genes identified as risk factors in genome‐wide association studies from human patients in the post‐genomic era are discussed.
Journal ArticleDOI

The Drosophila KIF1A Homolog unc-104 Is Important for Site-Specific Synapse Maturation.

TL;DR: Investigating the impact of partial loss-of-function of kinesin-3 on synapse maturation at the Drosophila neuromuscular junction (NMJ) finds defects in CAZ assembly and overexpression of Rab3 partially ameliorates synaptic phenotypes of unc-104bris larvae, suggesting that lack of presynaptic Rab3 contributes to defects in synapses maturation.