Maxime Rousseaux creator_dzzqbnofcbevzgjqdod2orw7hq

Given name Maxime
Surname Rousseaux

Releases

This creator has contributed to:

2018-03-19 Depleting Trim28 in adult mice is well tolerated and reduces levels of α-synuclein and tau
unknown status | post
doi:10.1101/284984
2017-07-12 Progress toward an integrated understanding of Parkinson's disease
published | article-journal
doi:10.12688/f1000research.11820.1
2018-06-04 Depleting Trim28 in adult mice is well tolerated and reduces levels of α-synuclein and tau
published | article-journal | CC-BY
doi:10.7554/elife.36768
2018-09-24 A Druggable Genome Screen Identifies Modifiers of α-Synuclein Levels via a Tiered Cross-Species Validation Approach
published | article-journal
doi:10.1523/jneurosci.0254-18.2018
2020-08-15 The role of TDP-43 mislocalization in amyotrophic lateral sclerosis
published | article-journal | CC-BY
doi:10.1186/s13024-020-00397-1
2022-09-10 Characterizing the differential distribution and targets of Sumo paralogs in the mouse brain
unknown status | post
doi:10.1101/2022.09.09.507035
2021-10-14 Constitutive nuclear accumulation of endogenous alpha-synuclein in mice causes motor dysfunction and cortical atrophy, independent of protein aggregation.
unknown status | post
doi:10.1101/2021.10.13.464123
2022-02-14 Constitutive nuclear accumulation of endogenous alpha-synuclein in mice causes motor impairment and cortical dysfunction, independent of protein aggregation
published | dataset | CC-BY
doi:10.5281/zenodo.6082270
2022-02-14 Constitutive nuclear accumulation of endogenous alpha-synuclein in mice causes motor impairment and cortical dysfunction, independent of protein aggregation
published | dataset | CC-BY
doi:10.5281/zenodo.6082269
2022-02-18 Constitutive nuclear accumulation of endogenous alpha-synuclein in mice causes motor impairment and cortical dysfunction, independent of protein aggregation
published | article-journal
doi:10.1093/hmg/ddac035
2021-03-11 Dual targeting of brain region‐specific kinases potentiates neurological rescue in Spinocerebellar ataxia type 1
published | article-journal
doi:10.15252/embj.2020106106