Annie Sittler
Overview
Explore the profile of Annie Sittler including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
12
Citations
3203
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Marinello M, Werner A, Giannone M, Tahiri K, Alves S, Tesson C, et al.
Dis Model Mech
. 2018 Dec;
12(1).
PMID: 30559154
Perturbation of protein homeostasis and aggregation of misfolded proteins is a major cause of many human diseases. A hallmark of the neurodegenerative disease spinocerebellar ataxia type 7 (SCA7) is the...
2.
Sittler A, Muriel M, Marinello M, Brice A, den Dunnen W, Alves S
Neuropathology
. 2017 Dec;
38(2):113-124.
PMID: 29218765
Autophagy, the major pathway for protein turnover, is critical to maintain cellular homeostasis and has been implicated in neurodegenerative diseases. The aim of this research was to analyze the expression...
3.
Hachigian L, Carmona V, Fenster R, Kulicke R, Heilbut A, Sittler A, et al.
Cell Rep
. 2017 Dec;
21(10):2688-2695.
PMID: 29212017
Alteration of corticostriatal glutamatergic function is an early pathophysiological change associated with Huntington's disease (HD). The factors that regulate the maintenance of corticostriatal glutamatergic synapses post-developmentally are not well understood....
4.
Alves S, Marais T, Biferi M, Furling D, Marinello M, Hachimi K, et al.
Mol Neurodegener
. 2016 Jul;
11(1):58.
PMID: 27465358
Background: We used lentiviral vectors (LVs) to generate a new SCA7 animal model overexpressing a truncated mutant ataxin-7 (MUT ATXN7) fragment in the mouse cerebellum, in order to characterize the...
5.
Klionsky D, Abdelmohsen K, Abe A, Abedin M, Abeliovich H, Arozena A, et al.
Autophagy
. 2016 Jan;
12(1):1-222.
PMID: 26799652
No abstract available.
6.
Tan J, Vance K, Varela M, Sirey T, Watson L, Curtis H, et al.
Nat Struct Mol Biol
. 2015 Mar;
22(3):272.
PMID: 25736092
No abstract available.
7.
Tan J, Vance K, Varela M, Sirey T, Watson L, Curtis H, et al.
Nat Struct Mol Biol
. 2014 Oct;
21(11):955-961.
PMID: 25306109
What causes the tissue-specific pathology of diseases resulting from mutations in housekeeping genes? Specifically, in spinocerebellar ataxia type 7 (SCA7), a neurodegenerative disorder caused by a CAG-repeat expansion in ATXN7...
8.
Alves S, Cormier-Dequaire F, Marinello M, Marais T, Muriel M, Beaumatin F, et al.
Acta Neuropathol
. 2014 May;
128(5):705-22.
PMID: 24859968
There is still no treatment for polyglutamine disorders, but clearance of mutant proteins might represent a potential therapeutic strategy. Autophagy, the major pathway for organelle and protein turnover, has been...
9.
Chort A, Alves S, Marinello M, Dufresnois B, Dornbierer J, Tesson C, et al.
Brain
. 2013 Mar;
136(Pt 6):1732-45.
PMID: 23518714
We showed previously, in a cell model of spinocerebellar ataxia 7, that interferon beta induces the expression of PML protein and the formation of PML protein nuclear bodies that degrade...
10.
Janer A, Werner A, Takahashi-Fujigasaki J, Daret A, Fujigasaki H, Takada K, et al.
Hum Mol Genet
. 2009 Oct;
19(1):181-95.
PMID: 19843541
Post-translational modification by SUMO (small ubiquitin-like modifier) was proposed to modulate the pathogenesis of several neurodegenerative diseases. Spinocerebellar ataxia type 7 (SCA7) is a neurodegenerative disorder, whose pathology is caused...