1 |
Weiss AR, Liguore WA, Brandon K, Wang X, Liu Z, Domire JS, Button D, Srinivasan S, Kroenke CD, McBride JL. A novel rhesus macaque model of Huntington's disease recapitulates key neuropathological changes along with motor and cognitive decline. Elife 2022;11:e77568. [PMID: 36205397 DOI: 10.7554/eLife.77568] [Reference Citation Analysis]
|
2 |
Comoy EE, Mikol J, Deslys J. Non-human primates in prion diseases. Cell Tissue Res. [DOI: 10.1007/s00441-022-03644-7] [Reference Citation Analysis]
|
3 |
Lunev E, Karan A, Egorova T, Bardina M. Adeno-Associated Viruses for Modeling Neurological Diseases in Animals: Achievements and Prospects. Biomedicines 2022;10:1140. [DOI: 10.3390/biomedicines10051140] [Reference Citation Analysis]
|
4 |
Yan Y, Zhang G, Wu C, Ren Q, Liu X, Huang F, Cao Y, Ye W. Structural Exploration of Polycationic Nanoparticles for siRNA Delivery. ACS Biomater Sci Eng 2022;8:1964-74. [PMID: 35380797 DOI: 10.1021/acsbiomaterials.2c00196] [Reference Citation Analysis]
|
5 |
Jansen-west K, Todd TW, Daughrity LM, Yue M, Tong J, Carlomagno Y, Del Rosso G, Kurti A, Jones CY, Dunmore JA, Castanedes-casey M, Dickson DW, Wszolek ZK, Fryer JD, Petrucelli L, Prudencio M. Plasma PolyQ-ATXN3 Levels Associate With Cerebellar Degeneration and Behavioral Abnormalities in a New AAV-Based SCA3 Mouse Model. Front Cell Dev Biol 2022;10:863089. [DOI: 10.3389/fcell.2022.863089] [Reference Citation Analysis]
|
6 |
Alpaugh M, Denis HL, Cicchetti F. Prion-like properties of the mutant huntingtin protein in living organisms: the evidence and the relevance. Mol Psychiatry 2021. [PMID: 34711942 DOI: 10.1038/s41380-021-01350-4] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
|
7 |
Ramírez-jarquín UN, Sharma M, Shahani N, Li Y, Boregowda S, Subramaniam S. Rhes protein transits from neuron to neuron and facilitates mutant huntingtin spreading in the brain.. [DOI: 10.1101/2021.08.27.457956] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
|
8 |
Margarita DC, Colombo L, Urszulax B, Amandine G, Natalia TE, Isabelle F, Hossain I, Daniela G, Anne E, Matthias M, Eline P. Transmission-selective muscle pathology induced by active propagation of mutant huntingtin across the human neuromuscular synapse.. [DOI: 10.1101/2021.07.28.454044] [Reference Citation Analysis]
|
9 |
Schindler F, Praedel N, Neuendorf N, Kunz S, Schnoegl S, Mason MA, Taxy BA, Bates GP, Khoshnan A, Priller J, Grimm J, Maier M, Boeddrich A, Wanker EE. Small, Seeding-Competent Huntingtin Fibrils Are Prominent Aggregate Species in Brains of zQ175 Huntington's Disease Knock-in Mice. Front Neurosci 2021;15:682172. [PMID: 34239412 DOI: 10.3389/fnins.2021.682172] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
|
10 |
Masnata M, Salem S, de Rus Jacquet A, Anwer M, Cicchetti F. Targeting Tau to Treat Clinical Features of Huntington's Disease. Front Neurol 2020;11:580732. [PMID: 33329322 DOI: 10.3389/fneur.2020.580732] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
|