Cargando…
Distinct Phospho-TDP-43 brain distribution in two cases of FTD, one associated with ALS
INTRODUCTION: TDP-43 is an intranuclear protein involved in many cellular processes. When altered, it shows a change in pattern of distribution, as well as in functioning, throughout the Central Nervous System structures. Frontotemporal Lobar Degeneration (FTLD) and Amyotrophic Lateral Sclerosis (AL...
Autores principales: | Guedes, Álvaro C.B., Santin, Ricardo, Costa, André S.R., Reiter, Keli C., Hilbig, Arlete, Fernandez, Liana L. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação de Neurologia Cognitiva e do Comportamento
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5674668/ https://www.ncbi.nlm.nih.gov/pubmed/29213521 http://dx.doi.org/10.1590/1980-57642016dn11-030006 |
Ejemplares similares
-
TDP-43 pathology disrupts nuclear pore complexes and nucleocytoplasmic transport in ALS/FTD
por: Chou, Ching-Chieh, et al.
Publicado: (2018) -
Disulfide cross-linked multimers of TDP-43 and spinal motoneuron loss in a TDP-43(A315T) ALS/FTD mouse model
por: Bargsted, Leslie, et al.
Publicado: (2017) -
TDP-43 represses cryptic exon inclusion in the FTD–ALS gene UNC13A
por: Ma, X. Rosa, et al.
Publicado: (2022) -
Mis-spliced transcripts generate de novo proteins in TDP-43-related ALS/FTD
por: Seddighi, Sahba, et al.
Publicado: (2023) -
Coexistence of perseveration and apathy in the TDP-43(Q331K) knock-in mouse model of ALS–FTD
por: Kim, Eosu, et al.
Publicado: (2020)