Detalhe da pesquisa
1.
Intrinsic mutant HTT-mediated defects in oligodendroglia cause myelination deficits and behavioral abnormalities in Huntington disease.
Proc Natl Acad Sci U S A
; 116(19): 9622-9627, 2019 05 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31015293
2.
Structural and molecular myelination deficits occur prior to neuronal loss in the YAC128 and BACHD models of Huntington disease.
Hum Mol Genet
; 25(13): 2621-2632, 2016 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27126634
3.
Impaired Remyelination in a Mouse Model of Huntington Disease.
Mol Neurobiol
; 56(10): 6873-6882, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30937636