Detalhe da pesquisa
1.
Induced-Pluripotent-Stem-Cell-Derived Primitive Macrophages Provide a Platform for Modeling Tissue-Resident Macrophage Differentiation and Function.
Immunity
; 47(1): 183-198.e6, 2017 07 18.
Artigo
Inglês
| MEDLINE | ID: mdl-28723550
2.
Oligodendroglia and myelin pathology in fragile X syndrome.
J Neurochem
; 2024 Jun 19.
Artigo
Inglês
| MEDLINE | ID: mdl-38898700
3.
Induced-Pluripotent-Stem-Cell-Derived Primitive Macrophages Provide a Platform for Modeling Tissue-Resident Macrophage Differentiation and Function.
Immunity
; 52(2): 417-418, 2020 Feb 18.
Artigo
Inglês
| MEDLINE | ID: mdl-32075730
4.
Gene expression profiles complement the analysis of genomic modifiers of the clinical onset of Huntington disease.
Hum Mol Genet
; 29(16): 2788-2802, 2020 09 29.
Artigo
Inglês
| MEDLINE | ID: mdl-32898862
5.
Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in GLS.
N Engl J Med
; 380(15): 1433-1441, 2019 04 11.
Artigo
Inglês
| MEDLINE | ID: mdl-30970188
6.
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
Inglês
| MEDLINE | ID: mdl-31015293
7.
Huntingtin confers fitness but is not embryonically essential in zebrafish development.
Dev Biol
; 458(1): 98-105, 2020 02 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31682806
8.
Urokinase plasminogen activator mediates changes in human astrocytes modeling fragile X syndrome.
Glia
; 69(12): 2947-2962, 2021 12.
Artigo
Inglês
| MEDLINE | ID: mdl-34427356
9.
Rescue of aberrant huntingtin palmitoylation ameliorates mutant huntingtin-induced toxicity.
Neurobiol Dis
; 158: 105479, 2021 10.
Artigo
Inglês
| MEDLINE | ID: mdl-34390831
10.
Early white matter pathology in the fornix of the limbic system in Huntington disease.
Acta Neuropathol
; 142(5): 791-806, 2021 11.
Artigo
Inglês
| MEDLINE | ID: mdl-34448021
11.
Reprint of: Manipulation of microbiota reveals altered callosal myelination and white matter plasticity in a model of Huntington disease.
Neurobiol Dis
; 135: 104744, 2020 02.
Artigo
Inglês
| MEDLINE | ID: mdl-31931139
12.
Narciclasine attenuates diet-induced obesity by promoting oxidative metabolism in skeletal muscle.
PLoS Biol
; 15(2): e1002597, 2017 02.
Artigo
Inglês
| MEDLINE | ID: mdl-28207742
13.
Manipulation of microbiota reveals altered callosal myelination and white matter plasticity in a model of Huntington disease.
Neurobiol Dis
; 127: 65-75, 2019 07.
Artigo
Inglês
| MEDLINE | ID: mdl-30802499
14.
A novel humanized mouse model of Huntington disease for preclinical development of therapeutics targeting mutant huntingtin alleles.
Hum Mol Genet
; 26(6): 1115-1132, 2017 03 15.
Artigo
Inglês
| MEDLINE | ID: mdl-28104789
15.
Interactome network analysis identifies multiple caspase-6 interactors involved in the pathogenesis of HD.
Hum Mol Genet
; 25(8): 1600-18, 2016 Apr 15.
Artigo
Inglês
| MEDLINE | ID: mdl-26908611
16.
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
Inglês
| MEDLINE | ID: mdl-27126634
17.
Connectomic imaging reveals Huntington-related pathological and pharmaceutical effects in a mouse model.
NMR Biomed
; 31(12): e4007, 2018 12.
Artigo
Inglês
| MEDLINE | ID: mdl-30260561
18.
Choosing an animal model for the study of Huntington's disease.
Nat Rev Neurosci
; 14(10): 708-21, 2013 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-24052178
19.
Partial rescue of some features of Huntington Disease in the genetic absence of caspase-6 in YAC128 mice.
Neurobiol Dis
; 76: 24-36, 2015 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-25583186
20.
Anti-semaphorin 4D immunotherapy ameliorates neuropathology and some cognitive impairment in the YAC128 mouse model of Huntington disease.
Neurobiol Dis
; 76: 46-56, 2015 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-25662335