Detalhe da pesquisa
1.
T-Cell-Intrinsic Receptor Interacting Protein 2 Regulates Pathogenic T Helper 17 Cell Differentiation.
Immunity
; 49(5): 873-885.e7, 2018 11 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-30366765
2.
C9orf72 in myeloid cells suppresses STING-induced inflammation.
Nature
; 585(7823): 96-101, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32814898
3.
MAPK/MAK/MRK overlapping kinase (MOK) controls microglial inflammatory/type-I IFN responses via Brd4 and is involved in ALS.
Proc Natl Acad Sci U S A
; 120(28): e2302143120, 2023 07 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37399380
4.
Debamestrocel multimodal effects on biomarker pathways in amyotrophic lateral sclerosis are linked to clinical outcomes.
Muscle Nerve
; 69(6): 719-729, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38593477
5.
Mitofusin 1 overexpression rescues the abnormal mitochondrial dynamics caused by the Mitofusin 2 K357T mutation in vitro.
J Peripher Nerv Syst
; 28(3): 329-340, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37220142
6.
A randomized placebo-controlled phase 3 study of mesenchymal stem cells induced to secrete high levels of neurotrophic factors in amyotrophic lateral sclerosis.
Muscle Nerve
; 65(3): 291-302, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34890069
7.
Sizing, stabilising, and cloning repeat-expansions for gene targeting constructs.
Methods
; 191: 15-22, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32721467
8.
Amyotrophic lateral sclerosis care and research in the United States during the COVID-19 pandemic: Challenges and opportunities.
Muscle Nerve
; 62(2): 182-186, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32445195
9.
Addressing heterogeneity in amyotrophic lateral sclerosis CLINICAL TRIALS.
Muscle Nerve
; 62(2): 156-166, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31899540
10.
Inflammation in ALS/FTD pathogenesis.
Acta Neuropathol
; 137(5): 715-730, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30465257
11.
Stem cell transplantation for amyotrophic lateral sclerosis.
Curr Opin Neurol
; 31(5): 655-661, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30080719
12.
MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signs.
Ann Neurol
; 79(3): 419-27, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26659848
13.
Prion-like nuclear aggregation of TDP-43 during heat shock is regulated by HSP40/70 chaperones.
Hum Mol Genet
; 23(1): 157-70, 2014 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23962724
14.
A dominant mutation in FBXO38 causes distal spinal muscular atrophy with calf predominance.
Am J Hum Genet
; 93(5): 976-83, 2013 Nov 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-24207122
15.
Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes.
Ann Neurol
; 77(1): 100-13, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25382069
16.
Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration.
Proc Natl Acad Sci U S A
; 110(47): E4530-9, 2013 Nov 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-24170860
17.
Sir-two-homolog 2 (Sirt2) modulates peripheral myelination through polarity protein Par-3/atypical protein kinase C (aPKC) signaling.
Proc Natl Acad Sci U S A
; 108(43): E952-61, 2011 Oct 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-21949390
18.
Mitofusin2 mutations disrupt axonal mitochondrial positioning and promote axon degeneration.
J Neurosci
; 32(12): 4145-55, 2012 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-22442078
19.
Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age.
Neurobiol Dis
; 58: 220-30, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23742762
20.
Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy.
Ann Neurol
; 71(3): 407-16, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22334415