Detalhe da pesquisa
1.
Retromer dysfunction in amyotrophic lateral sclerosis.
Proc Natl Acad Sci U S A
; 119(26): e2118755119, 2022 06 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35749364
2.
Improved synthesis and application of an alkyne-functionalized isoprenoid analogue to study the prenylomes of motor neurons, astrocytes and their stem cell progenitors.
Bioorg Chem
; 147: 107365, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38636436
3.
Patterns of TDP-43 Deposition in Brains with LRRK2 G2019S Mutations.
Mov Disord
; 38(8): 1541-1545, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37218402
4.
The two-century journey of Parkinson disease research.
Nat Rev Neurosci
; 18(4): 251-259, 2017 03 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-28303016
5.
Discussion of Research Priorities for Gait Disorders in Parkinson's Disease.
Mov Disord
; 37(2): 253-263, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34939221
6.
COVID-19 neuropathology at Columbia University Irving Medical Center/New York Presbyterian Hospital.
Brain
; 144(9): 2696-2708, 2021 10 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-33856027
7.
Recent Advances in the Development of Stem-Cell-Derived Dopaminergic Neuronal Transplant Therapies for Parkinson's Disease.
Mov Disord
; 36(8): 1772-1780, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33963552
8.
PINK1 Content in Mitochondria is Regulated by ER-Associated Degradation.
J Neurosci
; 39(36): 7074-7085, 2019 09 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31300519
9.
Addressing the Challenges of Clinical Research for Freezing of Gait in Parkinson's Disease.
Mov Disord
; 37(2): 264-267, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34939228
10.
Reply to: "Letter on Discussion of Gait Research".
Mov Disord
; 37(6): 1328, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35707827
11.
α-Synuclein-independent histopathological and motor deficits in mice lacking the endolysosomal Parkinsonism protein Atp13a2.
J Neurosci
; 35(14): 5724-42, 2015 Apr 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-25855184
12.
Cytosolic cleaved PINK1 represses Parkin translocation to mitochondria and mitophagy.
EMBO Rep
; 15(1): 86-93, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24357652
13.
α-Synuclein is localized to mitochondria-associated ER membranes.
J Neurosci
; 34(1): 249-59, 2014 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24381286
14.
A new role for α-synuclein in Parkinson's disease: Alteration of ER-mitochondrial communication.
Mov Disord
; 30(8): 1026-33, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25952565
15.
Mutant superoxide dismutase 1 (SOD1), a cause of amyotrophic lateral sclerosis, disrupts the recruitment of SMN, the spinal muscular atrophy protein to nuclear Cajal bodies.
Hum Mol Genet
; 21(15): 3421-34, 2012 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22581780
16.
Mitochondrial autophagy in cells with mtDNA mutations results from synergistic loss of transmembrane potential and mTORC1 inhibition.
Hum Mol Genet
; 21(5): 978-90, 2012 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22080835
17.
Mitophagy and Parkinson's disease: be eaten to stay healthy.
Mol Cell Neurosci
; 55: 37-43, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22926193
18.
Depletion of Mettl3 in cholinergic neurons causes adult-onset neuromuscular degeneration.
Cell Rep
; 43(4): 113999, 2024 Apr 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38554281
19.
Improved synthesis and application of an alkyne-functionalized isoprenoid analogue to study the prenylomes of motor neurons, astrocytes and their stem cell progenitors.
bioRxiv
; 2024 Mar 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38496415
20.
Mitochondrial dynamics and bioenergetic dysfunction is associated with synaptic alterations in mutant SOD1 motor neurons.
J Neurosci
; 32(1): 229-42, 2012 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-22219285