Detalhe da pesquisa
1.
Multiplying messages LRRK beneath Parkinson disease.
Cell
; 157(2): 291-293, 2014 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-24725399
2.
A pathogenic DYT-THAP1 dystonia mutation causes hypomyelination and loss of YY1 binding.
Hum Mol Genet
; 31(7): 1096-1104, 2022 03 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-34686877
3.
THAP1 modulates oligodendrocyte maturation by regulating ECM degradation in lysosomes.
Proc Natl Acad Sci U S A
; 118(31)2021 08 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34312226
4.
Hepatocytes Deficient in Nuclear Envelope Protein Lamina-associated Polypeptide 1 are an Ideal Mammalian System to Study Intranuclear Lipid Droplets.
J Lipid Res
; 63(10): 100277, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36100089
5.
α4ß2* Nicotinic Cholinergic Receptor Target Engagement in Parkinson Disease Gait-Balance Disorders.
Ann Neurol
; 90(1): 130-142, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33977560
6.
Oligodendrocyte and Extracellular Matrix Contributions to Central Nervous System Motor Function: Implications for Dystonia.
Mov Disord
; 37(3): 456-463, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34989453
7.
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
8.
TorsinA dysfunction causes persistent neuronal nuclear pore defects.
Hum Mol Genet
; 27(3): 407-420, 2018 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29186574
9.
Cholinergic system changes of falls and freezing of gait in Parkinson's disease.
Ann Neurol
; 85(4): 538-549, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30720884
10.
Lamina-associated polypeptide 1 is dispensable for embryonic myogenesis but required for postnatal skeletal muscle growth.
Hum Mol Genet
; 26(1): 65-78, 2017 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27798115
11.
Forebrain knock-out of torsinA reduces striatal free-water and impairs whole-brain functional connectivity in a symptomatic mouse model of DYT1 dystonia.
Neurobiol Dis
; 106: 124-132, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28673740
12.
A novel conditional knock-in approach defines molecular and circuit effects of the DYT1 dystonia mutation.
Hum Mol Genet
; 24(22): 6459-72, 2015 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26370418
13.
Access of torsinA to the inner nuclear membrane is activity dependent and regulated in the endoplasmic reticulum.
J Cell Sci
; 128(15): 2854-65, 2015 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26092934
14.
Reply to: "Letter on Discussion of Gait Research".
Mov Disord
; 37(6): 1328, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35707827
15.
Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia.
Cerebellum
; 16(2): 577-594, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27734238
16.
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
17.
Lamina-associated polypeptide 1: protein interactions and tissue-selective functions.
Semin Cell Dev Biol
; 29: 164-8, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24508913
18.
Endolysosomal dysfunction in Parkinson's disease: Recent developments and future challenges.
Mov Disord
; 31(10): 1433-1443, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27619535
19.
LRRK2 Parkinson disease mutations enhance its microtubule association.
Hum Mol Genet
; 21(4): 890-9, 2012 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22080837
20.
Cerebellothalamocortical pathway abnormalities in torsinA DYT1 knock-in mice.
Proc Natl Acad Sci U S A
; 108(16): 6638-43, 2011 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-21464304