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1.
Transcriptional Regulation of the Synaptic Vesicle Protein Synaptogyrin-3 (SYNGR3) Gene: The Effects of NURR1 on Its Expression.
Int J Mol Sci
; 23(7)2022 Mar 26.
Article
in English
| MEDLINE | ID: mdl-35409005
2.
Deficiency of Cks1 Leads to Learning and Long-Term Memory Defects and p27 Dependent Formation of Neuronal Cofilin Aggregates.
Cereb Cortex
; 27(1): 11-23, 2017 01 01.
Article
in English
| MEDLINE | ID: mdl-28365778
3.
Phos-tag analysis of Rab10 phosphorylation by LRRK2: a powerful assay for assessing kinase function and inhibitors.
Biochem J
; 473(17): 2671-85, 2016 09 01.
Article
in English
| MEDLINE | ID: mdl-27474410
4.
Modeling of Friedreich ataxia-related iron overloading cardiomyopathy using patient-specific-induced pluripotent stem cells.
Pflugers Arch
; 466(9): 1831-44, 2014 Sep.
Article
in English
| MEDLINE | ID: mdl-24327207
5.
A randomized controlled trial on the effects and acceptability of individual mindfulness techniques - meditation and yoga - on anxiety and depression in people with Parkinson's disease: a study protocol.
BMC Complement Med Ther
; 23(1): 241, 2023 Jul 17.
Article
in English
| MEDLINE | ID: mdl-37461018
6.
In vivoĀ overexpression of synaptogyrin-3 promotes striatal synapticĀ dopamineĀ uptakeĀ in LRRK2R1441G Ā mutant mouse model of Parkinson's disease.
Brain Behav
; 13(2): e2886, 2023 02.
Article
in English
| MEDLINE | ID: mdl-36624932
7.
LRRK2 mutant knock-in mouse models: therapeutic relevance in Parkinson's disease.
Transl Neurodegener
; 11(1): 10, 2022 02 14.
Article
in English
| MEDLINE | ID: mdl-35152914
8.
LRRK2, GBA and their interaction in the regulation of autophagy: implications on therapeutics in Parkinson's disease.
Transl Neurodegener
; 11(1): 5, 2022 01 31.
Article
in English
| MEDLINE | ID: mdl-35101134
9.
Long-term inhibition of mutant LRRK2 hyper-kinase activity reduced mouse brain α-synuclein oligomers without adverse effects.
NPJ Parkinsons Dis
; 8(1): 115, 2022 Sep 10.
Article
in English
| MEDLINE | ID: mdl-36088364
10.
Aberrant mitochondrial morphology and function associated with impaired mitophagy and DNM1L-MAPK/ERK signaling are found in aged mutant Parkinsonian LRRK2R1441G mice.
Autophagy
; 17(10): 3196-3220, 2021 10.
Article
in English
| MEDLINE | ID: mdl-33300446
11.
Age-dependent accumulation of oligomeric SNCA/α-synuclein from impaired degradation in mutant LRRK2 knockin mouse model of Parkinson disease: role for therapeutic activation of chaperone-mediated autophagy (CMA).
Autophagy
; 16(2): 347-370, 2020 02.
Article
in English
| MEDLINE | ID: mdl-30983487
12.
The interplay of aging, genetics and environmental factors in the pathogenesis of Parkinson's disease.
Transl Neurodegener
; 8: 23, 2019.
Article
in English
| MEDLINE | ID: mdl-31428316
13.
Combined LRRK2 mutation, aging and chronic low dose oral rotenone as a model of Parkinson's disease.
Sci Rep
; 7: 40887, 2017 01 18.
Article
in English
| MEDLINE | ID: mdl-28098219
14.
Revealing ecological risks of priority endocrine disrupting chemicals in four marine protected areas in Hong Kong through an integrative approach.
Environ Pollut
; 215: 103-112, 2016 Aug.
Article
in English
| MEDLINE | ID: mdl-27179329
15.
Efficient attenuation of Friedreich's ataxia (FRDA) cardiomyopathy by modulation of iron homeostasis-human induced pluripotent stem cell (hiPSC) as a drug screening platform for FRDA.
Int J Cardiol
; 203: 964-71, 2016 Jan 15.
Article
in English
| MEDLINE | ID: mdl-26625322
16.
Chronic adiponectin deficiency leads to Alzheimer's disease-like cognitive impairments and pathologies through AMPK inactivation and cerebral insulin resistance in aged mice.
Mol Neurodegener
; 11(1): 71, 2016 11 25.
Article
in English
| MEDLINE | ID: mdl-27884163
17.
PMCA4 (ATP2B4) mutation in familial spastic paraplegia causes delay in intracellular calcium extrusion.
Brain Behav
; 5(4): e00321, 2015 Apr.
Article
in English
| MEDLINE | ID: mdl-25798335
18.
Endothelin-1 overexpression exacerbate experimental allergic encephalomyelitis.
J Neuroimmunol
; 276(1-2): 64-70, 2014 Nov 15.
Article
in English
| MEDLINE | ID: mdl-25205217
19.
PMCA4 (ATP2B4) mutation in familial spastic paraplegia.
PLoS One
; 9(8): e104790, 2014.
Article
in English
| MEDLINE | ID: mdl-25119969
20.
LRRK2 R1441G mice are more liable to dopamine depletion and locomotor inactivity.
Ann Clin Transl Neurol
; 1(3): 199-208, 2014 Mar.
Article
in English
| MEDLINE | ID: mdl-25356398