Detalles de la búsqueda
1.
Effects of simvastatin on the expression of inducible nitric oxide synthase and brain-derived neurotrophic factor in a lipopolysaccharide-induced rat model of Parkinson disease.
Int J Neurosci
; 126(3): 278-86, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-26000813
2.
Screening for, andVariants in a Cohort of Chinese Patients with Charcot-Marie-Tooth / 中华医学杂志(英文版)
Chinese Medical Journal
; (24): 151-155, 2018.
Artículo
en Inglés
| WPRIM | ID: wpr-342073
3.
Influence of simvastatin on dopaminergic neurons of lipopolysaccharide-induced rat model of Parkinson's disease
Asian Pacific Journal of Tropical Medicine
; (12): 64-67, 2015.
Artículo
en Inglés
| WPRIM | ID: wpr-820400
4.
Influence of simvastatin on dopaminergic neurons of lipopolysaccharide-induced rat model of Parkinson's disease
Asian Pacific Journal of Tropical Medicine
; (12): 64-67, 2015.
Artículo
en Zh
| WPRIM | ID: wpr-951543
5.
Cloning and localization of A3IP -a novel protein that interacts with ataxin-3 / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 394-398, 2013.
Artículo
en Zh
| WPRIM | ID: wpr-237241
6.
Classification and molecular diagnostic procedure for Chacort-Marie-Tooth disease / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 553-557, 2012.
Artículo
en Zh
| WPRIM | ID: wpr-232258
7.
Functions of carboxyl-terminus of Hsc70 interacting protein and its role in neurodegenerative disease / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 426-430, 2012.
Artículo
en Zh
| WPRIM | ID: wpr-232283
8.
Recent advance in genetic study of hereditary autosomal recessive cerebellar ataxia / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 673-676, 2012.
Artículo
en Zh
| WPRIM | ID: wpr-232234
9.
Spinal muscular atrophy mimicking myotonic dystrophy: a case report and clinical, pathological and genetic analysis / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 455-458, 2012.
Artículo
en Zh
| WPRIM | ID: wpr-232276
10.
Fragile X-associated tremor/ataxia syndrome / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 52-55, 2011.
Artículo
en Zh
| WPRIM | ID: wpr-234319
11.
The effect of HSPB8 gene mutation on cell viability in Charcot-Marie-Tooth disease type 2L / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 528-531, 2011.
Artículo
en Zh
| WPRIM | ID: wpr-326899
12.
Cellular expression of (R127W)HSPB1 and its co-localization with neurofilament light chain / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 496-500, 2011.
Artículo
en Zh
| WPRIM | ID: wpr-326906
13.
Research progress in roles of microRNA in polyglutamine diseases / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 406-409, 2010.
Artículo
en Zh
| WPRIM | ID: wpr-234395
14.
Establishment and application of an analytical method for PINK1 gene exon copy number / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 158-161, 2010.
Artículo
en Zh
| WPRIM | ID: wpr-349021
15.
Polynucleotide repeat expansion of nine spinocerebellar ataxia subtypes and dentatorubral-pallidoluysian atrophy in healthy Chinese Han population / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 501-505, 2010.
Artículo
en Zh
| WPRIM | ID: wpr-234373
16.
Mutation analysis of ATP13A2 gene in Chinese patients with familial autosomal recessive early-onset parkinsonism / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 567-570, 2009.
Artículo
en Zh
| WPRIM | ID: wpr-287373
17.
Detection of the CAG trinucleotide repeats of MJD1 gene by recombinant DNA technology / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 406-409, 2009.
Artículo
en Zh
| WPRIM | ID: wpr-349066
18.
Blockade of the aberrant aggregation of alpha-synuclein in HEK293 cells induced by overexpression of wild-type alpha-synuclein by RNA interference / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 128-131, 2008.
Artículo
en Zh
| WPRIM | ID: wpr-229808
19.
Molecular basis of spinocerebellar ataxias subtype caused by nucleotide repeat expansion in noncoding region / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 293-296, 2008.
Artículo
en Zh
| WPRIM | ID: wpr-229770
20.
The advances in research on phosphorylation of polyglutamine disease / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 414-417, 2008.
Artículo
en Zh
| WPRIM | ID: wpr-308051