Detalles de la búsqueda
1.
Expression of truncated dystrophin cDNAs mediated by a lentiviral vector.
Neurol India
; 56(1): 52-6, 2008.
Artículo
en Inglés
| MEDLINE | ID: mdl-18310838
2.
Dysferlin mutation in a Chinese pedigree with Miyoshi myopathy.
Clin Neurol Neurosurg
; 108(4): 369-73, 2006 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-16023782
3.
Deletion and Duplication in the DMD Gene Detected by MLPA / 现代检验医学杂志
Journal of Modern Laboratory Medicine
; (4): 12-15, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-610917
4.
MicroRNA-146a C > G polymorphism and the risk of ischemic stroke: a meta-analysis / 国际脑血管病杂志
International Journal of Cerebrovascular Diseases
; (12): 336-342, 2016.
Artículo
en Zh
| WPRIM | ID: wpr-497554
5.
Analysis on A(TA)n TAA polymorphism of UGT1A1 gene promoter by fluorescence real-time quantitative PCR / 国际检验医学杂志
International Journal of Laboratory Medicine
; (12): 1806-1808, 2016.
Artículo
en Zh
| WPRIM | ID: wpr-494869
6.
The study of peripheral blood miR-29a/101 in the diagnosis of Alzheimer's disease / 中华行为医学与脑科学杂志
Chinese Journal of Behavioral Medicine and Brain Science
; (12): 1010-1014, 2016.
Artículo
en Zh
| WPRIM | ID: wpr-670343
7.
Correlation between methylenetetrahydrofolate reductase rs4846049 G/T polymorphism and ischemic stroke in a Chinese Han population / 国际脑血管病杂志
International Journal of Cerebrovascular Diseases
; (12): 709-714,715, 2016.
Artículo
en Zh
| WPRIM | ID: wpr-605301
8.
Association of R219K polymorphism in the ABCA1 gene with ischemic stroke in a Chinese Han population / 国际脑血管病杂志
International Journal of Cerebrovascular Diseases
; (12): 662-668, 2015.
Artículo
en Zh
| WPRIM | ID: wpr-480506
9.
Effect of cerebral ischemic preconditioning on the expressions of angiopoietin-1 and its receptor Tie-2 mRNA in cerebral ischemia in rats / 国际脑血管病杂志
International Journal of Cerebrovascular Diseases
; (12): 24-29, 2012.
Artículo
en Zh
| WPRIM | ID: wpr-418254
10.
Polymorphisms of (AC)n (AT)xTy in the upstream of β-globin gene in patients with mild β-thalassemia / 中华检验医学杂志
Chinese Journal of Laboratory Medicine
; (12): 32-36, 2012.
Artículo
en Zh
| WPRIM | ID: wpr-428250
11.
Chromosome aberration in a full-term neonate with low birth weight using microarray comparative genomic hybridization / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 550-554, 2008.
Artículo
en Zh
| WPRIM | ID: wpr-308019
12.
Expression of truncated dystrophin cDNAs mediated by a lentiviral vector.
Neurol India
; 2008 Jan-Mar; 56(1): 52-6
Artículo
en Inglés
| IMSEAR | ID: sea-121513
13.
Mutation analysis of dysferlin gene in a Chinese family with Miyoshi myopathy / 临床检验杂志
Chinese Journal of Clinical Laboratory Science
; (12)2006.
Artículo
en Zh
| WPRIM | ID: wpr-585721
14.
Dysferlin deficiency: the cause of limb-girdle muscular dystrophy 2B and Miyoshi myopathy in a Chinese pedigree / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 128-131, 2004.
Artículo
en Zh
| WPRIM | ID: wpr-329383
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