Detalles de la búsqueda
1.
Comparative Proteomic Analysis of Mature Pollen in Triploid and Diploid Populus deltoides.
Int J Mol Sci
; 17(9)2016 Sep 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-27598155
2.
The heat shock factor gene family in Salix suchowensis: a genome-wide survey and expression profiling during development and abiotic stresses.
Front Plant Sci
; 6: 748, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26442061
3.
Proteomic analysis and candidate allergenic proteins in Populus deltoides CL. "2KEN8" mature pollen.
Front Plant Sci
; 6: 548, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26284084
4.
Capsaicin inhibits experimental autoimmune neuritis in rats through inhibition of autophagy activity / 中国药理学通报
Chinese Pharmacological Bulletin
; (12): 191-197, 2018.
Artículo
en Zh
| WPRIM | ID: wpr-705016
5.
Linkage analysis of susceptibility loci in 2 target chromosomes in pedigrees with paranoid schizophrenia and undifferentiated schizophrenia / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 256-260, 2011.
Artículo
en Zh
| WPRIM | ID: wpr-326952
6.
Novel mutation of Y271H in EXT1 gene causes multiple exostoses / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 546-550, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-813843
7.
Mapping of pathogenic genes in a pedigree with autosomal dominant ichthyosis vulgaris / 中国医学科学院学报
Acta Academiae Medicinae Sinicae
; (6): 302-306, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-229984
8.
Isolation, culture and cryopreservation of cells derived from fetal appendages / 中华烧伤杂志
Chinese Journal of Burns
; (6): 447-450, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-347655
9.
Two novel mutations of the LDL receptor gene associated with familial hypercholesterolemia in a Chinese family / 中华医学杂志(英文版)
Chinese Medical Journal
; (24): 1694-1699, 2007.
Artículo
en Inglés
| WPRIM | ID: wpr-255524
10.
Identification of the origin of marker chromosome by comparative genomic hybridization / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 264-267, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-813896
11.
Biological characteristics and safety evaluation of endothelial progenitor cells from the umbilical cord blood / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 466-472, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-813859
12.
Azoospermia factor microdeletion on Y chromosome in patients with idiopathic azoospermia or severe oligozoospermia / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 241-245, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-813900
13.
Preimplantation genetic diagnosis of Duchenne muscular dystrophy by single cell triplex PCR / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 246-251, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-813899
14.
Fetal Membrane Derived Adherent Cells: a Novel Source for Mesenchymal Stem Cells / 中国生物工程杂志
China Biotechnology
; (12)2006.
Artículo
en Zh
| WPRIM | ID: wpr-685055
15.
Biotoxicology and biodynamics of silica nanoparticle / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 6-8, 2006.
Artículo
en Zh
| WPRIM | ID: wpr-813778
16.
Identification and clone of human Alzheimer's disease related gene nicastrin promoter / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 9-13, 2006.
Artículo
en Zh
| WPRIM | ID: wpr-813777
17.
A mutation 1633-26(C-->A) in EXT1 gene causes multiple exostoses / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 147-150, 2006.
Artículo
en Zh
| WPRIM | ID: wpr-263832
18.
Stable suppression of beta-catenin expression in prostate cancer cell line by retrovirus mediated RNAi / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 253-257, 2005.
Artículo
en Zh
| WPRIM | ID: wpr-813388
19.
Molecular analysis of SLC26A4 gene in a Chinese deafness family / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 376-379, 2005.
Artículo
en Inglés
| WPRIM | ID: wpr-280047
20.
A minidystrophin-EGFP fusion gene expressed in Cos-7 cells mediated by human source vector / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 493-496, 2005.
Artículo
en Inglés
| WPRIM | ID: wpr-280017