Detalhe da pesquisa
1.
[Shared functional modules for nasopharyngeal and oral squamous cell carcinoma identified by network analysis of transcriptomes].
Yi Chuan
; 41(2): 146-157, 2019 Feb 20.
Artigo
em Chinês
| MEDLINE | ID: mdl-30803945
2.
[Identification of gene functional modules shared by cancers based on biclustering].
Yi Chuan
; 35(3): 333-42, 2013 Mar.
Artigo
em Chinês
| MEDLINE | ID: mdl-23575539
3.
[Advances in development of gene-gene interaction analysis methods based on SNP data: a review].
Yi Chuan
; 35(12): 1331-9, 2013 Dec.
Artigo
em Chinês
| MEDLINE | ID: mdl-24645342
4.
Efficacy of combined treatment with albendazole and baicalein against eosinophilic meningitis induced by Angiostrongylus cantonensis in mice.
J Helminthol
; 85(1): 92-9, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20587113
5.
Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy.
BMC Med Genet
; 11: 79, 2010 May 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-20504331
6.
[Advances in genetics of restless legs syndrome].
Yi Chuan
; 31(7): 675-82, 2009 Jul.
Artigo
em Chinês
| MEDLINE | ID: mdl-19586871
7.
[Genetic relationships between Tuva population and the neighboring populations in the Altai Region of Xinjiang Uygur Autonomous Region].
Yi Chuan
; 31(8): 818-24, 2009 Aug.
Artigo
em Chinês
| MEDLINE | ID: mdl-19689942
8.
Rabies trend in China (1990-2007) and post-exposure prophylaxis in the Guangdong province.
BMC Infect Dis
; 8: 113, 2008 Aug 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-18717989
9.
GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects.
Acta Otolaryngol
; 128(3): 297-303, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18274916
10.
A novel mutation of POU3F4 causes congenital profound sensorineural hearing loss in a large Chinese family.
Laryngoscope
; 116(6): 944-50, 2006 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-16735904
11.
Decision forest analysis of large-scale sib-pair identical-by-decent profiles for locating the underlying disease genes for alcoholism in human.
Beijing Da Xue Xue Bao Yi Xue Ban
; 38(1): 71-3, 2006 Feb 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-16415971
12.
Novel strategies to identify relevant molecular signatures for complex human diseases based on data of identical-by-decent profiles and genomic context.
Beijing Da Xue Xue Bao Yi Xue Ban
; 38(1): 74-7, 2006 Feb 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-16415972
13.
[Analysis of diffuse large B-cell lymphoma heterogeneity based on coupled two-way clustering].
Yi Chuan
; 28(9): 1129-34, 2006 Sep.
Artigo
em Chinês
| MEDLINE | ID: mdl-16963424
14.
Identification of Risk Pathways and Functional Modules for Coronary Artery Disease Based on Genome-wide SNP Data.
Genomics Proteomics Bioinformatics
; 14(6): 349-356, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27965104
15.
Psychometric properties of the coronary heart disease scale of the quality-of-life instruments for chronic diseases (QLICD-CHD): an application to Cantonese patients.
Asia Pac J Public Health
; 27(2 Suppl): 100S-9S, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25352431
16.
Pathway-based analysis tools for complex diseases: a review.
Genomics Proteomics Bioinformatics
; 12(5): 210-20, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25462153
17.
A meta-analysis of the association between TNF-α -308G>A polymorphism and type 2 diabetes mellitus in Han Chinese population.
PLoS One
; 8(3): e59421, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23527193
18.
Laryngeal aerodynamic analysis in assisting with the diagnosis of muscle tension dysphonia.
J Voice
; 26(2): 177-81, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21550774
19.
Newborn hearing concurrent gene screening can improve care for hearing loss: a study on 14,913 Chinese newborns.
Int J Pediatr Otorhinolaryngol
; 75(4): 535-42, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21329993
20.
Association between polymorphisms in SOD1 and noise-induced hearing loss in Chinese workers.
Acta Otolaryngol
; 130(4): 477-86, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19895330