A K L Cheung
Overview
Explore the profile of A K L Cheung including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
5
Citations
103
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Cheung A, Huang Y, Chen M, Chen Z
Hong Kong Med J
. 2019 Nov;
25 Suppl 7(5):37-40.
PMID: 31761770
No abstract available.
2.
Chen M, Jia M, Ma Y, Luo H, Chen H, Yang C, et al.
Epidemiol Infect
. 2018 Mar;
146(6):775-781.
PMID: 29534773
Multiple human immunodeficiency virus (HIV)-1 genotypes in China were first discovered in Yunnan Province before disseminating throughout the country. As the HIV-1 epidemic continues to expand in Yunnan, genetic characteristics...
3.
Cheng Y, Ho R, Chan K, Kan R, Tung E, Lung H, et al.
Oncogene
. 2014 Oct;
34(32):4219-28.
PMID: 25347745
Zinc-finger, MYND-type containing 10 (ZMYND10), or more commonly called BLU, expression is frequently downregulated in nasopharyngeal carcinoma (NPC) and many other tumors due to promoter hypermethylation. Functional evidence shows that...
4.
Lung H, Man O, Yeung M, Ko J, Cheung A, Law E, et al.
Oncogene
. 2014 Mar;
34(7):878-89.
PMID: 24608426
Nasopharyngeal carcinoma (NPC) is a cancer that occurs in high frequency in Southern China. A previous functional complementation approach and the subsequent cDNA microarray analysis have identified that serum amyloid...
5.
Law E, Cheung A, Kashuba V, Pavlova T, Zabarovsky E, Lung H, et al.
Oncogene
. 2011 Jul;
31(6):728-38.
PMID: 21743496
Fibulin-2 (FBLN2) has been identified as a candidate tumor-suppressor gene in nasopharyngeal carcinoma (NPC). Originally identified through a chromosome 3 NotI genomic microarray screen, it shows frequent deletion or methylation...