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Title	Author(s)	Issue Date
ICOS regulates the generation and function of human CD4+ Treg in a CTLA-4 dependent manner Journal:PLoS ONE	Zheng, J Chan, PL Liu, Y Qin, G Xiang, Z Lam, KT Lewis, DB Lau, YL Tu, W	2013
Identical point mutation leading to low levels of mannose binding protein and poor C3b mediated opsonisation in Chinese and Caucasian populations Journal:Immunology Letters	Lipscombe, RJ Lau, YL Levinsky, RJ Sumiya, M Summerfield, JA Turner, MW	1992
Identification and evaluation of children with Autism Spectrum Disorder Proceeding/Conference:ICNA Symposium 2008 & Peking University International Forum on Child Neurology	Wong, VCN	2008
Identification and functional analysis of first heterozygous frameshift mutation in the GHRH gene in a Chinese boy with isolated growth hormone deficiency Journal:Gene	Wei, Shuoshuo Zhang, Mei Li, Yanying Yang, Wanling Zhang, Chuanpeng Liu, Fupeng Chen, Shuxiong Ban, Bo He, Dongye	20-May-2024
Identification and functional annotation of alternative splicing events using RNA sequencing in systemic lupus erythematosus	Zheng, Lichuan 鄭力川 Advisor(s):Yang, W Lau, YL	2021
Identification and functional studies of the protein interacting partners of Human Testis-specific Protein Y-linked Like 2 (TSPYL2) Gene Proceeding/Conference:Research Postgraduate Symposium, RPS 2007	Chiu, RPH Chan, SY	2007
Identification and prioritization of single nucleotide variation for Mendelian disorders from whole exome sequencing data	Zhang, Lu 张璐 Advisor(s):Yang, W Lau, YL	2012
Identification of 21 novel and 3 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes Proceeding/Conference:HUGO / HUGO-AP 2006	Lun, KS Lam, STS Tong, TMF Chung, BHY Li, YH Chan, HC Or, SF Lau, YL	2006
Identification of 21 novel and 3 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes Proceeding/Conference:Annual Congress of the Asian Society for Pediatric Research, ASPR 2006	Chung, BHY Lam, STS Tong, TMF Li, YH Lun, KS Chan, HC Or, SF Lau, YL	2006
Identification of 22q11.2 deletion in patients from adult congenital heart disease clinic - a missed burden in the transition care Proceeding/Conference:European Journal of Human Genetics	Chung, B Chow, P Liu, A Lee, P Wong, V Chan, K Tang, M Lun, KS Lau, ETK Cheung, YF Chau, KT Lau, YL	2013
Identification of 22q11.2 deletion in patients from adult congenital heart disease clinic: a missed and found burden in the transition care Proceeding/Conference:ASPR-PSM 2013 Joint Scientific Meeting	Chung, BHY	2013
Identification of 22q11.2 deletion in patients from adult congenital heart disease clinic: a missed burden in the transition care in Hong Kong Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013	Chung, B Chow, P Liu, A Lee, P Chan, K Tang, M Lau, E Cheung, YF Chau, KT Lau, YL	2013
Identification of 25 novel and 2 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes Proceeding/Conference:HKPS-HKPNA 2006 Joint Annual Scientific Meeting	Chung, BHY Lam, STS Tong, TMF Li, YH Lun, KS Chan, HC Or, SF Lau, YL	2006
Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups Journal:Nature Communications	Wang, YF Zhang, Y Lin, Z ZHANG, H Wang, TY CAO, Y Morris, DL Sheng, Y Yin, X Zhong, SL Gu, X LEI, Y He, J Wu, Q SHEN, J Yang, J Lam, TH Lin, JH Mai, Z GUO, M Tang, Y Chen, Y Song, Q Ban, B Mok, CC Cui, Y Lu, L Shen, N Sham, PC Lau, CS Smith, DK Vyse, TJ Zhang, X Lau, YL Yang, W	2021
Identification of 7 novel TGFBR2 (Transforming Growth Factor-Beta Receptor 2) mutations in Chinese with Marfan syndrome (MFS) and related phenotypes using denaturing high performance liquid chromatography (DHPLC) Proceeding/Conference:International Congress of Pediatrics, IPA 2007	Chung, BHY Li, YH Lam, STS Yang, W Lun, KS Lau, YL	2007
Identification of 7 novel TGFBR2 mutations in Chinese with marfan syndrome (MFS) and related phenotypes using DHPLC Proceeding/Conference:Congress of Asian Society for Pediatric Research, ASPR 2007	Chung, BHY Li, YH Lam, STS Yang, W Lun, KS Lau, YL	2007
Identification of 7 novel transforming growth factor β receptor 2 mutations in Chinese patients with marfan syndrome Proceeding/Conference:Pediatrics	Chung, BHY Li, YH Lam, STS Yang, W Lun, KS Lau, YL	2008
Identification of a CFTR founder mutations, c.3068T>G:p.I1023R, which causes protein trafficking defects in Chinese patients with cystic fibrosis Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Leung, KC Ying, D Mak, CCY Chen, XY Xu, W Yeung, KS Chu, WY Mok, TKG Chau, SKC McLuskey, J Ong, WPT Leong, HY Chan, YK Yang, W Chen, JH Li, AM Lau, YL Lee, SL Chung, BHY	2016
Identification of a novel homozygous missense mutation in ABR causing cerebellar hypoplasia with early lethality Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Leung, GKC Ying, D Shek, NWM Chu, WY Yeung, KS Tang, MHY Kan, SYA Chan, YK Ip, JKJ Yang, W Lau, YL Chung, BHY	2016
Identification of a Novel small-molecule inhibitor of avian influenza H5N1 virus through computational screening against neuraminidase Proceeding/Conference:Congress of Asia Society for Pediatric Research	An, J Law, HY Lee, DCW Yang, LH Poon, LLM Jones, SJM Lau, ASY	2009

Showing results 2506 to 2525 of 5524 < previous next >