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	Title	Author(s)	Issue Date	Views
	MNX1 (HLXB9) mutations in Currarino patients Journal:Journal of Pediatric Surgery	GarciaBarceló, MM Lui, VCH So, MT Miao, X Leon, TYY Yuan, ZW Ngan, ESW Ehsan, T Chung, HY Khong, Pl Wong, KKY Tam, PKH	2009	209
	Mutational analysis of SHH and GLI3 in anorectal malformations Journal:Birth Defects Research Part A - Clinical and Molecular Teratology	GarciaBarceló, MM Lui, VCH Miao, X So, MT Leon, TYY Yuan, ZW Li, L Liu, L Wang, B Sun, XB Huang, LM Tou, JF Ngan, ESW Cherny, SS Chan, KW Lee, KH Wang, W Wong, KKY Tam, PKH	2008	144
	Mutations in the NRG1 gene are associated with Hirschsprung disease Journal:Human Genetics	Tang, CSM Ngan, ESW Tang, WK So, MT Cheng, G Miao, XP Leon, TYY Leung, BMC Hui, KJWS Lui, VHC Chen, Y Chan, IHY Chung, HY Liu, XL Wong, KKY Sham, PC Cherny, SS Tam, PKH GarciaBarcelo, MM	2012	190
	MXD1 regulates the H9N2 and H1N1 influenza A virus–induced chemokine expression and their replications in human macrophage Journal:Journal of Leukocyte Biology	Yim, HCH Leon, TYY Li, JCB	2020	16
	No NRG1 V266L in Chinese patients with schizophrenia Journal:Psychiatric Genetics	GarciaBarceló, MM Miao, X Tang, CSM So, HC Tang, W Leon, TYY So, M Yip, B Chen, RYL Cheung, EFC Chen, EYH Li, T Tam, P Cherny, SS Sham, PC	2011	161
	Novel RET mutation produces a truncated RET receptor lacking the intracellular signaling domain in a 3-generation family with Hirschsprung disease Journal:Clinical Chemistry	Lui, VCH Leon, TYY GarciaBarcelo, MM Ganster, RW Chen, BLS Hutson, JM Tam, PKH	2005	283
	Perturbation of Hoxb5 Signaling in Vagal Neural Crests Down-Regulates Ret Leading to Intestinal Hypoganglionosis in Mice Journal:Gastroenterology	Lui, VCH Cheng, WWC Leon, TYY Lau, DKC GarciaBareclo, M Miao, XP Kam, MKM So, MT Chen, Y Wall, NA Sham, MH Tam, PKH	2008	206
	Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndrome Journal:Clinical Chemistry	GarciaBarceló, M So, MT Lau, DKC Leon, TYY Yuan, ZW Cai, WS Lui, VCH Fu, M Herbrick, JA Gutter, E Proud, V Li, L PierreLouis, J Aleck, K Van Heurn, E Belloni, E Scherer, SW Tam, PKH	2006	207
	Reduced RET expression in gut tissue of individuals carrying risk alleles of Hirschsprung's disease Journal:Human Molecular Genetics	Miao, X Leon, TYY Ngan, ESW So, MT Yuan, ZW Lui, VCH Chen, Y Wong, KKY Tam, PKH GarciaBarceló, M	2010	176
	A RET founder mutation in Chinese hirschsprung's patients Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2009	Cornes, BK Tang, CSM Leon, TYY So, MT Sham, PC Tam, PKH Garcia-Barcelo, MM	2009	149
	RET mutational spectrum in Hirschsprungs disease: evaluation of 601 Chinese patients Proceeding/Conference:International Congress of Human Genetics, ICHG 2011	Cherny, SS Garcia-Barcelo, MM Leon, TYY So, MT Sham, PC Tam, PKH	2011	171
	Role of RET and PHOX2B gene polymorphisms in risk of Hirschsprung's disease in Chinese population [9] Journal:Gut	Miao, X GarciaBarceló, MM So, MT Leon, TYY Lau, DKC Liu, TT Chan, EKW Lan, LCL Wong, KKY Lui, VCH Tam, PKH	2007	116
	Transcriptional regulation of RET by Nkx2-1, Phox2b, Sox10, and Pax3 Journal:Journal of Pediatric Surgery	Leon, TYY Ngan, ESW Poon, HC So, MT Lui, VCH Tam, PKH GarciaBarcelo, MM	2009	178
	TTF-1 and RET promoter SNPs: Regulation of RET transcription in Hirschsprung's disease Journal:Human Molecular Genetics	GarciaBarcelo, M Ganster, RW Lui, VCH Leon, TYY So, MT Lau, AMF Fu, M Sham, MH Knight, J Zannini, MS Sham, PC Tam, PKH	2005	188

Showing results 8 to 21 of 21 < previous