Results 1 to 19 of 19
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TypeTitleAuthor(s)YearViews
Functional analyses of RET mutations in Chinese hirschsprung disease patientsLeon, TYY; So, MT; Lui, VCH; Hofstra, RMW; Tam, PKH; Ngan, ESW; Garcia-Barcelo, MM2012149
 
Mutations in the NRG1 gene are associated with Hirschsprung diseaseTang, CSM; Ngan, ESW; Tang, WK; So, MT; Cheng, G; Miao, XP; Leon, TYY; Leung, BMC; Hui, KJWS; Lui, VHC; Chen, Y; Chan, IHY; Chung, PHY; Liu, XL; Wong, KKY; Sham, PC; Cherny, SS; Tam, PKH; GarciaBarcelo, MM2012245
 
No NRG1 V266L in Chinese patients with schizophreniaGarciaBarceló, MM; Miao, X; Tang, CS; So, HC; Tang, W; Leon, TYY; So, M; Yip, B; Chen, RYL; Cheung, EFC; Chen, EYH; Li, T; Tam, P; Cherny, SS; Sham, PC2011433
 
RET mutational spectrum in Hirschsprungs disease: evaluation of 601 Chinese patientsCherny, SS; Garcia-Barcelo, MM; Leon, TYY; So, MT; Sham, PC; Tam, PKH201193
 
Fine mapping of the NRG1 hirschsprung's disease locusTang, CSM; Tang, WK; So, MT; Miao, XP; Leung, BMC; Yip, BHK; Leon, TYY; Ngan, ESW; Lui, VCH; Chen, Y; Chan, IHY; Chung, PHY; Liu, XL; Wu, XZ; Wong, KKY; Sham, PC; Cherny, SS; Tam, PKH; GarciaBarceló, MM2011817
 
Reduced RET expression in gut tissue of individuals carrying risk alleles of Hirschsprung's diseaseMiao, X; Leon, TYY; Ngan, ESW; So, MT; Yuan, ZW; Lui, VCH; Chen, Y; Wong, KKY; Tam, PKH; GarciaBarceló, M2010923
 
Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese populationCornes, BK; Tang, CS; Leon, TYY; Hui, KJWS; So, MT; Miao, X; Cherny, SS; Sham, PC; Tam, PKH; GarciaBarcelo, MM2010700
 
A RET founder mutation in Chinese hirschsprung's patientsCornes, BK; Tang, CSM; Leon, TYY; So, MT; Sham, PC; Tam, PKH; Garcia-Barcelo, MM200991
 
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's diseaseGarcia-Barcelo, MM; Tang, CSM; Ngan, ESW; Lui, VCH; Chen, Y; So, MT; Leon, TYY; Miao, XP; Shum, CKY; Liu, FQ; Yeung, MY; Yuan, ZW; Guo, WH; Liu, L; Sun, XB; Huang, LM; Tou, JF; Song, YQ; Chan, D; Cheung, KMC; Wong, KKY; Cherny, SS; Sham, PC; Tam, PKH2009539
 
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's diseaseTam, PKH; Tang, CSM; Ngan, ESW; Lui, VCH; Chen, Y; So, MT; Leon, TYY; Miao, XP; Shum, CKY; Liu, FQ; Yeung, MY; Yuan, ZW; Guo, WH; Liu, L; Sun, XB; Huang, LM; Tou, JF; Song, YQ; Chan, D; Cheung, KMC; Wong, KKY; Cherny, SS; Sham, PC; Garcia-Barcelo, MM2009115
 
A germline mutation (A339V) in thyroid transcription factor-1 (TITF-1/NKX2.1) in patients with multinodular goiter and papillary thyroid carcinomaNgan, ESW; Lang, BHH; Liu, T; Shum, CKY; So, MT; Lau, DKC; Leon, TYY; Cherny, SS; Tsai, SY; Lo, CY; Khoo, US; Tam, PKH; GarciaBarceló, MM2009530
 
Transcriptional regulation of RET by Nkx2-1, Phox2b, Sox10, and Pax3Leon, TYY; Ngan, ESW; Poon, HC; So, MT; Lui, VCH; Tam, PKH; GarciaBarcelo, MM2009134
 
Perturbation of Hoxb5 Signaling in Vagal Neural Crests Down-Regulates Ret Leading to Intestinal Hypoganglionosis in MiceLui, VCH; Cheng, WWC; Leon, TYY; Lau, DKC; GarciaBareclo, M; Miao, XP; Kam, MKM; So, MT; Chen, Y; Wall, NA; Sham, MH; Tam, PKH2008206
 
Mutational analysis of SHH and GLI3 in anorectal malformationsGarciaBarceló, 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, PKH2008370
 
Evaluation of the thyroid transcription factor-1 gene (TITF1) as a Hirschsprung's disease locusGarciaBarceló, MM; Lau, DKC; Ngan, ESW; Leon, TYY; Liu, TT; So, MT; Miao, XP; Lui, VCC; Wong, KKY; Ganster, RW; Cass, DT; Croaker, GDH; Tam, PKH2007140
 
Role of RET and PHOX2B gene polymorphisms in risk of Hirschsprung's disease in Chinese population [9]Miao, X; GarciaBarceló, MM; So, MT; Leon, TYY; Lau, DKC; Liu, TT; Chan, EKW; Lan, LCL; Wong, KKY; Lui, VCH; Tam, PKH2007250
 
Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndromeGarciaBarceló, 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, PKH2006165
 
TTF-1 and RET promoter SNPs: Regulation of RET transcription in Hirschsprung's diseaseGarciaBarcelo, M; Ganster, RW; Lui, VCH; Leon, TYY; So, MT; Lau, AMF; Fu, M; Sham, MH; Knight, J; Zannini, MS; Sham, PC; Tam, PKH2005177
 
Novel RET mutation produces a truncated RET receptor lacking the intracellular signaling domain in a 3-generation family with Hirschsprung diseaseLui, VCH; Leon, TYY; GarciaBarcelo, MM; Ganster, RW; Chen, BLS; Hutson, JM; Tam, PKH200577
 
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