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Results 315 to 334 of 737
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TypeTitleAuthor(s)YearViews
Identification and characterization of human genes encoding Hprp3p and Hprp4p, interacting components of the spliceosomeWang, A; FormanKay, J; Luo, Y; Luo, M; Chow, YH; Plumb, J; Friesen, JD; Tsui, LC; Heng, HHQ; Woolford Jr, JL; Hu, J1997373
 
Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis geneRommens, JM; Zengerling, S; Burns, J; Melmer, G; Kerem, B; Plavsic, N; Zsiga, M; Kennedy, D; Markiewicz, D; Rozmahel, R; Riordan, JR; Buchwald, M; Tsui, L1988287
 
Identification of a 1300 kilobase deletion unit on chromosome 7q31.3 in invasive epithelial ovarian carcinomasEdelson, MI; Scherer, SW; Tsui, LC; Welch, WR; Bell, DA; Berkowitz, RS; Mok, SC1997111
 
Identification of a human LIM-Hox gene, hLH-2, aberrantly expressed in chronic myelogenous leukaemia and located on 9q33-34.1Wu, HK; Heng, HHQ; Siderovski, DP; Dong, WF; Okuno, Y; Shi, XM; Tsui, LC; Minden, MD1996118
 
Identification of a novel lipase gene mutated in lpd mice with hypertriglyceridemia and associated with dyslipidemia in humansWen, XY; Hegele, RA; Wang, J; Yan Wang, D; Cheung, J; Wilson, M; Yahyapour, M; Bai, Y; Zhuang, L; Skaug, J; Young, TK; Connelly, PW; Koop, BF; Tsui, LC; Stewart, AK2003710
 
Identification of a p.Ser81Arg encoding mutation in SLC2A10 gene of arterial tortuosity syndrome patients from 10 Qatari familiesFaiyazulHaque, M; Zaidi, SHE; Wahab, AA; Eltohami, A; AlMureikhi, MS; AlThani, G; Peltekova, VD; Tsui, LC; Teebi, AS2008135
 
Identification of a polymorphic DNA marker pDL32B (D12S7) and its localization to the long arm of chromosome 12, region q14.3-qterTsui, LC; Buchwald, M; Markiewicz, D; Kao, FT; Cai, GY; Law, ML1985288
 
Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndromeOsborne, LR; Campbell, T; Daradich, A; Scherer, SW; Tsui, LC1999184
 
Identification of a yeast artificial chromosome clone spanning a translocation breakpoint at 7q32.1 in a Smith-Lemli-Opitz syndrome patientAlley, TL; Gray, BA; Lee, SH; Scherer, SW; Tsui, LC; Tint, GS; Williams, CA; Zori, R; Wallace, MR1995275
 
Identification of an amplified gene cluster in glioma including two novel amplified genes isolated by exon trappingMueller, HW; Michel, A; Heckel, D; Fischer, U; Tönnes, M; Tsui, LC; Scherer, S; Zang, KD; Meese, E1997227
 
Identification of four new mutations in the cystic fibrosis transmembrane conductance regulator gene: I148T, L1077P, Y1092X, 2183AA→GBozon, D; Zielenski, J; Rininsland, F; Tsui, LC1994102
 
Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patientsOsborne, LR; Martindale, D; Scherer, SW; Shi, XM; Huizenga, J; Heng, HHQ; Costa, T; Pober, B; Lew, L; Brinkman, J; Rommens, J; Koop, B; Tsui, LC1996283
 
Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) geneZielenski, J; Bozon, D; Kerem, BS; Markiewicz, D; Durie, P; Rommens, JM; Tsui, LC1991323
 
Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis geneKerem, B; Zielenski, J; Markiewicz, D; Bozon, D; Gazit, E; Yahav, J; Kennedy, D; Riordan, JR; Collins, FS; Rommens, JM; Tsui, LC1990319
 
Identification of revertants for the cystic fibrosis ΔF508 mutation using STE6-CFTR chimeras in yeastTeem, JL; Berger, HA; Ostedgaard, LS; Rich, DP; Tsui, LC; Welsh, MJ1993246
 
Identification of six mutations (R31L, 441delA, 681delC, 1461ins4, W1089R, E1104X) in the cystic fibrosis transmembrane conductance regulator (CFTR) geneZielenski, J; Markiewicz, D; Chen, HS; Schappert, K; Seller, A; Durie, P; Corey, M; Tsui, LC1995284
 
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly.Belloni, E; Muenke, M; Roessler, E; Traverso, G; SiegelBartelt, J; Frumkin, A; Mitchell, HF; DonisKeller, H; Helms, C; Hing, AV; Heng, HH; Koop, B; Martindale, D; Rommens, JM; Tsui, LC; Scherer, SW1996363
 
Identification of the cystic fibrosis gene: Chromosome walking and jumpingRommens, JM; Iannuzzi, MC; Kerem, BS; Drumm, ML; Melmer, G; Dean, M; Rozmahel, R; Cole, JL; Kennedy, D; Hidaka, N; Zsiga, M; Buchwald, M; Riordan, JR; Tsui, LC; Collins, FS1989463
 
Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNARiordan, JR; Rommens, JM; Kerem, BS; Alon, N; Rozmahel, R; Grzelczak, Z; Zielinski, J; Lok, S; Plavsic, N; Chou, JL; Drumm, ML; Iannuzzi, MC; Collins, FS; Tsui, LC1989612
 
Identification of the cystic fibrosis gene: Genetic analysisKerem, BS; Rommens, JM; Buchanan, JA; Markiewicz, D; Cox, TK; Chakravarti, A; Buchwald, M; Tsui, LC1989311
 
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