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Results 58 to 77 of 737
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TypeTitleAuthor(s)YearViews
cAMP-inducible chloride conductance in mouse fibroblast lines stably expressing the human cystic fibrosis transmembrane conductance regulatorRommens, JM; Dho, S; Bear, CE; Kartner, N; Kennedy, D; Riordan, JR; Tsui, LC; Foskett, JK1991281
 
Carnosine as a protective factor in diabetic nephropathy: Association with a leucine repeat of the carnosinase gene CNDP1Janssen, B; Hohenadel, D; Brinkkoetter, P; Peters, V; Rind, N; Fischer, C; Rychlik, I; Cerna, M; Romzova, M; De Heer, E; Baelde, H; Bakker, SJL; Zirie, M; Rondeau, E; Mathieson, P; Saleem, MA; Meyer, J; Koppel, H; Sauerhoefer, S; Bartram, CR; Nawroth, P; Hammes, H-P; Yard, BA; Zschocke, J; Van Der Woude, FJ20058
 
Carpal instability after fracture of the lower end of the radiusChow, SP199139
 
Carpal malalignment following intra-articular fractures of the distal radius in a working populationO'flanagan, SJ; Ip, FK; Roberts, CJ; Chow, SP199549
 
Carrier detection and prenatal diagnosis of cystic fibrosis using an intragenic TA-repeat polymorphismMornet, E; Chateau, C; SimonBouy, B; Boue, J; Zielenski, J; Tsui, LC; Boue, A1992222
 
CFTR gene mutations and the pancreatic phenotypeDurie, PR; Ahmed, N; Corey, M; Zielenski, J; Ellis, L; Tullis, E; Tsui, LC1999123
 
CFTR gene variant for patients with congenital absence of vas deferens [3]Zielenski, J; Patrizio, P; Corey, M; Handelin, B; Markiewicz, D; Asch, R; Tsui, LC1995207
 
CFTR mutation detection by multiplex heteroduplex (mHET) analysis on MDE gel.Zielenski, J; Aznarez, I; Onay, T; Tzounzouris, J; Markiewicz, D; Tsui, LC2002113
 
Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: A cystic fibrosis mutation of Slavic origin common in Central and East EuropeDörk, T; Macek Jr, M; Mekus, F; Tümmler, B; Tzountzouris, J; Casals, T; Krebsová, A; Koudová, M; Sakmaryová, I; Macek Sr, M; Vávrová, V; Zemková, D; Ginter, E; Petrova, NV; Ivaschenko, T; Baranov, V; Witt, M; Pogorzelski, A; Bal, J; Zékanowsky, C; Wagner, K; Stuhrmann, M; Bauer, I; Seydewitz, HH; Neumann, T; Jakubiczka, S; Kraus, C; Thamm, B; Nechiporenko, M; Livshits, L; Mosse, N; Tsukerman, G; Kadási, L; RavnikGlavač, M; Glavač, D; Komel, R; Vouk, K; Kučinskas, V; Krumina, A; Teder, M; Kocheva, S; Efremov, GD; Onay, T; Kirdar, B; Malone, G; Schwarz, M; Zhou, Z; Friedman, KJ; Carles, S; Claustres, M; Bozon, D; Verlingue, C; Férec, C; Tzetis, M; Kanavakis, E; Cuppens, H; Bombieri, C; Pignatti, PF; Sangiuolo, F; Jordanova, A; Kusic, J; Radojkovič, D; Sertić, J; Richter, D; Rukavina, AS; Bjorck, E; Strandvik, B; Cardoso, H; Montgomery, M; Nakielna, B; Hughes, D; Estivill, X; Aznarez, I; Tullis, E; Tsui, LC; Zielenski, J2000487
 
Characterization of disease-associated mutations affecting an exonic splicing enhancer and two cryptic splice sites in exon 13 of the cystic fibrosis transmembrane conductance regulator geneAznarez, I; Chan, EM; Zielenski, J; Blencowe, BJ; Tsui, LC2003732
 
Characterization of the human beta-crystallin gene Hu beta A3/A1 reveals ancestral relationships among the beta gamma-crystallin superfamilyHogg, D; Tsui, L-C; Gorin, M; Breitman, ML1986424
 
Characterization of the promoter region of the cystic fibrosis transmembrane conductance regulator geneChou, JL; Rozmahel, R; Tsui, LC1991259
 
Characterization of the segmental duplication LCR7-20 in the human genomeLiu, X; Li, X; Li, M; Acimovic, YJ; Li, Z; Scherer, SW; Estivill, X; Tsui, LC2004933
 
Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb developmentCrackower, MA; Scherer, SW; Rommens, JM; Hui, CC; Poorkaj, P; Soder, S; Cobben, JM; Hudgins, L; Evans, JP; Tsui, LC1996636
 
Chinese students at an English-Language university: Prediction of academic performanceSpinks, JA; Ho, DYF198472
 
Cholesterol emboli may mimic systemic vasculitisPeat, DS; Mathieson, PW19965
 
Chromitite and ultramafic rock compositional zoning through a paleotransform fault, poum, new caledonia: a discussionMalpas, J; Robinson, PT; Zhou, MF199755
 
Chromosomal localization in mouse and human of the vasoactive intestinal peptide receptor type 2 gene: A possible contributor to the holoprosencephaly 3 phenotypeMackay, M; Fantes, J; Scherer, S; Boyle, S; West, K; Tsui, LC; Belloni, E; Lutz, E; Van Heyningen, V; Harmar, AJ1996306
 
Chromosomal localization of the human gene encoding the 51-kDa subunit of mitochondrial complex I (NDUFV1) to 11q13Ali, ST; Duncan, AMV; Schappert, K; Heng, HHQ; Tsui, L-C; Chow, W; Robinson, BH1993319
 
Chromosomal mapping of the second human CD8B gene locusZhang, XL; Heng, HHQ; Yang, Y; Tsui, LC; Parnes, JR; Chamberlain, JW199675
 
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