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Results: 1-12 |
Results: 12
Causes of microsatellite instability in colorectal tumors: implications for hereditary non-polyposis colorectal cancer screening
Authors: Potocnik, U Glavac, D Golouh, R Ravnik-Glavac, M
Citation: U. Potocnik et al., Causes of microsatellite instability in colorectal tumors: implications for hereditary non-polyposis colorectal cancer screening, CANC GENET, 126(2), 2001, pp. 85-96
The role of P-glycoprotein (MDR1) polymorphisms and mutations in colorectal cancer
Authors: Potocnik, U Glavac, MR Golouh, R Glavac, D
Citation: U. Potocnik et al., The role of P-glycoprotein (MDR1) polymorphisms and mutations in colorectal cancer, PFLUG ARCH, 442(6), 2001, pp. R182-R183
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 Europe
Authors: Dork, T Macek, M Mekus, F Tummler, B Tzountzouris, J Casals, T Krebsova, A Koudova, M Sakmaryova, I Macek, M Vavrova, V Zemkova, D Ginter, E Petrova, NV Ivaschenko, T Baranov, V Witt, M Pogorzelski, A Bal, J Zekanowsky, 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 Kadasi, L Ravnik-Glavac, M Glavac, D Komel, R Vouk, K Kucinskas, V Krumina, A Teder, M Kocheva, S Efremov, GD Onay, T Kirdar, B Malone, G Schwarz, M Zhou, ZQ Friedman, KJ Carles, S Claustres, M Bozon, D Verlingue, C Ferec, C Tzetis, M Kanavakis, E Cuppens, H Bombieri, C Pignatti, PF Sangiuolo, F Jordanova, A Kusic, J Radojkovic, D Sertic, 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, J
Citation: T. Dork et al., 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 Europe, HUM GENET, 106(3), 2000, pp. 259-268
Animal model in the study of colorectal carcinogenesis
Authors: Ravnik-Glavac, M Cerar, A Glavac, D
Citation: M. Ravnik-glavac et al., Animal model in the study of colorectal carcinogenesis, PFLUG ARCH, 440(5), 2000, pp. R55-R57
Screening methods for cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in non-human primates
Authors: Glavac, D Ravnik-Glavac, M Potocnik, U Dean, M Wine, J
Citation: D. Glavac et al., Screening methods for cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in non-human primates, PFLUG ARCH, 439(3), 2000, pp. R12-R13
Evaluation of microsatellite markers for efficient assessment of high microsatellite instabile colorectal tumors
Authors: Potocnik, U Glavac, D Golouh, R Ravnik-Glavac, M
Citation: U. Potocnik et al., Evaluation of microsatellite markers for efficient assessment of high microsatellite instabile colorectal tumors, PFLUG ARCH, 439(3), 2000, pp. R47-R49
Evidence that hereditary pancreatitis is genetically heterogeneous disorder
Authors: Ravnik-Glavac, M Dean, M di Sant'Agnese, P Chernick, M Kozelj, M Krizman, I Glavac, D
Citation: M. Ravnik-glavac et al., Evidence that hereditary pancreatitis is genetically heterogeneous disorder, PFLUG ARCH, 439(3), 2000, pp. R50-R52
Study of mutant and polyvariant mutant CFTR genes in patients with congenital absence of the vas deferens
Authors: Ravnik-Glavac, M Dean, M Glavac, D
Citation: M. Ravnik-glavac et al., Study of mutant and polyvariant mutant CFTR genes in patients with congenital absence of the vas deferens, PFLUG ARCH, 439(3), 2000, pp. R53-R55
Incidence of germline hMLH1 and hMSH2 mutations (HNPCC patients) among newly diagnosed colorectal cancers in a Slovenian population
Authors: Ravnik-Glavac, M Potocnik, L Glavac, D
Citation: M. Ravnik-glavac et al., Incidence of germline hMLH1 and hMSH2 mutations (HNPCC patients) among newly diagnosed colorectal cancers in a Slovenian population, J MED GENET, 37(7), 2000, pp. 533-536
VHL alterations in human clear cell renal cell carcinoma: Association withadvanced tumor stage and a novel hot spot mutation
Authors: Brauch, H Weirich, G Brieger, J Glavac, D Rodl, H Eichinger, M Feurer, M Weidt, E Puranakanitstha, C Neuhaus, C Pomer, S Brenner, W Schirmacher, P Storkel, S Rotter, M Masera, A Gugeler, N Decker, HJ
Citation: H. Brauch et al., VHL alterations in human clear cell renal cell carcinoma: Association withadvanced tumor stage and a novel hot spot mutation, CANCER RES, 60(7), 2000, pp. 1942-1948
Two novel missense mutations (R766M and R792G) in exon 13 of the CFTR genein a patient with congenital bilateral absence of the vas deferens
Authors: Ravnik-Glavac, M Dean, M Glavac, D
Citation: M. Ravnik-glavac et al., Two novel missense mutations (R766M and R792G) in exon 13 of the CFTR genein a patient with congenital bilateral absence of the vas deferens, HUMAN HERED, 50(5), 2000, pp. 318-319
A novel Q562X mutation identified in the hMLH1 gene in a Slovenian patientwith hereditary nonpolyposis colorectal cancer
Authors: Potocnik, U Glavac, D Golouh, R Ravnik-Glavac, M
Citation: U. Potocnik et al., A novel Q562X mutation identified in the hMLH1 gene in a Slovenian patientwith hereditary nonpolyposis colorectal cancer, HUMAN HERED, 50(2), 2000, pp. 140-141
Risultati: 1-12 |