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Results: 1-10 |
Results: 10
Cystic fibrosis mutations and associated haplotypes in Turkish cystic fibrosis patients
Authors: Onay, T Zielenski, J Topaloglu, O Gokgoz, N Kayserili, H Apak, MY Camcioglu, Y Cokugras, H Akcakaya, N Tsui, LC Kirdar, B
Citation: T. Onay et al., Cystic fibrosis mutations and associated haplotypes in Turkish cystic fibrosis patients, HUMAN BIOL, 73(2), 2001, pp. 191-203
Novel cystic fibrosis mutation (2215INSG) in two adolescent Taiwanese siblings
Authors: Wu, CL Shu, SG Zielenski, J Chiang, CD Tsui, LP
Citation: Cl. Wu et al., Novel cystic fibrosis mutation (2215INSG) in two adolescent Taiwanese siblings, J FORMOS ME, 99(7), 2000, pp. 564-567
An embryoprotective role for glucose-6-phosphate dehydrogenase in developmental oxidative stress and chemical teratogenesis
Authors: Nicol, CJ Zielenski, J Tsui, LC Wells, PG
Citation: Cj. Nicol et al., An embryoprotective role for glucose-6-phosphate dehydrogenase in developmental oxidative stress and chemical teratogenesis, FASEB J, 14(1), 2000, pp. 111-127
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
Spectrum of CFTR mutations in Mexican cystic fibrosis patients: identification of five novel mutations [W1098C, 846delT, P750L, 4160insGGGG and 297-1G -> A)
Authors: Orozco, L Velazquez, R Zielenski, J Tsui, LC Chavez, M Lezana, JL Saldana, Y Hernandez, E Carnevale, A
Citation: L. Orozco et al., Spectrum of CFTR mutations in Mexican cystic fibrosis patients: identification of five novel mutations [W1098C, 846delT, P750L, 4160insGGGG and 297-1G -> A), HUM GENET, 106(3), 2000, pp. 360-365
Cystic fibrosis gene mutations and infertile men with primary testicular failure
Authors: Mak, V Zielenski, J Tsui, LC Durie, P Zini, A Martin, S Longley, TB Jarvi, KA
Citation: V. Mak et al., Cystic fibrosis gene mutations and infertile men with primary testicular failure, HUM REPR, 15(2), 2000, pp. 436-439
Genotype and phenotype in cystic fibrosis
Authors: Zielenski, J
Citation: J. Zielenski, Genotype and phenotype in cystic fibrosis, RESPIRATION, 67(2), 2000, pp. 117-133
Mutations in the cystic fibrosis transmembrane regulator gene in patients with tropical calcific pancreatitis
Authors: Bhatia, E Durie, P Zielenski, J Lam, D Sikora, SS Choudhuri, G Tsui, LC
Citation: E. Bhatia et al., Mutations in the cystic fibrosis transmembrane regulator gene in patients with tropical calcific pancreatitis, AM J GASTRO, 95(12), 2000, pp. 3658-3659
Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13
Authors: Zielenski, J Corey, M Rozmahel, R Markiewicz, D Aznarez, I Casals, T Larriba, S Mercier, B Cutting, GR Krebsova, A Macek, M Langfelder-Schwind, E Marshall, BC DeCelie-Germana, J Claustres, M Palacio, A Bal, J Nowakowska, A Ferec, C Estivill, X Durie, P Tsui, LC
Citation: J. Zielenski et al., Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13, NAT GENET, 22(2), 1999, pp. 128-129
Proportion of cystic fibrosis gene mutations not detected by routine testing in men with obstructive azoospermia
Authors: Mak, V Zielenski, J Tsui, LC Durie, P Zini, A Martin, S Longley, TB Jarvi, KA
Citation: V. Mak et al., Proportion of cystic fibrosis gene mutations not detected by routine testing in men with obstructive azoospermia, J AM MED A, 281(23), 1999, pp. 2217-2224
Risultati: 1-10 |