AAAAAA

   
Results: 1-25 | 26-29
Results: 1-25/29
Regulated expression of the human CFTR gene in epithelial cells
Authors: Ye, L Chan, S Chow, YH Tsui, LC Hu, J
Citation: L. Ye et al., Regulated expression of the human CFTR gene in epithelial cells, MOL THER, 3(5), 2001, pp. 723-733
A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome
Authors: Osborne, LR Li, M Pober, B Chitayat, D Bodurtha, J Mandel, A Costa, T Grebe, T Cox, S Tsui, LC Scherer, SW
Citation: Lr. Osborne et al., A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome, NAT GENET, 29(3), 2001, pp. 321-325
Murine phosphatidylserine-specific phospholipase A1 (Ps-pla1) maps to Chromosome 16 but is distinct from the lpd (lipid defect) locus
Authors: Wen, XY Stewart, AK Skaug, J Wei, E Tsui, LC
Citation: Xy. Wen et al., Murine phosphatidylserine-specific phospholipase A1 (Ps-pla1) maps to Chromosome 16 but is distinct from the lpd (lipid defect) locus, MAMM GENOME, 12(2), 2001, pp. 129-132
Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31
Authors: Cheung, J Petek, E Nakabayashi, K Tsui, LC Vincent, JB Scherer, SW
Citation: J. Cheung et al., Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31, GENOMICS, 78(1-2), 2001, pp. 7-11
Comparative analysis of the gene-dense ACHE/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5
Authors: Wilson, MD Riemer, C Martindale, DW Schnupf, P Boright, AP Cheung, TL Hardy, DM Schwartz, S Scherer, SW Tsui, LC Miller, W Koop, BF
Citation: Md. Wilson et al., Comparative analysis of the gene-dense ACHE/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5, NUCL ACID R, 29(6), 2001, pp. 1352-1365
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
Molecular cytogenetic characterization of a critical region in bands 7q35-q36 commonly deleted in malignant myeloid disorders
Authors: Dohner, K Hehmann, U Brown, J Hetzel, C",Stewart,"Lowther, G Scholl, C Frohling, S Cuneo, A Tsui, LC Lichter, P Scherer, SW Dohner, H
Citation: K. Dohner et al., Molecular cytogenetic characterization of a critical region in bands 7q35-q36 commonly deleted in malignant myeloid disorders, HEMAT BLOOD, 40, 2001, pp. 15-19
Genome Canada update
Authors: Carty, A Tsui, LC
Citation: A. Carty et Lc. Tsui, Genome Canada update, NAT BIOTECH, 18(2), 2000, pp. 129-129
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
Involvement of the HLXB9 homeobox gene in Currarino syndrome
Authors: Belloni, E Martucciello, G Verderio, D Ponti, E Seri, M Jasonni, V Torre, M Ferrari, M Tsui, LC Scherer, SW
Citation: E. Belloni et al., Involvement of the HLXB9 homeobox gene in Currarino syndrome, AM J HU GEN, 66(1), 2000, pp. 312-319
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
Type II citrullinemia (citrin deficiency): A mysterious disease caused by a defect of calcium-binding mitochondrial carrier protein
Authors: Kobayashi, K Iijima, M Yasuda, T Sinasac, DS Yamaguchi, N Tsui, LC Scherer, SW Saheki, T
Citation: K. Kobayashi et al., Type II citrullinemia (citrin deficiency): A mysterious disease caused by a defect of calcium-binding mitochondrial carrier protein, CALCIUM: THE MOLECULAR BASIS OF CALCIUM ACTION IN BIOLOGY AND MEDICINE, 2000, pp. 565-587
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
The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein
Authors: Kobayashi, K Sinasac, DS Iijima, M Boright, AP Begum, L Lee, JR Yasuda, T Ikeda, S Hirano, R Terazono, H Crackower, MA Kondo, I Tsui, LC Scherer, SW Saheki, T
Citation: K. Kobayashi et al., The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein, NAT GENET, 22(2), 1999, pp. 159-163
Dysregulation of cyclin dependent kinase 6 expression in splenic marginal zone lymphoma through chromosome 7q translocations
Authors: Corcoran, MM Mould, SJ Orchard, JA Ibbotson, RE Chapman, RM Boright, AP Platt, C Tsui, LC Scherer, SW Oscier, DG
Citation: Mm. Corcoran et al., Dysregulation of cyclin dependent kinase 6 expression in splenic marginal zone lymphoma through chromosome 7q translocations, ONCOGENE, 18(46), 1999, pp. 6271-6277
Genomic structure of the adult-onset type II citrullinemia gene, SLC25A13,and cloning and expression of its mouse homologue
Authors: Sinasac, DS Crackower, MA Lee, JR Kobayashi, K Saheki, T Scherer, SW Tsui, LC
Citation: Ds. Sinasac et al., Genomic structure of the adult-onset type II citrullinemia gene, SLC25A13,and cloning and expression of its mouse homologue, GENOMICS, 62(2), 1999, pp. 289-292
Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome
Authors: Osborne, LR Campbell, T Daradich, A Scherer, SW Tsui, LC
Citation: Lr. Osborne et al., Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome, GENOMICS, 57(2), 1999, pp. 279-284
Cloning and characterization of two cytoplasmic dynein intermediate chain genes in mouse and human
Authors: Crackower, MA Sinasac, DS Xia, J Motoyama, J Prochazka, M Rommens, JM Scherer, SW Tsui, LC
Citation: Ma. Crackower et al., Cloning and characterization of two cytoplasmic dynein intermediate chain genes in mouse and human, GENOMICS, 55(3), 1999, pp. 257-267
Generation and chromosome mapping of expressed sequence tags (ESTs) from ahuman infant thymus
Authors: Hwang, MY Kang, YJ Kim, YH Scherer, SW Tsui, LC Sohn, U
Citation: My. Hwang et al., Generation and chromosome mapping of expressed sequence tags (ESTs) from ahuman infant thymus, GENOME, 42(3), 1999, pp. 457-464
Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24
Authors: Crackower, MA Sinasac, DS Lee, JR Herbrick, JA Tsui, LC Scherer, SW
Citation: Ma. Crackower et al., Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24, CYTOG C GEN, 87(3-4), 1999, pp. 197-198
Physical mapping of a tandem duplication on the long arm of chromosome 7 associated with a multidrug resistant phenotype
Authors: de Silva, MG Kantharidis, P Scherer, SW Rayeroux, K Campbell, L Tsui, LC Zalcberg, JR
Citation: Mg. De Silva et al., Physical mapping of a tandem duplication on the long arm of chromosome 7 associated with a multidrug resistant phenotype, CANC GENET, 110(1), 1999, pp. 28-33
Genome scan for linkage to Gilles de la Tourette syndrome
Authors: Barr, CL Wigg, KG Pakstis, AJ Kurlan, R Pauls, D Kidd, KK Tsui, LC Landor, P
Citation: Cl. Barr et al., Genome scan for linkage to Gilles de la Tourette syndrome, AM J MED G, 88(4), 1999, pp. 437-445
Risultati: 1-25 | 26-29