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Results: 1-25 | 26-27
Results: 1-25/27
Thirteen UDPglucuronosyltransferase genes are encoded at the human UGT1 gene complex locus
Authors: Gong, QH Cho, JW Huang, T Potter, C Gholami, N Basu, NK Kubota, S Carvalho, S Pennington, MW Owens, IS Popescu, NC
Citation: Qh. Gong et al., Thirteen UDPglucuronosyltransferase genes are encoded at the human UGT1 gene complex locus, PHARMACOGEN, 11(4), 2001, pp. 357-368
Human breast cancer cells generated by oncogenic transformation of primarymammary epithelial cells
Authors: Elenbaas, B Spirio, L Koerner, F Fleming, MD Zimonjic, DB Donaher, JL Popescu, NC Hahn, WC Weinberg, RA
Citation: B. Elenbaas et al., Human breast cancer cells generated by oncogenic transformation of primarymammary epithelial cells, GENE DEV, 15(1), 2001, pp. 50-65
UGRP1, a uteroglobin/clara cell secretory protein-related protein, is a novel lung-enriched downstream target gene for the T/EBP/NKX2.1 homeodomain transcription factor
Authors: Niimi, T Keck-Waggoner, CL Popescu, NC Zhou, YH Levitt, RC Kimura, S
Citation: T. Niimi et al., UGRP1, a uteroglobin/clara cell secretory protein-related protein, is a novel lung-enriched downstream target gene for the T/EBP/NKX2.1 homeodomain transcription factor, MOL ENDOCR, 15(11), 2001, pp. 2021-2036
Integration of a c-myc transgene results in disruption of the mouse Gtf2ird1 gene, the homologue of the human GTF2IRD1 gene hemizygously deleted in Williams-Beuren syndrome
Authors: Durkin, ME Keck-Waggoner, CL Popescu, NC Thorgeirsson, SS
Citation: Me. Durkin et al., Integration of a c-myc transgene results in disruption of the mouse Gtf2ird1 gene, the homologue of the human GTF2IRD1 gene hemizygously deleted in Williams-Beuren syndrome, GENOMICS, 73(1), 2001, pp. 20-27
Novel genomic imbalances and chromosome translocations involving c-myc gene in Burkitt's lymphoma
Authors: Zimonjic, DB Keck-Waggoner, C Popescu, NC
Citation: Db. Zimonjic et al., Novel genomic imbalances and chromosome translocations involving c-myc gene in Burkitt's lymphoma, LEUKEMIA, 15(10), 2001, pp. 1582-1588
Identification of rat mammary tumor-1 gene (RMT-1), which is highly expressed in rat mammary tumors
Authors: Chiou, S Yoo, J Loh, KC Guzman, RC Gopinath, GR Rajkumar, L Chou, YC Yang, J Popescu, NC Nandi, S
Citation: S. Chiou et al., Identification of rat mammary tumor-1 gene (RMT-1), which is highly expressed in rat mammary tumors, CANCER LETT, 174(1), 2001, pp. 45-55
DNA amplification associated with double minutes originating from chromosome 19 in mouse hepatocellular carcinoma
Authors: Zimonjic, DB Zhang, H Shan, Z Factor, V Trent, J Thorgeirsson, SS Popescu, NC
Citation: Db. Zimonjic et al., DNA amplification associated with double minutes originating from chromosome 19 in mouse hepatocellular carcinoma, CYTOG C GEN, 93(1-2), 2001, pp. 114-116
claudin-18, a novel downstream target gene for the T/EBP/NKX2.1 homeodomain transcription factor, encodes lung- and stomach-specific isoforms throughalternative splicing
Authors: Niimi, T Nagashima, K Ward, JM Minoo, P Zimonjic, DB Popescu, NC Kimura, S
Citation: T. Niimi et al., claudin-18, a novel downstream target gene for the T/EBP/NKX2.1 homeodomain transcription factor, encodes lung- and stomach-specific isoforms throughalternative splicing, MOL CELL B, 21(21), 2001, pp. 7380-7390
Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma
Authors: Espinoza, LA Neto, JB Popescu, NC Casartelli, C
Citation: La. Espinoza et al., Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma, CANC GENET, 131(1), 2001, pp. 79-81
Human mitochondrial topoisomerase I
Authors: Zhang, HL Barcelo, JM Lee, B Kohlhagen, G Zimonjic, DB Popescu, NC Pommier, Y
Citation: Hl. Zhang et al., Human mitochondrial topoisomerase I, P NAS US, 98(19), 2001, pp. 10608-10613
Profile of genetic alterations and tumorigenicity of human breast cancer cells
Authors: Zimonjic, DB Keck-Waggoner, CL Yuan, BZ Kraus, MH Popescu, NC
Citation: Db. Zimonjic et al., Profile of genetic alterations and tumorigenicity of human breast cancer cells, INT J ONCOL, 16(2), 2000, pp. 221-230
Assignment of the MDM2 binding protein gene (MTBP) to human chromosome band 8q24 by in situ hybridization
Authors: Boyd, MT Zimonjic, DB Popescu, NC Athwal, R Haines, DS
Citation: Mt. Boyd et al., Assignment of the MDM2 binding protein gene (MTBP) to human chromosome band 8q24 by in situ hybridization, CYTOG C GEN, 90(1-2), 2000, pp. 64-65
Assignment of the mitochondrial aldehyde dehydrogenase gene (Aldh2) to mouse chromosome 5 by fluorescence in situ hybridization
Authors: Jeong, KS Song, BJ Keck-Waggoner, CL Huh, CG Popescu, NC
Citation: Ks. Jeong et al., Assignment of the mitochondrial aldehyde dehydrogenase gene (Aldh2) to mouse chromosome 5 by fluorescence in situ hybridization, CYTOG C GEN, 89(1-2), 2000, pp. 54-55
Assignment of WDR7 (alias TRAG, TGF-beta resistance associated gene) to orthologous regions of human chromosome 18q21.1 -> q22 and mouse chromosome 18D.1-E.3 by fluorescence in situ hybridization
Authors: Sanders, S Keck-Waggoner, CL Zimonjic, DB Popescu, NC Thorgeirsson, SS
Citation: S. Sanders et al., Assignment of WDR7 (alias TRAG, TGF-beta resistance associated gene) to orthologous regions of human chromosome 18q21.1 -> q22 and mouse chromosome 18D.1-E.3 by fluorescence in situ hybridization, CYTOG C GEN, 88(3-4), 2000, pp. 324-325
Vitamin E reduces chromosomal damage and inhibits hepatic tumor formation in a transgenic mouse model
Authors: Factor, VM Laskowska, D Jensen, MR Woitach, JT Popescu, NC Thorgeirsson, SS
Citation: Vm. Factor et al., Vitamin E reduces chromosomal damage and inhibits hepatic tumor formation in a transgenic mouse model, P NAS US, 97(5), 2000, pp. 2196-2201
Acquired, nonrandom chromosomal abnormalities associated with the development of acute promyelocytic leukemia in transgenic mice
Authors: Zimonjic, DB Pollock, JL Westervelt, P Popescu, NC Ley, TJ
Citation: Db. Zimonjic et al., Acquired, nonrandom chromosomal abnormalities associated with the development of acute promyelocytic leukemia in transgenic mice, P NAS US, 97(24), 2000, pp. 13306-13311
Alterations of the FHIT gene in human hepatocellular carcinoma
Authors: Yuan, BZ Keck-Waggoner, C Zimonjic, DB Thorgeirsson, SS Popescu, NC
Citation: Bz. Yuan et al., Alterations of the FHIT gene in human hepatocellular carcinoma, CANCER RES, 60(4), 2000, pp. 1049-1053
Human FRAG1 encodes a novel membrane-spanning protein that localizes to chromosome 11p15.5, a region of frequent loss of heterozygosity in cancer
Authors: Lorenzi, MV Castagnino, P Aaronson, DC Lieb, DC Lee, CC Keck, CL Popescu, NC Miki, T
Citation: Mv. Lorenzi et al., Human FRAG1 encodes a novel membrane-spanning protein that localizes to chromosome 11p15.5, a region of frequent loss of heterozygosity in cancer, GENOMICS, 62(1), 1999, pp. 59-66
Palmitoyl-protein thioesterase gene expression in the developing mouse brain and retina: Implications for early loss of vision in infantile neuronal ceroid lipofuscinosis
Authors: Zhang, ZJ Mandal, AK Wang, N Keck, CL Zimonjic, DB Popescu, NC Mukherjee, AB
Citation: Zj. Zhang et al., Palmitoyl-protein thioesterase gene expression in the developing mouse brain and retina: Implications for early loss of vision in infantile neuronal ceroid lipofuscinosis, GENE, 231(1-2), 1999, pp. 203-211
Assignment and cloning of mouse Arhgap7 to chromosome 8A4-B2, a conserved syntenic region of human chromosome 8p22 -> p21
Authors: Yuan, BZ Yang, Y Keck-Waggoner, CL Zimonjic, DB Thorgeirsson, SS Popescu, NC
Citation: Bz. Yuan et al., Assignment and cloning of mouse Arhgap7 to chromosome 8A4-B2, a conserved syntenic region of human chromosome 8p22 -> p21, CYTOG C GEN, 87(3-4), 1999, pp. 189-190
Assignment of the Bog gene (RBBP9) to syntenic regions of mouse chromosome2G1-H1 and human chromosome 20p11.2 by fluorescence in situ hybridization
Authors: Woitach, JT Hong, R Keck, CL Zimonjic, DB Popescu, NC Thorgeirsson, SS
Citation: Jt. Woitach et al., Assignment of the Bog gene (RBBP9) to syntenic regions of mouse chromosome2G1-H1 and human chromosome 20p11.2 by fluorescence in situ hybridization, CYTOG C GEN, 85(3-4), 1999, pp. 252-253
Novel recurrent genetic imbalances in human hepatocellular carcinoma cell lines identified by comparative genomic hybridization
Authors: Zimonjic, DB Keck, CL Thorgeirsson, SS Popescu, NC
Citation: Db. Zimonjic et al., Novel recurrent genetic imbalances in human hepatocellular carcinoma cell lines identified by comparative genomic hybridization, HEPATOLOGY, 29(4), 1999, pp. 1208-1214
Nonrandom breakpoints of unbalanced chromosome translocations in human hepatocellular carcinoma cell lines
Authors: Keck, CL Zimonjic, DB Yuan, BZ Thorgeirsson, SS Popescu, NC
Citation: Cl. Keck et al., Nonrandom breakpoints of unbalanced chromosome translocations in human hepatocellular carcinoma cell lines, CANC GENET, 111(1), 1999, pp. 37-44
Recurrent alterations of the short arm of chromosome 3 define a tumor suppressor region in rat mammary tumor cells
Authors: Popescu, NC Greiner, JW
Citation: Nc. Popescu et Jw. Greiner, Recurrent alterations of the short arm of chromosome 3 define a tumor suppressor region in rat mammary tumor cells, CARCINOGENE, 20(10), 1999, pp. 2033-2036
Flavone acetic acid induces a G2/M cell cycle arrest in mammary carcinoma cells
Authors: Panaro, NJ Popescu, NC Harris, SR Thorgeirsson, UP
Citation: Nj. Panaro et al., Flavone acetic acid induces a G2/M cell cycle arrest in mammary carcinoma cells, BR J CANC, 80(12), 1999, pp. 1905-1911
Risultati: 1-25 | 26-27