Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Debbie H Svendsrud"'
Autor:
Malin Lando, Marit Holden, Linn C Bergersen, Debbie H Svendsrud, Trond Stokke, Kolbein Sundfør, Ingrid K Glad, Gunnar B Kristensen, Heidi Lyng
Publikováno v:
PLoS Genetics, Vol 5, Iss 11, p e1000719 (2009)
Integrative analysis of gene dosage, expression, and ontology (GO) data was performed to discover driver genes in the carcinogenesis and chemoradioresistance of cervical cancers. Gene dosage and expression profiles of 102 locally advanced cervical ca
Externí odkaz:
https://doaj.org/article/e4e6bd4517c540658eebd15dd8257ae6
Publikováno v:
Cancer Letters. 267:18-25
7,8-dihydro-8-oxo-guanine (8-oxoG) is a mutagenic DNA lesion that is induced by ultraviolet A (UVA) radiation. 8-oxoG results in increased frequency of GC-->TA transversion mutations. UVA-induced mutant frequency was measured in the guanine phosphori
Autor:
Aage Haugen, Vidar Skaug, David H. Phillips, Hein te Riele, Shanbeh Zienolddiny, David Ryberg, Alan Hewer, Debbie H. Svendsrud, Einar Eilertsen
Publikováno v:
International Journal of Cancer. 118:2899-2902
Msh2 deficiency increases susceptibility to benzo[a]pyrene-induced lymphomagenesis DNA mismatch repair (MMR) is essential for repair of single-base mismatches and insertion/deletion loops. MMR proteins also participate in cellular response to DNA dam
Autor:
E A Sivertsen, David Mu, Stine H. Kresse, Paula M. DeAngelis, Debbie H. Svendsrud, L. Smedshammer, Eivind Galteland, Leonardo A. Meza-Zepeda, Ola Myklebost, Zhenhe Suo, Trond Stokke
Publikováno v:
Leukemia. 19:2313-2323
Gain of chromosome 18q and translocation t(14;18) are] frequently found in B-cell non-Hodgkin's lymphomas (B-NHL). Increased BCL2 transcription and BCL2 protein expression have been suggested to be the result of the gain. We utilized FISH, PCR and ar
Autor:
Odd Terje Brustugun, Ane Skjønsberg, Heidi Lyng, Debbie H. Svendsrud, Kolbein Sundfør, Trond Stokke, Gunnar B. Kristensen, Paula M. De Angelis, Marzieh Beigi
Publikováno v:
International Journal of Cancer. 111:358-366
Intratumor heterogeneity in chromosomal aberrations is believed to represent a major challenge in the treatment of cancer. The aim of our work was to assess the chromosomal heterogeneity of advanced cervical carcinomas and to distinguish aberrations
Publikováno v:
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 452:91-100
Nickel(II) is a human carcinogen causing respiratory cancers. The purpose of this study was to determine whether Ni(II) may induce microsatellite mutations in human cells. We transfected the three human lung tumor cell lines A427, HCC15 and NCI-H2009
Autor:
Shan Zienolddiny, Aage Haugen, Vidar Skaug, Debbie H. Svendsrud, David Ryberg, Steen Mollerup
Publikováno v:
Toxicology Letters. :233-237
Gene-environment interactions are thought to be critical for several diseases such as cancer, diabetes, heart disease and asthma. Cancer is a result of multiple gene-environment interactions occurring over several decades. During tumor development th
Autor:
Trevor Clancy, Kolbein Sundfør, Debbie H. Svendsrud, Malin Lando, Heidi Lyng, Ruth Holm, Cathinka Halle, Marit Holden, Gunnar B. Kristensen
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 17(16)
Purpose: We compared the prognostic significance of ectodomain isoforms of the epidermal growth factor receptor (EGFR), which lack the tyrosine kinase (TK) domain, with that of the full-length receptor and its autophosphorylation status in cervical c
Autor:
Tayeba Ali, Ruth Holm, Heidi Lyng, Jahn M. Nesland, Debbie H. Svendsrud, Gunnar B. Kristensen
Publikováno v:
Oncology reports. 22(1)
14-3-3 sigma (sigma) sequesters the cdc2-cyclin B1 complex in the cytoplasm resulting in G2 arrest. Inactivation and reduced expression of 14-3-3sigma have been reported in a varity of cancers. In the present study, we investigated the expression of
Autor:
Marit Holden, Ingrid K. Glad, Debbie H. Svendsrud, Heidi Lyng, Mark A. van de Wiel, Arnoldo Frigessi
Publikováno v:
Nucleic Acids Research
Nucleic Acids Research, 33(17):e143, 1-13. Oxford University Press
Frigessi, A, van de Wiel, M A, Holden, M, Svendsrud, D H, Glad, I K & Lyng, H 2005, ' Genome-wide estimation of transcript concentrations from spotted cDNA microarray data ', Nucleic Acids Research, vol. 33, no. 17, e143, pp. 1-13 . https://doi.org/10.1093/nar/gni141
Nucleic Acids Research-Methods Online, 33(17)
Nucleic Acids Research, 33(17):e143, 1-13. Oxford University Press
Frigessi, A, van de Wiel, M A, Holden, M, Svendsrud, D H, Glad, I K & Lyng, H 2005, ' Genome-wide estimation of transcript concentrations from spotted cDNA microarray data ', Nucleic Acids Research, vol. 33, no. 17, e143, pp. 1-13 . https://doi.org/10.1093/nar/gni141
Nucleic Acids Research-Methods Online, 33(17)
A method providing absolute transcript concentrations from spotted microarray intensity data is presented. Number of transcripts per microg total RNA, mRNA or per cell, are obtained for each gene, enabling comparisons of transcript levels within and