Search Results - "Steingrimsdottir, H"

The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms by Oddsson, A, Kristinsson, S Y, Helgason, H, Gudbjartsson, D F, Masson, G, Sigurdsson, A, Jonasdottir, A, Steingrimsdottir, H, Vidarsson, B, Reykdal, S, Eyjolfsson, G I, Olafsson, I, Onundarson, P T, Runarsson, G, Sigurdardottir, O, Kong, A, Rafnar, T, Sulem, P, Thorsteinsdottir, U, Stefansson, K

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Molecular and biochemical characterization of xrs mutants defective in Ku80 by Singleton, B. K., Priestley, A., Steingrimsdottir, H., Gell, D., Blunt, T., Jackson, S. P., Lehmann, A. R., Jeggo, P. A.

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Role of p16/MTS1, cyclin D1 and RB in primary oral cancer and oral cancer cell lines by SARTOR, M, STEINGRIMSDOTTIR, H, ELAMIN, F, GÄKEN, J, WARNAKULASURIYA, S, PARTRIDGE, M, THAKKER, N, JOHNSON, N. W, TAVASSOLI, M

“…One of the most important components of G1 checkpoint is the retinoblastoma protein (pRB110). The activity of pRB is regulated by its phosphorylation, which is…”
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Immune reconstitution after autologous hematopoietic stem cell transplantation in relation to underlying disease, type of high-dose therapy and infectious complications by Steingrimsdottir, H, Gruber, A, Bjorkholm, M, Svensson, A, Hansson, M

“…Department of Medicine, Division of Hematology, Karolinska Hospital, SE-171 76 Stockholm, Sweden. hlif@hotmail.com BACKGROUND AND OBJECTIVES: Autologous…”
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Mutations which alter splicing in the human hypoxanthine-guanine phosphoribosyltransferase gene by Steingrimsdottir, H., Rowley, G., Dorado, G., Cole, J., Lehmann, A.R.

“…A large proportion of mutations at the human hprt locus result in aberrant splicing of the hprt mRNA. We have been able to relate the mutation to the splicing…”
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Prevalence of human papillomavirus infection in premalignant and malignant lesions of the oral cavity in U.K. subjects: a novel method of detection by Elamin, F, Steingrimsdottir, H, Wanakulasuriya, S, Johnson, N, Tavassoli, M

“…To evaluate the possible role of human papillomavirus (HPV) in oral neoplasms, 28 oral squamous cell carcinomas (SCC) and 12 potentially malignant lesions were…”
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Loss of heterozygosity on chromosome 5q in ovarian cancer is frequently accompanied by TP53 mutation and identifies a tumour suppressor gene locus at 5q13.1-21 by TAVASSOLI, M, STEINGRIMSDOTTIR, H, PIERCE, E, JIANG, X, ALAGOZ, M, FARZANEH, F, CAMPBELL, I. G

“…Forty-nine ovarian tumours were examined for loss of heterozygosity (LOH) on chromosome 5 using eight microsatellite markers spanning both arms, including one…”
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p53 aberrations in oral submucous fibrosis and oral squamous cell carcinoma detected by immunocytochemistry and PCR-SSCP by Trivedy, C., Warnakulasuriya, K. A. A. S., Tavassoli, M., Steingrimsdottir, H., Penhallow, J., Maher, R., Johnson, N. W.

“…Trivedy C, Warnakulasuriya KAAS, Tavassoli M, Steingrimsdottir H, Penhallow J, Maher R, Johnson NW: p53 aberrations in oral submucous fibrosis and oral…”
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Bortezomib consolidation after autologous stem cell transplantation in multiple myeloma: a Nordic Myeloma Study Group randomized phase 3 trial by Mellqvist, Ulf-Henrik, Gimsing, Peter, Hjertner, Oyvind, Lenhoff, Stig, Laane, Edward, Remes, Kari, Steingrimsdottir, Hlif, Abildgaard, Niels, Ahlberg, Lucia, Blimark, Cecilie, Dahl, Inger Marie, Forsberg, Karin, Gedde-Dahl, Tobias, Gregersen, Henrik, Gruber, Astrid, Guldbrandsen, Nina, Haukås, Einar, Carlson, Kristina, Kvam, Ann Kristin, Nahi, Hareth, Lindås, Roald, Andersen, Niels Frost, Turesson, Ingemar, Waage, Anders, Westin, Jan

“…The Nordic Myeloma Study Group conducted an open randomized trial to compare bortezomib as consolidation therapy given after high-dose therapy and autologous…”
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Molecular analysis of ultraviolet-induced mutations in a xeroderma pigmentosum cell line by Dorado, G, Steingrimsdottir, H, Arlett, C F, Lehmann, A R

“…We have isolated and characterized 47 ultraviolet light-induced hprt mutants from a simian virus 40-transformed excision-repair-deficient xeroderma pigmentosum…”
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Detection of p53 mutations in oral cancer samples using a sensitive PCR-based method by Steingrimsdottir, H, Penhallow, J, Farzaneh, F, Johnson, N, Tavassoli, M

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U.v.-hypermutability of xeroderma pigmentosum cells demonstrated with a DNA-based mutation system by Steingrimsdottir, H, Beare, D, Carr, A M, Cole, J, Lehmann, A R

“…We have developed a DNA-based system, to detect mutations at restriction sites without any selection in culture. DNA is exhaustively digested with a…”
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Bone disease in monoclonal gammopathy of undetermined significance: results from a screened population-based study by Thorsteinsdottir, Sigrun, Lund, Sigrun H., Lindqvist, Ebba K., Thordardottir, Marianna, Sigurdsson, Gunnar, Costello, Rene, Burton, Debra, Steingrimsdottir, Hlif, Gudnason, Vilmundur, Eiriksdottir, Gudny, Siggeirsdottir, Kristin, Harris, Tamara B., Landgren, Ola, Kristinsson, Sigurdur Y.

“…Previous studies have shown that individuals with monoclonal gammopathy of undetermined significance (MGUS) have an increased risk of fractures, although the…”
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Inactivation of a transfected gene in human fibroblasts can occur by deletion, amplification, phenotypic switching, or methylation by GEBARA, M. M, DREVON, C, HARCOURT, S. A, STEINGRIMSDOTTIR, H, JAMES, M. R, BURKE, J. F, ARLETT, C. F, LEHMANN, A. R

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Mutant sequences in the rpsL gene of Escherichia coli B/r: mechanistic implications for spontaneous and ultraviolet light mutagenesis by Timms, A R, Steingrimsdottir, H, Lehmann, A R, Bridges, B A

“…Mutants able to grow in the presence of 1.2 mg/ml streptomycin were isolated from Escherichia coli WP2 after exposure to ultraviolet light (UV) or in the…”
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BONE DISEASE IN MONOCLONAL GAMMOPATHY OF UNDETERMINED SIGNIFICANCE: RESULTS FROM A SCREENED POPULATION-BASED STUDY by Thorsteinsdottir, S, Lund, SH, Lindqvist, E, Sigurdsson, G, Costello, R, Burton, D, Steingrimsdottir, H, Launer, LJ, Gudnason, V, Eiriksdottir, G, Siggeirsdottir, K, Harris, TB, Landgren, O, Kristinsson, SY

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Molecular Analysis of Mutations in the CSB(ERCC6) Gene in Patients with Cockayne Syndrome by Mallery, Donna L., Tanganelli, Bianca, Colella, Stefano, Steingrimsdottir, Herdis, van Gool, Alain J., Troelstra, Christine, Stefanini, Miria, Lehmann, Alan R.

“…Cockayne syndrome is a multisystem sun-sensitive genetic disorder associated with a specific defect in the ability to perform transcription-coupled repair of…”
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HPRT somatic mutation data by Cole, J, Green, M H, Stephens, G, Waugh, A P, Beare, D, Steingrimsdottir, H, Bridges, B A

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Monoclonal gammopathy: natural history studied with a retrospective approach by Steingrimsdottir, Hlif, Haraldsdottir, Vilhelmina, Olafsson, Isleifur, Gudnason, Vilmundur, Ogmundsdottir, Helga M

“…From the Landspitali University Hospital, Department of Clinical Hematology (HS, VH); Landspitali University Hospital, Department of Clinical Chemistry (IO);…”
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Bioavailability of Aciclovir after Oral Administration of Aciclovir and Its Prodrug Valaciclovir to Patients with Leukopenia after Chemotherapy by STEINGRIMSDOTTIR, H, GRUBER, A, PALM, C, GRIMFORS, G, KALIN, M, EKSBORG, S

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