Mutations which alter splicing in the human hypoxanthine-guanine phosphoribosyltransferase gene.

Por Steingrimsdottir, H, Rowley, G, Dorado, G, Cole, J, Lehmann, A R
Publicado em 1992

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.

Por Tavassoli, M., Steingrimsdottir, H., Pierce, E., Jiang, X., Alagoz, M., Farzaneh, F., Campbell, I. G.
Publicado em 1996

Molecular and biochemical characterization of xrs mutants defective in Ku80.

Por Singleton, B K, Priestley, A, Steingrimsdottir, H, Gell, D, Blunt, T, Jackson, S P, Lehmann, A R, Jeggo, P A
Publicado em 1997

Role of p16/MTS1, cyclin D1 and RB in primary oral cancer and oral cancer cell lines

Por Sartor, M, Steingrimsdottir, H, Elamin, F, Gäken, J, Warnakulasuriya, S, Partridge, M, Thakker, N, Johnson, N W, Tavassoli, M
Publicado em 1999

Molecular analysis of mutations in the CSB (ERCC6) gene in patients with Cockayne syndrome.

Por Mallery, D L, Tanganelli, B, Colella, S, Steingrimsdottir, H, van Gool, A J, Troelstra, C, Stefanini, M, Lehmann, A R
Publicado em 1998

Inactivation of a transfected gene in human fibroblasts can occur by deletion, amplification, phenotypic switching, or methylation.

Por Gebara, M M, Drevon, C, Harcourt, S A, Steingrimsdottir, H, James, M R, Burke, J F, Arlett, C F, Lehmann, A R
Publicado em 1987

The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms

Por Oddsson, A, Kristinsson, S Y, Helgason, H, Gudbjartsson, D F, Masson, G, Sigurdsson, A, Jonasdottir, 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
Publicado em 2014