AAAAAA

   
Results: 1-19 |
Results: 19
Relative frequency and morphology of cancers in carriers of germline TP53 mutations
Authors: Birch, JM Alston, RD McNally, RJQ Evans, DGR Kelsey, AM Harris, M Eden, OB Varley, JM
Citation: Jm. Birch et al., Relative frequency and morphology of cancers in carriers of germline TP53 mutations, ONCOGENE, 20(34), 2001, pp. 4621-4628
Characterization of germline TP53 splicing mutations and their genetic andfunctional analysis
Authors: Varley, JM Attwooll, C White, G McGown, G Thorncroft, M Kelsey, AM Greaves, M Boyle, J Birch, JM
Citation: Jm. Varley et al., Characterization of germline TP53 splicing mutations and their genetic andfunctional analysis, ONCOGENE, 20(21), 2001, pp. 2647-2654
Significance of intron 6 sequence variations in the TP53 gene in Li-Fraumeni syndrome
Authors: Varley, JM McGown, G Thorncroft, M Kelsey, AM Birch, JM
Citation: Jm. Varley et al., Significance of intron 6 sequence variations in the TP53 gene in Li-Fraumeni syndrome, CANC GENET, 129(1), 2001, pp. 85-87
Destabilization of CHK2 by a missense mutation associated with Li-Fraumenisyndrome
Authors: Lee, SB Kim, SH Bell, DW Wahrer, DCR Schiripo, TA Jorczak, MM Sgroi, DC Garber, JE Li, FP Nichols, KE Varley, JM Godwin, AK Shannon, KM Harlow, E Haber, DA
Citation: Sb. Lee et al., Destabilization of CHK2 by a missense mutation associated with Li-Fraumenisyndrome, CANCER RES, 61(22), 2001, pp. 8062-8067
Correspondence re: A. Rothfuss et al., Induced micronucleus frequencies inperipheral blood lymphocytes as a screening test for carriers of a BRCA1 mutation in breast cancer families. Cancer Res., 60 : 390-394, 2000.
Authors: Baria, K Warren, C Roberts, SA West, CML Evans, DGR Varley, JM Scott, D
Citation: K. Baria et al., Correspondence re: A. Rothfuss et al., Induced micronucleus frequencies inperipheral blood lymphocytes as a screening test for carriers of a BRCA1 mutation in breast cancer families. Cancer Res., 60 : 390-394, 2000., CANCER RES, 61(15), 2001, pp. 5948-5949
The relationship between radiation-induced G(1) arrest and chromosome aberrations in Li-Fraumeni fibroblasts with or without germline TP53 mutations
Authors: Boyle, JM Spreadborough, A Greaves, MJ Birch, JM Varley, JM Scott, D
Citation: Jm. Boyle et al., The relationship between radiation-induced G(1) arrest and chromosome aberrations in Li-Fraumeni fibroblasts with or without germline TP53 mutations, BR J CANC, 85(2), 2001, pp. 293-296
Immunohistochemical analysis of expression and allelotype of mismatch repair genes (hMLH1 and hMSH2) in bladder cancer
Authors: Kassem, HS Varley, JM Hamam, SM Margison, GP
Citation: Hs. Kassem et al., Immunohistochemical analysis of expression and allelotype of mismatch repair genes (hMLH1 and hMSH2) in bladder cancer, BR J CANC, 84(3), 2001, pp. 321-328
Assignment of TTC4 to human chromosome band 1p31.3 and a pseudogene TTC4P to 7p14 -> p13 by in situ hybridization
Authors: Hey, Y Brintnell, B James, LA Varley, JM
Citation: Y. Hey et al., Assignment of TTC4 to human chromosome band 1p31.3 and a pseudogene TTC4P to 7p14 -> p13 by in situ hybridization, CYTOG C GEN, 88(3-4), 2000, pp. 272-274
Genomic structure and expression profile of LPHH1, a 7TM gene variably expressed in breast cancer cell lines
Authors: White, GRM Varley, JM Heighway, J
Citation: Grm. White et al., Genomic structure and expression profile of LPHH1, a 7TM gene variably expressed in breast cancer cell lines, BBA-GENE ST, 1491(1-3), 2000, pp. 75-92
Genomic alterations associated with loss of heterozygosity for TP53 in Li -Fraumeni syndrome fibroblasts
Authors: Burt, EC James, LA Greaves, MJ Birch, JM Boyle, JM Varley, JM
Citation: Ec. Burt et al., Genomic alterations associated with loss of heterozygosity for TP53 in Li -Fraumeni syndrome fibroblasts, BR J CANC, 83(4), 2000, pp. 467-472
Identification of a novel fusion gene involving hTAF(II)68 and CHN from a t(9;17)(q22;q11.2) translocation in an extraskeletal myxoid chondrosarcoma
Authors: Attwooll, C Tariq, M Harris, M Coyne, JD Telford, N Varley, JM
Citation: C. Attwooll et al., Identification of a novel fusion gene involving hTAF(II)68 and CHN from a t(9;17)(q22;q11.2) translocation in an extraskeletal myxoid chondrosarcoma, ONCOGENE, 18(52), 1999, pp. 7599-7601
Isolation and characterization of a human homologue of the latrophilin gene from a region of 1p31.1 implicated in breast cancer (vol 17, pg 3513, 1998)
Authors: White, GRM Varley, JM Heighway, J
Citation: Grm. White et al., Isolation and characterization of a human homologue of the latrophilin gene from a region of 1p31.1 implicated in breast cancer (vol 17, pg 3513, 1998), ONCOGENE, 18(12), 1999, pp. 2167-2167
Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome
Authors: Bell, DW Varley, JM Szydlo, TE Kang, DH Wahrer, DCR Shannon, KE Lubratovich, M Verselis, SJ Isselbacher, KJ Fraumeni, JF Birch, JM Li, FP Garber, JE Haber, DA
Citation: Dw. Bell et al., Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome, SCIENCE, 286(5449), 1999, pp. 2528-2531
Human papillomavirus type 16 E6 variants in cervical carcinoma: relationship to host genetic factors and clinical parameters
Authors: Brady, CS Duggan-Keen, MF Davidson, JA Varley, JM Stern, PL
Citation: Cs. Brady et al., Human papillomavirus type 16 E6 variants in cervical carcinoma: relationship to host genetic factors and clinical parameters, J GEN VIROL, 80, 1999, pp. 3233-3240
Highly consistent genetic alterations in childhood adrenocortical tumours detected by comparative genomic hybridization
Authors: James, LA Kelsey, AM Birch, JM Varley, JM
Citation: La. James et al., Highly consistent genetic alterations in childhood adrenocortical tumours detected by comparative genomic hybridization, BR J CANC, 81(2), 1999, pp. 300-304
Exclusion of the genes CDKN2 and PTEN as causative gene defects in Li-Fraumeni syndrome
Authors: Burt, EC McGown, G Thorncroft, M James, LA Birch, JM Varley, JM
Citation: Ec. Burt et al., Exclusion of the genes CDKN2 and PTEN as causative gene defects in Li-Fraumeni syndrome, BR J CANC, 80(1-2), 1999, pp. 9-10
Radiation-induced G(1) arrest is not defective in fibroblasts from Li-Fraumeni families without TP53 mutations
Authors: Boyle, JM Greaves, MJ Camplejohn, RS Birch, JM Roberts, SA Varley, JM
Citation: Jm. Boyle et al., Radiation-induced G(1) arrest is not defective in fibroblasts from Li-Fraumeni families without TP53 mutations, BR J CANC, 79(11-12), 1999, pp. 1657-1664
Are there low-penetrance TP53 alleles? Evidence from childhood adrenocortical tumors
Authors: Varley, JM McGown, G Thorncroft, M James, LA Margison, GP Forster, G Evans, DGR Harris, M Kelsey, AM Birch, JM
Citation: Jm. Varley et al., Are there low-penetrance TP53 alleles? Evidence from childhood adrenocortical tumors, AM J HU GEN, 65(4), 1999, pp. 995-1006
Isolation and characterization of a human homologue of the latrophilin gene from a region of 1p31.1 implicated in breast cancer
Authors: While, GRM Varley, JM Heighway, J
Citation: Grm. While et al., Isolation and characterization of a human homologue of the latrophilin gene from a region of 1p31.1 implicated in breast cancer, ONCOGENE, 17(26), 1998, pp. 3513-3519
Risultati: 1-19 |