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The following research has been published in 2005 using tissue specimens supplied by ABN-Oncology-affiliated tissue banks:
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Astuti D., Latif F., Wagner K., Gentle D., Cooper W.N., Catchpoole D.R., Grundy R., Ferguson-Smith A.C. and Maher E. (2005) “Epigenetic alteration at the DLK-GTL2 imprinted domain in human neoplasia provides evidence for trans interaction between DLK1 and GTL2.”, British Journal of Cancer 92, 1574-1580 |
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Gorringe, KL., Boussioutas, A., The Melbourne Gastric Cancer Group, Peter Mac Microarray Facility, Bowtell, DDL. (2005) 'Novel regions of chromosomal amplification at 6p21, 5p13, and 12q14 in gastric cancer identified by array comparative genomic hybridization', Genes, Chromosomes and Cancer 42(3): 247-259 |
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Henson J.D., et al. (2005) "A robust assay for alternative lengthening of telomeres in tumours shows the significance if alternative lengthening of telomeres in sarcomas and astrocytomas”, Clinical Cancer Research 11, 217-225 |
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Phelan CM, Dapic V, Tice B, Favis R, Kwan E, Barany F, Manoukian S, Radice P, van der Luijt RB, van Nesselrooij BP, Chenevix-Trench G, kConFab, Caldes T, de la Hoya M, Lindquist S, Tavtigian SV, Goldgar D, Borg A, Narod SA, Monteiro AN. (2005) 'Classification of BRCA1 missense variants of unknown clinical significance'. Journal of Medical Genetics 42(2):138-46 |
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Sven Bilke, Qing-Rong Chen, Frank Westerman, Manfred Schwab, Daniel Catchpoole, Javed Khan ‘Inferring a Tumour Progression Model for Neuroblastoma from Genomic data’ Journal of Clinical Oncology 23(29),2005 |
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Margetts C.D.E., Astuti D., Gentle D.C., Cooper W.N., Cascon A., Catchpoole D.R., Robledo M., Neumann H.P.H., Latif F. and Maher E.R. (2005) “Epigenetic analysis of HIC1, CASP8, FLIP, TSP1, DcR1, DcR2, DR4, DR5, KvDMR1, H19 and preferential 11p15.5 maternal allele loss in VHL and sporadic phaeochromocytomas.”, Endocrine-Related Cancer 12, 161-172 |
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Chenevix-Trench, G., Sinilnikova, O.M., Suthers, G., Pandeya, N., Mazoyer, S., Sambrook, J.F., Goldup, S., Goldgar, D.E., Lynch, H.T., Lenoir, G.M., Cheetham, G. and kConFab . (2005) 'Ratio of male to female births in the offspring of BRCA1 and BRCA2 carriers'. Familial Cancer 4(2):73-5 |
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Phillips, K-A., Butow, P.N., Stewart, A.E., Chang, J-H., Weideman, P.C., Price, M.A., McLachlan, S.A., kConFab Investigators , Lindeman , G.J., McKay, M., Friedlander, M.L., Hopper, J.L. (2005) 'Predictors of participation in clinical and psychosocial follow up of the kConFab breast cancer family cohort'. Familial Cancer 4(2):105-13 |
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Aghmesheh, M., Edwards, L., Clarke, C.L., Byth, K., Katzenellenbogen, B.S., Russell, P.J., Friedlander, M., Tucker, K.M. and deFazio, A.(2005) 'Expression of steroid hormone receptors in BRCA1 -associated ovarian carcinomas'. Gynecologic Oncology 97: 16-25 |
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Spurdle, A.B., Antoniou, A., Duffy, D., Pandeya, N., Keleman, L., Chen, X., Peock, S., Cook, M., Smith, P.L., Purdie, D., Newman, B., Dite, G., Apicella, C., Southey, M., Giles, G.G., Hopper, J., kConFab , EMBRACE, Chenevix-Trench, G. and Easton, D. (2005) 'The androgen receptor CAG repeat polymorphism and modification of breast cancer risk in BRCA1 and BRCA2 mutation carriers'. Breast Cancer Research 7 :R176-R183 |
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Jekimovs, C., Chen, X., Arnold, J., Gatei, M., Richard, D.J., kConFab Investigators, Spurdle, A.B., Khanna, K.K. and Chenevix-Trench , G. (2005) 'Low frequency of CHEK2 1100delC in multiple-case breast cancer families from Australia: functional analysis in heterozygous individuals'. British Journal of Cancer 92(4):784-901 |
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Woodward, A.M., Gonclaves dos Santos Silva, A., Davis, T., kConFab, Kirk, J.A., Leary, J.A. (2005) 'Frequency of large genomic deletions and rearrangements in the BRCA1 and BRCA2 genes in genetically heterogeneous mutation negative families at high risk of developing breast and ovarian cancer in Australia', Journal of Medical Genetics 42(5):e3 |
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Thompson, D., Marsh, A., Chen, X., Antoniou, A., Jenkins, M., Wayne, T., Tesoriero, A., Milne, R., Spurdle, A.B., Thorstenson, Y., Southey, M., Giles, G.G., kConFab Investigators, Khanna, K.K., Sambrook, J.F., Oefner, P., Goldgar, D., Hopper, J., Easton, D. and Chenevix-Trench, G. (2005) 'Two ATM variants and breast cancer risk'. Human Mutation 25:594-595 |
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Lovelock, P., Healey, S., Au, W., Sum, E., Tesoriero, A., Wong, E.M., Hinson, S., Brinkworth, R., Bekessy, A., Diez, O., Izatt, L., Solomon, E., Jenkins, M., Renard, H., Hopper , J., Waring, P. kConFab, Tavtigian, S., Goldgar, D., Lindeman, G., Visvader, J., Couch, F., Henderson, B., Southey, M., Chenevix-Trench, G., Spurdle, A., Brown, M. (2005) 'Genetic, functional and histopathological evaluation of two C-terminal BRCA1 missense variants'. Journal of Medical Genetics June 2 (e-pub) |
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Wardrop, S.L., kConFab and Brown, M.A. (2005) 'Identification of Two Evolutionarily Conserved and Functional Regulatory Elements in Intron 2 of the Human BRCA1 Gene'. Genomics 86(3):316-28 |
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Robinson BWS, Creaney J, Lake R, Nowak A, Musk AW, de Klerk N, Winzell P, Hellstrom KE, Hellstrom I. (2005) 'Soluble mesothelin-related protein – A blood test for mesothelioma'. Lung Cancer 49,S1:S109-S111. |
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Mitchell, G., Antill, Y.C., Murray, W., Kirk, J., Salisbury, E., Lindeman, G.J., Di Iulio, J., Milner, A.D., Devereaux, L., Phillips, K. (2005) ‘ Nipple aspiration and ductal lavage in women with a germline BRCA1 or BRCA2 mutation’, Breast Cancer Research 7:R1122-R1131 |
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Creaney J, Robinson BWS. (2005) 'Detection of mesothelioma in asbestos exposed individuals: The potential role of soluble mesothelin related protein'. Hematol Oncol Clin North Am. Dec;19(6):1025-40 |
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Lewis, A.G.V., Flanagan, J., Marsh, A., Pupo, G., Mann, G., Spurdle, A.B., Lindeman, G.J., Visvader, J.E., Brown, M., Chenevix-Trench, G. for the Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer (2005). 'Mutation analysis of FANCD2,BRIP1/BACH1, LMO4 and STN in familial breast cancer'. Breast Cancer Research 7(6):R1005-R1016 |
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Morgan T., Atkins G.J., Trivett, M.K., Johnson, S.A., Kansara, M., Schlicht, S., Slavin, J.L., Simmons, P., Dickinson, I., Powell, G.J., Choong, P.F.M., and Thomas, D.M. (2005) 'Molecular profiling of giant cell tumor of bone and the osteoclastic localization of RANKL'. American Journal of Pathology 167(1): 117-28. |
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Tesoriero, A.A., Wong. E.M., Jenkins, M., Hopper, J.L. kConFab , Brown, M., Chenevix - Trench, G., Spurdle, A.B. and Southey, M.C. (2005) 'Molecular characterization and cancer risk associated with BRCA1 and BRCA2 splice site variants identified in multiple case breast cancer families'. Human Mutation 26(5): 495 |
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A combined meeting of kConFab, AOCS, ACCFS and the Family Cancer Clinics of Australia and New Zealand September 2005. Hereditary Cancer in Clinical Practice 3.4 S1-37 |
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Last Update on:
Wednesday 23-Jan-2008 4:28 PM
© Copyright: Australasian Biospecimen Network (ABN)
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