1995 Research Publications

Pathology

Books and Chapters

Kakulas, B.A. and Cooper, B.J. Experimental and animal models of human neuromuscular disease, Disorders of Voluntary Muscle, eds J. Walton, G. Karpati, D. Hilton-Jones, Edinburgh, Churchill Livingstone, 1: pp 437-496 (1995)

Kakulas, B.A. Animal Models of Amyotropic Lateral Sclerosis. A Discussion, Pathogenesis and Therapy of Amyotrophic Lateral Sclerosis, eds G. Serratrice, T. Munsat, Philadelphia, Lippincott-Raven Publishers, 68: pp 89-91 (1995)

Journal Articles

Anderson, J.E., Mitchell, C.A., Mcgeachie, J.K. and Grounds, M.D.The Time Course of Basic Fibroblast Growth Factor Expression in Crush-Injured Skeletal Muscles of SJL/J and BALB/c Mice, Experimental Cell Research, 216: pp 325-334 (1995)

Ashman, R.B., Bolitho, E.M. and Fulurija, A. Cytokine mRNA in Brain Tissue from Mice that Show Strain-Dependent Differences in the Severity of Lesions Induced by Systemic Infection with Candida albicans Yeast, The Journal of Infectious Diseases, 172: pp 823-830 (1995)

Chirila, T.V., Sharp, C., Moore, S.R., Davies, M.J., Constable, I.J., Hong, Y., Vijayasekaran, S., Humphrey, M.F., Dalton, P.D., Tahija, S.G., Maley, M.A.L. and Cuypers, M.J.H. Synthetic hydrogel as an artificial vitreous body. A one-year animal study of its effects on the retina, Cells and Materials, 5:1, pp 83-96 (1995)

Dix, B.R., Robbins, P.D., Spagnolo, D.V., Padovan, G.L., House, A.K. and Iacopetta, B.J. Clonal Analysis of Colorectal Tumors using K-ras and P53 Gene Mutations as Markers, Diagnostic Molecular Pathology, 4: pp 261-265 (1995)

Eyre, H., Akkari, P.A., Wilton, S.D., Callen, D.C., Baker, E. and Laing, N.G.Assignment of the human skeletal muscle a-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridization, Cytogenetics and Cell Genetics, 69: pp 15-17 (1995)

Farr, T.J., Lai, C.M., Beilharz, M.W., Papadimitriou, J., Riches, K., Rossi, E., Garcia-Webb, P. and Klinken, S.P. A rapid fatal erythroleukemia caused by J2E cells can be treated ex vivo with erythropoietin, Leukemia, 9: pp 900-907 (1995)

Hahnel, R. Prospective study of stromelysin-3 expression in breast cancer biopsies and disease-free survival, International Journal of Oncology, 7: pp 1315-1318 (1995)

Harvey, J.M., Sterrett, G.F., Parsons, R.W., Fitzgerald, C.J., Jamrozik, K., Dewar, J.M., Byrne, M.J., Ingram, D.M. and Sheiner, H.M. Breast cancer in Western Australia in 1989: IV. Summary of histopathological assessment in 655 cases, Pathology, 27: pp 12-17 (1995)

Harvey, J.M., De Klerk, N.H., Robbins, P.D. and Sterrett, G.F. Histological grading of breast cancer: a study of reproducibility of consensus grading, The Breast, 4: pp 297-300 (1995)

Hunt, C.C.J., Eyre, H.J., Akkari, P.A., Meredith, C., Dorosz, S.M., Wilton, S.D., Callen, D.F., Laing, N.G. and Baker, E.Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation, Cytogenetics and Cell Genetics, 71: pp 94-95 (1995)

Jongpiputvanich, S., Walsh, P.J. and Kakulas, B.A. Minicores and congenital fibre type disproportion observed in a family, Journal of Paediatrics & Child Health, 31: pp 253-257 (1995)

Kay, P.H., Taylor, J., Kees, U.R., Baker, D.L. and Spagnolo, D.V. Myf-3 hypermethylation in malignant lymphoproliferative disorders, International Journal of Cancer, 62: pp 797-799 (1995)

Kay, P.H., Mitchell, C.A., Akkari, A. and Papadimitriou, J.M. Association of an unusual form of a Pax7-like gene with increased efficiency of skeletal muscle regeneration, Gene, 163: pp 171-177 (1995)

Keil, U., Busfield, S.J., Farr, T.J., Papadimitriou, J., Green, A.R., Begley, C.G. and Klinken, S.P. Emergence of Myeloid Cells from Cultures of J2E Erythroid Cells is linked with Karyotypic Abnormalities, Cell Growth and Differentiation, 6:April, pp 439-448 (1995)

Kricker, A., Armstrong, B.K., English, D.R. and Heenan, P.J. A dose-response curve for sun exposure and basal cell carcinoma, International Journal of Cancer, 60: pp 482-488 (1995)

Kricker, A., Armstrong, B.K., English, D.R. and Heenan, P.J. Does intermittent sun exposure cause basal cell carcinoma? A case-control study in Western Australia, International Journal of Cancer, 60: pp 489-494 (1995)

Lai, C.M., Swaminathan, N., Beilharz, M.W., Papadimitriou, J.M. and Klinken, S.P. Interferon-a Inhibits Erythropoietin-Induced Proliferation, but Not Differentiation, and Restricts Erythroleukemia Development, Journal of Interferon and Cytokine Research, 15: pp 669-675 (1995)

Laing, N.G., Love, D.R., Haan, E., Wilton, S.D., Akkari, P.A., Dorosz, S., Boundy, K., Kneebone, C., Blumbergs, P., White, S. and Watkins, H. A mutation in the a tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy, Nature Genetics, 9:January, pp 75-79 (1995)

Laing, N.G., Kakulas, B.A., Laing, B.A., Meredith, C., Wilton, S.D., Robbins, P., Honeyman, K., Dorosz, S., Kozman, H. and Mastaglia, F.L. Autosomal Dominant Distal Myopathy: Linkage to Chromosome 14, American Journal of Human Genetics, 56: pp 422-427 (1995)

Lynch, D.M. and Kay, P.H. Studies on the Polymorphism of the Fifth Component of Complement in Laboratory Mice, Experimental and Clinical Immunogenetics, 12: pp 253-260 (1995)

Maley, M.A.L., Davies, M.J. and Grounds, M.D. Extracellular Matrix, Growth Factors, Genetics: Their Influence on Cell Proliferation and Myotube Formation in Primary Cultures of Adult Mouse Skeletal Muscle, Experimental Cell Research, 219: pp 169-179 (1995)

Marlow, S.A., Kay, P.H. and Papadimitriou, J.M. Polymorphism of the murine inhibitor of differentiation-controlling gene, Id, Gene, 153: pp 281-282 (1995)

Marlow, S.A., Kay, P.H. and Papadimitriou, J.M. Myo-D1 alleles distinguish between Mm domesticus and Mm musculus, Mouse Genome, 93: pp 436-438 (1995)

Mcgeachie, J.K. and Grounds, M.D. Retarded myogenic cell replication in regenerating skeletal muscles of old mice: an autoradiographic study in young and old BALB/c and SJL/J mice, Cell and Tissue Research, 280: pp 277-282 (1995)

Mitchell, C.A., Grounds, M.D. and Papadimitriou, J.M. The genotype of bone marrow-derived inflammatory cells does not account for differences in skeletal muscle regeneration between SJL/J and BALB/c mice, Cell and Tissue Research, 280: pp 407-413 (1995)

Papadopulos-Eleopulos, E., Turner, V.F., Papadimitriou, J.M. and Causer, D. Factor VIII, HIV and AIDS in haemophiliacs: an analysis of their relationship, Genetica, 95: pp 25-50 (1995)

Papadopulos-Eleopulos, E., Turner, V.F., Papadimitriou, J.M., Causer, D., Hedland-Thomas, B. and Page, B.A.P. A critical analysis of the HIV-T4-cell-AIDS hypothesis, Genetica, 95: pp 5-24 (1995)

Robbins, P., Segal, A., Narula, S., Stokes, B., Lee, M., Thomas, W., Caterina, P., Sinclair, I.and Spagnolo, D. Central Neurocytoma. A Clinicopathological, Immunohistochemical and Ultrastructural Study of 7 Cases, Pathology Research and Practice, 191: pp 100-111 (1995)

Robbins, P.D., Pinder, S., De Klerk, N.H., Dawkins, H., Harvey, J., Sterrett, G.F., Ellis, I. and Elston, C.W. Histological Grading of Breast Carcinomas: A Study of Interobserver Agreement, Human Pathology, 26:8 (August), pp 873-879 (1995)

Skender-Kalnenas, T.M., English, D.R. and Heenan, P.J. Benign melanocytic lesions: Risk markers or precursors of cutaneous melanoma?, Journal of the American Academy of Dermatology, 33:6, pp 1000-1007 (1995)

Sparrow, L.E., Soong, R., Dawkins, H.J.S., Iacopetta, B.J. and Heenan, P.J. p53 gene mutation and expression in naevi and melanomas, Melanoma Research, 5: pp 93-100 (1995)

Sparrow, L.E., English, D.R., Heenan, P.J., Dawkins, H.J.S. and Taran, J.Prognostic significance of p53 overexpression in thin melanomas, Melanoma Research, 5: pp 387-392 (1995)

Wallgren-Pettersson, C., Van Langen, I.M., Laing, N.G., Faure, S., De La chapelle, A., Avela, K., Marchand, S., Kolehmainen, J., Tahvanainen, E., Juul Hansen, F., Muntoni, F., Dubowitz, V. and De Visser, M. A gene for autosomal recessive namaline myopathy assigned to chromosome 2q by linkage analysis, Neuromuscular Disorders, 5:6, pp 441-443 (1995)

Williams, V., De Klerk, N.H., Whitaker, D., Musk, A.W. and Shilkin, K.B.Asbestos Bodies in Lung Tissue Following Exposure to Crocidolite, American Journal of Industrial Medicine, 28: pp 489-495 (1995)

Wilton, S. and Lim, L. Rapid identification of ApoE alleles by multiple-single-strand conformation polymorphism (SSCP) analysis, Trends in Genetics, 11:9, p 341 (1995)

Wilton, S.D., Eyre, H., Akkari, P.A., Watkins, H.C., Macrae, C., Laing, N.G. and Callen, D.C. Assignment of the human a-tropomyosin gene TPM3 to 1q22-q23 by fluorescence in situ hybridisation, Cytogenetics and Cell Genetics, 68: pp 122-124 (1995)

Zheng, M.H., Lau, T.T.A., Prince, R., Criddle, A., Wysocki, S., Beilharz, M., Papadimitriou, J.M. and Wood, D.J. 17b-Estradiol Suppresses Gene Expression of Tartrate-Resistant Acid Phosphatase and Carbonic Anhydrase II in Ovariectomized Rats, Calcified Tissue International, 56: pp 166-169 (1995)

Zheng, M.H., Fan, Y., Panicker, A., Smith, A., Robertson, T., Wysocki, S., Robbins, P., Papadimitriou, J.M. and Wood, D.J. Detection of mRNAs for Urokinase-Type Plasminogen Activator, Its Receptor, and Type 1 Inhibitor in Giant Cell Tumors of Bone with In Situ Hybridization, American Journal of Pathology, 147:6 December, pp 1559-1566 (1995)

Conference Publications

Ashman, R.B. Acute susceptibility of aging mice to candida albicans infection, and the protective effect of immunization, III International Mycological Symposium "Pathogenesis, Diagnostics and Therapy of Mycoses and Mycogenic Allergy", St Petersburg, Russian Central Mycology Laboratory, 1: p 16 (1995)

Dench, J., Wilton, S., Yeung, L., Nicholson, G. and Laing, N.G. Molecular investigations of Cu/Zn superoxide dismutase (SOD1) amyotrophic lateral sclerosis, Human Genetics Society of Australasia. 19th Annual Scientific Meeting. Genes and Development., Surrey Hills NSW, Human Genetics Society of Australasia, 8 No 2 August: p 23 (1995)

Fabian, V.A., Jones, T.M., Wilton, S.D. and Kakulas, B.A. Apolipoprotein E and Alzheimer's disease, Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology of Disease, Jakarta Indonesia, Organising Committee. Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology, 1: p 40 (1995)

Fan, Y., Beilharz, M.W., Maley, M.A. and Grounds, M.D. The use of Y-chromosome specific probes to monitor the movement and survival of cells in myoblast transplantation studies, Fifteenth Annual Meeting of the Australian Neuroscience Society, Perth, Australian Neuroscience Society, 6: p 147 (1995)

Grounds, M.D., Maley, M.A.L. and Vague, M.J. The interaction of extracellular matrix and growth factors on primary cultures of adult skeletal muscle, Fifteenth Annual Meeting of the Australian Neuroscience Society, Perth, Australian Neuroscience Society, 6: p 57 (1995)

Hunt, C.C.J., Eyre, H.J., Akkari, P.A., Meredith, C., Dorosz, S.M., Wilton, S.D., Callen, D.F., Laing, N.G. and Baker, E. Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation, Fifteenth Annual Meeting of the Australian Neuroscience Society, Perth, Australian Neuroscience Society, 6: p 232 (1995)

Jacobsen, P.F., Kay, P.H. and Butler, T.L. The role of DNA methylation in horizontal transmission of neoplasia, 1995 South Pacific Congress, Hamilton Central Queensland, Australian Institute of Medical Scientists, 16: p 165 (1995)

Kakulas, B.A., Kaelan, C. and Tizard, B.K. The problem - the neuropathology of spinal cord injury, Fifteenth Annual Meeting of the Australian Neuroscience Society, Perth, Australian Neuroscience Society, 6: pp 28-29 (1995)

Laing, N.G., Eyre, H.J., Callen, D.F., Wilton, S.D., Akkari, P.A., Dorosz, S.M., Gunn, H.C., Hunt, C.C.J., Lim, L., Meredith, C. and Baker, E. Inherited diseases of skeletal and cardiac muscle associated with contractile proteins, Human Genetics Society of Australasia. 19th Annual Scientific Meeting. Genes and Development., Surry Hills NSW, Human Genetics Society of Australasia, 8 No 2 August: p 58 (1995)

Lorimer, R.L., Gubbay, A.D., Tizard, B.K. and Kakulas, B.A. The neuropathology of spinal cord injury: traumatic demyelination and remyelination, Regional Scientific Meeting of the International Medical Society of Paraplegia, Limassol Cyprus, International Medical Society of Paraplegia, 1: p 27 (1995)

Mears, M.E., Laing, N.G., Goldblatt, J. and Kakulas, B.A. Adoption and genetic risk: the detrimental effects of non-disclosure, Human Genetics Society of Australasia. 19th Annual Scientific Meeting. Genes and Development., Surry Hills NSW, Human Genetics Society of Australasia, 8 No 2 August: p 40 (1995)

Mok, D. and Hahnel, R. Retinoic acid receptors in breast cancer biopsies, Fifth International Congress on Hormones and Cancer, Quebec City, Medical Research Council of Canada, 1: p 109 (1995)

Pearce, D.J., Randall, A.G., Kent, G.N., Will, R.K. and Garcia-Webb, P. Size fractionation of hydroxypyridinium species in urine, The XII International Conference on Calcium Regulating Hormones, New York, International Bone and Mineral Society, 16 No 1 (Supplement) January: pp 180S-180S (1995)

Randall, A.G., Price, R.I., Retallack, R.W., Stewart, G., Will, R.K., Kent, G.N., Garcia-Webb, P., Pearce, D.J., Fisher, E., Stuckey, B.G., Gutteridge, D.H., Bhagat, C.I. and Prince, R.L. Bone turnover marker response to treatment of Paget's disease with pamidronate, The XII International Conference on Calcium Regulating Hormones, New York, International Bone and Mineral Society, 16 No 1 (Supplement) January: pp 211S-211S (1995)

Stanton, J.L. and Laing, N.G. Detection of the neurotrophins BDNF, NGF and NT-3 and the receptor, trkB, in E11 chick embryonic spinal cord, Fifteenth Annual Meeting of the Australian Neuroscience Society, Perth, Australian Neuroscience Society, 6: p 141 (1995)

Wilton, S., Dye, D. and Laing, N.G. Revertant Fibres: a possible genetic therapy for duchenne muscular dystrophy, Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology of Disease, Jakarta Indonesia, Organising Committee. Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology, 1: p 69 (1995)

Wilton, S., Akkari, A., Boundy, K., Kneebone, C., Blumberg, P., White, S., Watkins, H., Love, D. and Laing, N.G. An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy, Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology of Disease, Jakarta Indonesia, Organising Committee. Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology, 1: p 122 (1995)

Others

Akkari, A., Wilton, S., Dorosz, S., Callen, D., Eyre, H., Baker, L., Lim, L., Hunt, C. and Laing, N. Localization of the tropomyosin genes, 17th Annual Conference on The Organisation and Expression of the Genome, 1: pp Poster1.1-Poster1.1, Lorne Victoria (1995)

Butler, T.L., Jacobsen, P.F. and Kay, P.H. An In Vivo Model of Horizontal Transmission of Neoplasia and the Role of DNA Methylation in Neoplastic Progression, Sixteenth Annual Neuroscience Colloquium of Western Australia, 1: p 14, Perth (1995)

Davis, M.R., Stell, R., Laing, N.G. and Kakulas, B.A. Late onset Kennedy's disease - very mild clinical features associated with an intermediate sized androgen receptor CAG trinucleotide repeat expansion, Sixteenth Annual Neuroscience Colloquium of Western Australia, 1: p 16, Perth (1995)

Dench, J., Wilton, S., Yeung, L., Nicholson, G., Kakulas, B. and Laing, N.G. Superoxide dismutase (SOD1) mutations in amyotrophic lateral sclerosis (ALS), Sixteenth Annual Neuroscience Colloquium of Western Australia, 1: p 17, Perth(1995)

Dix, B.R., Robbins, P., Soong, R., Jenner, D., House, A.K., Iacopetta, B.J. and General Surgeons The common molecular genetic alterations in Dukes' B and C colorectal carcinomas are not short-term prognostic indicators of survival, 7th Lorne Cancer Conference, 1: pp Poster 28-Poster 28, Melbourne (1995)

Fabian, V.A., Wood, B., Crowley, P., Taran, J. and Kakulas, B.A. Herpes zoster brachial plexus neuritis: a neuropathological case study, Sixteenth Annual Neuroscience Colloquium of Western Australia, 1: p 18, Perth(1995)

Fletcher, S., Lim, L., Dye, D. and Wilton, S. "Snap-back" SSCP: specific introduction of conformational changes for mutation detection, Combined Biological Sciences Meeting, 1: p P62, Perth (1995)

Fletcher, S., Lim, L., Dye, D. and Wilton, S. "Snap-back" SSCP: specific introduction of conformational changes for mutation detection, The Fifth Annual Queenstown Molecular Biology Meeting, 1: p 124, Queenstown New Zealand (1995)

Harker, N.A., Laing, N.G. and Kakulas, B.A. Genetic analysis of spinal muscular atrophy families using linkage and direct mutation detection, Sixteenth Annual Neuroscience Colloquium of Western Australia, 1: p 11, Perth (1995)

Johnsen, R.D., Laing, N.G., Silberstein, E.P. and Kakulas, B.A. Expression of the 50 KD dystrophin associated glycoprotein (adhalin) in normal and dystrophic human muscle, Sixteenth Annual Neuroscience Colloquium of Western Australia, 1: p 22, Perth (1995)

Lai, M., Robertson, T., Vijayasekaran, S., Seydel, U., Constable, I. and Rakoczy, P.E. Development of an animal model for eye diseases induced by debris accumulation in the Retinal Pigment Epithelial cells, Combined Biological Sciences Meeting, 1: p P58, Perth (1995)

Maley, M.A.L., Lawson-Smith, M., Davies, M.J., Bolitho, E.M., Robertson, T.A., Mcgeachie, J.K. and Grounds, M.D. Techniques for increasing the sensitivity of detection for antigens present at low levels in muscle: tissue sections and cell cultures, Combined Biological Sciences Meeting, 1: p P64, Perth (1995)

Smith, K.L., Pauletti, G., Robbins, P.D., Dawkins, H.J.S., Papadimitriou, J.M., Redmond, S.L., Harvey, J.M., Sterrett, G.F. and Slamon, D. c-erb B-2 amplifications in breast cancer: detection in formalin-fixed paraffin-embedded tissue by fluorescent in situ hybridisation (FISH), 7th Lorne Cancer Conference, 1: pp Poster 128-Poster 128, Melbourne (1995)

Sparrow, L.E., Soong, R., Dawkins, H.J.S., Iacopetta, B.J. and Heenan, P.J. p53 gene mutation and expression in naevi and melanomas, 7th Lorne Cancer Conference, 1: pp Poster 133-Poster 133, Melbourne (1995)

Stepien, E., Tizard, B. and Kakulas, B. A method for neuronal tracing in human SCI, Sixteenth Annual Neuroscience Colloquium of Western Australia, 1: p 25, Perth (1995)

Tan, P., Wilton, S.D., Akkari, P.A., Sharp, M., Allen, J., Laing, N.G. and Huxtable, C. Frameshift mutation in ovine muscular disease, Combined Biological Sciences Meeting, 1: p P24, Perth (1995)

Tan, P., Wilton, S.D., Akkari, P.A., Sharp, M., Allen, J., Huxtable, C. and Laing, N.G. A splice-site mutation causes ovine McArdle's disease, Sixteenth Annual Neuroscience Colloquium of Western Australia, 1: p 5, Perth (1995)

Taylor, J.R. and Kakulas, B.A. Acute injuries to Dorsal Root Ganglia, Combined Meeting of Spine Society of Australia and Neurosurgical Society of Australasia, 1: p 33, Perth (1995)

Wilton, S., Laing, N.G. and Dye, D. Revertant fibres: a genetic therapy for duchenne muscular dystrophy?, Combined Biological Sciences Meeting, 1: p P61, Perth (1995)

Wilton, S., Lim, L. and Kelloway, L. Rapid identification of ApoE alleles by multiplex SSCP analysis, Combined Biological Sciences Meeting, 1: p P72, Perth (1995)

Wilton, S., Laing, N.G., Akkari, A., Dorosz, S., Boundy, K., Kneebone, C., Blumberg, P., White, S., Watkins, H. and Love, D. Autosomal dominant nemaline myopathy - positional cloning to a mutation in tropomyosin 3, The Fifth Annual Queenstown Molecular Biology Meeting, 1: p 29, Queenstown New Zealand (1995)

Wilton, S., Laing, N.G., Akkari, A., Dorosz, S., Boundy, K., Kneebone, C., Blumberg, P., White, S., Watkins, H. and Love, D. An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy, 17th Annual Conference on The Organisation and Expression of the Genome, 1: pp Symposium 10.3-Symposium 10.3, Lorne Victoria (1995)

Wilton, S., Laing, N.G. and Dye, D. Revertant fibres: a genetic therapy for duchenne muscular dystrophy?, Sixteenth Annual Neuroscience Colloquium of Western Australia, 1: p 27, Perth (1995)

Yovich, S., Seydel, U., Collier, F., Papadimitriou, J.M., Nicholson, G.C., Wood, D.J. and Zheng, M.H. The role of osteoclast polarisation in bone resorption, Combined Biological Sciences Meeting, 1: p P30, Perth (1995)

Zheng, M.H., Fan, Y., Wysocki, S.J., Papadimitriou, J.M. and Wood, D.J. Detection of urokinase-type plasminogen activator, its receptor and type 1 inhibitor mRNAs in giant cell tumours of bone, 7th Lorne Cancer Conference, 1: pp Poster 168-Poster 168, Melbourne (1995)