Catalog Home Page

Publications: Howell, John

Export as [feed] RSS
Group by: Publication Type | Year
Number of items: 43.

Journal Article

Howell, J.Mc.C., Walker, K.R., Creed, K.E., Dunton, E., Davies, L., Quinlivan, R. and Karpati, G. (2013) Phosphorylase re-expression, increase in the force of contraction and decreased fatigue following notexin-induced muscle damage and regeneration in the ovine model of McArdle disease. Neuromuscular Disorders, 24 (2). pp. 167-177.

Howell, J.Mc.C., Walker, K.R., Davies, L., Dunton, E., Everaardt, A., Laing, N. and Karpati, G. (2008) Adenovirus and adeno-associated virus-mediated delivery of human myophosphorylase cDNA and LacZ cDNA to muscle in the ovine model of McArdle’s disease: Expression and re-expression of glycogen phosphorylase. Neuromuscular Disorders, 18 (3). pp. 248-258.

Yuasa, K., Yoshimura, M., Urasawa, N., Ohshima, S., Howell, J.M., Nakamura, A., Hijikata, T., Miyagoe-Suzuki, Y. and Takeda, S. (2007) Injection of a recombinant AAV serotype 2 into canine skeletal muscles evokes strong immune responses against transgene products. Gene Therapy, 14 (17). pp. 1249-1260.

O'Hara, A.J., Collins, T. and Howell, J.M. (2002) Gingival eruption cysts induced by cyclosporine administration to neonatal dogs. Journal of Clinical Periodontology, 29 (6). pp. 507-513.

Fletcher, S., Ly, T., Duff, R.M., Howell, J.Mc.C. and Wilton, S.D. (2001) Cryptic splicing involving the splice site mutation in the canine model of Duchenne muscular dystrophy. Neuromuscular Disorders, 11 (3). pp. 239-243.

Fletcher, S., Carville, K.S., Howell, J.M., Mann, C.J. and Wilton, S.D. (2001) Evaluation of a short interspersed nucleotide element in the 3' untranslated region of the defective dystrophin gene of dogs with muscular dystrophy. American Journal of Veterinary Research, 62 (12). pp. 1964-1968.

O'Hara, A.J., Howell, J.Mc.C., Taplin, R.H., Fletcher, S., Lloyd, F., Kakulas, B., Lochmüller, H. and Karpati, G. (2001) The spread of transgene expression at the site of gene construct injection. Muscle & Nerve, 24 (4). pp. 488-495.

Fletcher, S., Wilton, S.D. and Howell, J.Mc.C. (2000) Gene therapy and molecular approaches to the treatment of hereditary muscular disorders. Current Opinion in Neurology, 13 (5). pp. 553-560.

Pari, G., Crerar, M.M., Nalbantoglu, J., Shoubridge, E., Jani, A., Tsujino, S., Shanske, S., DiMauro, S., Howell, J.M. and Karpati, G. (1999) Myophosphorylase gene transfer in McArdle's disease myoblasts in vitro. Neurology, 53 (6). pp. 1352-4.

Honeyman, K., Carville, K.S., Howell, J.M., Fletcher, S. and Wilton, S.D. (1999) Development of a snapback method of single-strand conformation polymorphism analysis for genotyping Golden Retrievers for the X-linked muscular dystrophy allele. American Journal of Veterinary Research, 60 (6). pp. 734-7.

Honeyman, K., Carville, K.S., Howell, J.M., Fletcher, S. and Wilton, S.D. (1999) Development of a snapback method of single-strand conformation polymorphism analysis for genotyping Golden Retrievers for the X-linked muscular dystrophy allele. American Journal of Veterinary Research, 60 (6). pp. 734-7.

Howell, J.M. (1999) Is there a future for gene therapy? Neuromuscular Disorders, 9 (2). pp. 102-107.

Howell, J.M., Fletcher, S., O'Hara, A., Johnsen, R.D., Lloyd, F. and Kakulas, B.A. (1998) Direct dystrophin and reporter gene transfer into dog muscle in vivo. Muscle & Nerve, 21 (2). pp. 159-165.

Howell, J.M., Lochmüller, H., O'Hara, A., Fletcher, S., Kakulas, B.A., Massie, B., Nalbantoglu, J. and Karpati, G. (1998) High-level dystrophin expression after adenovirus-mediated dystrophin minigene transfer to skeletal muscle of dystrophic dogs: Prolongation of expression with immunosuppression. Human Gene Therapy, 9 (5). pp. 629-634.

Colbourne, C.M., Raidal, S.L., Yovich, J.V., Howell, J.M. and Richardson, J.L. (1997) Cervical diskospondylitis in two horses. Australian Veterinary Journal, 75 (7). pp. 477-479.

Howell, J.Mc.C., Fletcher, S., Kakulas, B.A., O'Hara, M., Lochmuller, H. and Karpati, G. (1997) Use of the dog model for Duchenne muscular dystrophy in gene therapy trials. Neuromuscular Disorders, 7 (5). pp. 325-328.

Bartlett, R.J., Winand, N.J., Secore, S.L., Singer, J.T., Fletcher, S., Wilton, S., Bogan, D.J., Metcalf-Bogan, J.R., Bartlett, W.T., Howell, J.M., Cooper, B.J. and Kornegay, J.N. (1996) Mutation segregation and rapid carrier detection of X-linked muscular dystrophy in dogs. American Journal of Veterinary Research, 57 (5). pp. 650-654.

Palmer, D.G., Dorling, P.R. and Howell, J.Mc.C. (1994) Bovine glycogenosis type II: The molecular defect in shorthorn cattle. Neuromuscular Disorders, 4 (1). pp. 39-48.

Deol, H.S., Howell, J.Mc.C. and Dorling, P.R. (1994) Effect of the ingestion of heliotrope and copper on the concentration of zinc, selenium and molybdenum in the liver of sheep. Journal of Comparative Pathology, 110 (3). pp. 303-307.

Howell, J.Mc.C. and Mercer, J.F.B. (1994) The pathology and trace element status of the toxic milk mutant mouse. Journal of Comparative Pathology, 110 (1). pp. 37-47.

Howell, J.Mc.C., Shunxiang, Y. and Gawthorne, J.M. (1993) Effect of thiomolybdate and ammonium molybdate in pregnant guinea pigs and their offspring. Research in Veterinary Science, 55 (2). pp. 224-230.

Colbourne, C.M., Bolton, J.R., Mills, J.N., Whitaker, D., Yovich, J.V. and Howell, J.Mc.C. (1992) Mesothelioma in horses. Australian Veterinary Journal, 69 (11). pp. 275-278.

Deol, H.S., Howell, J.Mc.C., Dorling, P.R. and Symonds, H.W. (1992) The effect of copper and heliotrope on the composition of bile in sheep. Research in Veterinary Science, 53 (3). pp. 324-330.

Howell, J.Mc.C., Deol, H.S., Dorling, P.R. and Thomas, J.B. (1991) Experimental copper and heliotrope intoxication in sheep: morphological changes. Journal of Comparative Pathology, 105 (1). pp. 49-74.

Riley, C.B., Yovich, J.V. and Howell, J.Mc.C. (1991) Malignant mast cell tumours in horses. Australian Veterinary Journal, 68 (10). pp. 346-347.

Howell, J.Mc.C., Dorling, P.R., Shelton, J.N., Taylor, E.G., Palmer, D.G and Di Marco, P.N. (1991) Natural bone marrow transplantation in cattle with Pompe's disease. Neuromuscular Disorders, 1 (6). pp. 449-454.

Howell, J.Mc.C. and Kumaratilake, J.S. (1990) Effect of intravenously administered tetrathiomolybdate on plasma copper concentrations of Copper-loaded sheep. Journal of Comparative Pathology, 103 (3). pp. 321-334.

Kumaratilake, J.S. and Howell, J.Mc.C. (1989) Intracellular distribution of copper in the liver of copper-loaded sheep--a subcellular fractionation study. Journal of Comparative Pathology, 101 (2). pp. 161-76.

Kumaratilake, J.S. and Howell, J.Mc.C. (1989) Intravenously administered tetra-thiomolybdate and the removal of copper from the liver of copper-loaded sheep. Journal of Comparative Pathology, 101 (2). pp. 177-99.

Kumaratilake, J.S. and Howell, J.Mc.C. (1989) Lysosomes in the pathogenesis of liver injury in chronic copper poisoned sheep: an ultrastructural and morphometric study. Journal of Comparative Pathology, 100 (4). pp. 381-90.

Gooneratne, S.R, Gawthorne, J.M. and Howell, J.Mc.C. (1989) Distribution of Cu, Zn, and Fe in the soluble fraction of the kidney in normal, copper-poisoned, and thiomolybdate-treated sheep. Journal of Inorganic Biochemistry, 35 (1). pp. 37-53.

Gooneratne, S.R, Howell, J.Mc.C., Gawthorne, J.M. and Kumaratilake, J.S. (1989) Subcellular distribution of copper in the kidneys of normal, copper-poisoned, and thiomolybdate-treated sheep. Journal of Inorganic Biochemistry, 35 (1). pp. 23-36.

Kumaratilake, J.S. and Howell, J.Mc.C. (1987) Effects of intravenously administered tetra-thiomolybdate on the distribution of copper in the liver and kidney of copper loaded sheep: a histochemical study. Research in Veterinary Science, 42 (2). pp. 154-161.

Howell, J.Mc.C., Dorling, P.R., Dimarco, P.N. and Taylor, E.G. (1987) Multiple implantation of normal amnion into cattle with generalized glycogenosis type II. Journal of Inherited Metabolic Disease, 10 (1). pp. 3-10.

Gooneratne, S.R, Howell, J.Mc.C. and Aughey, E. (1986) An ultrastructural study of the kidney of normal, copper poisoned and thiomolybdate-treated sheep. Journal of Comparative Pathology, 96 (6). pp. 593-612.

Di Marco, P.N., Howell, J.Mc.C. and Dorling, P.R. (1985) Bovine generalised glycogenosis type II. Uptake of lysosomal alpha-glucosidase by cultured skeletal muscle and reversal of glycogen accumulation. FEBS Letters, 190 (2). pp. 301-4.

Gooneratne, S.R, Howell, J.Mc.C. and Gawthorne, J.M. (1985) Distribution of copper in the kidney of sheep after thiomolybdate administration. Nutrition Research, 5 (SUPPL. 1). S-546-S-554.

Di Marco, P.N., Howell, J.Mc.C. and Dorling, P.R. (1984) Bovine glycogenosis type II. Biochemical and morphological characteristics of skeletal muscle in culture. Neuropathology and Applied Neurobiology, 10 (5). pp. 379-95.

Howell, J.Mc.C., Dorling, P.R. and Cook, R.D. (1984) The effect of age on biochemical and morphological changes in the semitendinosus muscle of cattle with generalized glycogenosis type II. Neuropathology and Applied Neurobiology, 10 (4). pp. 255-266.

Conference Item

Fletcher, S., Ly, T., Duff, R.M., Howell, J.M., Mann, C.J. and Wilton, S.D. (2001) Cryptic splicing involving the splice site mutation in the canine model of Duchenne Muscular Dystrophy. In: 2nd Meeting of the Australasian Gene Therapy Society, 27 - 29 April 2001, Sydney, Australia.

Howell, J.M., Pari, G., Davies, L., Fletcher, S., Wilton, S.D., Collins, T., Crerar, M.M., Nalbantoglu, J., Shoubridge, E., Jani, A., Tsujino, S., Shankse, S., Kakulas, B.A., DiMauro, S. and Karpati, G. (1999) Investigations of gene therapy for McArdle's disease using the sheep model. In: 4th International Congress of the World Muscle Society, 14 - 16 October 1999, Antalya, Turkey.

Carville, K., Mann, C., Schatzberg, S., Sharp, N., Howell, J.Mc.C. and Wilton, S. (1997) Sequence of full-length dystrophin CDNA and several revertant fibres from muscles of golden retriever dogs. In: 8th Annual Combined Biological Sciences Meeting, 15 August 1997, Perth, Western Australia.

Mann, C.J., Fletcher, S., Wilton, S.D. and Howell, J.Mc.C. (1996) Use of the GRMD model to study gene and genetic therapies for muscular dystrophy. In: 7th Annual Combined Biological Sciences Meeting, 19 August 1996, Perth, Western Australia.

This list was generated on Sun Apr 20 05:22:57 2014 IST.