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Article

Ho, Gladys, Reichardt, Juergen, and Christodoulou, John (2013) In vitro read-through of phenylalanine hydroxylase (PAH) nonsense mutations using aminoglycosides: a potential therapy for phenylketonuria. Journal of Inherited Metabolic Diseases, 36 (6). pp. 955-959.

Togo, Yumiko , Takahashi, Katsu, Saito, Kazuyuki, Kiso, Honoka, Huang, Boyen, Tsukamoto, Hiroko, Hyon, Suong-Hyu, and Bessho, Kazuhisa (2013) Aldehyded dextran and ε-poly(l-lysine) hydrogel as nonviral gene carrier. Stem Cells International, 2013. pp. 1-5.

Huang, B., Takahashi, K., Sakata-Goto, T., Kiso, H., Togo, Y., Saito, K., Tsukamoto, H., Sugai, M., Akira, S., Shimizu, A., and Bessho, K. (2013) Phenotypes of CCAAT/enhancer-binding protein beta deficiency: hyperdontia and elongated coronoid process. Oral Diseases, 19 (2). pp. 144-150.

Sakata-Goto, Tomoko, Takahashi, Katsu, Kiso, Honoka, Huang, Boyen, Tsukamoto, Hiroko, Takemoto, Mitsuru, Hayashi, Tatsunari, Sugai, Manabu, Nakamura, Takashi, Yokota, Yoshifumi, Shimizu, Akira, Slavkin, Harold, and Bessho, Kazuhisa (2012) Id2 controls chondrogenesis acting downstream of BMP signaling during maxillary morphogenesis. Bone, 50 (1). pp. 69-78.

Sondhi, Dolan, Johnson, Linda, Purpura, Keith, Monette, Sebastien, Souweidane, Mark M., Kaplitt, Michael G., Kosofsky, Barry, Yohay, Kaleb, Ballon, Douglas, Dyke, Jonathan, Kaminsky, Stephen M., Hackett, Neil R., and Crystal, Ronald G. (2012) Long-term expression and safety of administration of AAVrh.10hCLN2 to the brain of rats and nonhuman primates for the treatment of late infantile neuronal ceroid lipofuscinosis. Human Gene Therapy Methods, 23 (5). pp. 324-335.

Tiong, Keith, Cotterill, Andrew, and Falhammar, Henrik (2010) Adult case of partial trisomy 9q. BMC Medical Genetics, 11 (26). pp. 1-5.

Warren, William D., and Gorringe, Kylie L. (2006) A molecular model for sporadic human aneuploidy. Trends in Genetics, 22 (4). pp. 218-224.

Towner, Rheal A., Hashimoto, Hisanori, and Summers, Phillip M. (2000) Non-invasive in vivo magnetic resonance imaging assessment of acute aflatoxin B1 hepatotoxicity in rats. Biochimica et Biophysica Acta, 1475 (3). pp. 314-320.

Kamitani, Atsushi, Wong, Zilla Y.H., Dickson, Phillip, van Herwerden, Lynne, Raven, Joan, Forbes, Andrew B., Abramson, Michael J., Walters, E. Haydn, and Harrap, Stephen B. (1997) Absence of genetic linkage of chromosome 5q31 with asthma and atopy in the general population. Thorax, 52 (9). pp. 816-817.

Wong, Zilla Y.H., Tsonis, Dina, van Herwerden, Lynne, Raven, Joan, Forbes, Andrew, Abramson, Michael J., Walters, E. Haydn, and Harrap, Stephen B. (1997) Linkage analysis of bronchial hyperreactivity and atopy with chromosome 11q13. Electrophoresis, 18 (9). pp. 1641-1645.

van Herwerden, Lynne, Harrap, Stephen B., Wong, Zilla Y.H., Abrahamson, Michael J., Kutin, Jozica J., Forbes, Andrew B., Raven, Joan, Lanigan, Anna, and Walters, E. Haydn (1995) Linkage of high-affinity IgE receptor gene with bronchial hyperreactivity, even in absence of atopy. Lancet, 346 (8985). pp. 1262-1265.

Woodman, B.F., Jordan, M.A., Moller, L.I., Cartwright, J.D., and De Ravel, T.J.L. (1995) The Pallister-Killian syndrome in an African individual. Genetic Counseling, 6 (1). pp. 33-36.

Reardon, W., van Herwerden, L., Rose, C., Jones, B., Malcolm, S., and Winter, R.M. (1994) Crouzon syndrome is not linked to craniosynostosis loci at 7p and 5qter. Journal of Medical Genetics, 31 (3). pp. 219-221.

van Herwerden, Lynne, Rose, Charlotte S.P., Reardon, William, Brueton, Louise A., Weissenbach, Jean, Malcolm, Sue, and Winter, Robin M. (1994) Evidence for locus heterogeneity in acrocephalosyndactyly: a refined localization for the Saethre-Chotzen syndrome locus on distal chromosome 7p-- and exclusion of Jackson-Weiss syndrome from craniosynostosis loci on 7p and 5q. American Journal of Human Genetics, 54. pp. 669-674.

Chotai, Kokila A., Brueton, Louise A., van Herwerden, Lyn, Garrett, Christine, Hinkel, Georg K., Schinzel, Albert, Mueller, Robert F., Speleman, Frank, and Winter, Robin M. (1994) Six cases of 7p deletion: clinical, cytogenetic, and molecular studies. American Journal of Medical Genetics, 51 (3). pp. 270-276.

Chotai, K.A., Brueton, L., van Herwerden, L., and Winter, R.M. (1992) Eight cases of 7p deletion: clinical features, cytogenetic findings, and molecular studies. Journal of Medical Genetics, 29 (4). pp. 283-284.

Brueton, Louise A., Chotai, Kokila A., van Herwerden, Lynne, Schinzel, Albert, and Winter, Robin M. (1992) The acrocallosal syndrome and Greig syndrome are not allelic disorders. Journal of Medical Genetics, 29 (9). pp. 635-637.

Brueton, L.A., van Herwerden, L., Chotai, K.A., and Winter, R.M. (1992) The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7p. Journal of Medical Genetics, 29 (10). pp. 681-685.

Book Chapter

Takahashi, Katsu, Kiso, Honoka, Saito, Kazuyuki, Togo, Yumiko, Tsukamoto, Hiroko, Huang, Boyen, and Besho, Kazuhisa (2013) Feasibility of gene therapy for tooth regeneration by stimulation of a third dentition. In: Martin, Francisco, (ed.) Gene therapy: tools and potential applications. InTech, Rijeka, Croatia, pp. 727-744.

Thesis

Jordan, Margaret Agnes (2011) Dissecting the genetics of autoimmune diseases. PhD thesis, James Cook University.

This list was generated on Wed Apr 23 18:50:39 2014 EST.