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2024 Conference Publication How the Australian Functional Genomics Network (AFGN) contributes to improved patient careScott, Hamish S., Matotek, Ebony, Mattiske, Tessa, Bryson-Richardson, Robert J., Smyth, Ian, Gecz, Jozef, Christodoulou, John, Palpant, Nathan, Smith, Kelly, Warr, Coral, Bennetts, Bruce, Thomas, Paul, Bowles, Josephine, Hilliard, Massimo, Hime, Gary, Hool, Livia, Quinn, Leonie, Wolvetang, Ernst, Jamieson, Robyn, Baynam, Gareth, Dudding-Byth, Tracy, Tan, Tiong Yang, Milnes, Di, Wallis, Mathew, Palmer, Elizabeth, Patel, Chirag, Jones, Kristi, Tam, Patrick, Stark, Zornitza ... Sinclair, Andrew (2024). How the Australian Functional Genomics Network (AFGN) contributes to improved patient care. Pathology Update 2024, Adelaide, SA, Australia, 1-3 March 2024. Oxford, United Kingdom: Elsevier. doi: 10.1016/j.pathol.2023.12.084 |
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2024 Conference Publication Variants in SART3 cause a novel spliceosomopathy characterised by failure of testis development and neuronal defectsAyers, Katie, Eggers, Stefanie, Rollo, Ben, Smith, Katherine, Davidson, Nadia, Siddall, Nicole, Zhao, Liang, Bowles, Josephine, Weiss, Karin, Zanni, Ginevra, Burglen, Lydie, Ben Shachar, Shay, Rosensaft, Jenny, Raas-Rothschild, Annick, Jorgensen, Anne, Schittenhelm, Ralf, Huang, Cheng, Robevska, Gorjana, van den Bergen, Jocelyn, Casagranda, Franca, Cyza, Justyna, Pachernegg, Svenja, Wright, David, Bahlo, Melanie, Oshlack, Alicia, O'Brien, Terence, Kwan, Patrick, Koopman, Peter, Hime, Gary ... Sinclair, Andrew (2024). Variants in SART3 cause a novel spliceosomopathy characterised by failure of testis development and neuronal defects. 56th Annual Conference of the European Society of Human Genetics (ESHG), Glasgow, Scotland, 10-13 June 2023. London, United Kingdom: Nature Publishing Group. |
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2018 Conference Publication Gene editing of the multi-copy H2A.B gene family by a single pair of TALENs in miceAnuar, Nur Diana, Field, Matt, Kurscheid, Sebastian, Zhang, Lei, Rebar, Edward, Gregory, Philip, Bowles, Josephine, Koopman, Peter, Tremethick, David J. and Soboleva, Tatiana (2018). Gene editing of the multi-copy H2A.B gene family by a single pair of TALENs in mice. LONDON: BIOMED CENTRAL LTD. |
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2009 Conference Publication Sex fate determination in the germ lineBowles, Josephine, Feng, Chun-Wei, Davidson, Tara and Koopman, Peter (2009). Sex fate determination in the germ line. 42nd Annual Meeting of the Society for the Study of Reproduction, Pittsburgh PA, 8-22 July 2009. United States: Society for the Study of Reproduction. |
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2006 Conference Publication The production of male of-only offspring in beef cattle - a proof of principle projectFarkas, D., Bowles, J., Lehnert, S.A. and Koopman, P.A. (2006). The production of male of-only offspring in beef cattle - a proof of principle project. 7th Transgenic Technology Meeting (TT2007), Brisbane, Qld, Australia, 12-14 February, 2007. Dordrecht,The Netherlands: Springer. doi: 10.1007/s11248-006-9047-x |
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2005 Conference Publication The PCNA-associated factor KIAA0101/p15(PAF) binds the potential tumour suppressor product p33ING1Simpson, F., van Bueren, Lammerts K., Fowles, L., Berkman, J., Butterfield, N., Bowles, J., Adolphe, C., Simms, L., Young, J., Walsh, M. and Wicking, C. (2005). The PCNA-associated factor KIAA0101/p15(PAF) binds the potential tumour suppressor product p33ING1. Unknown, Unknown, Unknown. Amsterdam, Netherlands: Elsevier Science. |
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2005 Conference Publication Entry of mouse embryonic germ cells into meiosis is induced by retinoic acidBowles, J., Knight, D., Smith, C., Wilson, M., Wilhelm, D., Richman, J., Rossant, J. and Koopman, P. (2005). Entry of mouse embryonic germ cells into meiosis is induced by retinoic acid. |
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2005 Conference Publication Entry of germ cells into meiosis is induced by retinoic acid in miceKoopman, P., Knight, D., Smith, C., Wilson, M., Wilhelm, D., Richman, J., Rossant, J. and Bowles, J. (2005). Entry of germ cells into meiosis is induced by retinoic acid in mice. |
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2003 Conference Publication Dppa3 is a marker of pluripotency and has a human homologue that is expressed in germ cell tumoursBowles, J., Teasdale, R. D., James, K. M. and Koopman, P. A. (2003). Dppa3 is a marker of pluripotency and has a human homologue that is expressed in germ cell tumours. Vertebrate Sex Determination, Kona, Hawaii, 24-28 March, 2003. Basil, Switzerland: Karger. doi: 10.1159/000074346 |
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2002 Conference Publication Expression-based strategies for discovery of genes involved in testis and ovary developmentKoopman, P.A., Bullejos Martin, M., Loffler, K.A. and Bowles, J. (2002). Expression-based strategies for discovery of genes involved in testis and ovary development. The genetics and biology of sex determination, Novartis Foundation, London, 1-3 May, 2001. Chichester, West Sussex, England ; New York, NY: Wiley & Sons. |
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2001 Conference Publication Assessment of candidate ovarian-determining genes.Loffler, KA, Bowles, J and Koopman, P (2001). Assessment of candidate ovarian-determining genes.. SAN DIEGO: ACADEMIC PRESS INC. |
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2001 Conference Publication Searching for missing pieces of the sex-determination puzzleBullejos Martin, M., Bowles, J. and Koopman, P. A. (2001). Searching for missing pieces of the sex-determination puzzle. USA: Wiley-Liss Inc.. doi: 10.1002/jez.1095 |
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2001 Conference Publication Regulation of male sexual development by Sry and Sox9Koopman, P., Bullejos, M. and Bowles, J. (2001). Regulation of male sexual development by Sry and Sox9. New York: John Wiley & Sons, Inc.. doi: 10.1002/jez.1089 |
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1999 Conference Publication Mouse SRY requires a CAG repeat domain for male sex determinationBowles, J., Cooper, L., Berkman, J. and Koopman, P. (1999). Mouse SRY requires a CAG repeat domain for male sex determination. -, -, 1999. Chicago, IL United States: University of Chicago Press. |
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1996 Conference Publication Aetiology of the skeletal dysmorphology syndrome campomelic dysplasia: Expression of the Sox9 gene during chondrogenesis in mouse embryosWheatley, Susan, Wright, Edwina, Jeske, Yvette, Mccormack, Andrew, Bowles, Josephine and Koopman, Peter (1996). Aetiology of the skeletal dysmorphology syndrome campomelic dysplasia: Expression of the Sox9 gene during chondrogenesis in mouse embryos. Conference on Molecular and Developmental Biology of Cartilage, Bethesda, MD, United States, 27-30 September 1995. Hoboken, NJ, United States: Wiley-Blackwell Publishing. doi: 10.1111/j.1749-6632.1996.tb56306.x |
