Publications by: Helmut Butzkueven

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Number of items: 5.

Field, Judith, Shahijanian, Fernando, Schibeci, Stephen, Australia and New Zealand MS Genetics Consortium, (ANZgene), Johnson, Laura, Gresle, Melissa, Laverick, Louise, Parnell, Grant, Stewart, Graeme, McKay, Fiona, Kilpatrick, Trevor, Butzkueven, Helmut, and Booth, David (2015) The MS risk allele of CD40 is associated with reduced cell-membrane bound expression in antigen presenting cells: implications for gene function. PLoS ONE, 10 (6). pp. 1-14.

Gu, Ben J., Field, Judith, Dutertre, Sébastien, Ou, Amber, Kilpatrick, Trevor J., Lechner-Scott, Jeannette, Scott, Rodney, Lea, Rodney, Taylor, Bruce V., Stankovich, Jim, Butzkueven, Helmut, Gresle, Melissa, Laws, Simon M., Petrou, Steven, Hoffjan, Sabine, Akkad, Denis A., Graham, Colin A., Hawkins, Stanley, Bedri, Sahl Khalid, Glaser, Anna, Hillert, Jan, Matute, Carlos, Antiguedad, Alfredo, Wiley, James S., and ANZgene Consortium inlcuding Alan G. Baxter, (2015) A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis. Human Molecular Genetics, 24 (19). pp. 5644-5654.

Gresle, Melissa M., Schulz, Katrin, Jonas, Anna, Perreau, Victoria M., Cipriani, Tania, Baxter, Alan G., Miranda-Hernandez, Socorro, Field, Judith, Jokubaitis, Vilija G., Cherny, Robert, Volitakis, Irene, David, Samuel, Kilpatrick, Trevor J., and Butzkueven, Helmut (2014) Ceruloplasmin gene-deficient mice with experimental autoimmune encephalomyelitis show attenuated early disease evolution. Journal of Neuroscience Research, 92 (6). pp. 732-742.

Shahijanian, Fernando, Parnell, Grant P., McKay, Fiona C., Gatt, Prudence N., Shojoei, Maryam, O'Connor, Kate S., Schibeci, Stephen D., Brilot, Fabienne, Liddle, Christopher, Batten, Marcel, Baxter, Alan, Kermode, Allan, Carrol, William, Butzkueven, Helmut, Vucic, Steve, Wiley, James, Field, Judith, Tajouri, Lotti, Griffiths, Lyn, Barnett, Michael, Scott, Rodney, Lechner-Scott, Jeannette, Moscato, Pablo, Broadley, Simon, Slee, Mark, Kilpatrick, Trevor, Taylor, Bruce, Charlesworth, Jac, Brown, Matt, Mason, Deborah, Graeme, Stewart J., and Booth, David R. (2014) The CYP27B1 variant associated with an increased risk of autoimmune disease is underexpressed in tolerizing dendritic cells. Human Molecular Genetics, 23 (6). pp. 1425-1434.

Jordan, Margaret A., Field, Judith, Butzkueven, Helmut, and Baxter, Alan G. (2014) Genetic predisposition, humans. In: Rose, Noel R., and Mackay, Ian R., (eds.) The Autoimmune Diseases. Elsevier, Boston, MA, USA, pp. 341-364.

This list was generated on Tue May 23 03:18:39 2017 AEST.