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2010

Journal Article

Syntaxin 5 is required for copper homeostasis in Drosophila and mammals

Norgate, Melanie, Southon, Adam, Greenough, Mark, Cater, Michael, Farlow, Ashley, Batterham, Philip, Bush Ashley I., Subramaniam, V. Nathan, Burke, Richard and Camakaris, James (2010). Syntaxin 5 is required for copper homeostasis in Drosophila and mammals. PLoS One, 5 (12) e14303, e14303-1-e14303-10. doi: 10.1371/journal.pone.0014303

Syntaxin 5 is required for copper homeostasis in Drosophila and mammals

2010

Journal Article

Transferrin receptor 1: A ferritin receptor as well?

Wallace, Daniel F., McDonald, Cameron and Subramaniam, V. Nathan (2010). Transferrin receptor 1: A ferritin receptor as well?. Gastroenterology, 139 (3), 1052-1053. doi: 10.1053/j.gastro.2010.07.030

Transferrin receptor 1: A ferritin receptor as well?

2010

Journal Article

Centrobin regulates the assembly of functional mitotic spindles

Jeffery, J. M., Urquhart, A. J., Subramaniam, V. N., Parton, R.G. and Khanna, K.K. (2010). Centrobin regulates the assembly of functional mitotic spindles. Oncogene, 29 (18), 2649-2658. doi: 10.1038/onc.2010.37

Centrobin regulates the assembly of functional mitotic spindles

2010

Journal Article

Increased iron stores correlate with worse disease outcomes in a mouse model of schistosomiasis infection

McDonald, Cameron J., Jones, Malcolm K., Wallace, Daniel F., Summerville, Lesa, Nawaratna, Sujeevi and Subramaniam, V. Nathan (2010). Increased iron stores correlate with worse disease outcomes in a mouse model of schistosomiasis infection. PLoS One, 5 (3) e9594, 1-7. doi: 10.1371/journal.pone.0009594

Increased iron stores correlate with worse disease outcomes in a mouse model of schistosomiasis infection

2010

Conference Publication

G80S-linked ferroportin disease: classical ferroportin disease in an Australian family of Asian descent and reclassification of the mutant as iron transport defective

Subramaniam, V. N., Mcdonald, C. J., Ostini, L., Bell, S. J., Demediuk, B. and Wallace, D. F. (2010). G80S-linked ferroportin disease: classical ferroportin disease in an Australian family of Asian descent and reclassification of the mutant as iron transport defective. Australian Gastroenterology Week 2010, Broadbeach, QLD, Australia, 20-23 October 2010. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/j.1440-1746.2010.06450.x

G80S-linked ferroportin disease: classical ferroportin disease in an Australian family of Asian descent and reclassification of the mutant as iron transport defective

2010

Journal Article

Functional analysis and theoretical modeling of ferroportin reveals clustering of mutations according to phenotype

Wallace, Daniel F., Harris, Jonathan M. and Subramaniam, V. Nathan (2010). Functional analysis and theoretical modeling of ferroportin reveals clustering of mutations according to phenotype. American Journal of Physiology: Cell Physiology, 298 (1), C75-C84. doi: 10.1152/ajpcell.00621.2008

Functional analysis and theoretical modeling of ferroportin reveals clustering of mutations according to phenotype

2010

Conference Publication

Hereditary iron overload in the Asia Pacific: first identification of ferroportin disease in a Vietnamese family

Subramaniam, V. N., Mcdonald, C. J., Ostini, L., Bell, S. J., Demediuk, B. and Wallace, D. F. (2010). Hereditary iron overload in the Asia Pacific: first identification of ferroportin disease in a Vietnamese family. Gastroenterology in Asia Pacific - Excellence in the New Decade, Kuala Lumpa, Malaysia, 19-22 September 2010. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/j.1440-1746.2009.06464.x

Hereditary iron overload in the Asia Pacific: first identification of ferroportin disease in a Vietnamese family

2010

Conference Publication

Clinical expression of HFE-associated haemochromatosis in subjects under 40 years of age

Dixon, J. L., Watt, E. E., Ramm, G. A., Subrmaniam, V. N., Powell, L. W. and Anderson, G. J. (2010). Clinical expression of HFE-associated haemochromatosis in subjects under 40 years of age. Australian Gastroenterology Week 2010, Gold Coast , QLD Australia, 20-23 October 2010. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/j.1440-1746.2010.06451.x

Clinical expression of HFE-associated haemochromatosis in subjects under 40 years of age

2010

Conference Publication

Blunted hepcidin response to inflammation in the absence of Hfe and Tfr2

Wallace, D. F., Mcdonald, C. J., Ostini, L. and Subramaniam, V. N. (2010). Blunted hepcidin response to inflammation in the absence of Hfe and Tfr2. Australian Gastroenterology Week 2010, Gold Coast, QLD, Australia, 20 -23 October 2010. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/j.1440-1746.2010.06450.x

Blunted hepcidin response to inflammation in the absence of Hfe and Tfr2

2009

Journal Article

Combined deletion of Hfe and transferrin receptor 2 in mice leads to marked dysregulation of hepcidin and iron overload

Wallace, Daniel F., Summerville, Lesa, Crampton, Emily M., Frazer, David M., Anderson, Gregory J. and Subramaniam, V. Nathan (2009). Combined deletion of Hfe and transferrin receptor 2 in mice leads to marked dysregulation of hepcidin and iron overload. Hepatology, 50 (6), 1992-2000. doi: 10.1002/hep.23198

Combined deletion of Hfe and transferrin receptor 2 in mice leads to marked dysregulation of hepcidin and iron overload

2009

Journal Article

Co-factors in liver disease: The role of HFE-related hereditary hemochromatosis and iron

Wallace, Daniel F. and Subramaniam, V. Nathan (2009). Co-factors in liver disease: The role of HFE-related hereditary hemochromatosis and iron. Biochimica et Biophysica Acta - General Subjects, 1790 (7), 663-670. doi: 10.1016/j.bbagen.2008.09.002

Co-factors in liver disease: The role of HFE-related hereditary hemochromatosis and iron

2009

Journal Article

Carrier-Mediated Thyroid Hormone Transport into Placenta by Placental Transthyretin

Landers, Kelly A., McKinnon, Brett D., Li, Huika, Subramaniam, V. Nathan, Mortimer, Robin H. and Richard, Kerry (2009). Carrier-Mediated Thyroid Hormone Transport into Placenta by Placental Transthyretin. Journal of Clinical Endocrinology and Metabolism, 94 (7), 2610-2616. doi: 10.1210/jc.2009-0048

Carrier-Mediated Thyroid Hormone Transport into Placenta by Placental Transthyretin

2009

Journal Article

Lymphotoxin-beta receptor signaling regulates hepatic stellate cell function and wound healing in a murine model of chronic liver injury

Ruddell, Richard G., Knight, Belinda, Tirnitz-Parker, Janina E. E., Akhurst, Barbara, Summerville, Lesa, Subramaniam, V. Nathan, Olynyk, John K. and Ramm, Grant A. (2009). Lymphotoxin-beta receptor signaling regulates hepatic stellate cell function and wound healing in a murine model of chronic liver injury. Hepatology, 49 (1), 227-239. doi: 10.1002/hep.22597

Lymphotoxin-beta receptor signaling regulates hepatic stellate cell function and wound healing in a murine model of chronic liver injury

2009

Journal Article

Hepcidin Regulation by HFE and TFR2: Is It Enough to Give a Hepatocyte a Complex?

Wallace, Daniel F., Trinder, Debbie and Subramaniam, V. Nathan (2009). Hepcidin Regulation by HFE and TFR2: Is It Enough to Give a Hepatocyte a Complex?. Gastroenterology, 137 (3), 1173-1175. doi: 10.1053/j.gastro.2009.07.009

Hepcidin Regulation by HFE and TFR2: Is It Enough to Give a Hepatocyte a Complex?

2009

Journal Article

Identification of Ferritin Receptors: Their Role in Iron Homeostasis, Hepatic Injury, and Inflammation

Ramm, Grant A., Ruddell, Richard G. and Subramaniam, V. Nathan (2009). Identification of Ferritin Receptors: Their Role in Iron Homeostasis, Hepatic Injury, and Inflammation. Gastroenterology, 137 (5), 1849-1851. doi: 10.1053/j.gastro.2009.09.037

Identification of Ferritin Receptors: Their Role in Iron Homeostasis, Hepatic Injury, and Inflammation

2009

Journal Article

Serum hyaluronic acid with serum ferritin accurately predicts cirrhosis and reduces the need for liver biopsy in C282Y hemochromatosis

Crawford, D. H. G., Murphy, T. L., Ramm, L. E., Fletcher, L. M., Clouston, AD, Anderson, G. J., Subramaniam, V. N., Powell, L. W. and Ramm, G. A. (2009). Serum hyaluronic acid with serum ferritin accurately predicts cirrhosis and reduces the need for liver biopsy in C282Y hemochromatosis. Hepatology, 49 (2), 418-425. doi: 10.1002/hep.22650

Serum hyaluronic acid with serum ferritin accurately predicts cirrhosis and reduces the need for liver biopsy in C282Y hemochromatosis

2009

Journal Article

Regulation of Iron Homeostasis: Is It All in the HBD?

Subramaniam, V. Nathan (2009). Regulation of Iron Homeostasis: Is It All in the HBD?. Gastroenterology, 136 (4), 1449-1451. doi: 10.1053/j.gastro.2009.02.034

Regulation of Iron Homeostasis: Is It All in the HBD?

2008

Journal Article

Juvenile iron overload: Advances, but no answers

Walker, Nicole A., Crawford, Darrell H.G., Subramaniam, V. Nathan and Wallace, Daniel F. (2008). Juvenile iron overload: Advances, but no answers. Journal of Pediatrics, 153 (4), 588-588. doi: 10.1016/j.jpeds.2008.06.005

Juvenile iron overload: Advances, but no answers

2008

Journal Article

Kupffer cells modulate iron homeostasis in mice via regulation of hepcidin expression

Theurl, Milan, Theurl, Igor, Hochegger, Kathrin, Obrist, Peter, Subramaniam, Nathan, van Rooijen, Nico, Schuemann, Klaus and Weiss, Guenter (2008). Kupffer cells modulate iron homeostasis in mice via regulation of hepcidin expression. Journal of Molecular Medicine, 86 (7), 825-835. doi: 10.1007/s00109-008-0346-y

Kupffer cells modulate iron homeostasis in mice via regulation of hepcidin expression

2008

Journal Article

Defective trafficking and localization of mutated transferrin receptor 2: Implications for type 3 hereditary hemochromatosis

Wallace, Daniel F., Summerville, Lesa, Crampton, Emily M. and Subramaniam, V. Nathan (2008). Defective trafficking and localization of mutated transferrin receptor 2: Implications for type 3 hereditary hemochromatosis. American Journal of Physiology - Cell Physiology, 294 (2), C383-C390. doi: 10.1152/ajpcell.00492.2007

Defective trafficking and localization of mutated transferrin receptor 2: Implications for type 3 hereditary hemochromatosis