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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?

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?

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

2007

Journal Article

Non-HFE haemochromatosis

Wallace, Daniel F. and Subramaniam, V. Nathan (2007). Non-HFE haemochromatosis. World Journal of Gastroenterology, 13 (35), 4690-4698. doi: 10.3748/wjg.v13.i35.4690

Non-HFE haemochromatosis

2007

Journal Article

A novel mutation in ferroportin implicated in iron overload

Wallace, Daniel F., Dixon, Jeannette L., Ramm, Grant A., Anderson, Gregory J., Powell, Lawrie W. and Subramaniam, V. Nathan (2007). A novel mutation in ferroportin implicated in iron overload. Journal of Hepatology, 46 (5), 921-926. doi: 10.1016/j.jhep.2007.01.033

A novel mutation in ferroportin implicated in iron overload

2007

Journal Article

Targeted disruption of the hepatic transferrin receptor 2 gene in mice leads to iron overload

Wallace, Daniel F., Summerville, Lesa and Subramaniam, V. Nathan (2007). Targeted disruption of the hepatic transferrin receptor 2 gene in mice leads to iron overload. Gastroenterology, 132 (1), 301-310. doi: 10.1053/j.gastro.2006.11.028

Targeted disruption of the hepatic transferrin receptor 2 gene in mice leads to iron overload

2006

Journal Article

The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis

Walsh, Alissa, Dixon, Jeannette L., Ramm, Grant A., Hewett, David G., Lincoln, Douglas J., Anderson, Gregory J., Subramaniam, V. Nathan, Dodemaide, Julian, Cavanaugh, Juleen A., Bassett, Mark L. and Powell, Lawrie W. (2006). The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis. Clinical Gastroenterology and Hepatology, 4 (11), 1403-1410. doi: 10.1016/j.cgh.2006.07.009

The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis

2006

Journal Article

Clinical expression of C282Y hornozygous HFE haernochromatosis at 14 years of age

Rossi, Enrico, Wallace, Daniel F., Subramaniam, V. Nathan, St Pierre, Timothy G., Mews, Catherine and Jeffrey, Gary P. (2006). Clinical expression of C282Y hornozygous HFE haernochromatosis at 14 years of age. Annals of Clinical Biochemistry, 43 (3), 233-236. doi: 10.1258/000456306776865197

Clinical expression of C282Y hornozygous HFE haernochromatosis at 14 years of age

2006

Journal Article

Purification and partial characterisation of recombinant human hepcidin

Wallace, Daniel F., Jones, Marc D., Pedersen, Palle, Rivas, Lucy, Sly, Lindsay I. and Subramaniam, V. Nathan (2006). Purification and partial characterisation of recombinant human hepcidin. Biochimie, 88 (1), 31-37. doi: 10.1016/j.biochi.2005.07.003

Purification and partial characterisation of recombinant human hepcidin

2006

Journal Article

Screening for hemochromatosis in asymptomatic subjects with or without a family history

Powell, Lawrie W., Dixon, Jeannette L., Ramm, Grant A., Purdie, David M., Lincoln, Douglas J., Anderson, Gregory J., Subramaniam, V. Nathan, Hewett, David G., Searle, Jeffrey W., Fletcher, Linda M., Crawford, Darrell H., Rodgers, Helen, Allen, Katrina J., Cavanaugh, Juleen A. and Bassett, Mark L. (2006). Screening for hemochromatosis in asymptomatic subjects with or without a family history. Archives of Internal Medicine, 166 (3), 294-301. doi: 10.1001/archinte.166.3.294

Screening for hemochromatosis in asymptomatic subjects with or without a family history

2005

Journal Article

Prohepcidin localises to the Golgi compartment and secretory pathway in hepatocytes

Wallace, Daniel F., Summerville, Lesa, Lusby, Patricia E. and Subramaniam, V. Nathan (2005). Prohepcidin localises to the Golgi compartment and secretory pathway in hepatocytes. Journal of Hepatology, 43 (4), 720-728. doi: 10.1016/j.jhep.2005.02.047

Prohepcidin localises to the Golgi compartment and secretory pathway in hepatocytes

2005

Journal Article

First phenotypic description of transferrin receptor 2 knockout mouse, and the role of hepcidin

Wallace, D. F., Summerville, L., Lusby, P. E. and Subramaniam, V. N. (2005). First phenotypic description of transferrin receptor 2 knockout mouse, and the role of hepcidin. Gut, 54 (7), 980-986. doi: 10.1136/gut.2004.062018

First phenotypic description of transferrin receptor 2 knockout mouse, and the role of hepcidin

2005

Journal Article

Identification of ferroportin disease in the Indian subcontinent

Wallace, D. F., Browett, P., Wong, P., Kua, H., Ameratunga, R. and Subramaniam, V. N. (2005). Identification of ferroportin disease in the Indian subcontinent. Gut, 54 (4), 567-568. doi: 10.1136/gut.2004.060988

Identification of ferroportin disease in the Indian subcontinent

2005

Journal Article

Mammalian Bet3 functions as a cytosolic factor participating in transport from the ER to the Golgi apparatus

Loh, Eva, Peter, Frank, Subramaniam, V. Nathan and Hong, Wanjin (2005). Mammalian Bet3 functions as a cytosolic factor participating in transport from the ER to the Golgi apparatus. Journal of Cell Science, 118 (6), 1209-1222. doi: 10.1242/jcs.01723

Mammalian Bet3 functions as a cytosolic factor participating in transport from the ER to the Golgi apparatus

2005

Journal Article

Hemojuvelin (HJV)-associated hemochromatosis: Analysis of HJV and HFE mutations and iron overload in three families

Wallace, Daniel F., Dixon, Jeannette L., Ramm, Grant A., Anderson, Gregory J., Powell, Lawrie W. and Subramaniam, Nathan (2005). Hemojuvelin (HJV)-associated hemochromatosis: Analysis of HJV and HFE mutations and iron overload in three families. Haematologica, 90 (2), 254-255.

Hemojuvelin (HJV)-associated hemochromatosis: Analysis of HJV and HFE mutations and iron overload in three families

2005

Journal Article

Ferroportin disease due to the A77D mutation in Australia

Subramaniam, V. N., Wallace, D. F., Dixon, J. L., Fletcher, L. M. and Crawford, D. H. (2005). Ferroportin disease due to the A77D mutation in Australia. Gut, 54 (7), 1048-1049. doi: 10.1136/gut.2005.069021

Ferroportin disease due to the A77D mutation in Australia

2004

Journal Article

Genetic disorders in gastroenterology and hepatology - HFE gene and hemochromatosis

Ramm, G. A., Subramaniam, V. N. and Powell, L. W. (2004). Genetic disorders in gastroenterology and hepatology - HFE gene and hemochromatosis. Journal of Gastroenterology and Hepatology, 19 (6), 712-712. doi: 10.1111/j.0815-9319.2004.03499.x

Genetic disorders in gastroenterology and hepatology - HFE gene and hemochromatosis