Honorary Professor

Nathan Subramaniam

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Availability

Honorary Professor Nathan Subramaniam is:
Available for supervision

Fields of research

Biological Sciences Clinical sciences Oncology and carcinogenesis

Qualifications

  • PhD, Purdue University USA
  • BSc, Rajasthan University India
  • MSc, Bombay University India

Search Professor Nathan Subramaniam’s works on UQ eSpace

211 works between 1991 and 2024
All (211) Journal Article (130) Book Chapter (2) Conference Publication (79)

141 - 160 of 211 works

2008

Conference Publication

Combined deletion of HFE and transferrin receptor 2 results in a dramatic disruption in hepcidin regulation and severe iron overload

Subramaniam, V. N., Summerville, L., Crampton, E. M., Frazer, D. M., Anderson, G. J. and Wallace, D. F. (2008). Combined deletion of HFE and transferrin receptor 2 results in a dramatic disruption in hepcidin regulation and severe iron overload. Australian Gastroenterology Week, Brisbane, QLD, Austalia, 22-25 October 2008. Richmond, Vic., Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/j.1440-1746.2008.05613.x

Combined deletion of HFE and transferrin receptor 2 results in a dramatic disruption in hepcidin regulation and severe iron overload

2008

Conference Publication

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

Crawford, Darrell H., Murphy, Therese L., Ramm, Louise E., Fletcher, Linda M., Clouston, Andrew D., Anderson, Gregory J., Subramaniam, V. Nathan, Powell, Lawrie W. and Ramm, Grant A. (2008). Serum hyaluronic acid with serum ferritin accurately predicts cirrhosis and reduces the need for liver biopsy in C282Y hemochromatosis. The Liver Meeting 2008: 59th Annual Meeting of the American Association for the Study of Liver Diseases (AASLD), San Francisco, CA, U.S.A., 31 October-4 November 2008. Hoboken, NJ, U.S.A.: John Wiley & Sons. doi: 10.1002/hep.22641

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

2008

Conference Publication

Functional consequences of disease causing mutations in the juvenile haemochromatosis gene

Wallace, D. F., Leddy, E., Summerville, L., Crampton, E. M. and Subramaniam, V. N. (2008). Functional consequences of disease causing mutations in the juvenile haemochromatosis gene. Australian Gastroenterology Week, Brisbane, QLD, Austalia, 22-25 October 2008. Richmond, Vic., Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/j.1440-1746.2008.05613.x

Functional consequences of disease causing mutations in the juvenile haemochromatosis gene

2008

Conference Publication

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, A. D., Anderson, G. J., Subramaniam, V. N., Powell, L. W. and Ramm, G. A. (2008). Serum hyaluronic acid with serum ferritin accurately predicts cirrhosis and reduces the need for liver biopsy in C282Y hemochromatosis. AGW 2008: Australian Gastroenterology Week 08, Brisbane, QLD, Australia, 22-25 October 2008. MALDEN: WILEY-BLACKWELL PUBLISHING, INC. doi: 10.1111/j.1440-1746.2008.05613.x

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

Conference Publication

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

Theurl, M., Theurl, I., Hochegger, K., Obrist, P., Subramaniam, N., van Rooijen, N., Schuemann, K. and Weiss, G. (2007). Kupffer cells modulate iron homeostasis in mice via regulation of hepcidin expression. HOBOKEN: WILEY-LISS.

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

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

Conference Publication

Ferroportin : Membrane topologyand characterisation of mutations

Wallace, D. F. and Subramaniam, V. N. (2007). Ferroportin : Membrane topologyand characterisation of mutations. International BioIron Society Meeting, Kyoto, Japan, 1-6 April 2007. Hoboken, NJ, United States: John Wiley & Sons, Inc.. doi: 10.1002/ajh.20964

Ferroportin : Membrane topologyand characterisation of mutations

2007

Conference Publication

Disease causing mutations of transferrin receptor 2 cause its intracellular retention

Subramaniam, V. N., Summerville, L. and Wallace, D. F. (2007). Disease causing mutations of transferrin receptor 2 cause its intracellular retention. International BioIron Society Meeting, Kyoto, Japan, 1-6 April 2007. Hoboken, NJ, United States: John Wiley & Sons, Inc.. doi: 10.1002/ajh.20964

Disease causing mutations of transferrin receptor 2 cause its intracellular retention

2007

Conference Publication

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

Wallace, D. F., Summerville, L. and Subramaniam, V. N. (2007). Targeted disruption of the hepatic transferrin receptor 2 gene in mice leads to iron overload. 42th Annual Meeting of the European Association for the Study of the Liver, Barcelona, Spain, 11-15 April 2007. AMSTERDAM: Elsevier. doi: 10.1016/S0168-8278(07)61717-6

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

2007

Conference Publication

Liver-specific deletion of the transferrin receptor 2 gene in mice leads to iron overload

Subramaniam, V. N., Summerville, L. and Wallace, D. F. (2007). Liver-specific deletion of the transferrin receptor 2 gene in mice leads to iron overload. International BioIron Society Meeting, Kyoto, Japan, 1-6 April 2007. Hoboken, NJ, United States: John Wiley & Sons, Inc.. doi: 10.1002/ajh.20964

Liver-specific deletion of the 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

Conference Publication

Liver-specific deletion of the transferrin receptor 2 gene causes iron overload implicating the liver in regulation of iron homeostasis

Wallace, D. F., Summerville, L. and Subramaniam, V. N. (2006). Liver-specific deletion of the transferrin receptor 2 gene causes iron overload implicating the liver in regulation of iron homeostasis. OXFORD: BLACKWELL PUBLISHING.

Liver-specific deletion of the transferrin receptor 2 gene causes iron overload implicating the liver in regulation of iron homeostasis

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

Conference Publication

The clinical relevance of compound heterozygosity for the haemochromatosis mutations (C282Y/H63D)

Walsh, A., Dixon, J. L., Ranun, G. A., Hewett, D. G., Lincoln, D., Anderson, G. L., Subramaniam, N., Dodermaide, J., Bassett, M. and Powell, L. (2006). The clinical relevance of compound heterozygosity for the haemochromatosis mutations (C282Y/H63D). Digestive Disease Week Meeting/107th Annual Meeting of the American Gastroenterlogical Association, Los Angeles, CA, United States, 20-25 May 2006. PHILADELPHIA: W.B. Saunders.

The clinical relevance of compound heterozygosity for the haemochromatosis mutations (C282Y/H63D)

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

Conference Publication

Liver-specific deletion of the transferrin receptor 2 gene causes iron overload implicating the liver in regulation of iron homeostasis

Wallace, D. F., Summerville, L. and Subramaniam, V. N. (2006). Liver-specific deletion of the transferrin receptor 2 gene causes iron overload implicating the liver in regulation of iron homeostasis. Australian Gastroenterology Week, Adelaide, SA, Australia, 11-14 October 2006. Richmond, Vic., Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/j.1440-1746.2006.04689.x

Liver-specific deletion of the transferrin receptor 2 gene causes iron overload implicating the liver in regulation of iron homeostasis

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

Past funding

  • 2014 - 2019
    Immunotherapeutic Approaches for Hepatocellular Carcinoma
    Gallipoli Medical Research Foundation
    Open grant

Availability

Honorary Professor Nathan Subramaniam is:
Available for supervision

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Supervision history

Completed supervision

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