Subramaniam VN - Search Results

1

Iron loading and oxidative stress in the Atm-/- mouse liver.

McDonald CJ, Ostini L, Wallace DF, John AN, Watters DJ, Subramaniam VN. McDonald CJ, et al. Among authors: subramaniam vn. Am J Physiol Gastrointest Liver Physiol. 2011 Apr;300(4):G554-60. doi: 10.1152/ajpgi.00486.2010. Epub 2011 Feb 3. Am J Physiol Gastrointest Liver Physiol. 2011. PMID: 21292994 Free article.

2

Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y.

Wallace DF, Walker AP, Pietrangelo A, Clare M, Bomford AB, Dixon JL, Powell LW, Subramaniam VN, Dooley JS. Wallace DF, et al. Among authors: subramaniam vn. J Hepatol. 2002 Apr;36(4):474-9. doi: 10.1016/s0168-8278(01)00304-x. J Hepatol. 2002. PMID: 11943417

3

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis.

Wallace DF, Pedersen P, Dixon JL, Stephenson P, Searle JW, Powell LW, Subramaniam VN. Wallace DF, et al. Among authors: subramaniam vn. Blood. 2002 Jul 15;100(2):692-4. doi: 10.1182/blood.v100.2.692. Blood. 2002. PMID: 12091366 Free article.

4

Molecular and cellular characterization of transferrin receptor 2.

Subramaniam VN, Summerville L, Wallace DF. Subramaniam VN, et al. Cell Biochem Biophys. 2002;36(2-3):235-9. doi: 10.1385/CBB:36:2-3:235. Cell Biochem Biophys. 2002. PMID: 12139409 Review.

5

Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homoeostasis.

Bridle KR, Frazer DM, Wilkins SJ, Dixon JL, Purdie DM, Crawford DH, Subramaniam VN, Powell LW, Anderson GJ, Ramm GA. Bridle KR, et al. Among authors: subramaniam vn. Lancet. 2003 Feb 22;361(9358):669-73. doi: 10.1016/S0140-6736(03)12602-5. Lancet. 2003. PMID: 12606179

6

A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient.

Arden KE, Wallace DF, Dixon JL, Summerville L, Searle JW, Anderson GJ, Ramm GA, Powell LW, Subramaniam VN. Arden KE, et al. Among authors: subramaniam vn. Gut. 2003 Aug;52(8):1215-7. doi: 10.1136/gut.52.8.1215. Gut. 2003. PMID: 12865285 Free PMC article.

7

Autosomal dominant iron overload due to a novel mutation of ferroportin1 associated with parenchymal iron loading and cirrhosis.

Wallace DF, Clark RM, Harley HA, Subramaniam VN. Wallace DF, et al. Among authors: subramaniam vn. J Hepatol. 2004 Apr;40(4):710-3. doi: 10.1016/j.jhep.2003.12.008. J Hepatol. 2004. PMID: 15030991

8

Inactivation of the murine Transferrin Receptor 2 gene using the Cre recombinase: loxP system.

Wallace DF, Tonks ID, Zournazi A, Kay GF, Subramaniam VN. Wallace DF, et al. Among authors: subramaniam vn. Genesis. 2004 May;39(1):38-41. doi: 10.1002/gene.20023. Genesis. 2004. PMID: 15124225

9

Identification of ferroportin disease in the Indian subcontinent.

Wallace DF, Browett P, Wong P, Kua H, Ameratunga R, Subramaniam VN. Wallace DF, et al. Among authors: subramaniam vn. Gut. 2005 Apr;54(4):567-8. doi: 10.1136/gut.2004.060988. Gut. 2005. PMID: 15753550 Free PMC article. No abstract available.

10

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

Wallace DF, Summerville L, Lusby PE, Subramaniam VN. Wallace DF, et al. Among authors: subramaniam vn. Gut. 2005 Jul;54(7):980-6. doi: 10.1136/gut.2004.062018. Gut. 2005. PMID: 15951546 Free PMC article.

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