Cox TM - Search Results

1

Typical type 2 diabetes mellitus and HFE gene mutations: a population-based case - control study.

Halsall DJ, McFarlane I, Luan J, Cox TM, Wareham NJ. Halsall DJ, et al. Among authors: cox tm. Hum Mol Genet. 2003 Jun 15;12(12):1361-5. doi: 10.1093/hmg/ddg149. Hum Mol Genet. 2003. PMID: 12783844

2

Hemochromatosis--neonatal and young subjects.

Cox TM, Halsall DJ. Cox TM, et al. Blood Cells Mol Dis. 2002 Nov-Dec;29(3):411-7. doi: 10.1006/bcmd.2002.0580. Blood Cells Mol Dis. 2002. PMID: 12547231 Review.

3

Co-localization of the mammalian hemochromatosis gene product (HFE) and a newly identified transferrin receptor (TfR2) in intestinal tissue and cells.

Griffiths WJ, Cox TM. Griffiths WJ, et al. Among authors: cox tm. J Histochem Cytochem. 2003 May;51(5):613-24. doi: 10.1177/002215540305100507. J Histochem Cytochem. 2003. PMID: 12704209

4

Primary iron overload with inappropriate hepcidin expression in V162del ferroportin disease.

Zoller H, McFarlane I, Theurl I, Stadlmann S, Nemeth E, Oxley D, Ganz T, Halsall DJ, Cox TM, Vogel W. Zoller H, et al. Among authors: cox tm. Hepatology. 2005 Aug;42(2):466-72. doi: 10.1002/hep.20775. Hepatology. 2005. PMID: 15986403

5

Clinical evaluation of chemokine and enzymatic biomarkers of Gaucher disease.

Deegan PB, Moran MT, McFarlane I, Schofield JP, Boot RG, Aerts JM, Cox TM. Deegan PB, et al. Among authors: cox tm. Blood Cells Mol Dis. 2005 Sep-Oct;35(2):259-67. doi: 10.1016/j.bcmd.2005.05.005. Blood Cells Mol Dis. 2005. PMID: 16125420

6

Clinical presentation and molecular pathophysiology of autosomal dominant hemochromatosis caused by a novel ferroportin mutation.

Griffiths WJ, Mayr R, McFarlane I, Hermann M, Halsall DJ, Zoller H, Cox TM. Griffiths WJ, et al. Among authors: cox tm. Hepatology. 2010 Mar;51(3):788-95. doi: 10.1002/hep.23377. Hepatology. 2010. PMID: 19937651

7

Potential biomarkers of osteonecrosis in Gaucher disease.

Pavlova EV, Deegan PB, Tindall J, McFarlane I, Mehta A, Hughes D, Wraith JE, Cox TM. Pavlova EV, et al. Among authors: cox tm. Blood Cells Mol Dis. 2011 Jan 15;46(1):27-33. doi: 10.1016/j.bcmd.2010.10.010. Epub 2010 Nov 13. Blood Cells Mol Dis. 2011. PMID: 21075651

8

Identification of mutations in SLC40A1 that affect ferroportin function and phenotype of human ferroportin iron overload.

Mayr R, Griffiths WJ, Hermann M, McFarlane I, Halsall DJ, Finkenstedt A, Douds A, Davies SE, Janecke AR, Vogel W, Cox TM, Zoller H. Mayr R, et al. Among authors: cox tm. Gastroenterology. 2011 Jun;140(7):2056-63, 2063.e1. doi: 10.1053/j.gastro.2011.02.064. Epub 2011 Mar 9. Gastroenterology. 2011. PMID: 21396368

9

Hemochromatosis: genetic testing and clinical practice.

Zoller H, Cox TM. Zoller H, et al. Among authors: cox tm. Clin Gastroenterol Hepatol. 2005 Oct;3(10):945-58. doi: 10.1016/s1542-3565(05)00607-5. Clin Gastroenterol Hepatol. 2005. PMID: 16234038 Review.

10

Adeno-associated virus-mediated expression of β-hexosaminidase prevents neuronal loss in the Sandhoff mouse brain.

Sargeant TJ, Wang S, Bradley J, Smith NJ, Raha AA, McNair R, Ziegler RJ, Cheng SH, Cox TM, Cachón-González MB. Sargeant TJ, et al. Among authors: cox tm. Hum Mol Genet. 2011 Nov 15;20(22):4371-80. doi: 10.1093/hmg/ddr364. Epub 2011 Aug 18. Hum Mol Genet. 2011. PMID: 21852247

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