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Items: 1 to 50 of 103

1.

Interim assessment of liver damage in patients with sickle cell disease using new non-invasive techniques.

Drasar E, Fitzpatrick E, Gardner K, Awogbade M, Dhawan A, Bomford A, Suddle A, Thein SL.

Br J Haematol. 2017 Feb;176(4):643-650. doi: 10.1111/bjh.14462. Epub 2016 Dec 16.

2.

CD44 as a Potential Screening Marker for Preliminary Differentiation Between Congenital Dyserythropoietic Anemia Type II and Hereditary Spherocytosis.

Singleton BK, Ahmed M, Green CA, Heimpel H, Woźniak MJ, Ranjha L, Seeney F, Bomford A, Mehta P, Guest A, Mushens R, King MJ.

Cytometry B Clin Cytom. 2018 Mar;94(2):312-326. doi: 10.1002/cyto.b.21488. Epub 2016 Nov 23.

3.

Expression and cellular localization of hepcidin mRNA and protein in normal rat brain.

Raha-Chowdhury R, Raha AA, Forostyak S, Zhao JW, Stott SR, Bomford A.

BMC Neurosci. 2015 Apr 21;16:24. doi: 10.1186/s12868-015-0161-7.

4.

How we treat sickle hepatopathy and liver transplantation in adults.

Gardner K, Suddle A, Kane P, O'Grady J, Heaton N, Bomford A, Thein SL.

Blood. 2014 Apr 10;123(15):2302-7. doi: 10.1182/blood-2013-12-542076. Epub 2014 Feb 24. Review.

5.

The systemic iron-regulatory proteins hepcidin and ferroportin are reduced in the brain in Alzheimer's disease.

Raha AA, Vaishnav RA, Friedland RP, Bomford A, Raha-Chowdhury R.

Acta Neuropathol Commun. 2013 Sep 3;1:55. doi: 10.1186/2051-5960-1-55.

6.

The association of pretransplant ferritin level with waiting list and post-transplant survival. Does ferritin actually predict outcome?

Al-Freah MA, Kriese S, Foxton MR, Quaglia A, Bomford A, Heaton ND, O'Grady JG, Agarwal K, Wendon JA, Heneghan MA.

Transpl Int. 2013 Nov;26(11):1070-9. doi: 10.1111/tri.12164.

7.

Two novel mutations in the L ferritin coding sequence associated with benign hyperferritinaemia unmasked by glycosylated ferritin assay.

Thurlow V, Vadher B, Bomford A, DeLord C, Kannengiesser C, Beaumont C, Grandchamp B.

Ann Clin Biochem. 2012 May;49(Pt 3):302-5. doi: 10.1258/acb.2011.011229. Epub 2012 Apr 25.

PMID:
22535864
8.

Peritoneal macrophages from patients with cirrhotic ascites show impaired phagocytosis and vigorous respiratory burst.

Ahmed AM, Bomford A, Nouri-Aria KT, Davies T, Smith R, Williams R.

Results Immunol. 2011 Sep 1;1(1):53-9. doi: 10.1016/j.rinim.2011.08.004. eCollection 2011.

9.

The iron-chelating potential of silybin in patients with hereditary haemochromatosis.

Hutchinson C, Bomford A, Geissler CA.

Eur J Clin Nutr. 2010 Oct;64(10):1239-41. doi: 10.1038/ejcn.2010.136. Epub 2010 Jul 14.

10.

Quantitation of hepcidin in serum using ultra-high-pressure liquid chromatography and a linear ion trap mass spectrometer.

Bansal SS, Abbate V, Bomford A, Halket JM, Macdougall IC, Thein SL, Hider RC.

Rapid Commun Mass Spectrom. 2010 May 15;24(9):1251-9. doi: 10.1002/rcm.4512.

PMID:
20391595
11.

Outcome of liver transplantation in hereditary hemochromatosis.

Dar FS, Faraj W, Zaman MB, Bartlett A, Bomford A, O'Sullivan A, O'Grady J, Heneghan M, Rela M, Heaton ND.

Transpl Int. 2009 Jul;22(7):717-24. doi: 10.1111/j.1432-2277.2009.00863.x. Epub 2009 Mar 16.

12.

Quantification of hepcidin using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.

Bansal SS, Halket JM, Fusova J, Bomford A, Simpson RJ, Vasavda N, Thein SL, Hider RC.

Rapid Commun Mass Spectrom. 2009 Jun;23(11):1531-42. doi: 10.1002/rcm.4033.

PMID:
19399775
13.

Quantitation of hepcidin in human urine by liquid chromatography-mass spectrometry.

Bansal SS, Halket JM, Bomford A, Simpson RJ, Vasavda N, Thein SL, Hider RC.

Anal Biochem. 2009 Jan 15;384(2):245-53. doi: 10.1016/j.ab.2008.09.045. Epub 2008 Oct 5.

PMID:
18951868
14.

Evaluation of risk factors in the development of hepatocellular carcinoma in autoimmune hepatitis: Implications for follow-up and screening.

Yeoman AD, Al-Chalabi T, Karani JB, Quaglia A, Devlin J, Mieli-Vergani G, Bomford A, O'Grady JG, Harrison PM, Heneghan MA.

Hepatology. 2008 Sep;48(3):863-70. doi: 10.1002/hep.22432.

PMID:
18752332
15.

Post-prandial iron absorption in humans: comparison between HFE genotypes and iron deficiency anaemia.

Hutchinson C, Conway RE, Bomford A, Hider RC, Powell JJ, Geissler CA.

Clin Nutr. 2008 Apr;27(2):258-63. doi: 10.1016/j.clnu.2007.12.007. Epub 2008 Feb 13.

PMID:
18276042
16.

Hepatic dysfunction in sickle cell disease: a new system of classification based on global assessment.

Berry PA, Cross TJ, Thein SL, Portmann BC, Wendon JA, Karani JB, Heneghan MA, Bomford A.

Clin Gastroenterol Hepatol. 2007 Dec;5(12):1469-76; quiz 1369. Epub 2007 Sep 27.

PMID:
17900995
17.

Proton pump inhibitors suppress absorption of dietary non-haem iron in hereditary haemochromatosis.

Hutchinson C, Geissler CA, Powell JJ, Bomford A.

Gut. 2007 Sep;56(9):1291-5. Epub 2007 Mar 7.

18.

Antioxidants versus corticosteroids in the treatment of severe alcoholic hepatitis--a randomised clinical trial.

Phillips M, Curtis H, Portmann B, Donaldson N, Bomford A, O'Grady J.

J Hepatol. 2006 Apr;44(4):784-90. Epub 2005 Dec 20.

PMID:
16469404
19.

Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.

Merryweather-Clarke AT, Cadet E, Bomford A, Capron D, Viprakasit V, Miller A, McHugh PJ, Chapman RW, Pointon JJ, Wimhurst VL, Livesey KJ, Tanphaichitr V, Rochette J, Robson KJ.

Hum Mol Genet. 2003 Sep 1;12(17):2241-7. Epub 2003 Jul 15.

PMID:
12915468
20.
21.

Non HFE-related haemochromatosis: exclusion of the 1q21 zinc-iron regulated transporter-like (ZIRTL) gene in juvenile haemochromatosis.

Sebastiani G, Wallace DF, Lioumi M, Goutos I, Mitchell WA, Bomford AB, Dhillon AP, Dooley JS, Ragoussis J, Walker AP.

J Hepatol. 2003 Mar;38(3):376-7. No abstract available.

PMID:
12586309
22.

Genetics of haemochromatosis.

Bomford A.

Lancet. 2002 Nov 23;360(9346):1673-81. Review.

PMID:
12457803
23.

Iron transport across cell membranes: molecular understanding of duodenal and placental iron uptake.

Srai SK, Bomford A, McArdle HJ.

Best Pract Res Clin Haematol. 2002 Jun;15(2):243-59. Review.

PMID:
12401306
24.

Down-regulation of liver iron-regulatory protein 1 in haemochromatosis.

Neonaki M, Graham DC, White KN, Bomford A.

Biochem Soc Trans. 2002 Aug;30(4):726-8.

PMID:
12196178
25.

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.

J Hepatol. 2002 Apr;36(4):474-9.

PMID:
11943417
26.

An iron-regulated ferric reductase associated with the absorption of dietary iron.

McKie AT, Barrow D, Latunde-Dada GO, Rolfs A, Sager G, Mudaly E, Mudaly M, Richardson C, Barlow D, Bomford A, Peters TJ, Raja KB, Shirali S, Hediger MA, Farzaneh F, Simpson RJ.

Science. 2001 Mar 2;291(5509):1755-9. Epub 2001 Feb 1.

27.

Hepatic expression of hepatocyte growth factor gene mRNA in acute liver failure.

Harrison P, Gove C, Bomford A.

Dig Dis Sci. 2000 Oct;45(10):1913-20.

PMID:
11117560
29.

A novel duodenal iron-regulated transporter, IREG1, implicated in the basolateral transfer of iron to the circulation.

McKie AT, Marciani P, Rolfs A, Brennan K, Wehr K, Barrow D, Miret S, Bomford A, Peters TJ, Farzaneh F, Hediger MA, Hentze MW, Simpson RJ.

Mol Cell. 2000 Feb;5(2):299-309.

30.

Mechanism of regulation of HGF/SF gene expression in fibroblasts by TGF-beta1.

Harrison P, Bradley L, Bomford A.

Biochem Biophys Res Commun. 2000 Apr 29;271(1):203-11.

PMID:
10777703
31.

The human and mouse GATA-6 genes utilize two promoters and two initiation codons.

Brewer A, Gove C, Davies A, McNulty C, Barrow D, Koutsourakis M, Farzaneh F, Pizzey J, Bomford A, Patient R.

J Biol Chem. 1999 Dec 31;274(53):38004-16.

32.

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis Consortium.

Merryweather-Clarke AT, Pointon JJ, Shearman JD, Robson KJ, Jouanolle AM, Mosser A, David V, Le Gall JY, Halsall DJ, Elsey TS, Kelly A, Cox TM, Clare M, Bomford A, Vandwalle JL, Rochette J, Borot N, Coppin H, Roth MP, Ryan E, Crowe J, Totaro A, Gasparini P, Roetto A, Walker AP, et al.

Nat Genet. 1999 Nov;23(3):271. No abstract available.

PMID:
10545942
33.

Hepatocellular carcinoma arising in the absence of cirrhosis in genetic haemochromatosis: three case reports and review of literature.

Goh J, Callagy G, McEntee G, O'Keane JC, Bomford A, Crowe J.

Eur J Gastroenterol Hepatol. 1999 Aug;11(8):915-9. Review.

PMID:
10514128
34.

Atypical haemochromatosis: phenotypic spectrum and beta2-microglobulin candidate gene analysis.

Walker AP, Wallace DF, Partridge J, Bomford AB, Dooley JS.

J Med Genet. 1999 Jul;36(7):537-41.

35.

p53 mutations in british patients with hepatocellular carcinoma: clustering in genetic hemochromatosis.

Vautier G, Bomford AB, Portmann BC, Metivier E, Williams R, Ryder SD.

Gastroenterology. 1999 Jul;117(1):154-60.

PMID:
10381922
36.

A 6p22 reference map of leukocyte DNA: exclusion of rearrangement in four cases of atypical haemochromatosis.

Wallace DF, Partridge J, Robertson A, Simpson VM, Worwood M, Bomford AB, Volz A, Ziegler A, Dooley JS, Walker AP.

Eur J Hum Genet. 1998 Sep-Oct;6(5):523-6.

37.

Hemochromatosis-related mutation detection.

Merryweather-Clarke AT, Shearman JD, Robson KJ, Pointon JJ, Liu YT, Bomford A, Dooley J, Walker AP, Worwood M.

Blood. 1998 Apr 1;91(7):2620-1. No abstract available.

38.

Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis.

Datz C, Lalloz MR, Vogel W, Graziadei I, Hackl F, Vautier G, Layton DM, Maier-Dobersberger T, Ferenci P, Penner E, Sandhofer F, Bomford A, Paulweber B.

J Hepatol. 1997 Nov;27(5):773-9.

PMID:
9382962
39.

Isolation, characterization, and functional studies of rat liver iron regulatory protein 1.

Eisenstein RS, Barton HA, Pettingell WH Jr, Bomford AB.

Arch Biochem Biophys. 1997 Jul 1;343(1):81-91.

PMID:
9210649
40.

Haemochromatosis: a gene at last?

Robson KJ, Shearman JD, Merryweather-Clarke AT, Pointon JJ, Rosenberg WM, Walker AP, Dooley JS, Bomford A, Raha-Chowdhury R, Worwood M.

J Med Genet. 1997 Feb;34(2):148-51. No abstract available.

41.

Over-expression of GATA-6 in Xenopus embryos blocks differentiation of heart precursors.

Gove C, Walmsley M, Nijjar S, Bertwistle D, Guille M, Partington G, Bomford A, Patient R.

EMBO J. 1997 Jan 15;16(2):355-68. Erratum in: EMBO J 1997 Apr 1;16(7):1806-7.

42.

A duodenal mucosal abnormality in the reduction of Fe(III) in patients with genetic haemochromatosis.

Raja KB, Pountney D, Bomford A, Przemioslo R, Sherman D, Simpson RJ, Williams R, Peters TJ.

Gut. 1996 May;38(5):765-9.

43.

Conformational analysis of pentapeptide sequences matching a proposed recognition motif for lysosomal degradation.

Gorinsky B, Laskowski RA, Lee DA, Bomford A.

Biochim Biophys Acta. 1996 Apr 16;1293(2):243-53.

PMID:
8620036
44.

Relationship between duodenal cytosolic aconitase activity and iron status in the mouse.

Rabie A, Simpson RJ, Bomford A, Cunninghame-Graham D, Peters TJ.

Biochim Biophys Acta. 1995 Dec 14;1245(3):414-20.

PMID:
8541321
45.

New polymorphic microsatellite markers place the haemochromatosis gene telomeric to D6S105.

Raha-Chowdhury R, Bowen DJ, Stone C, Pointon JJ, Terwilliger JD, Shearman JD, Robson KJ, Bomford A, Worwood M.

Hum Mol Genet. 1995 Oct;4(10):1869-74.

PMID:
8595409
46.

Hepatic and extrahepatic hepatitis C virus replication in relation to response to interferon therapy.

Saleh MG, Tibbs CJ, Koskinas J, Pereira LM, Bomford AB, Portmann BC, McFarlane IG, Williams R.

Hepatology. 1994 Dec;20(6):1399-404. Erratum in: Hepatology 1995 Mar;21(3):900.

PMID:
7982638
47.

Antibodies to atypical mycobacteria in primary biliary cirrhosis.

O'Donohue J, McFarlane B, Bomford A, Yates M, Williams R.

J Hepatol. 1994 Nov;21(5):887-9.

PMID:
7890908
48.

Metal ions catalytic for free radical reactions in the plasma of patients with fulminant hepatic failure.

Evans PJ, Evans RW, Bomford A, Williams R, Halliwell B.

Free Radic Res. 1994 Mar;20(3):139-44.

PMID:
8019638
49.

Iterative endocytosis of transferrin by K562 cells.

Young SP, Bomford A.

Biochem J. 1994 Feb 15;298 ( Pt 1):165-70.

50.

Reversibility of hypogonadotrophic hypogonadism associated with genetic haemochromatosis.

Cundy T, Butler J, Bomford A, Williams R.

Clin Endocrinol (Oxf). 1993 Jun;38(6):617-20.

PMID:
8334747

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