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Items: 1 to 50 of 124

1.

PD-L1 and calcitriol dependent liposomal antigen-specific regulation of systemic inflammatory autoimmune disease.

Galea R, Nel H, Talekar M, Liu X, Ooi JD, Huynh M, Hadjigol S, Robson KJ, Ting YT, Cole S, Cochlin K, Hitchcock S, Zeng B, Yekollu S, Boks M, Goh N, Roberts H, Rossjohn J, Reid HH, Boyd BJ, Malaviya R, Shealy DJ, Baker DG, Madakamutil L, Kitching AR, O'Sullivan BJ, Thomas R.

JCI Insight. 2019 Sep 5. pii: 126025. doi: 10.1172/jci.insight.126025. [Epub ahead of print]

2.

Scientific Business Abstracts of the 112th Annual Meeting of the Association of Physicians of Great Britain and Ireland.

Chauhan A, Lalor T, Watson S, Adams D, Farrah TE, Anand A, Kimmitt R, Mills NL, Webb DJ, Dhaun N, Kalla R, Adams A, Vatn S, Bonfliglio F, Nimmo E, Kennedy N, Ventham N, Vatn M, Ricanek P, Halfvarson J, Soderhollm J, Pierik M, Torkvist L, Gomollon F, Gut I, Jahnsen J, Satsangi J, Body R, Almashali M, McDowell G, Taylor P, Lacey A, Rees A, Dayan C, Lazarus J, Nelson S, Okosieme O, Corcoran D, Young R, Ciadella P, McCartney P, Bajrangee A, Hennigan B, Collison D, Carrick D, Shaukat A, Good R, Watkins S, McEntegart M, Watt J, Welsh P, Sattar N, McConnachie A, Oldroyd K, Berry C, Parks T, Auckland K, Mentzer AJ, Kado J, Mirabel MM, Kauwe JK, Robson KJ, Mittal B, Steer AC, Hill AVS, Akbar M, Forrester M, Virlan AT, Gilmour A, Wallace C, Paterson C, Reid D, Siebert S, Porter D, Liversidge J, McInnes I, Goodyear C, Athwal V, Pritchett J, Zaitoun A, Irving W, Guha IN, Hanley NA, Hanley KP, Briggs T, Reynolds J, Rice G, Bondet V, Bruce E, Crow Y, Duffy D, Parker B, Bruce I, Martin K, Pritchett J, Aoibheann Mullan M, Llewellyn J, Athwal V, Zeef L, Farrow S, Streuli C, Henderson N, Friedman S, Hanley N, Hanley KP.

QJM. 2018 Dec 1;111(12):920-924. doi: 10.1093/qjmed/hcy193. No abstract available.

PMID:
31222346
3.

HLA and kidney disease: from associations to mechanisms.

Robson KJ, Ooi JD, Holdsworth SR, Rossjohn J, Kitching AR.

Nat Rev Nephrol. 2018 Oct;14(10):636-655. doi: 10.1038/s41581-018-0057-8. Review.

PMID:
30206339
4.

Language continuity despite population replacement in Remote Oceania.

Posth C, Nägele K, Colleran H, Valentin F, Bedford S, Kami KW, Shing R, Buckley H, Kinaston R, Walworth M, Clark GR, Reepmeyer C, Flexner J, Maric T, Moser J, Gresky J, Kiko L, Robson KJ, Auckland K, Oppenheimer SJ, Hill AVS, Mentzer AJ, Zech J, Petchey F, Roberts P, Jeong C, Gray RD, Krause J, Powell A.

Nat Ecol Evol. 2018 Apr;2(4):731-740. doi: 10.1038/s41559-018-0498-2. Epub 2018 Feb 27.

5.

Thrombotic microangiopathy associated with intravenous injection of extended-release oxycodone.

Robson KJ, Clucas D, Filshie R, Nandurkar H.

BMJ Case Rep. 2017 Jul 17;2017. pii: bcr-2017-220977. doi: 10.1136/bcr-2017-220977.

6.

Association between a common immunoglobulin heavy chain allele and rheumatic heart disease risk in Oceania.

Parks T, Mirabel MM, Kado J, Auckland K, Nowak J, Rautanen A, Mentzer AJ, Marijon E, Jouven X, Perman ML, Cua T, Kauwe JK, Allen JB, Taylor H, Robson KJ, Deane CM, Steer AC, Hill AVS; Pacific Islands Rheumatic Heart Disease Genetics Network.

Nat Commun. 2017 May 11;8:14946. doi: 10.1038/ncomms14946.

7.

Henoch-Schönlein purpura following Yersinia enterocolitica infection.

Ngu K, Robson KJ, Goodman DJ.

Med J Aust. 2017 Mar 6;206(4):160. No abstract available.

PMID:
28253462
8.

Distinct gene expression program dynamics during erythropoiesis from human induced pluripotent stem cells compared with adult and cord blood progenitors.

Merryweather-Clarke AT, Tipping AJ, Lamikanra AA, Fa R, Abu-Jamous B, Tsang HP, Carpenter L, Robson KJ, Nandi AK, Roberts DJ.

BMC Genomics. 2016 Oct 21;17(1):817.

9.

Phase-contrast and magnification radiography at diagnostic X-ray energies using a pseudo-microfocus X-ray source.

Kotre CJ, Robson KJ.

Br J Radiol. 2014 Jul;87(1039):20130734. doi: 10.1259/bjr.20130734. Epub 2014 Apr 29.

10.

Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.

Breuss M, Heng JI, Poirier K, Tian G, Jaglin XH, Qu Z, Braun A, Gstrein T, Ngo L, Haas M, Bahi-Buisson N, Moutard ML, Passemard S, Verloes A, Gressens P, Xie Y, Robson KJ, Rani DS, Thangaraj K, Clausen T, Chelly J, Cowan NJ, Keays DA.

Cell Rep. 2012 Dec 27;2(6):1554-62. doi: 10.1016/j.celrep.2012.11.017. Epub 2012 Dec 13.

11.

Global gene expression analysis of human erythroid progenitors.

Merryweather-Clarke AT, Atzberger A, Soneji S, Gray N, Clark K, Waugh C, McGowan SJ, Taylor S, Nandi AK, Wood WG, Roberts DJ, Higgs DR, Buckle VJ, Robson KJ.

Blood. 2011 Mar 31;117(13):e96-108. doi: 10.1182/blood-2010-07-290825. Epub 2011 Jan 26. Erratum in: Blood. 2011 Dec 22;118(26):6993.

12.

Factors influencing disease phenotype and penetrance in HFE haemochromatosis.

Rochette J, Le Gac G, Lassoued K, Férec C, Robson KJ.

Hum Genet. 2010 Sep;128(3):233-48. doi: 10.1007/s00439-010-0852-1. Epub 2010 Jul 6. Review.

PMID:
20607553
13.

Advances in mammographic imaging.

Robson KJ.

Br J Radiol. 2010 Apr;83(988):273-5. doi: 10.1259/bjr/97865299. Epub 2010 Mar 11.

14.

In vitro binding of HFE to the cation-independent mannose-6 phosphate receptor.

Schimanski LM, Drakesmith H, Sweetland E, Bastin J, Rezgui D, Edelmann M, Kessler B, Merryweather-Clarke AT, Robson KJ, Townsend AR.

Blood Cells Mol Dis. 2009 Sep-Oct;43(2):180-93. doi: 10.1016/j.bcmd.2009.03.010. Epub 2009 May 31.

PMID:
19487139
15.

A novel HFE mutation (c.del478) results in nonsense-mediated decay of the mutant transcript in a hemochromatosis patient.

Pointon JJ, Lok CY, Shearman JD, Suckling RJ, Rochette J, Merryweather-Clarke AT, Robson KJ.

Blood Cells Mol Dis. 2009 Sep-Oct;43(2):194-8. doi: 10.1016/j.bcmd.2009.04.007. Epub 2009 May 24.

PMID:
19477142
16.

Iron overload in the Asian community.

Lok CY, Merryweather-Clarke AT, Viprakasit V, Chinthammitr Y, Srichairatanakool S, Limwongse C, Oleesky D, Robins AJ, Hudson J, Wai P, Premawardhena A, de Silva HJ, Dassanayake A, McKeown C, Jackson M, Gama R, Khan N, Newman W, Banait G, Chilton A, Wilson-Morkeh I, Weatherall DJ, Robson KJ.

Blood. 2009 Jul 2;114(1):20-5. doi: 10.1182/blood-2009-01-199109. Epub 2009 Apr 2.

17.

Malarial anemia and STAT6.

Robson KJ, Weatherall DJ.

Haematologica. 2009 Feb;94(2):157-9. doi: 10.3324/haematol.2008.002311. Review. No abstract available.

18.

An investigation into the effects of suboptimal viewing conditions in screen-film mammography.

Robson KJ.

Br J Radiol. 2008 Mar;81(963):219-31. doi: 10.1259/bjr/16470646.

PMID:
18270296
19.
20.

Iron genes, iron load and risk of Alzheimer's disease.

Lehmann DJ, Worwood M, Ellis R, Wimhurst VL, Merryweather-Clarke AT, Warden DR, Smith AD, Robson KJ.

J Med Genet. 2006 Oct;43(10):e52.

21.

The Thrombospondin-related Protein Family of Apicomplexan Parasites: The Gears of the Cell Invasion Machinery.

Naitza S, Spano F, Robson KJ, Crisanti A.

Parasitol Today. 1998 Dec;14(12):479-84.

PMID:
17040860
22.

Cellular reactivity to the p. Falciparum protein trap in adult kenyans: novel epitopes, complex cytokine patterns, and the impact of natural antigenic variation.

Flanagan KL, Plebanski M, Odhiambo K, Sheu E, Mwangi T, Gelder C, Hart K, Kortok M, Lowe B, Robson KJ, Marsh K, Hill AV.

Am J Trop Med Hyg. 2006 Mar;74(3):367-75.

PMID:
16525093
23.

Gene symbol: DCYTB/CYBRD1. Disease: primary iron overload.

Zaahl MG, Merryweather-Clarke AT, Kotze MJ, van der Merwe S, Warnich L, Robson KJ.

Hum Genet. 2005 Dec;118(3-4):549. No abstract available.

PMID:
16521312
24.

Gene symbol: DCYTB/CYBRD1. Disease: primary iron overload.

Zaahl MG, Merryweather-Clarke AT, Kotze MJ, van der Merwe S, Warnich L, Robson KJ.

Hum Genet. 2005 Dec;118(3-4):548-9. No abstract available.

PMID:
16521311
25.

Gene symbol: SLC40A1. Disease: primary iron overload.

Zaahl MG, Merryweather-Clarke AT, Kotze MJ, van der Merwe S, Warnich L, Robson KJ.

Hum Genet. 2005 Dec;118(3-4):547. No abstract available.

PMID:
16521305
26.

Gene symbol: DCYTB/CYBRD1. Disease: primary iron overload.

Zaahl MG, Merryweather-Clarke AT, Kotze MJ, van der Merwe S, Warnich L, Robson KJ.

Hum Genet. 2005 Dec;118(3-4):546. No abstract available.

PMID:
16521301
27.

Pilot study into optimisation of viewing conditions for electronically displayed images.

Robson KJ, Kotre CJ.

Radiat Prot Dosimetry. 2005;117(1-3):298-303. Epub 2006 Feb 3.

PMID:
16461502
28.

Multifactorial iron man.

Robson KJ, Drakesmith H.

Digestion. 2005;72(1):22-4. Epub 2005 Aug 10. No abstract available.

29.

Gene symbol: SLC40A1. Disease: Primary iron overload.

Zaahl MG, Merryweather-Clarke AT, Kotze MJ, van der Merwe S, Warnich L, Robson KJ.

Hum Genet. 2005 May;116(6):541. No abstract available.

PMID:
15991323
30.

Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?

Cadet E, Capron D, Gallet M, Omanga-Léké ML, Boutignon H, Julier C, Robson KJ, Rochette J.

J Med Genet. 2005 May;42(5):390-5.

31.

Resistance to hepcidin is conferred by hemochromatosis-associated mutations of ferroportin.

Drakesmith H, Schimanski LM, Ormerod E, Merryweather-Clarke AT, Viprakasit V, Edwards JP, Sweetland E, Bastin JM, Cowley D, Chinthammitr Y, Robson KJ, Townsend AR.

Blood. 2005 Aug 1;106(3):1092-7. Epub 2005 Apr 14.

32.

In vitro functional analysis of human ferroportin (FPN) and hemochromatosis-associated FPN mutations.

Schimanski LM, Drakesmith H, Merryweather-Clarke AT, Viprakasit V, Edwards JP, Sweetland E, Bastin JM, Cowley D, Chinthammitr Y, Robson KJ, Townsend AR.

Blood. 2005 May 15;105(10):4096-102. Epub 2005 Feb 3.

33.

Inverse associations of human leukocyte antigen and malaria parasite types in two West African populations.

Young K, Frodsham A, Doumbo OK, Gupta S, Dolo A, Hu JT, Robson KJ, Crisanti A, Hill AV, Gilbert SC.

Infect Immun. 2005 Feb;73(2):953-5.

34.

Mammographic image restoration using maximum entropy deconvolution.

Jannetta A, Jackson JC, Kotre CJ, Birch IP, Robson KJ, Padgett R.

Phys Med Biol. 2004 Nov 7;49(21):4997-5010.

PMID:
15584533
35.

Recent advances in understanding haemochromatosis: a transition state.

Robson KJ, Merryweather-Clarke AT, Cadet E, Viprakasit V, Zaahl MG, Pointon JJ, Weatherall DJ, Rochette J.

J Med Genet. 2004 Oct;41(10):721-30. Review. Erratum in: J Med Genet. 2004 Dec;41(12):959.

36.

Analysis of genes implicated in iron regulation in individuals presenting with primary iron overload.

Zaahl MG, Merryweather-Clarke AT, Kotze MJ, van der Merwe S, Warnich L, Robson KJ.

Hum Genet. 2004 Oct;115(5):409-17. Epub 2004 Aug 24.

PMID:
15338274
37.

The origin and spread of the HFE-C282Y haemochromatosis mutation.

Distante S, Robson KJ, Graham-Campbell J, Arnaiz-Villena A, Brissot P, Worwood M.

Hum Genet. 2004 Sep;115(4):269-79.

PMID:
15290237
38.

Application of low dose rate pulsed fluoroscopy in cardiac pacing and electrophysiology: patient dose and image quality implications.

Kotre CJ, Charlton S, Robson KJ, Birch IP, Willis SP, Thornley M.

Br J Radiol. 2004 Jul;77(919):597-9.

PMID:
15238407
39.

Expression of the SLC11A1 (NRAMP1) 5'-(GT)n repeat: opposite effect in the presence of -237C-->T.

Zaahl MG, Robson KJ, Warnich L, Kotze MJ.

Blood Cells Mol Dis. 2004 Jul-Aug;33(1):45-50.

PMID:
15223010
40.

Hepcidin and its role in iron absorption.

Robson KJ.

Gut. 2004 May;53(5):617-9. Review.

41.

Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease.

Robson KJ, Lehmann DJ, Wimhurst VL, Livesey KJ, Combrinck M, Merryweather-Clarke AT, Warden DR, Smith AD.

J Med Genet. 2004 Apr;41(4):261-5.

42.

The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading.

Livesey KJ, Wimhurst VL, Carter K, Worwood M, Cadet E, Rochette J, Roberts AG, Pointon JJ, Merryweather-Clarke AT, Bassett ML, Jouanolle AM, Mosser A, David V, Poulton J, Robson KJ.

J Med Genet. 2004 Jan;41(1):6-10.

43.

A Plasmodium falciparum candidate vaccine based on a six-antigen polyprotein encoded by recombinant poxviruses.

Prieur E, Gilbert SC, Schneider J, Moore AC, Sheu EG, Goonetilleke N, Robson KJ, Hill AV.

Proc Natl Acad Sci U S A. 2004 Jan 6;101(1):290-5. Epub 2003 Dec 23.

44.

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
45.

Hemochromatosis gene (HFE) mutations in South East Asia: a potential for iron overload.

Pointon JJ, Viprakasit V, Miles KL, Livesey KJ, Steiner M, O'Riordan S, Hien TT, Merryweather-Clarke AT, Robson KJ.

Blood Cells Mol Dis. 2003 May-Jun;30(3):302-6.

PMID:
12737949
46.

A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosis.

Cadet E, Capron D, Perez AS, Crépin SN, Arlot S, Ducroix JP, Dautréaux M, Fardellone P, Leflon P, Merryweather-Clarke AT, Livesey KJ, Pointon JJ, Rose P, Harcourt J, Emery J, Sueur JM, Feyt R, Robson KJ, Rochette J.

J Intern Med. 2003 Feb;253(2):217-24.

47.

A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4.

Roetto A, Merryweather-Clarke AT, Daraio F, Livesey K, Pointon JJ, Barbabietola G, Piga A, Mackie PH, Robson KJ, Camaschella C.

Blood. 2002 Jul 15;100(2):733-4. No abstract available.

48.
49.

Eruptive vellus hair cysts presenting as multiple periorbital papules in a 13-year-old boy.

Reep MD, Robson KJ.

Pediatr Dermatol. 2002 Jan-Feb;19(1):26-7.

PMID:
11860565
50.

A prime-boost immunisation regimen using DNA followed by recombinant modified vaccinia virus Ankara induces strong cellular immune responses against the Plasmodium falciparum TRAP antigen in chimpanzees.

Schneider J, Langermans JA, Gilbert SC, Blanchard TJ, Twigg S, Naitza S, Hannan CM, Aidoo M, Crisanti A, Robson KJ, Smith GL, Hill AV, Thomas AW.

Vaccine. 2001 Sep 14;19(32):4595-602.

PMID:
11535306

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