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Items: 34

1.

Association between relative age effect and organisational practices of American youth football.

Jones C, Visek AJ, Barron MJ, Hyman M, Chandran A.

J Sports Sci. 2019 May;37(10):1146-1153. doi: 10.1080/02640414.2018.1546545. Epub 2018 Dec 11.

PMID:
30526349
2.

Aged human skin accumulates mast cells with altered functionality that localize to macrophages and vasoactive intestinal peptide-positive nerve fibres.

Pilkington SM, Barron MJ, Watson REB, Griffiths CEM, Bulfone-Paus S.

Br J Dermatol. 2019 Apr;180(4):849-858. doi: 10.1111/bjd.17268. Epub 2018 Dec 6.

PMID:
30291626
3.

Multifactorial examination of sex-differences in head injuries and concussions among collegiate soccer players: NCAA ISS, 2004-2009.

Chandran A, Barron MJ, Westerman BJ, DiPietro L.

Inj Epidemiol. 2017 Oct 25;4(1):28. doi: 10.1186/s40621-017-0127-6.

4.

The Unfolded Protein Response in Amelogenesis and Enamel Pathologies.

Brookes SJ, Barron MJ, Dixon MJ, Kirkham J.

Front Physiol. 2017 Sep 8;8:653. doi: 10.3389/fphys.2017.00653. eCollection 2017. Review.

5.

Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stress.

Brookes SJ, Barron MJ, Smith CEL, Poulter JA, Mighell AJ, Inglehearn CF, Brown CJ, Rodd H, Kirkham J, Dixon MJ.

Hum Mol Genet. 2017 May 15;26(10):1863-1876. doi: 10.1093/hmg/ddx090.

6.

Time Trends in Incidence and Severity of Injury Among Collegiate Soccer Players in the United States: NCAA Injury Surveillance System, 1990-1996 and 2004-2009.

Chandran A, Barron MJ, Westerman BJ, DiPietro L.

Am J Sports Med. 2016 Dec;44(12):3237-3242. Epub 2016 Aug 15.

PMID:
27528613
7.

Entry mechanisms of herpes simplex virus 1 into murine epidermis: involvement of nectin-1 and herpesvirus entry mediator as cellular receptors.

Petermann P, Thier K, Rahn E, Rixon FJ, Bloch W, Özcelik S, Krummenacher C, Barron MJ, Dixon MJ, Scheu S, Pfeffer K, Knebel-Mörsdorf D.

J Virol. 2015 Jan;89(1):262-74. doi: 10.1128/JVI.02917-14. Epub 2014 Oct 15.

8.

Endoplasmic reticulum stress in amelogenesis imperfecta and phenotypic rescue using 4-phenylbutyrate.

Brookes SJ, Barron MJ, Boot-Handford R, Kirkham J, Dixon MJ.

Hum Mol Genet. 2014 May 1;23(9):2468-80. doi: 10.1093/hmg/ddt642. Epub 2013 Dec 20.

9.

Perfusion flow enhances osteogenic gene expression and the infiltration of osteoblasts and endothelial cells into three-dimensional calcium phosphate scaffolds.

Barron MJ, Goldman J, Tsai CJ, Donahue SW.

Int J Biomater. 2012;2012:915620. doi: 10.1155/2012/915620. Epub 2012 Sep 4.

10.

Phenotype-genotype correlations in mouse models of amelogenesis imperfecta caused by Amelx and Enam mutations.

Coxon TL, Brook AH, Barron MJ, Smith RN.

Cells Tissues Organs. 2012;196(5):420-30. doi: 10.1159/000336440. Epub 2012 Jun 28.

11.

Is the 32-kDa fragment the functional enamelin unit in all species?

Brookes SJ, Kingswell NJ, Barron MJ, Dixon MJ, Kirkham J.

Eur J Oral Sci. 2011 Dec;119 Suppl 1:345-50. doi: 10.1111/j.1600-0722.2011.00869.x.

12.

Differences in the accumulation of mitochondrial defects with age in mice and humans.

Greaves LC, Barron MJ, Campbell-Shiel G, Kirkwood TB, Turnbull DM.

Mech Ageing Dev. 2011 Nov-Dec;132(11-12):588-91. doi: 10.1016/j.mad.2011.10.004. Epub 2011 Oct 12.

PMID:
22015485
13.

Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome.

O'Sullivan J, Bitu CC, Daly SB, Urquhart JE, Barron MJ, Bhaskar SS, Martelli-Júnior H, dos Santos Neto PE, Mansilla MA, Murray JC, Coletta RD, Black GC, Dixon MJ.

Am J Hum Genet. 2011 May 13;88(5):616-20. doi: 10.1016/j.ajhg.2011.04.005. Epub 2011 May 5.

14.

CASE 3-2010 Dynamic partial obstruction of the tricuspid valve inlet produced by anterior mediastinal aspergillosis invading the right atrium.

Hansen TN, Plambeck CJ, Barron MJ, Pagel PS, DeAnda A, Neustein S.

J Cardiothorac Vasc Anesth. 2010 Jun;24(3):506-12. doi: 10.1053/j.jvca.2010.02.022. No abstract available.

PMID:
20510248
15.

Mechanical stimulation mediates gene expression in MC3T3 osteoblastic cells differently in 2D and 3D environments.

Barron MJ, Tsai CJ, Donahue SW.

J Biomech Eng. 2010 Apr;132(4):041005. doi: 10.1115/1.4001162.

PMID:
20387968
16.

Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO.

Greaves LC, Yu-Wai-Man P, Blakely EL, Krishnan KJ, Beadle NE, Kerin J, Barron MJ, Griffiths PG, Dickinson AJ, Turnbull DM, Taylor RW.

Invest Ophthalmol Vis Sci. 2010 Jul;51(7):3340-6. doi: 10.1167/iovs.09-4659. Epub 2010 Feb 17.

17.

Defects in multiple complexes of the respiratory chain are present in ageing human colonic crypts.

Greaves LC, Barron MJ, Plusa S, Kirkwood TB, Mathers JC, Taylor RW, Turnbull DM.

Exp Gerontol. 2010 Aug;45(7-8):573-9. doi: 10.1016/j.exger.2010.01.013. Epub 2010 Jan 22.

18.

A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta.

Barron MJ, Brookes SJ, Kirkham J, Shore RC, Hunt C, Mironov A, Kingswell NJ, Maycock J, Shuttleworth CA, Dixon MJ.

Hum Mol Genet. 2010 Apr 1;19(7):1230-47. doi: 10.1093/hmg/ddq001. Epub 2010 Jan 12.

19.

Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia.

Barron MJ, McDonnell ST, Mackie I, Dixon MJ.

Orphanet J Rare Dis. 2008 Nov 20;3:31. doi: 10.1186/1750-1172-3-31. Review.

20.

Novel mutations in GJA1 cause oculodentodigital syndrome.

Fenwick A, Richardson RJ, Butterworth J, Barron MJ, Dixon MJ.

J Dent Res. 2008 Nov;87(11):1021-6.

21.

The cell adhesion molecule nectin-1 is critical for normal enamel formation in mice.

Barron MJ, Brookes SJ, Draper CE, Garrod D, Kirkham J, Shore RC, Dixon MJ.

Hum Mol Genet. 2008 Nov 15;17(22):3509-20. doi: 10.1093/hmg/ddn243. Epub 2008 Aug 14.

22.

Gastrointestinal tract involvement associated with the 3243A>G mitochondrial DNA mutation.

Betts J, Barron MJ, Needham SJ, Schaefer AM, Taylor RW, Turnbull DM.

Neurology. 2008 Apr 8;70(15):1290-2. doi: 10.1212/01.wnl.0000308940.38092.74. No abstract available.

PMID:
18391161
23.

Time-loss and non-time-loss injuries in youth football players.

Dompier TP, Powell JW, Barron MJ, Moore MT.

J Athl Train. 2007 Jul-Sep;42(3):395-402.

24.

Validation of a noninvasive maturity estimate relative to skeletal age in youth football players.

Malina RM, Dompier TP, Powell JW, Barron MJ, Moore MT.

Clin J Sport Med. 2007 Sep;17(5):362-8.

PMID:
17873548
25.

Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions.

Taivassalo T, Gardner JL, Taylor RW, Schaefer AM, Newman J, Barron MJ, Haller RG, Turnbull DM.

Brain. 2006 Dec;129(Pt 12):3391-401. Epub 2006 Nov 3.

PMID:
17085458
26.

Mitochondrial DNA mutations are established in human colonic stem cells, and mutated clones expand by crypt fission.

Greaves LC, Preston SL, Tadrous PJ, Taylor RW, Barron MJ, Oukrif D, Leedham SJ, Deheragoda M, Sasieni P, Novelli MR, Jankowski JA, Turnbull DM, Wright NA, McDonald SA.

Proc Natl Acad Sci U S A. 2006 Jan 17;103(3):714-9. Epub 2006 Jan 6.

27.

Cytochrome c oxidase deficient muscle fibres: substantial variation in their proportions within skeletal muscles from patients with mitochondrial myopathy.

Barron MJ, Chinnery PF, Howel D, Blakely EL, Schaefer AM, Taylor RW, Turnbull DM.

Neuromuscul Disord. 2005 Nov;15(11):768-74. Epub 2005 Sep 28.

PMID:
16198107
28.

Familial myopathy: new insights into the T14709C mitochondrial tRNA mutation.

McFarland R, Schaefer AM, Gardner JL, Lynn S, Hayes CM, Barron MJ, Walker M, Chinnery PF, Taylor RW, Turnbull DM.

Ann Neurol. 2004 Apr;55(4):478-84.

PMID:
15048886
29.

The diagnosis of mitochondrial muscle disease.

Taylor RW, Schaefer AM, Barron MJ, McFarland R, Turnbull DM.

Neuromuscul Disord. 2004 Apr;14(4):237-45. Review.

PMID:
15019701
30.
31.

Mitochondrial DNA mutations in human colonic crypt stem cells.

Taylor RW, Barron MJ, Borthwick GM, Gospel A, Chinnery PF, Samuels DC, Taylor GA, Plusa SM, Needham SJ, Greaves LC, Kirkwood TB, Turnbull DM.

J Clin Invest. 2003 Nov;112(9):1351-60.

32.

A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.

Taylor RW, Giordano C, Davidson MM, d'Amati G, Bain H, Hayes CM, Leonard H, Barron MJ, Casali C, Santorelli FM, Hirano M, Lightowlers RN, DiMauro S, Turnbull DM.

J Am Coll Cardiol. 2003 May 21;41(10):1786-96.

33.

Mitochondrial abnormalities in ageing macular photoreceptors.

Barron MJ, Johnson MA, Andrews RM, Clarke MP, Griffiths PG, Bristow E, He LP, Durham S, Turnbull DM.

Invest Ophthalmol Vis Sci. 2001 Nov;42(12):3016-22.

PMID:
11687550
34.

Influence of electrical stimulation of the tibialis anterior muscle in paraplegic subjects. 2. Morphological and histochemical properties.

Rochester L, Barron MJ, Chandler CS, Sutton RA, Miller S, Johnson MA.

Paraplegia. 1995 Sep;33(9):514-22.

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