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    Results: 16

    1.

    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. Review.PMID: 19021896 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    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.PMID: 18946008 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    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. Epub 2008 Aug 14.PMID: 18703497 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    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. No abstract available. PMID: 18391161 [PubMed - indexed for MEDLINE]Related articles

    5.

    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.PMID: 18059996 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    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 [PubMed - indexed for MEDLINE]Related articles

    7.

    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 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    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.PMID: 16407113 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    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 [PubMed - indexed for MEDLINE]Related articles

    10.

    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 [PubMed - indexed for MEDLINE]Related articles

    11.

    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 [PubMed - indexed for MEDLINE]Related articles

    12.

    The distributions of mitochondria and sodium channels reflect the specific energy requirements and conduction properties of the human optic nerve head.

    Barron MJ, Griffiths P, Turnbull DM, Bates D, Nichols P.

    Br J Ophthalmol. 2004 Feb;88(2):286-90.PMID: 14736793 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    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.PMID: 14597761 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    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.PMID: 12767666 [PubMed - indexed for MEDLINE]Related articles

    15.

    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 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    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.PMID: 8524604 [PubMed - indexed for MEDLINE]Related articles

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