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Items: 1 to 50 of 169

1.

Infographic: Injury and illness, the 2016 Olympic Games.

Soligard T, Steffen K, Palmer D, Alonso JM, Bahr R, Lopes AD, Dvorak J, Grant ME, Meeuwisse W, Mountjoy M, Costa LOP, Salmina N, Budgett R, Engebretsen L.

Br J Sports Med. 2019 Apr;53(7):404-405. doi: 10.1136/bjsports-2018-099090. Epub 2018 Feb 10. No abstract available.

PMID:
29440038
2.

Sports injury and illness incidence in the Rio de Janeiro 2016 Olympic Summer Games: A prospective study of 11274 athletes from 207 countries.

Soligard T, Steffen K, Palmer D, Alonso JM, Bahr R, Lopes AD, Dvorak J, Grant ME, Meeuwisse W, Mountjoy M, Pena Costa LO, Salmina N, Budgett R, Engebretsen L.

Br J Sports Med. 2017 Sep;51(17):1265-1271. doi: 10.1136/bjsports-2017-097956. Epub 2017 Jul 29.

PMID:
28756389
3.

Sports injuries and illnesses in the Sochi 2014 Olympic Winter Games.

Soligard T, Steffen K, Palmer-Green D, Aubry M, Grant ME, Meeuwisse W, Mountjoy M, Budgett R, Engebretsen L.

Br J Sports Med. 2015 Apr;49(7):441-7. doi: 10.1136/bjsports-2014-094538. Epub 2015 Jan 28.

PMID:
25631542
4.

Using criteria-based interview models for assessing clinical expertise to select physiotherapists at major multisport games.

Phillips N, Grant ME, Booth L, Glasgow P.

Br J Sports Med. 2015 Mar;49(5):312-7. doi: 10.1136/bjsports-2014-094176. Epub 2015 Jan 6.

PMID:
25564006
5.

The role of sports physiotherapy at the London 2012 Olympic Games.

Grant ME, Steffen K, Glasgow P, Phillips N, Booth L, Galligan M.

Br J Sports Med. 2014 Jan;48(1):63-70. doi: 10.1136/bjsports-2013-093169.

PMID:
24334506
6.

Online virtual patients - A driver for change in medical and healthcare professional education in developing countries?

Dewhurst D, Borgstein E, Grant ME, Begg M.

Med Teach. 2009 Aug;31(8):721-4.

PMID:
19811208
7.

The epigenetic origins of mental retardation.

Grant ME.

Clin Genet. 2008 Jun;73(6):528-30. doi: 10.1111/j.1399-0004.2008.00979_1.x. Epub 2008 Apr 22. Review. No abstract available.

PMID:
18435797
8.

Severe hyponatremia and Schmidt's syndrome.

Wehbe E, Grant ME.

Clin Exp Nephrol. 2008 Jun;12(3):211-4. doi: 10.1007/s10157-008-0035-8. Epub 2008 Feb 20. Review.

PMID:
18283521
9.

From collagen chemistry towards cell therapy - a personal journey.

Grant ME.

Int J Exp Pathol. 2007 Aug;88(4):203-14. Review.

10.

Apoptosis of terminal hypertrophic chondrocytes in an in vitro model of endochondral ossification.

Cheung JO, Grant ME, Jones CJ, Hoyland JA, Freemont AJ, Hillarby MC.

J Pathol. 2003 Nov;201(3):496-503.

PMID:
14595763
11.

An enhancer complex confers both high-level and cell-specific expression of the human type X collagen gene.

Chambers D, Young DA, Howard C, Thomas JT, Boam DS, Grant ME, Wallis GA, Boot-Handford RP.

FEBS Lett. 2002 Nov 20;531(3):505-8.

12.

Blood analysis at the point of care: issues in application for use in critically ill patients.

Giuliano KK, Grant ME.

AACN Clin Issues. 2002 May;13(2):204-20. Review.

PMID:
12011593
13.

Coordinated expression of matrix Gla protein is required during endochondral ossification for chondrocyte survival.

Newman B, Gigout LI, Sudre L, Grant ME, Wallis GA.

J Cell Biol. 2001 Aug 6;154(3):659-66.

14.

Mutations in the region encoding the von Willebrand factor A domain of matrilin-3 are associated with multiple epiphyseal dysplasia.

Chapman KL, Mortier GR, Chapman K, Loughlin J, Grant ME, Briggs MD.

Nat Genet. 2001 Aug;28(4):393-6.

PMID:
11479597
15.

A novel cell culture model of chondrocyte differentiation during mammalian endochondral ossification.

Cheung JO, Hillarby MC, Ayad S, Hoyland JA, Jones CJ, Denton J, Thomas JT, Wallis GA, Grant ME.

J Bone Miner Res. 2001 Feb;16(2):309-18.

16.

Matrix Gla protein is differentially expressed during the deposition of a calcified matrix by vascular pericytes.

Canfield AE, Doherty MJ, Kelly V, Newman B, Farrington C, Grant ME, Boot-Handford RP.

FEBS Lett. 2000 Dec 29;487(2):267-71.

17.

Cartilage oligomeric matrix protein interacts with type IX collagen, and disruptions to these interactions identify a pathogenetic mechanism in a bone dysplasia family.

Holden P, Meadows RS, Chapman KL, Grant ME, Kadler KE, Briggs MD.

J Biol Chem. 2001 Feb 23;276(8):6046-55. Epub 2000 Nov 21.

18.
19.

Identification of genes expressed during the osteogenic differentiation of vascular pericytes in vitro.

Doherty M, Boot-Handford RP, Grant ME, Canfield AE.

Biochem Soc Trans. 1998 Feb;26(1):S4. No abstract available.

PMID:
10909762
20.

The ribosomal protein QM is expressed differentially during vertebrate endochondral bone development.

Green H, Canfield AE, Hillarby MC, Grant ME, Boot-Handford RP, Freemont AJ, Wallis GA.

J Bone Miner Res. 2000 Jun;15(6):1066-75.

21.

Role of pericytes in vascular calcification: a review.

Canfield AE, Doherty MJ, Wood AC, Farrington C, Ashton B, Begum N, Harvey B, Poole A, Grant ME, Boot-Handford RP.

Z Kardiol. 2000;89 Suppl 2:20-7. Review.

PMID:
10769400
22.

Identification of novel pro-alpha2(IX) collagen gene mutations in two families with distinctive oligo-epiphyseal forms of multiple epiphyseal dysplasia.

Holden P, Canty EG, Mortier GR, Zabel B, Spranger J, Carr A, Grant ME, Loughlin JA, Briggs MD.

Am J Hum Genet. 1999 Jul;65(1):31-8.

23.

The bcl-2 knockout mouse exhibits marked changes in osteoblast phenotype and collagen deposition in bone as well as a mild growth plate phenotype.

Boot-Handford RP, Michaelidis TM, Hillarby MC, Zambelli A, Denton J, Hoyland JA, Freemont AJ, Grant ME, Wallis GA.

Int J Exp Pathol. 1998 Oct;79(5):329-35.

24.

Vascular pericytes express osteogenic potential in vitro and in vivo.

Doherty MJ, Ashton BA, Walsh S, Beresford JN, Grant ME, Canfield AE.

J Bone Miner Res. 1998 May;13(5):828-38.

25.

The expression of types X and VI collagen and fibrillin in rat mandibular condylar cartilage. Response to mastication forces.

Salo LA, Hoyland J, Ayad S, Kielty CM, Freemont A, Pirttiniemi P, Kantomaa T, Grant ME, Thomas JT.

Acta Odontol Scand. 1996 Oct;54(5):295-302.

PMID:
8923923
26.

Localization of gene expression during endochondral ossification.

Hillarby MC, King KE, Brady G, Grant ME, Wallis GA, Boot-Handford RP.

Ann N Y Acad Sci. 1996 Jun 8;785:263-6. No abstract available.

PMID:
8702149
27.

Sequence elements within intron 1 of the human collagen X gene do not contribute to the regulation of gene expression.

Chambers D, Thomas JT, Boam D, Wallis GA, Grant ME, Boot-Handford RP.

Ann N Y Acad Sci. 1996 Jun 8;785:227-30. No abstract available.

PMID:
8702136
28.

Mutations within the gene encoding the alpha 1 (X) chain of type X collagen (COL10A1) cause metaphyseal chondrodysplasia type Schmid but not several other forms of metaphyseal chondrodysplasia.

Wallis GA, Rash B, Sykes B, Bonaventure J, Maroteaux P, Zabel B, Wynne-Davies R, Grant ME, Boot-Handford RP.

J Med Genet. 1996 Jun;33(6):450-7.

29.

Sequence comparison of three mammalian type-X collagen promoters and preliminary functional analysis of the human promoter.

Thomas JT, Sweetman WA, Cresswell CJ, Wallis GA, Grant ME, Boot-Handford RP.

Gene. 1995 Jul 28;160(2):291-6.

PMID:
7642113
30.

The complete cDNA derived sequence of the rat prolyl 4-hydroxylase alpha subunit.

Hopkinson I, Smith SA, Donne A, Gregory H, Franklin TJ, Grant ME, Rosamond J.

Gene. 1994 Nov 18;149(2):391-2.

PMID:
7959029
31.

Cartilage collagens: strategies for the study of their organisation and expression in the extracellular matrix.

Thomas JT, Ayad S, Grant ME.

Ann Rheum Dis. 1994 Aug;53(8):488-96. Review. No abstract available.

33.
34.

Distribution of the matrix metalloproteinases stromelysin, gelatinases A and B, and collagenase in Crohn's disease and normal intestine.

Bailey CJ, Hembry RM, Alexander A, Irving MH, Grant ME, Shuttleworth CA.

J Clin Pathol. 1994 Feb;47(2):113-6.

35.

Intron-exon structure, alternative use of promoter and expression of the mouse collagen X gene, Col10a-1.

Kong RY, Kwan KM, Lau ET, Thomas JT, Boot-Handford RP, Grant ME, Cheah KS.

Eur J Biochem. 1993 Apr 1;213(1):99-111.

37.

Microfibrillar assemblies of foetal bovine skin. Developmental expression and relative abundance of type VI collagen and fibrillin.

Kielty CM, Berry L, Whittaker SP, Grant ME, Shuttleworth CA.

Matrix. 1993 Mar;13(2):103-12.

PMID:
8492740
40.

The financial and clinical impact of redraws due to inadequate heelstick.

Grant ME, Mueller R.

Neonatal Intensive Care. 1993 Jan-Feb;6(1):23-6. No abstract available.

PMID:
10148082
41.

Attachment of human vascular smooth muscles cells to intact microfibrillar assemblies of collagen VI and fibrillin.

Kielty CM, Whittaker SP, Grant ME, Shuttleworth CA.

J Cell Sci. 1992 Oct;103 ( Pt 2):445-51.

42.

SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasia.

Sweetman WA, Rash B, Sykes B, Beighton P, Hecht JT, Zabel B, Thomas JT, Boot-Handford R, Grant ME, Wallis GA.

Am J Hum Genet. 1992 Oct;51(4):841-9.

43.
44.

Aortic endothelial cell heterogeneity in vitro. Lack of association between morphological phenotype and collagen biosynthesis.

Canfield AE, Wren FE, Schor SL, Grant ME, Schor AM.

J Cell Sci. 1992 Aug;102 ( Pt 4):807-14.

45.

Type VI collagen microfibrils: evidence for a structural association with hyaluronan.

Kielty CM, Whittaker SP, Grant ME, Shuttleworth CA.

J Cell Biol. 1992 Aug;118(4):979-90.

46.
47.

Bone-marrow-derived chondrogenesis in vitro.

Berry L, Grant ME, McClure J, Rooney P.

J Cell Sci. 1992 Feb;101 ( Pt 2):333-42.

48.

Aortic endothelial cells in culture: factors which modulate their morphological and biosynthetic phenotypes.

Canfield AE, Sutton AB, Schor SL, Grant ME, Schor AM.

EXS. 1992;61:158-66. No abstract available.

PMID:
1617228
49.

The human collagen X gene. Complete primary translated sequence and chromosomal localization.

Thomas JT, Cresswell CJ, Rash B, Nicolai H, Jones T, Solomon E, Grant ME, Boot-Handford RP.

Biochem J. 1991 Dec 15;280 ( Pt 3):617-23.

50.

The human collagen X gene: complete primary sequence and re-expression in osteoarthritis.

Thomas JT, Cresswell CJ, Rash B, Hoyland J, Freemont AJ, Grant ME, Boot-Handford RP.

Biochem Soc Trans. 1991 Nov;19(4):804-8. No abstract available.

PMID:
1794562

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