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    Results: 23

    1.

    The Helix-II epitope: a cautionary tale from a cartilage biomarker based on an invalid collagen sequence.

    Eyre DR, Weis MA.

    Osteoarthritis Cartilage. 2009 Apr;17(4):423-6. Epub 2009 Mar 5.PMID: 19248751 [PubMed - in process]Related articles

    2.

    Differences in chain usage and cross-linking specificities of cartilage type V/XI collagen isoforms with age and tissue.

    Wu JJ, Weis MA, Kim LS, Carter BG, Eyre DR.

    J Biol Chem. 2009 Feb 27;284(9):5539-45. Epub 2008 Dec 22.PMID: 19103590 [PubMed - indexed for MEDLINE]Related articles

    3.

    Advances in collagen cross-link analysis.

    Eyre DR, Weis MA, Wu JJ.

    Methods. 2008 May;45(1):65-74.PMID: 18442706 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    From surveillance to action: early gains from the National Violent Death Reporting System.

    Campbell R, Weis MA, Millet L, Powell V, Hull-Jilly D, Hackman H.

    Inj Prev. 2006 Dec;12 Suppl 2:ii6-ii9. Review.PMID: 17170175 [PubMed - indexed for MEDLINE]Related articles

    5.

    Using NVDRS data for suicide prevention: promising practices in seven states.

    Powell V, Barber CW, Hedegaard H, Hempstead K, Hull-Jilly D, Shen X, Thorpe GE, Weis MA.

    Inj Prev. 2006 Dec;12 Suppl 2:ii28-ii32.PMID: 17170167 [PubMed - indexed for MEDLINE]Related articles

    6.

    An exploration of human services system contacts prior to suicide in South Carolina: an expansion of the South Carolina Violent Death Reporting System.

    Weis MA, Bradberry C, Carter LP, Ferguson J, Kozareva D.

    Inj Prev. 2006 Dec;12 Suppl 2:ii17-ii21.PMID: 17170165 [PubMed - indexed for MEDLINE]Related articles

    7.

    Rough endoplasmic reticulum abnormalities in a patient with spondyloepimetaphyseal dysplasia with scoliosis, joint laxity, and finger deformities.

    Shapiro F, Mulhern H, Weis MA, Eyre D.

    Ultrastruct Pathol. 2006 Sep-Oct;30(5):393-400.PMID: 17090519 [PubMed - indexed for MEDLINE]Related articles

    8.

    Articular cartilage collagen: an irreplaceable framework?

    Eyre DR, Weis MA, Wu JJ.

    Eur Cell Mater. 2006 Nov 2;12:57-63. Review.PMID: 17083085 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Acetabular augmentation at six- to 30-year follow-up. A biochemical and histological analysis.

    Diab M, Clark JM, Weis MA, Eyre DR.

    J Bone Joint Surg Br. 2005 Jan;87(1):32-5.PMID: 15686234 [PubMed - indexed for MEDLINE]Related articles

    10.

    Covalent cross-linking of the NC1 domain of collagen type IX to collagen type II in cartilage.

    Eyre DR, Pietka T, Weis MA, Wu JJ.

    J Biol Chem. 2004 Jan 23;279(4):2568-74. Epub 2003 Nov 5.PMID: 14602708 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Matrix deposition of tryptophan-containing allelic variants of type IX collagen in developing human cartilage.

    Matsui Y, Wu JJ, Weis MA, Pietka T, Eyre DR.

    Matrix Biol. 2003 Apr;22(2):123-9.PMID: 12782139 [PubMed - indexed for MEDLINE]Related articles

    12.

    Recent developments in cartilage research: matrix biology of the collagen II/IX/XI heterofibril network.

    Eyre DR, Wu JJ, Fernandes RJ, Pietka TA, Weis MA.

    Biochem Soc Trans. 2002 Nov;30(Pt 6):893-9. Review.PMID: 12440941 [PubMed - indexed for MEDLINE]Related articles

    14.

    Incorporation of structurally defective type II collagen into cartilage matrix in kniest chondrodysplasia.

    Fernandes RJ, Wilkin DJ, Weis MA, Wilcox WR, Cohn DH, Rimoin DL, Eyre DR.

    Arch Biochem Biophys. 1998 Jul 15;355(2):282-90.PMID: 9675039 [PubMed - indexed for MEDLINE]Related articles

    15.

    Structurally abnormal type II collagen in a severe form of Kniest dysplasia caused by an exon 24 skipping mutation.

    Weis MA, Wilkin DJ, Kim HJ, Wilcox WR, Lachman RS, Rimoin DL, Cohn DH, Eyre DR.

    J Biol Chem. 1998 Feb 20;273(8):4761-8.PMID: 9468540 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Dominant mutations in the type II collagen gene, COL2A1, produce spondyloepimetaphyseal dysplasia, Strudwick type.

    Tiller GE, Polumbo PA, Weis MA, Bogaert R, Lachman RS, Cohn DH, Rimoin DL, Eyre DR.

    Nat Genet. 1995 Sep;11(1):87-9.PMID: 7550321 [PubMed - indexed for MEDLINE]Related articles

    17.

    An RNA-splicing mutation (G+5IVS20) in the type II collagen gene (COL2A1) in a family with spondyloepiphyseal dysplasia congenita.

    Tiller GE, Weis MA, Polumbo PA, Gruber HE, Rimoin DL, Cohn DH, Eyre DR.

    Am J Hum Genet. 1995 Feb;56(2):388-95.PMID: 7847372 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Collagen crosslinks and mineral crystallinity in bone of patients with osteogenesis imperfecta.

    Vetter U, Weis MA, Mörike M, Eanes ED, Eyre DR.

    J Bone Miner Res. 1993 Feb;8(2):133-7.PMID: 8442432 [PubMed - indexed for MEDLINE]Related articles

    19.

    An amino acid substitution (Gly853-->Glu) in the collagen alpha 1(II) chain produces hypochondrogenesis.

    Bogaert R, Tiller GE, Weis MA, Gruber HE, Rimoin DL, Cohn DH, Eyre DR.

    J Biol Chem. 1992 Nov 5;267(31):22522-6.PMID: 1429602 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    A specific immunoassay for monitoring human bone resorption: quantitation of type I collagen cross-linked N-telopeptides in urine.

    Hanson DA, Weis MA, Bollen AM, Maslan SL, Singer FR, Eyre DR.

    J Bone Miner Res. 1992 Nov;7(11):1251-8.PMID: 1466251 [PubMed - indexed for MEDLINE]Related articles

    21.

    The cartilage collagens and joint degeneration.

    Eyre DR, Wu JJ, Woods PE, Weis MA.

    Br J Rheumatol. 1991;30 Suppl 1:10-5. Review. No abstract available. PMID: 1991234 [PubMed - indexed for MEDLINE]Related articles

    22.

    Cartilage expression of a type II collagen mutation in an inherited form of osteoarthritis associated with a mild chondrodysplasia.

    Eyre DR, Weis MA, Moskowitz RW.

    J Clin Invest. 1991 Jan;87(1):357-61.PMID: 1985108 [PubMed - indexed for MEDLINE]Related articlesFree article

    23.

    Osteogenesis imperfecta. The position of substitution for glycine by cysteine in the triple helical domain of the pro alpha 1(I) chains of type I collagen determines the clinical phenotype.

    Starman BJ, Eyre D, Charbonneau H, Harrylock M, Weis MA, Weiss L, Graham JM Jr, Byers PH.

    J Clin Invest. 1989 Oct;84(4):1206-14.PMID: 2794057 [PubMed - indexed for MEDLINE]Related articlesFree article

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