Articular cartilage collagen: an irreplaceable framework? von Eyre, D R, Weis, M A, Wu, J-J

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Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix von Valli, M, Barnes, AM, Gallanti, A, Cabral, WA, Viglio, S, Weis, MA, Makareeva, E, Eyre, D, Leikin, S, Antoniazzi, F, Marini, JC, Mottes, M

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Evidence for enhanced collagen type III deposition focally in the territorial matrix of osteoarthritic hip articular cartilage von Hosseininia, S, Weis, M.A, Rai, J, Kim, L, Funk, S, Dahlberg, L.E, Eyre, D.R

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The Helix-II epitope: a cautionary tale from a cartilage biomarker based on an invalid collagen sequence von Eyre, D.R, Weis, M.A

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Dominant mutations in the type II collagen gene, COL2A1 , produce spondyloepimetaphyseal dysplasia, Strudwick type von Tiller, George E, Polumbo, Paula A, Weis, Mary Ann, Bogaert, Ray, Lachman, Ralph S, Cohn, Daniel H, Rimoin, David L, Eyre, David R

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An exploration of human services system contacts prior to suicide in South Carolina: an expansion of the South Carolina Violent Death Reporting System von Weis, M A, Bradberry, C, Carter, L P, Ferguson, J, Kozareva, D

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HIF-1α metabolically controls collagen synthesis and modification in chondrocytes von Stegen, Steve, Laperre, Kjell, Eelen, Guy, Rinaldi, Gianmarco, Fraisl, Peter, Torrekens, Sophie, Van Looveren, Riet, Loopmans, Shauni, Bultynck, Geert, Vinckier, Stefan, Meersman, Filip, Maxwell, Patrick H., Rai, Jyoti, Weis, MaryAnn, Eyre, David R., Ghesquière, Bart, Fendt, Sarah-Maria, Carmeliet, Peter, Carmeliet, Geert

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An amino acid substitution (Gly853-->Glu) in the collagen alpha 1(II) chain produces hypochondrogenesis von Bogaert, R, Tiller, G E, Weis, M A, Gruber, H E, Rimoin, D L, Cohn, D H, Eyre, D R

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Cartilage expression of a type II collagen mutation in an inherited form of osteoarthritis associated with a mild chondrodysplasia von EYRE, D. R, WEIS, M. A, MOSKOWITZ, R. W

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Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen von Schwarze, Ulrike, Cundy, Tim, Pyott, Shawna M, Christiansen, Helena E, Hegde, Madhuri R, Bank, Ruud A, Pals, Gerard, Ankala, Arunkanth, Conneely, Karen, Seaver, Laurie, Yandow, Suzanne M, Raney, Ellen, Babovic-Vuksanovic, Dusica, Stoler, Joan, Ben-Neriah, Ziva, Segel, Reeval, Lieberman, Sari, Siderius, Liesbeth, Al-Aqeel, Aida, Hannibal, Mark, Hudgins, Louanne, McPherson, Elizabeth, Clemens, Michele, Sussman, Michael D, Steiner, Robert D, Mahan, John, Smith, Rosemarie, Anyane-Yeboa, Kwame, Wynn, Julia, Chong, Karen, Uster, Tami, Aftimos, Salim, Sutton, V Reid, Davis, Elaine C, Kim, Lammy S, Weis, Mary Ann, Eyre, David, Byers, Peter H

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An RNA-splicing mutation (G+5IVS20) in the type II collagen gene (COL2AI) in a family with spondyloepiphyseal dysplasia congenita von TILLER, G. E, WEIS, M. A, POLUMBO, P. A, GRUBER, H. E, RIMOIN, D. L, COHN, D. H, EYRE, D. R

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Using NVDRS data for suicide prevention: promising practices in seven states von Powell, V, Barber, C W, Hedegaard, H, Hempstead, K, Hull-Jilly, D, Shen, X, Thorpe, G E, Weis, M A

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From surveillance to action: early gains from the National Violent Death Reporting System von Campbell, R, Weis, M A, Millet, L, Powell, V, Hull-Jilly, D, Hackman, H

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Gain-of-function mutation of microRNA-140 in human skeletal dysplasia von Grigelioniene, Giedre, Suzuki, Hiroshi I., Taylan, Fulya, Mirzamohammadi, Fatemeh, Borochowitz, Zvi U., Ayturk, Ugur M., Tzur, Shay, Horemuzova, Eva, Lindstrand, Anna, Weis, Mary Ann, Grigelionis, Gintautas, Hammarsjö, Anna, Marsk, Elin, Nordgren, Ann, Nordenskjöld, Magnus, Eyre, David R., Warman, Matthew L., Nishimura, Gen, Sharp, Phillip A., Kobayashi, Tatsuya

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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 p... von Starman, B J, Eyre, D, Charbonneau, H, Harrylock, M, Weis, M A, Weiss, L, Graham, Jr, J M, Byers, P H

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Acetabular augmentation at six- to 30-year follow-up : A biochemical and histological analysis von DIAB, M, CLARK, J. M, WEIS, M. A, EYRE, D. R

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COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay von Marom, Ronit, Burrage, Lindsay C., Venditti, Rossella, Clément, Aurélie, Blanco-Sánchez, Bernardo, Jain, Mahim, Scott, Daryl A., Rosenfeld, Jill A., Sutton, V. Reid, Shinawi, Marwan, Mirzaa, Ghayda, DeVile, Catherine, Roberts, Rowenna, Calder, Alistair D., Allgrove, Jeremy, Grafe, Ingo, Lanza, Denise G., Li, Xiaohui, Joeng, Kyu Sang, Lee, Yi-Chien, Song, I-Wen, Sliepka, Joseph M., Batkovskyte, Dominyka, Washington, Megan, Dawson, Brian C., Jin, Zixue, Jiang, Ming-Ming, Chen, Shan, Chen, Yuqing, Tran, Alyssa A., Emrick, Lisa T., Murdock, David R., Hanchard, Neil A., Zapata, Gladys E., Mehta, Nitesh R., Weis, Mary Ann, Scott, Abbey A., Tremp, Brenna A., Phillips, Jennifer B., Wegner, Jeremy, Taylor-Miller, Tashunka, Gibbs, Richard A., Muzny, Donna M., Jhangiani, Shalini N., Hicks, John, Stottmann, Rolf W., Dickinson, Mary E., Seavitt, John R., Heaney, Jason D., Eyre, David R., Westerfield, Monte, De Matteis, Maria Antonietta, Lee, Brendan

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Structurally Abnormal Type II Collagen in a Severe Form of Kniest Dysplasia Caused by an Exon 24 Skipping Mutation von Weis, M A, Wilkin, D J, Kim, H J, Wilcox, W R, Lachman, R S, Rimoin, D L, Cohn, D H, Eyre, D R

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People in nuclear medicine: an interview with Arthur M. Weis von Weis, A M

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Incorporation of Structurally Defective Type II Collagen into Cartilage Matrix in Kniest Chondrodysplasia von Fernandes, Russell J., Wilkin, Douglas J., Weis, Mary Ann, Wilcox, William R., Cohn, Daniel H., Rimoin, David L., Eyre, David R.

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