Eyre DR. Biomarkers of joint disease, injury and repair: Where are we? ICRS ’10, Sitges/Barcelona, Spain 2010. ICRS 2010.pdf
Weis MA, Hudson DM, Kim L, Scott M, Wu J-J, Eyre DR. Location of 3-hydroxyproline residues in collagen types I, II, III and V/XI implies a role in fibril supramolecular assembly. J. Biol. Chem. 2010; 285(4):2580-2590. PubMed
Barnes AM, Carter EM, Cabral WA, Weis MA, Chang W, Makareeva E, Leikin S, Rotimi CN, Eyre DR, Raggio CL, Marini JC. Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding. N. Engl. J. Med. 2010; 362:521-528. NEJM OA 0907705.pdf
Christiansen HE, Schwarze U, Pyott SM, Abdulrahman A, Al Balwi M, Alrasheed S, Pepin MG, Weis MA, Eyre DR, Byers P. Homozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfecta. Amer. J. Hum. Genet. 2010; 86:389-398. PubMed
Alanay Y, Avaygan H, Camacho N, Utine GE, Boduroglu K, Aktas D, Alikasifoglu M, Tuncbilek E, Orhan D, Bakar FT, Zabel B, Superti-Furga A, Bruckner-Tuderman L, Curry CJ, Pyott S, Byers PH, Eyre DR, Baldridge D, Lee B, Merrill AE, Davis EC, Cohn DH, Akarsu N, Krakow D. Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta. Am. J. Hum. Genet. 2010; 86:551-559. PubMed
Eyre DR, Weis MA, Wu J-J. Maturation of collagen ketoimine cross-links by an alternative mechanism to pyridinoline formation in cartilage. J. Biol. Chem. 2010; 285:16675-16682. PubMed
Wu J-J, Weis MA, Kim LS, Eyre DR. Type III collagen: A fibril network modifier in articular cartilage. J. Biol. Chem. 2010; 285:18537-18544. PubMed
Baldridge D, Lennington J, Homan EP, Jiang M, Munivez E, Bertin TK, Keene D, Pyott S, Byers PH, Weis M, Eyre DR, Lee B, Morello R. Generalized Connective Tissue Disease Due to Loss of Crtap expression. PLoS One 2010; 5(5):e10560. PubMed
Alanay Y, Avaygan H, Camacho N, Utine GE, Boduroglu K, Aktas D, Alikasifoglu M, Tuncbilek E, Orhan D, Bakar FT, Zabel B, Superti-Furga A, Bruckner-Tuderman L, Curry CJ, Pyott S, Byers PH, Eyre DR, Baldridge D, Lee B, Merrill AE, Davis EC, Cohn DH, Akarsu N, Krakow D. Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imprefecta. Am. J. Hum. Genet. 2010; 87:572-573. PubMed
Tompson SW, Bacino CA, Safina NP, Bober MB, Proud VK, Funari T, Wangler MF, Nevarez L, Ala-Kokko L, Wilcox WR, Eyre DR, Krakow D, Cohn DH. Fibrochondrogenesis results from mutations in the COL11A1 type XI collage gene. Am. J. Hum. Genet. 2010; 87:708-712. PubMed
Kraus VB, Burnett B, Coindreau J, Cottrell S, Eyre DR, Gendreau M, Gardiner J, Garnero P, Hardin J, Henrotin Y, Heinegard D, Ko A, Lohmander S, Matthews G, Menetski J, Moskowitz R, Persiani S, Poole AR, Rousseau JC, Todman M. Application of biomarkers in the development of drugs intended for the treatment of osteoarthritis. Osteoarth. Cart. 2010.
