Boot-Handford R
Int J Exp Pathol. 2019; 100(1):4-11.
PMID: 30912609
PMC: 6463393.
DOI: 10.1111/iep.12311.
Byerly M, Petersen P, Ramamurthy S, Seldin M, Lei X, Provost E
J Biol Chem. 2013; 289(7):4055-69.
PMID: 24366864
PMC: 3924272.
DOI: 10.1074/jbc.M113.506956.
Seldin M, Tan S, Wong G
Rev Endocr Metab Disord. 2013; 15(2):111-23.
PMID: 23963681
PMC: 3931758.
DOI: 10.1007/s11154-013-9255-7.
Wei Z, Seldin M, Natarajan N, Djemal D, Peterson J, Wong G
J Biol Chem. 2013; 288(15):10214-29.
PMID: 23449976
PMC: 3624406.
DOI: 10.1074/jbc.M113.458711.
Colombatti A, Spessotto P, Doliana R, Mongiat M, Bressan G, Esposito G
Front Immunol. 2012; 2:93.
PMID: 22566882
PMC: 3342094.
DOI: 10.3389/fimmu.2011.00093.
Academic and molecular matrices: a study of the transformations of connective tissue research at the University of Manchester (1947-1996).
Garcia-Sancho M
Stud Hist Philos Biol Biomed Sci. 2011; 42(2):233-45.
PMID: 21486662
PMC: 3677089.
DOI: 10.1016/j.shpsc.2010.12.007.
From collagen chemistry towards cell therapy - a personal journey.
Grant M
Int J Exp Pathol. 2007; 88(4):203-14.
PMID: 17696900
PMC: 2517318.
DOI: 10.1111/j.1365-2613.2007.00537.x.
Deletions in the COL10A1 gene are not associated with skeletal changes in dogs.
Young A, Ryun J, Bannasch D
Mamm Genome. 2006; 17(7):761-8.
PMID: 16845471
DOI: 10.1007/s00335-005-0163-3.
Partial characterization of cell-type X collagen interactions.
Luckman S, Rees E, Kwan A
Biochem J. 2003; 372(Pt 2):485-93.
PMID: 12617725
PMC: 1223416.
DOI: 10.1042/BJ20021572.
Mutation of the type X collagen gene (COL10A1) causes spondylometaphyseal dysplasia.
Ikegawa S, Nishimura G, Nagai T, Hasegawa T, Ohashi H, Nakamura Y
Am J Hum Genet. 1998; 63(6):1659-62.
PMID: 9837818
PMC: 1377637.
DOI: 10.1086/302158.
A nonsense mutation in the carboxyl-terminal domain of type X collagen causes haploinsufficiency in schmid metaphyseal chondrodysplasia.
Chan D, Weng Y, Graham H, Sillence D, Bateman J
J Clin Invest. 1998; 101(7):1490-9.
PMID: 9525992
PMC: 508727.
DOI: 10.1172/JCI1976.
Partial characterization of the C-terminal non-collagenous domain (NC1) of collagen type X.
Barber R, Kwan A
Biochem J. 1996; 320 ( Pt 2):479-85.
PMID: 8973556
PMC: 1217955.
DOI: 10.1042/bj3200479.
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 G, Rash B, Sykes B, Bonaventure J, Maroteaux P, Zabel B
J Med Genet. 1996; 33(6):450-7.
PMID: 8782043
PMC: 1050629.
DOI: 10.1136/jmg.33.6.450.
The mouse collagen X gene: complete nucleotide sequence, exon structure and expression pattern.
Elima K, Eerola I, Rosati R, Metsaranta M, Garofalo S, Perala M
Biochem J. 1993; 289 ( Pt 1):247-53.
PMID: 8424763
PMC: 1132157.
DOI: 10.1042/bj2890247.
Characterization of an intronless collagen gene family in the marine sponge Microciona prolifera.
Aho S, Turakainen H, Onnela M, Boedtker H
Proc Natl Acad Sci U S A. 1993; 90(15):7288-92.
PMID: 8346246
PMC: 47122.
DOI: 10.1073/pnas.90.15.7288.
Amino acid substitutions of conserved residues in the carboxyl-terminal domain of the alpha 1(X) chain of type X collagen occur in two unrelated families with metaphyseal chondrodysplasia type Schmid.
Wallis G, Rash B, Sweetman W, Thomas J, Super M, Evans G
Am J Hum Genet. 1994; 54(2):169-78.
PMID: 8304336
PMC: 1918153.
Reconstitution of the folding pathway of collagen in a cell-free system: formation of correctly aligned and hydroxylated triple helices.
Middleton R, Bulleid N
Biochem J. 1993; 296 ( Pt 2):511-7.
PMID: 8257444
PMC: 1137724.
DOI: 10.1042/bj2960511.
Beta-sheet secondary structure of the trimeric globular domain of C1q of complement and collagen types VIII and X by Fourier-transform infrared spectroscopy and averaged structure predictions.
Smith K, Haris P, Chapman D, Reid K, Perkins S
Biochem J. 1994; 301 ( Pt 1):249-56.
PMID: 8037678
PMC: 1137169.
DOI: 10.1042/bj3010249.
Cartilage collagens: strategies for the study of their organisation and expression in the extracellular matrix.
Thomas J, Ayad S, Grant M
Ann Rheum Dis. 1994; 53(8):488-96.
PMID: 7944631
PMC: 1005385.
DOI: 10.1136/ard.53.8.488.
Mutations in three subdomains of the carboxy-terminal region of collagen type X account for most of the Schmid metaphyseal dysplasias.
Bonaventure J, Chaminade F, Maroteaux P
Hum Genet. 1995; 96(1):58-64.
PMID: 7607655
DOI: 10.1007/BF00214187.