Cole WG - Search Results

1

Chondrocyte cell death and intracellular distribution of COMP and type IX collagen in the pseudoachondroplasia growth plate.

Hecht JT, Makitie O, Hayes E, Haynes R, Susic M, Montufar-Solis D, Duke PJ, Cole WG. Hecht JT, et al. Among authors: cole wg. J Orthop Res. 2004 Jul;22(4):759-67. doi: 10.1016/j.orthres.2003.11.010. J Orthop Res. 2004. PMID: 15183431 Free article.

2

Early-onset metaphyseal chondrodysplasia type Schmid associated with a COL10A1 frame-shift mutation and impaired trimerization of wild-type α1(X) protein chains.

Mäkitie O, Susic M, Cole WG. Mäkitie O, et al. Among authors: cole wg. J Orthop Res. 2010 Nov;28(11):1497-501. doi: 10.1002/jor.21161. J Orthop Res. 2010. PMID: 20872587 Free article.

3

COMP mutations, chondrocyte function and cartilage matrix.

Hecht JT, Hayes E, Haynes R, Cole WG. Hecht JT, et al. Among authors: cole wg. Matrix Biol. 2005 Jan;23(8):525-33. doi: 10.1016/j.matbio.2004.09.006. Epub 2004 Nov 18. Matrix Biol. 2005. PMID: 15694129

4

Schmid type of metaphyseal chondrodysplasia and COL10A1 mutations--findings in 10 patients.

Mäkitie O, Susic M, Ward L, Barclay C, Glorieux FH, Cole WG. Mäkitie O, et al. Among authors: cole wg. Am J Med Genet A. 2005 Sep 1;137A(3):241-8. doi: 10.1002/ajmg.a.30855. Am J Med Genet A. 2005. PMID: 16088909

5

Cell-type specific trafficking of expressed mutant COMP in a cell culture model for PSACH.

Chen TL, Stevens JW, Cole WG, Hecht JT, Vertel BM. Chen TL, et al. Among authors: cole wg. Matrix Biol. 2004 Nov;23(7):433-44. doi: 10.1016/j.matbio.2004.09.005. Matrix Biol. 2004. PMID: 15579310

6

Differentiation-induced loss of heparan sulfate in human exostosis derived chondrocytes.

Hecht JT, Hayes E, Haynes R, Cole WG, Long RJ, Farach-Carson MC, Carson DD. Hecht JT, et al. Among authors: cole wg. Differentiation. 2005 Jun;73(5):212-21. doi: 10.1111/j.1432-0436.2005.00025.x. Differentiation. 2005. PMID: 16026543

7

Heparan sulfate abnormalities in exostosis growth plates.

Hecht JT, Hall CR, Snuggs M, Hayes E, Haynes R, Cole WG. Hecht JT, et al. Among authors: cole wg. Bone. 2002 Jul;31(1):199-204. doi: 10.1016/s8756-3282(02)00796-2. Bone. 2002. PMID: 12110435

8

Early-onset osteoarthritis due to otospondylomegaepiphyseal dysplasia in a family with a novel splicing mutation of the COL11A2 gene.

Avcin T, Makitie O, Susic M, Miller S, Thorne C, Tenenbaum J, Laxer RM, Cole WG. Avcin T, et al. Among authors: cole wg. J Rheumatol. 2008 May;35(5):920-6. Epub 2008 Mar 15. J Rheumatol. 2008. PMID: 18381781

9

Mutations in the known genes are not the major cause of MED; distinctive phenotypic entities among patients with no identified mutations.

Jakkula E, Mäkitie O, Czarny-Ratajczak M, Jackson GC, Damignani R, Susic M, Briggs MD, Cole WG, Ala-Kokko L. Jakkula E, et al. Among authors: cole wg. Eur J Hum Genet. 2005 Mar;13(3):292-301. doi: 10.1038/sj.ejhg.5201314. Eur J Hum Genet. 2005. PMID: 15523498

10

Clinical and radiographic findings in multiple epiphyseal dysplasia caused by MATN3 mutations: description of 12 patients.

Mäkitie O, Mortier GR, Czarny-Ratajczak M, Wright MJ, Suri M, Rogala P, Freund M, Jackson GC, Jakkula E, Ala-Kokko L, Briggs MD, Cole WG. Mäkitie O, et al. Among authors: cole wg. Am J Med Genet A. 2004 Mar 15;125A(3):278-84. doi: 10.1002/ajmg.a.20486. Am J Med Genet A. 2004. PMID: 14994237

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