Publications

Found 4 results
Filters: Author is S.S. Wang  [Clear All Filters]
2011
L. H. Cao, Wang, L. B., Wang, S. S., Ma, H. W., Ji, C. Y., and Luo, Y., Identification of novel and recurrent mutations in the calcium binding type III repeats of cartilage oligomeric matrix protein in patients with pseudoachondroplasia, vol. 10, pp. 955-963, 2011.
Ballo R, Briggs MD, Cohn DH, Knowlton RG, et al. (1997). Multiple epiphyseal dysplasia, ribbing type: a novel point mutation in the COMP gene in a South African family. Am. J. Med. Genet. 68: 396-400. doi:10.1002/(SICI)1096-8628(19970211)68:4<396::AID-AJMG4>3.0.CO;2-K Briggs MD and Chapman KL (2002). Pseudoachondroplasia and multiple epiphyseal dysplasia: mutation review, molecular interactions, and genotype to phenotype correlations. Hum. Mutat. 19: 465-478. doi:10.1002/humu.10066 PMid:11968079 Briggs MD, Mortier GR, Cole WG, King LM, et al. (1998). Diverse mutations in the gene for cartilage oligomeric matrix protein in the pseudoachondroplasia-multiple epiphyseal dysplasia disease spectrum. Am. J. Hum. Genet. 62: 311- 319. doi:10.1086/301713 PMid:9463320 Budde B, Blumbach K, Ylostalo J, Zaucke F, et al. (2005). Altered integration of matrilin-3 into cartilage extracellular matrix in the absence of collagen IX. Mol. Cell Biol. 25: 10465-10478. doi:10.1128/MCB.25.23.10465-10478.2005 PMid:16287859    PMCid:1291247 Chen FH, Herndon ME, Patel N, Hecht JT, et al. (2007). Interaction of cartilage oligomeric matrix protein/thrombospondin 5 with aggrecan. J. Biol. Chem. 282: 24591-24598. doi:10.1074/jbc.M611390200 PMid:17588949    PMCid:2905148 Chen H, Deere M, Hecht JT and Lawler J (2000). Cartilage oligomeric matrix protein is a calcium-binding protein, and a mutation in its type 3 repeats causes conformational changes. J. Biol. Chem. 275: 26538-26544. doi:10.1074/jbc.M909780199 PMid:10852928 Chen TLL, Posey KL, Hecht JT and Vertel BM (2008). COMP mutations: domain-dependent relationship between abnormal chondrocyte trafficking and clinical PSACH and MED phenotypes. J. Cell Biochem. 103: 778-787. doi:10.1002/jcb.21445 PMid:17570134 Deere M, Sanford T, Ferguson HL, Daniels K, et al. (1998). Identification of twelve mutations in cartilage oligomeric matrix protein (COMP) in patients with pseudoachondroplasia. Am. J. Med. Genet. 80: 510-513. doi:10.1002/(SICI)1096-8628(19981228)80:5<510::AID-AJMG14>3.0.CO;2-F Deere M, Sanford T, Francomano CA, Daniels K, et al. (1999). Identification of nine novel mutations in cartilage oligomeric matrix protein in patients with pseudoachondroplasia and multiple epiphyseal dysplasia. Am. J. Med. Genet. 85: 486-490. doi:10.1002/(SICI)1096-8628(19990827)85:5<486::AID-AJMG10>3.0.CO;2-O Fairbank HA (1946). Dysplasia epiphysealis multiplex. Proc. R. Soc. Med. 39: 315-317. PMCid:2181808 Hashimoto Y, Tomiyama T, Yamano Y and Mori H (2003). Mutation (D472Y) in the type 3 repeat domain of cartilage oligomeric matrix protein affects its early vesicle trafficking in endoplasmic reticulum and induces apoptosis. Am. J. Pathol. 163: 101-110. doi:10.1016/S0002-9440(10)63634-6 Hecht JT, Makitie O, Hayes E, Haynes R, et al. (2004). Chondrocyte cell death and intracellular distribution of COMP and type IX collagen in the pseudoachondroplasia growth plate. J. Orthop. Res. 22: 759-767. doi:10.1016/j.orthres.2003.11.010 PMid:15183431 Hecht JT, Hayes E, Haynes R and Cole WG (2005). COMP mutations, chondrocyte function and cartilage matrix. Matrix Biol. 23: 525-533. doi:10.1016/j.matbio.2004.09.006 PMid:15694129 Hedbom E, Antonsson P, Hjerpe A, Aeschlimann D, et al. (1992). Cartilage matrix proteins. An acidic oligomeric protein (COMP) detected only in cartilage. J. Biol. Chem. 267: 6132-6136. PMid:1556121 Hou J, Putkey JA and Hecht JT (2000). Delta 469 mutation in the type 3 repeat calcium binding domain of cartilage oligomeric matrix protein (COMP) disrupts calcium binding. Cell Calcium 27: 309-314. doi:10.1054/ceca.2000.0125 PMid:11013461 Ikegawa S, Ohashi H, Nishimura G, Kim KC, et al. (1998). Novel and recurrent COMP (cartilage oligomeric matrix protein) mutations in pseudoachondroplasia and multiple epiphyseal dysplasia. Hum. Genet. 103: 633-638. doi:10.1007/s004390050883 PMid:9921895 Kennedy J, Jackson G, Ramsden S, Taylor J, et al. (2005a). COMP mutation screening as an aid for the clinical diagnosis and counselling of patients with a suspected diagnosis of pseudoachondroplasia or multiple epiphyseal dysplasia. Eur. J. Hum. Genet. 13: 547-555. doi:10.1038/sj.ejhg.5201374 PMid:15756302    PMCid:2673054 Kennedy J, Jackson GC, Barker FS, Nundlall S, et al. (2005b). Novel and recurrent mutations in the C-terminal domain of COMP cluster in two distinct regions and result in a spectrum of phenotypes within the pseudoachondroplasia - multiple epiphyseal dysplasia disease group. Hum. Mutat. 25: 593-594. doi:10.1002/humu.9342 PMid:15880723 Kleerekoper Q, Hecht JT and Putkey JA (2002). Disease-causing mutations in cartilage oligomeric matrix protein cause an unstructured Ca2+ binding domain. J. Biol. Chem. 277: 10581-10589. doi:10.1074/jbc.M109944200 PMid:11782471 Kozlowski K (1976). Pseudoachondroplastic dysplasia (Maroteaux-Lamy): a critical analysis. Australas. Radiol. 20: 255-269. doi:10.1111/j.1440-1673.1976.tb02033.x PMid:828853 Kwak YH, Roh JY, Lee KS, Park HW, et al. (2009). Altered synthesis of cartilage-specific proteoglycans by mutant human cartilage oligomeric matrix protein. Clin. Orthop. Surg. 1: 181-187. doi:10.4055/cios.2009.1.4.181 PMid:19956474    PMCid:2784957 Loughlin J, Irven C, Mustafa Z, Briggs MD, et al. (1998). Identification of five novel mutations in cartilage oligomeric matrix protein gene in pseudoachondroplasia and multiple epiphyseal dysplasia. Hum. Mutat. (Suppl 1): S10-S17. doi:10.1002/humu.1380110105 Mabuchi A, Haga N, Ikeda T, Manabe N, et al. (2001). Novel mutation in exon 18 of the cartilage oligomeric matrix protein gene causes a severe pseudoachondroplasia. Am. J. Med. Genet. 104: 135-139. doi:10.1002/ajmg.10067 PMid:11746044 Mabuchi A, Manabe N, Haga N, Kitoh H, et al. (2003). Novel types of COMP mutations and genotype-phenotype association in pseudoachondroplasia and multiple epiphyseal dysplasia. Hum. Genet. 112: 84-90. doi:10.1007/s00439-002-0845-9 PMid:12483304 Mabuchi A, Momohara S, Ohashi H, Takatori Y, et al. (2004). Circulating COMP is decreased in pseudoachondroplasia and multiple epiphyseal dysplasia patients carrying COMP mutations. Am. J. Med. Genet. A 129A: 35-38. doi:10.1002/ajmg.a.30164 PMid:15266613 Maddox BK, Mokashi A, Keene DR and Bachinger HP (2000). A cartilage oligomeric matrix protein mutation associated with pseudoachondroplasia changes the structural and functional properties of the type 3 domain. J. Biol. Chem. 275: 11412-11417. doi:10.1074/jbc.275.15.11412 PMid:10753957 Malashkevich VN, Kammerer RA, Efimov VP, Schulthess T, et al. (1996). The crystal structure of a five-stranded coiled coil in COMP: a prototype ion channel? Science 274: 761-765. doi:10.1126/science.274.5288.761 PMid:8864111 Merritt TM, Bick R, Poindexter BJ, Alcorn JL, et al. (2007). Unique matrix structure in the rough endoplasmic reticulum cisternae of pseudoachondroplasia chondrocytes. Am. J. Pathol. 170: 293-300. doi:10.2353/ajpath.2007.060530 PMid:17200202    PMCid:1762700 Nakashima E, Mabuchi A, Kubota M, Ishikiriyama S, et al. (2005). Novel and recurrent exon 13 mutations of COMP in pseudoachondroplasia. Am. J. Med. Genet. A 132A: 108-109. doi:10.1002/ajmg.a.30348 PMid:15523619 Newton G, Weremowicz S, Morton CC, Copeland NG, et al. (1994). Characterization of human and mouse cartilage oligomeric matrix protein. Genomics 24: 435-439. doi:10.1006/geno.1994.1649 PMid:7713493 Oldberg A, Antonsson P, Lindblom K and Heinegard D (1992). COMP (cartilage oligomeric matrix protein) is structurally related to the thrombospondins. J. Biol. Chem. 267: 22346-22350. PMid:1429587 Piróg-Garcia KA, Meadows RS, Knowles L, Heinegard D, et al. (2007). Reduced cell proliferation and increased apoptosis are significant pathological mechanisms in a murine model of mild pseudoachondroplasia resulting from a mutation in the C-terminal domain of COMP. Hum. Mol. Genet. 16: 2072-2088. doi:10.1093/hmg/ddm155 PMid:17588960    PMCid:2674228 Schmitz M, Becker A, Schmitz A, Weirich C, et al. (2006). Disruption of extracellular matrix structure may cause pseudoachondroplasia phenotypes in the absence of impaired cartilage oligomeric matrix protein secretion. J. Biol. Chem. 281: 32587-32595. doi:10.1074/jbc.M601976200 PMid:16928687 Schmitz M, Niehoff A, Miosge N, Smyth N, et al. (2008). Transgenic mice expressing D469Delta mutated cartilage oligomeric matrix protein (COMP) show growth plate abnormalities and sternal malformations. Matrix Biol. 27: 67-85. doi:10.1016/j.matbio.2007.08.001 PMid:17889519 Tufan AC, Satiroglu-Tufan NL, Jackson GC, Semerci CN, et al. (2007). Serum or plasma cartilage oligomeric matrix protein concentration as a diagnostic marker in pseudoachondroplasia: differential diagnosis of a family. Eur. J. Hum. Genet. 15: 1023-1028. doi:10.1038/sj.ejhg.5201882 PMid:17579668 Unger S and Hecht JT (2001). Pseudoachondroplasia and multiple epiphyseal dysplasia: new etiologic developments. Am. J. Med. Genet. 106: 244-250. doi:10.1002/ajmg.10234 PMid:11891674 Vranka J, Mokashi A, Keene DR, Tufa S, et al. (2001). Selective intracellular retention of extracellular matrix proteins and chaperones associated with pseudoachondroplasia. Matrix Biol. 20: 439-450. doi:10.1016/S0945-053X(01)00148-2 Zankl A, Jackson GC, Crettol LM, Taylor J, et al. (2007). Preselection of cases through expert clinical and radiological review significantly increases mutation detection rate in multiple epiphyseal dysplasia. Eur. J. Hum. Genet. 15: 150-154. doi:10.1038/sj.ejhg.5201744 PMid:17133256    PMCid:2670452