Citations for
1ADAMTS2, EDS7C
Multiple congenital skull fractures as a presentation of Ehlers-Danlos syndrome type VIIC.
Bar-Yosef O, Polak-Charcon S, Hoffman C, Feldman ZP, Frydman M, Kuint J.
Am J Med Genet A 146A(23):3054-7. 2008
2ADAMTS2, TIMP3
TIMP-3 inhibits the procollagen N-proteinase ADAMTS-2.
Wang WM, Ge G, Lim NH, Nagase H, Greenspan DS.
Biochem J 398(3):515-9. 2006
3ADAMTS2, EDS7C
The natural history, including orofacial features of three patients with Ehlers-Danlos syndrome, dermatosparaxis type (EDS type VIIC).
Malfait F, De Coster P, Hausser I, van Essen AJ, Franck P, Colige A, Nusgens B, Martens L, De Paepe A.
Am J Med Genet 131A(1):18-28. 2004
4EDS7C, ADAMTS2
Novel types of mutation responsible for the dermatosparactic type of Ehlers-Danlos syndrome (Type VIIC) and common polymorphisms in the ADAMTS2 gene.
Colige A, Nuytinck L, Hausser I, van Essen AJ, Thiry M, Herens C, Ades LC, Malfait F, Paepe AD, Franck P, Wolff G, Oosterwijk JC, Smitt JH, Lapiere CM, Nusgens BV.
J Invest Dermatol 123(4):656-63. 2004
5ADAMTS1, ADAMTS2, ADAMTS3, ADAMTS4, ADAMTS5, ADAMTS6, ADAMTS7, ADAMTS8, ADAMTS9, TIMP3
Expression of ADAMTS metalloproteinases in the retinal pigment epithelium derived cell line ARPE-19: transcriptional regulation by TNFalpha.
Bevitt DJ, Mohamed J, Catterall JB, Li Z, Arris CE, Hiscott P, Sheridan C, Langton KP, Barker MD, Clarke MP, McKie N.
Biochim Biophys Acta 1626(1-3):83-91. 2003
6ADAMTS2, ADAMTS14, ADAMTS3
Cloning and characterization of ADAMTS-14, a novel ADAMTS displaying high homology with ADAMTS-2 and ADAMTS-3.
Colige A, Vandenberghe I, Thiry M, Lambert CA, Van Beeumen J, Li SW, Prockop DJ, Lapiere CM, Nusgens BV.
J Biol Chem 277(8):5756-66. Epub 2001 Dec 07. 2002
7ADAMTS1, ADAMTS2, ADAMTS5, ADAMTS6, ADAMTS7
ADAM-TS5, ADAM-TS6, and ADAM-TS7, novel members of a new family of zinc metalloproteases. General features and genomic distribution of the ADAM-TS family.
Hurskainen TL, et al.
J Biol Chem 274(36):25555-63 1999
8ADAMTS2, ADAMTS4, ADAMTS3
ADAMTS: a novel family of proteases with an ADAM protease domain and thrombospondin 1 repeats.
Tang BL, et al.
FEBS Lett 445(2-3):223-5. Review. No abstract available 1999
9ADAMTS2, EDS7C
Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene.
Colige A, Sieron AL, Li SW, Schwarze U, Petty E, Wertelecki W, Wilcox W, Krakow D, Cohn DH, Reardon W, Byers PH, Lapiere CM, Prockop DJ, Nusgens BV.
Am J Hum Genet 65(2):308-17. 1999