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