Citations for
1ADAMTS10, ADAMTS17, ADAMTSL4, FBN1, WMSAR, WMSL
Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature.
Morales J, Al-Sharif L, Khalil DS, Shinwari JM, Bavi P, Al-Mahrouqi RA, Al-Rajhi A, Alkuraya FS, Meyer BF, Al Tassan N.
Am J Hum Genet 85(5):558-68.PMID: 19836009 2009
2ADAMTS16, ADAMTS17, MMP28, TIMP2
Expression profiling of metalloproteinases and their inhibitors in synovium and cartilage.
Davidson RK, Waters JG, Kevorkian L, Darrah C, Cooper A, Donell ST, Clark IM.
Arthritis Res Ther 8(4):R124.PMID: 16859525 2006
3ADAMTS17
Protease degradomics: mass spectrometry discovery of protease substrates and the CLIP-CHIP, a dedicated DNA microarray of all human proteases and inhibitors.
Overall CM, Tam EM, Kappelhoff R, Connor A, Ewart T, Morrison CJ, Puente X, López-Otín C, Seth A.
Biol Chem 385(6):493-504.PMID: 15255181 2004
4ADAMTS14, ADAMTS15, ADAMTS16, ADAMTS17, ADAMTS18, ADAMTS19
Cloning, expression analysis, and structural characterization of seven novel human ADAMTSs, a family of metalloproteinases with disintegrin and thrombospondin-1 domains.
Cal S, Obaya AJ, Llamazares M, Garabaya C, Quesada V, Lopez-Otin C.
Gene 283(1-2):49-62. 2002