| LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development Y Gong, RB Slee, N Fukai, G Rawadi, S Roman-Roman, AM Reginato, ... Cell 107 (4), 513-523, 2001 | 2667 | 2001 |
| Impaired endochondral ossification and angiogenesis in mice deficient in membrane-type matrix metalloproteinase I Z Zhou, SS Apte, R Soininen, R Cao, GY Baaklini, RW Rauser, J Wang, ... Proceedings of the National Academy of Sciences 97 (8), 4052-4057, 2000 | 935 | 2000 |
| A disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif (ADAMTS) superfamily: functions and mechanisms SS Apte Journal of Biological Chemistry 284 (46), 31493-31497, 2009 | 553 | 2009 |
| Matrix metalloproteinases: old dogs with new tricks RPT Somerville, SA Oblander, SS Apte Genome biology 4, 1-11, 2003 | 454 | 2003 |
| The Gene Structure of Tissue Inhibitor of Metalloproteinases (TIMP)-3 and Its Inhibitory Activities Define the Distinct TIMP Gene Family∗ SS Apte, BR Olsen, G Murphy Journal of Biological Chemistry 270 (24), 14313-14318, 1995 | 409 | 1995 |
| Characterization of ADAMTS-9 and ADAMTS-20 as a distinct ADAMTS subfamily related to Caenorhabditis elegans GON-1 RPT Somerville, JM Longpre, KA Jungers, JM Engle, M Ross, S Evanko, ... Journal of Biological Chemistry 278 (11), 9503-9513, 2003 | 389 | 2003 |
| Inhibition of angiogenesis by tissue inhibitor of metalloproteinase-3. B Anand-Apte, MS Pepper, E Voest, R Montesano, B Olsen, G Murphy, ... Investigative ophthalmology & visual science 38 (5), 817-823, 1997 | 356 | 1997 |
| A disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motifs: the ADAMTS family SS Apte The international journal of biochemistry & cell biology 36 (6), 981-985, 2004 | 334 | 2004 |
| A type X collagen mutation causes Schmid metaphyseal chondrodysplasia ML Warman, M Abbott, SS Apte, T Hefferon, I McIntosh, DH Cohn, ... Nature genetics 5 (1), 79-82, 1993 | 317 | 1993 |
| Cloning of the cDNA encoding human tissue inhibitor of metalloproteinases-3 (TIMP-3) and mapping of the TIMP3 gene to chromosome 22 SS Apte, MG Mattei, BR Olsen Genomics 19 (1), 86-90, 1994 | 312 | 1994 |
| Identification and characterization of a novel human matrix metalloproteinase with unique structural characteristics, chromosomal location, and tissue distribution AM Pendás, V Knäuper, XS Puente, E Llano, MG Mattei, S Apte, ... Journal of Biological Chemistry 272 (7), 4281-4286, 1997 | 311 | 1997 |
| Procollagen II amino propeptide processing by ADAMTS-3: insights on dermatosparaxis RJ Fernandes, S Hirohata, JM Engle, A Colige, DH Cohn, DR Eyre, ... Journal of Biological Chemistry 276 (34), 31502-31509, 2001 | 289 | 2001 |
| Acanthamoeba keratitis: multicentre survey in England 1992–6 CF Radford, OJ Lehmann, JKG Dart British journal of ophthalmology 82 (12), 1387-1392, 1998 | 282 | 1998 |
| Murine tissue inhibitor of metalloproteinases—4 (Timp—4): cDNA isolation and expression in adult mouse tissues 1 KJ Leco, SS Apte, GT Taniguchi, SP Hawkes, R Khokha, GA Schultz, ... FEBS letters 401 (2-3), 213-217, 1997 | 264 | 1997 |
| ADAMTS metalloproteases generate active versican fragments that regulate interdigital web regression DR McCulloch, CM Nelson, LJ Dixon, DL Silver, JD Wylie, V Lindner, ... Developmental cell 17 (5), 687-698, 2009 | 263 | 2009 |
| ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-β bioavailability regulation C Le Goff, F Morice-Picard, N Dagoneau, LW Wang, C Perrot, YJ Crow, ... Nature genetics 40 (9), 1119-1123, 2008 | 252 | 2008 |
| 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* 210 TL Hurskainen, S Hirohata, MF Seldin, SS Apte Journal of Biological Chemistry 274 (36), 25555-25563, 1999 | 251 | 1999 |
| Loss of MMP-2 disrupts skeletal and craniofacial development and results in decreased bone mineralization, joint erosion and defects in osteoblast and osteoclast growth RA Mosig, O Dowling, A DiFeo, MCM Ramirez, IC Parker, E Abe, J Diouri, ... Human molecular genetics 16 (9), 1113-1123, 2007 | 249 | 2007 |
| Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias C Le Goff, C Mahaut, LW Wang, S Allali, A Abhyankar, S Jensen, ... The American Journal of Human Genetics 89 (1), 7-14, 2011 | 240 | 2011 |
| Egr-1 mediates extracellular matrix-driven transcription of membrane type 1 matrix metalloproteinase in endothelium TL Haas, D Stitelman, SJ Davis, SS Apte, JA Madri Journal of Biological Chemistry 274 (32), 22679-22685, 1999 | 233 | 1999 |
