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Positionally cloned gene for a novel glomerular protein—nephrin—is mutated in congenital nephrotic syndrome M Kestilä, U Lenkkeri, M Männikkö, J Lamerdin, P McCready, H Putaala, ... Molecular cell 1 (4), 575-582, 1998 | 2347 | 1998 |
Isolation and characterization of type IV procollagen, laminin, and heparan sulfate proteoglycan from the EHS sarcoma HK Kleinman, ML McGarvey, LA Liotta, PG Robey, K Tryggvason, ... Biochemistry 21 (24), 6188-6193, 1982 | 1536 | 1982 |
Alport's syndrome, Goodpasture's syndrome, and type IV collagen BG Hudson, K Tryggvason, M Sundaramoorthy, EG Neilson New England Journal of Medicine 348 (25), 2543-2556, 2003 | 1176 | 2003 |
A simplified laminin nomenclature M Aumailley, L Bruckner-Tuderman, WG Carter, R Deutzmann, D Edgar, ... Matrix biology 24 (5), 326-332, 2005 | 1103 | 2005 |
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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 | 940 | 2000 |
A new nomenclature for the laminins RE Burgeson, M Chiquet, R Deutzmann, P Ekblom, J Engel, H Kleinman, ... Matrix Biology 14 (3), 209-211, 1994 | 939 | 1994 |
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X-linked Alport syndrome natural history in 195 families and genotype-phenotype correlations in males JP JAIS, B KNEBELMANN, I GIATRAS, M DE MARCHI, G RIZZONI, ... Journal of the American Society of Nephrology 11 (4), 649-657, 2000 | 900* | 2000 |
Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy A Helbling-Leclerc, X Zhang, H Topaloglu, C Cruaud, F Tesson, ... Nature genetics 11 (2), 216-218, 1995 | 753 | 1995 |
Hereditary proteinuria syndromes and mechanisms of proteinuria K Tryggvason, J Patrakka, J Wartiovaara New England Journal of Medicine 354 (13), 1387-1401, 2006 | 747 | 2006 |
Structure of human pro-matrix metalloproteinase-2: activation mechanism revealed E Morgunova, A Tuuttila, U Bergmann, M Isupov, Y Lindqvist, G Schneider, ... Science 284 (5420), 1667-1670, 1999 | 745 | 1999 |
Genomic instability in laminopathy-based premature aging B Liu, J Wang, KM Chan, WM Tjia, W Deng, X Guan, J Huang, KM Li, ... Nature medicine 11 (7), 780-785, 2005 | 734 | 2005 |
Proteolytic degradation of extracellular matrix in tumor invasion K Tryggvason, M Höyhtyä, T Salo Biochimica et Biophysica Acta (BBA)-Reviews on Cancer 907 (3), 191-217, 1987 | 694 | 1987 |
Long-term self-renewal of human pluripotent stem cells on human recombinant laminin-511 S Rodin, A Domogatskaya, S Ström, EM Hansson, KR Chien, J Inzunza, ... Nature biotechnology 28 (6), 611, 2010 | 660 | 2010 |
Defective prelamin A processing and muscular and adipocyte alterations in Zmpste24 metalloproteinase–deficient mice AM Pendás, Z Zhou, J Cadiñanos, JMP Freije, J Wang, K Hultenby, ... Nature genetics 31 (1), 94-99, 2002 | 649 | 2002 |
The vascular basement membrane: a niche for insulin gene expression and β cell proliferation G Nikolova, N Jabs, I Konstantinova, A Domogatskaya, K Tryggvason, ... Developmental cell 10 (3), 397-405, 2006 | 627 | 2006 |
The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death H Putaala, R Soininen, P Kilpeläinen, J Wartiovaara, K Tryggvason Human molecular genetics 10 (1), 1-8, 2001 | 608 | 2001 |
Cloning of a novel bacteria-binding receptor structurally related to scavenger receptors and expressed in a subset of macrophages O Elomaa, M Kangas, C Sahlberg, J Tuukkanen, R Sormunen, A Liakka, ... Cell 80 (4), 603-609, 1995 | 593 | 1995 |