| The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB JD Fine, RAJ Eady, EA Bauer, JW Bauer, L Bruckner-Tuderman, ... Journal of the American Academy of Dermatology 58 (6), 931-950, 2008 | 1287 | 2008 |
| Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification JD Fine, L Bruckner-Tuderman, RAJ Eady, EA Bauer, JW Bauer, C Has, ... Journal of the American Academy of Dermatology 70 (6), 1103-1126, 2014 | 1188 | 2014 |
| A simplified laminin nomenclature M Aumailley, L Bruckner-Tuderman, WG Carter, R Deutzmann, D Edgar, ... Matrix biology 24 (5), 326-332, 2005 | 1168 | 2005 |
| Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility C Has, JW Bauer, C Bodemer, MC Bolling, L Bruckner‐Tuderman, A Diem, ... British Journal of Dermatology 183 (4), 614-627, 2020 | 865 | 2020 |
| Intrinsic aging vs. photoaging: a comparative histopathological, immunohistochemical, and ultrastructural study of skin M El‐Domyati, S Attia, F Saleh, D Brown, DE Birk, F Gasparro, H Ahmad, ... Experimental dermatology 11 (5), 398-405, 2002 | 770 | 2002 |
| Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa JD Fine, RAJ Eady, EA Bauer, RA Briggaman, L Bruckner-Tuderman, ... Journal of the American Academy of Dermatology 42 (6), 1051-1066, 2000 | 599 | 2000 |
| Targeted disruption of the pemphigus vulgaris antigen (desmoglein 3) gene in mice causes loss of keratinocyte cell adhesion with a phenotype similar to pemphigus vulgaris PJ Koch, MG Mahoney, H Ishikawa, L Pulkkinen, J Uitto, L Shultz, ... The Journal of cell biology 137 (5), 1091-1102, 1997 | 530 | 1997 |
| Pseudoxanthoma elasticum: Mutations in the MRP6 gene encoding a transmembrane ATP-binding cassette (ABC) transporter F Ringpfeil, MG Lebwohl, AM Christiano, J Uitto Proceedings of the National Academy of Sciences 97 (11), 6001-6006, 2000 | 499 | 2000 |
| Keloids: The paradigm of skin fibrosis—Pathomechanisms and treatment JP Andrews, J Marttala, E Macarak, J Rosenbloom, J Uitto Matrix Biology 51, 37-46, 2016 | 494 | 2016 |
| The role of elastin and collagen in cutaneous aging: intrinsic aging versus photoexposure. J Uitto Journal of drugs in dermatology: JDD 7 (2 Suppl), s12-6, 2008 | 481 | 2008 |
| Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome G Richard, F Rouan, CE Willoughby, N Brown, P Chung, M Ryynänen, ... The American Journal of Human Genetics 70 (5), 1341-1348, 2002 | 471 | 2002 |
| Plectin deficiency results in muscular dystrophy with epidermolysis bullosa FJD Smith, RAJ Eady, IM Leigh, JR McMillan, EL Rugg, DP Kelsell, ... Nature genetics 13 (4), 450-457, 1996 | 466 | 1996 |
| Integrin β4 mutations associated with junctional epidermolysis bullosa with pyloric atresia F Vidal, D Aberdam, C Miquel, AM Christiano, L Pulkkinen, J Uitto, ... Nature genetics 10 (2), 229-234, 1995 | 466 | 1995 |
| Novel function for beta 1 integrins in keratinocyte cell-cell interactions. H Larjava, J Peltonen, SK Akiyama, SS Yamada, HR Gralnick, J Uitto, ... The Journal of cell biology 110 (3), 803-815, 1990 | 441 | 1990 |
| Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris A Kljuic, H Bazzi, JP Sundberg, A Martinez-Mir, R O'Shaughnessy, ... Cell 113 (2), 249-260, 2003 | 438 | 2003 |
| Biostimulation of wound healing by lasers: experimental approaches in animal models and in fibroblast cultures PR ABERGEL, RF Lyons, JC Castel, RM Dwyer, J Uitto Dermatologic Surgery 13 (2), 127-133, 1987 | 428 | 1987 |
| Mutations in the 180–kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa JA McGrath, B Gatalica, AM Christiano, K Si, K Owaribe, JR McMillan, ... Nature genetics 11 (1), 83-86, 1995 | 416 | 1995 |
| Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization. WH McLean, L Pulkkinen, FJ Smith, EL Rugg, EB Lane, F Bullrich, ... Genes & development 10 (14), 1724-1735, 1996 | 408 | 1996 |
| Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the γ2 subunit of nicein/kalinin (LAMININ–5) D Aberdam, MF Galliano, J Vailly, L Pulkkinen, J Bonifas, AM Christiano, ... Nature genetics 6 (3), 299-304, 1994 | 406 | 1994 |
| An AP-1 Binding Sequence Is Essential for Regulation of the Human α2 (I) Collagen (COL1A2) Promoter Activity by Transforming Growth Factor-β (∗) KY Chung, A Agarwal, J Uitto, A Mauviel Journal of Biological Chemistry 271 (6), 3272-3278, 1996 | 402 | 1996 |
