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Medline Title Search (Dupuytren + Elastin)

Selected Publications

  • Almine, J. F., Wise, S. G., Hiob, M., Singh, N. K., Tiwari, K. K., Vali, S., … Weiss, A. S. (2013). Elastin sequences trigger transient proinflammatory responses by human dermal fibroblasts. FASEB Journal, 27(9), 3455–3465. (PDF)
  • Barroso, B., Abello, N., & Bischoff, R. (2006). Study of human lung elastin degradation by different elastases using high-performance liquid chromatography/mass spectrometry. Analytical Biochemistry, 358(2), 216–224. (PDF)
  • Baydanoff, S., Nicoloff, G., & Alexiev, C. (1987). Age-related changes in anti-elastin antibodies in serum from normal and atherosclerotic subjects. Atherosclerosis, 63(2–3), 267–271. (PDF)
  • Brouwer, B. De, Drent, M., Ouweland, J. M. W. Van Den, Wijnen, P. A., Moorsel, C. H. M. Van, Bekers, O., … Janssen, R. (2018). Increased circulating desmosine and age-dependent elastinolysis in idiopathic pulmonary fibrosis, 1–4. (PDF)
  • Durand, E., Fournier, B., Couty, L., Lemitre, M., Achouh, P., Julia, P., … Lafont, A. (2012). Endoluminal gingival fibroblast transfer reduces the size of rabbit carotid aneurisms via elastin repair. Arteriosclerosis, Thrombosis, and Vascular Biology, 32(8), 1892–1901. (PDF)
  • Hansen, N. U. B., Karsdal, M. A., Brockbank, S., Cruwys, S., Rønnow, S., & Leeming, D. J. (2016). Tissue turnover of collagen type I, III and elastin is elevated in the PCLS model of IPF and can be restored back to vehicle levels using a phosphodiesterase inhibitor. Respiratory Research, 17(1), 1–10. (PDF)
  • Hirsch, E., & Ghigo, A. (2014). Elastin degradation and ensuing inflammation as emerging keys to atherosclerosis. Cardiovascular Research, 102(1), 1–2. (PDF)
  • Hong YJ, Kim J, et al (2012). Serum elastin-derived peptides and anti-elastin antibody in patients with systemic sclerosis. Journal of Korean Medical Science, 27(5), 484–488. (PDF)
  • Ingram, J. L., Slade, D., Church, T. D., Francisco, D., Heck, K., Wesley Sigmon, R., … Kraft, M. (2016). Role of matrix metalloproteinases-1 and-2 in interleukin-13-suppressed elastin in airway fibroblasts in asthma. American Journal of Respiratory Cell and Molecular Biology, 54(1), 41–50. (PDF)
  • Lee, S. M., Chiang, S. H., Wang, H. Y., Wu, P. S., & Lin, C. C. (2015). Curcumin enhances the production of major structural components of elastic fibers, elastin, and fibrillin-1, in normal human fibroblast cells. Bioscience, Biotechnology and Biochemistry, 79(2), 247–252. (PDF)
  • Luisetti, M., Ma, S., Iadarola, P., Stone, P. J., Viglio, S., Casado, B., … Turino, G. M. (2008). Desmosine as a biomarker of elastin degradation in COPD: Current status and future directions. European Respiratory Journal, 32(5), 1146–1157. (PDF)
  • Ma, S., Turino, G. M., & Lin, Y. Y. (2011). Quantitation of desmosine and isodesmosine in urine, plasma, and sputum by LC-MS/MS as biomarkers for elastin degradation. Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences, 879(21), 1893–1898. (PDF)
  • Ma, S., Lin, Y. Y., Cantor, J. O., Chapman, K. R., Sandhaus, R. A., Fries, M., … Turino, G. M. (2017). The Effect of Alpha-1 Proteinase Inhibitor on Biomarkers of Elastin Degradation in Alpha-1 Antitrypsin Deficiency : An Analysis of the RAPID / RAPID Extension Trials. Journal of the COPD Foundation, 4(1), 34–44. (PDF)
  • Melling, M., Karimian-Teherani, D., Mostler, S., Behnam, M., Sobal, G., & Menzel, E. J. (2000). Changes of biochemical and biomechanical properties in Dupuytren disease. Arch Pathol Lab Med, 124(9), 1275–1281. (PDF)
  • Menzel, E. J., Neumuller, J., Rietsch, A., & Millesi, H. (1994). Connective Tissue Autoantibodies in Dupuytren’s Disease: Associations with HLA DR3. In Dupuytren’s Disease Pathobiochemistry and Clinical Management (pp. 49–61). (PDF)
  • Millesi, H. (1974). The Clinical And Morphological Course Of Dupuytren’s Disease. In J. Hueston & R. Tubiana (Eds.), Dupuytren’s Disease (pp. 49–60). Grune& Stratton, London. (PDF)
  • Millesi, H., Reihserner, R., Menzel, J., Hamilton, G., & Mallinger, R. (1994). Changes in the Biochemical Properties of Diseased Tissue as Pathogenetic Factors in Dupuytren’s Contracture. In Dupuytren’s Disease Pathobiochemistry and Clinical Management (pp. 178–189). Springer-Verlag. (PDF)
  • Millesi, H., Reihsner, R., Hamilton, G., Mallinger, R., & Menzel, E. J. (1995). Biomechanical properties of normal tendons, normal palmar aponeuroses, and tissues from patients with Dupuytren’s disease subjected to elastase and chondroitinase treatment. Clin Biomech (Bristol, Avon), 10(1), 29–35. (PDF)
  • Millesi, H., Reihsner, R., Hamilton, G., Mallinger, R., & Menzel, E. J. (1995). Biomechanical properties of normal tendons, normal palmar aponeuroses and palmar aponeuroses from patients with Dupuytren’s disease subjected to elastase and chondroitinase treatment. Connect Tissue Res, 31(2), 109–115. (PDF)
  • Millesi, H., Reihsner, R., Eberhard, D., Mallinger, R., Hamilton, G., & Menzel, E. J. (1997). The mechanical properties of the palmar aponeurosis and their significance for the pathogenesis of dupuytren’s contracture. Journal of Hand Surgery: European Volume, 22(4), 510–517. (PDF)
  • Millesi, H. (2012). Basic Thoughts on Dupuytren’s Contracture. In C. E. et al. (eds.) (Ed.), Dupuytren’s Disease and Related Hyperproliferative Disorders (pp. 21–26). Springer-Verlag Berlin Heidelberg. (PDF)
  • Neumüller, J., Menzel, J., & Millesi, H. (1994). Prevalence of HLA-DR3 and autoantibodies to connective tissue components in Dupuytren’s contracture. Clinical Immunology and Immunopathology, 71(2), 142–148. (PDF)
  • Robert, L., & Labat-Robert, J. (2014). Circulating elastin peptides, role in vascular pathology. Pathologie Biologie, 62(6), 337–341. (PDF)
  • Shemesh, S., Sidon, E., Kaisler, E., Sheinis, D., Velkes, S., Ohana, N., & Benayahu, D. (2017). Diabetes mellitus is associated with increased elastin fiber loss in ligamentum flavum of patients with lumbar spinal canal stenosis: results of a pilot histological study. European Spine Journal, 1–9. (PDF)
  • Skjøt-Arkil, H., Clausen, R. E., Nguyen, Q. H. T., Wang, Y., Zheng, Q., Martinez, F. J., … Karsdal, M. A. (2012). Measurement of MMP-9 and -12 degraded elastin (ELM) provides unique information on lung tissue degradation. BMC Pulmonary Medicine, 12. (PDF)
  • Smith, E. R., Tomlinson, L. A., Ford, M. L., McMahon, L. P., Rajkumar, C., & Holt, S. G. (2012). Elastin degradation is associated with progressive aortic stiffening and all-cause mortality in predialysis chronic kidney disease. Hypertension, 59(5), 973–978. (PDF)
  • Stein, F., Pezess, M. P., Robert, L., & Poullain, N. (1965). Anti-elastin antibodies in normal and pathological human sera. Nature, 207(994), 312–313. (PDF)
  • Stewart, S., Malto, M., Sandberg, L., & Colburn, K. K. (1994). Increased serum levels of anti-elastin antibodies in patients with Peyronie’s disease. J Urol, 152(1), 105–106. (PDF)
  • Stone, P. J., Korn, J. H., North, H., Lally, E. V, Miller, L. C., Tucker, L. B., … Franzblau, C. (1995). Cross-linked elastin and collagen degradation products in the urine of patients with scleroderma. Arthritis and Rheumatism, 38(4), 517–524. (PDF)
  • Turino, G. M., Lin, Y. Y., He, J., Cantor, J. O., & Ma, S. (2012). Elastin degradation: An effective biomarker in COPD. COPD: Journal of Chronic Obstructive Pulmonary Disease, 9(4), 435–438. (PDF)
  • Tyrkkö J and Viljanto J (1975) Significance of histopathological findings in Dupuytren’s contracture. Annales chirurgiae et gynaecologiae Fenniae 64(5). 1975/01/01.: 288–291. (PDF)
  • Tzvetanov, P., Hegde, V., Al-Hashel, J. Y., Atanasova, M., Sohal, A. P. S., & Rousseff, R. T. (2014). Abnormal levels of serum anti-elastin antibodies in patients with symptomatic carotid stenosis. Clinical Neurology and Neurosurgery, 116, 9–12. (PDF)
  • Viglio, S., Annovazzi, L., Luisetti, M., Stolk, J., Casado, B., & Iadarola, P. (2007). Progress in the methodological strategies for the detection in real samples of desmosine and isodesmosine, two biological markers of elastin degradation. Journal of Separation Science, 30(2), 202–213. (PDF)
  • Zhang, J., Wu, L., Feng, M. xiang, Sexton, P., Bai, C. xue, Qu, J. ming, … Black, P. N. (2011). Pulmonary fibroblasts from COPD patients show an impaired response of elastin synthesis to TGF-ß1. Respiratory Physiology and Neurobiology, 177(3), 236–240. (PDF)