Sengle group  
Publication

Bookchapters
  1. Sengle, G., Charbonneau, N.L., Ono, R.N., and Sakai, L.Y. Connective tissue pathways that regulate growth factors. Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism 7, 27-32 (2008)
  2. Sengle, G, and Sakai, L.Y. Connective Tissue Pathways That Regulate Growth Factors. Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism, 8th edition, in press
Originial publications
  1. Sengle, G., Tufa, S.F., Sakai, L.Y., Zulliger, M.A., and Keene, D.R. A Correlative Method for Imaging Identical Regions of Samples by Micro-CT, Light Microscopy and Electron Microscopy: Imaging Adipose Tissue in a Model System. J. Histochem Cytochem. 2012 Dec 20, in press
  2. Sengle, G., Tsutsui, K., Keene, D.R., Tufa, S.F., Carlson, E.J., Charbonneau, N.L., Ono, R.N., Sasaki, T., Wirtz, M.K., Samples, J.R., Fessler, L.I., Fessler, J.H., Sekiguchi, K., Hayflick, S.J., and Sakai, L.Y. Microenvironmental regulation by fibrillin-1. PLoS Genet. 8, e1002425 (2012).
  3. Sengle, G., Ono, R.N., Sasaki, T., and Sakai, L.Y. Prodomains of transforming growth factor {beta} (TGF{beta}) superfamily members specify different functions: Extracellular Matrix interactions and growth factor bioavailability. J. Biol. Chem. 286, 5087-99 (2011)
  4. Nistala, H., Lee-Arteaga, S., Smaldone, S., Siciliano, G., Carta, L., Ono, R.N., Sengle, G., Arteaga-Solis, E., Levasseur, R., Ducy, P., Sakai, L.Y., Karsenty, G., and Ramirez, F. Fibrillin-1 and -2 differentially modulate endogenous TGF-β and BMP bioavailability during bone formation. J. Cell Biol. 190, 1107-21 (2010)
  5. Charbonneau, N.L., Carlson, E.J., Tufa, S., Sengle, G., Manalo, E.C., Carlberg, V.M., Ramirez, F., Keene, D.R., and Sakai, L.Y. In vivo studies of mutant fibrillin-1 microfibrils. J. Biol. Chem. 285, 24943-55 (2010)
  6. Tsutsui, K., Manabe, R., Yamada, T., Nakano, I., Oguri, Y., Keene, D.R., Sengle, G., Sakai, L.Y., and Sekiguchi, K. ADAMTSL-6 is a novel extracellular matrix protein that binds to fibrillin-1 and promotes fibrillin-1 fibril formation. J. Biol. Chem. 285, 4870-82 (2010)
  7. Ono, R.N., Sengle, G., Charbonneau, N.L., Carlberg, V., Bächinger, H.P., Sasaki, T., Lee-Arteaga, S., Zilberberg, L., Rifkin, D.B., Ramirez, F., Chu, M.L., and Sakai, L.Y. Latent transforming growth factor beta-binding proteins and fibulins compete for fibrillin-1 and exhibit exquisite specificities in binding sites. J. Biol. Chem. 284, 16872-81 (2009)
  8. Sengle, G., Ono, R.N., Lyons, K.M., Bächinger, H.P., and Sakai, L.Y. A new model for growth factor activation: type II receptors compete with the prodomain for BMP-7. J. Mol. Biol. 381, 1025-39 (2008)
  9. Sengle, G., Charbonneau, N.L., Ono, R.N., Sasaki, T., Alvarez, J., Keene, D.R., Bächinger, H.P., and Sakai, L.Y. Targeting of bone morphogenetic protein growth factor complexes to fibrillin. J. Biol. Chem. 283, 13874-88 (2008)
  10. Kuo, C.L., Isogai, Z., Keene, D.R., Hazeki, N., Ono, R.N., Sengle, G., Bächinger, H.P., and Sakai, L.Y. Effects of fibrillin-1 degradation on microfibril ultrastructure. J. Biol. Chem. 282, 4007-20 (2007)


19 Februar 2013
Gerhard Sengle
Institute for Biochemistry II, Joseph-Stelzmann-Strasse 52, D50931 Cologne
Suggestions and wishes: Budi Tunggal
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