Concepedia

PPIB Mutations Cause Severe Osteogenesis Imperfecta

Fleur S. van Dijk, I. M. Nesbitt, Eline H. Zwikstra, Peter G. J. Nikkels, Sander R. Piersma, Silvina A. Fratantoni, Connie R. Jiménez, Margriet Huizer, Alice C. Morsman, Jan M. Cobben,

The American Journal of Human Genetics · 2009 · 299 citations · 17 references

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17

Mass Spectrometric Sequencing of Proteins from Silver-Stained Polyacrylamide Gels

Andrej Shevchenko, Matthias Wilm, Ole Vorm et al. · Analytical Chemistry · 1996 · 9.1K citations

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Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta

Wayne A. Cabral, Weizhong Chang, Aileen M. Barnes et al. · Nature Genetics · 2007 · 483 citations · Full text

, , +10

Deficiency of Cartilage-Associated Protein in Recessive Lethal Osteogenesis Imperfecta

Aileen M. Barnes, Weizhong Chang, Roy Morello et al. · New England Journal of Medicine · 2006 · 350 citations · Full text

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Cyclosporin A slows collagen triple-helix formation in vivo: indirect evidence for a physiologic role of peptidyl-prolyl cis-trans-isomerase.

B Steinmann, Peter Brückner, Andrea Superti‐Furga · Journal of Biological Chemistry · 1991 · 318 citations · Full text

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Human cyclophilin B: a second cyclophilin gene encodes a peptidyl-prolyl isomerase with a signal sequence.

Edwin R. Price, Lynne D. Zydowsky, M J Jin et al. · Proceedings of the National Academy of Sciences · 1991 · 318 citations

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