Fetuin-A deficiency is associated with infantile cortical hyperostosis (Caffey disease)

The serum protein α2–Heremans-Schmid glycoprotein/fetuin-A is a systemically acting inhibitor of ectopic calcification

Cora Schäfer, Alexander Heiss, Anke Schwarz et al. · Journal of Clinical Investigation · 2003 · 904 citations · Full text

Medicine, Biochemistry, Nephrology +16

Fetuin/α2-HS Glycoprotein Is a Transforming Growth Factor-β Type II Receptor Mimic and Cytokine Antagonist

Michael Demetriou, Christoph A. Binkert, Balram Sukhu et al. · Journal of Biological Chemistry · 1996 · 280 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +17

α2-HS Glycoprotein/Fetuin, a Transforming Growth Factor-β/Bone Morphogenetic Protein Antagonist, Regulates Postnatal Bone Growth and Remodeling

Melanie Szweras, Danmei Liu, Emily A. Partridge et al. · Journal of Biological Chemistry · 2002 · 217 citations · Full text

Medicine, Developmental Biology, Bone Metabolism +16

A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders

Robert Gensure, Outi Mäkitie, Catherine Barclay et al. · Journal of Clinical Investigation · 2005 · 165 citations · Full text

Life Sciences, Molecular Biology, Molecular Genetics +16

Regulation of Osteogenesis by Fetuin

Christoph A. Binkert, Michael Demetriou, Balram Sukhu et al. · Journal of Biological Chemistry · 1999 · 131 citations · Full text

Medicine, Cell Biology, Nutritional Sciences +10