Mechanism of FGF23 processing in fibrous dysplasia

Biochemistry, Genetics and Molecular Biology

• Dysplasia 100%
• Fibroblast Growth Factor 23 100%
• Furin 50%
• Glycosylation 30%
• Cyclic Adenosine Monophosphate 30%
• Stromal Cell 20%
• Rickets 20%
• C-Terminus 10%
• Autosomal Dominant Inheritance 10%
• Osteoblast 10%
• Osteocyte 10%
• Vitamin D 10%
• Autosomal Recessive Inheritance 10%
• Primary Cell 10%
• Glycosyltransferase 10%
• Protein G 10%
• Small GTPase 10%

Keyphrases

• Fibroblast Growth Factor 23 (FGF23) 100%
• Fibrous Dysplasia 100%
• Fibrous Dysplasia of Bone 31%
• Cyclic Adenosine Monophosphate (cAMP) 15%
• Furin 15%
• Glycosylation 10%
• Human Mesenchymal Stem Cells (hMSCs) 10%
• Furin Activity 10%
• Vitamin D 5%
• Osteoblast 5%
• Phosphate 5%
• Primary Cells 5%
• X-linked 5%
• Osteocyte 5%
• Autosomal Recessive 5%
• Glycosyltransferase 5%
• Blood Specimen 5%
• O-glycosylation 5%
• Activating mutation 5%
• Small G Protein 5%
• Hyperostosis 5%
• Hypophosphatemia 5%
• Autosomal Dominant Hypophosphatemic Rickets 5%
• Tumoral Calcinosis 5%
• N-acetylglucosaminyltransferase 5%
• Hypophosphatemic Rickets 5%