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University of Arkansas for Medical Sciences
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Proteasomal degradation of Runx2 shortens parathyroid hormone-induced anti-apoptotic signaling in osteoblasts. A putative explanation for why intermittent administration is needed for bone anabolism.
Bellido T, Ali AA, Plotkin LI, Fu Q, Gubrij I, Roberson PK, Weinstein RS, O'Brien CA, Manolagas SC, Jilka RL. Proteasomal degradation of Runx2 shortens parathyroid hormone-induced anti-apoptotic signaling in osteoblasts. A putative explanation for why intermittent administration is needed for bone anabolism. J Biol Chem. 2003 Dec 12; 278(50):50259-72.
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PubMed
subject areas
Animals
Apoptosis
bcl-Associated Death Protein
Blotting, Western
Bone Resorption
Calcium
Carrier Proteins
Cells, Cultured
Core Binding Factor Alpha 1 Subunit
Culture Media, Conditioned
Cyclic AMP Response Element-Binding Protein
Cyclic AMP-Dependent Protein Kinases
Cysteine Endopeptidases
Dactinomycin
Female
HeLa Cells
Humans
Kinetics
Membrane Glycoproteins
Mice
Mice, Inbred C57BL
Models, Biological
Models, Genetic
Multienzyme Complexes
Neoplasm Proteins
Osteoblasts
Parathyroid Hormone
Phosphorylation
Proteasome Endopeptidase Complex
Proto-Oncogene Proteins c-bcl-2
RANK Ligand
Receptor Activator of Nuclear Factor-kappa B
RNA
RNA, Messenger
Signal Transduction
Time Factors
Transcription Factors
Transcription, Genetic
authors with profiles
Qiang Fu
Stavros Manolagas
Robert Weinstein
Paula Roberson
Teresita Bellido