Omar M E Albagha Selected Research

hereditary expansile Polyostotic osteolytic dysplasia

1/2021

Insertion Mutation in Tnfrsf11a Causes a Paget's Disease-Like Phenotype in Heterozygous Mice and Osteopetrosis in Homozygous Mice.

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Omar M E Albagha Research Topics

Disease

7	Osteoporosis 08/2009 - 03/2003
1	Ischemic Stroke 03/2022
1	Stroke (Strokes) 03/2022
1	Bone Resorption 01/2022
1	Familial Paget's disease of bone 01/2021
1	hereditary expansile Polyostotic osteolytic dysplasia 01/2021
1	Colorectal Neoplasms (Colorectal Cancer) 01/2014
1	Hypophosphatemic Rickets 08/2010
1	Genetic Predisposition to Disease (Genetic Predisposition) 06/2008
1	Necrosis 06/2008
1	Bone Diseases (Bone Disease) 03/2003

Drug/Important Bio-Agent (IBA)

1	RNA (Ribonucleic Acid)IBA 03/2022
1	MicroRNAs (MicroRNA)IBA 03/2022
1	Biomarkers (Surrogate Marker)IBA 03/2022
1	MineralsIBA 01/2022
1	Receptor Activator of Nuclear Factor-kappa B (TRANCE-R)IBA 01/2021
1	Nonsense Codon (Nonsense Mutation)IBA 01/2014
1	Phosphates (Orthophosphate)IBA 08/2010
1	Proteins (Proteins, Gene)FDA Link 08/2009
1	Collagen Type I (Type I Collagen)IBA 08/2009
1	Diphosphonates (Bisphosphonates)IBA 03/2009
1	RANK LigandIBA 06/2008
1	Vitamin D FDA LinkGeneric 11/2006
1	Estrogen Receptor alphaIBA 11/2004
1	Tumor Necrosis Factor Receptors (Tumor Necrosis Factor Receptor)IBA 11/2004
1	Genetic Markers (Genetic Marker)IBA 03/2003