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2. Analysis of mouse models with loss or mutations in Nbr1 demonstrate an age-dependent high bone mass due to altered osteoblast activity

Author

Caroline A. Whitehouse, Gareth O. Richards, Katie Marchbank, N McGowan, Timothy M. Skerry, Agamemnon E. Grigoriadis, John Burford, Ellen Solomon, A. Horner, Paul T. Sharpe, and Sarah Waters

Subjects
medicine.medical_specialty, Histology, medicine.anatomical_structure, Endocrinology, Physiology, Chemistry, Endocrinology, Diabetes and Metabolism, Internal medicine, medicine, Osteoblast, Age dependent, Bone mass
Published
2010
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