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David G. Monroe

Endocrine Research Unit

Guggenheim 7-11A

Mayo Clinic

200 First Street SW

[email]@mayo.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Endocrine Research Unit, Guggenheim 7-11A, Mayo Clinic, 200 First Street SW. 2012
  • Department of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine, Rochester, Minnesota 55905, USA. 2005 - 2010
  • Department of Molecular Biology and Biochemistry, Mayo Clinic and Mayo Foundation, 200 1st Avenue SW, Rochester, USA. 2003

References

  1. Examination of ERα Signaling Pathways in Bone of Mutant Mouse Models Reveals the Importance of ERE-Dependent Signaling. Chokalingam, K., Roforth, M.M., Nicks, K.M., McGregor, U., Fraser, D., Khosla, S., Monroe, D.G. Endocrinology (2012) [Pubmed]
  2. Retinoblastoma binding protein-1 (RBP1) is a Runx2 coactivator and promotes osteoblastic differentiation. Monroe, D.G., Hawse, J.R., Subramaniam, M., Spelsberg, T.C. BMC. Musculoskelet. Disord (2010) [Pubmed]
  3. Estrogen receptor isoform-specific regulation of the retinoblastoma-binding protein 1 (RBBP1) gene: roles of AF1 and enhancer elements. Monroe, D.G., Secreto, F.J., Hawse, J.R., Subramaniam, M., Khosla, S., Spelsberg, T.C. J. Biol. Chem. (2006) [Pubmed]
  4. Estrogen receptor alpha and beta heterodimers exert unique effects on estrogen- and tamoxifen-dependent gene expression in human U2OS osteosarcoma cells. Monroe, D.G., Secreto, F.J., Subramaniam, M., Getz, B.J., Khosla, S., Spelsberg, T.C. Mol. Endocrinol. (2005) [Pubmed]
  5. Mutual antagonism of estrogen receptors alpha and beta and their preferred interactions with steroid receptor coactivators in human osteoblastic cell lines. Monroe, D.G., Johnsen, S.A., Subramaniam, M., Getz, B.J., Khosla, S., Riggs, B.L., Spelsberg, T.C. J. Endocrinol. (2003) [Pubmed]
 
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