Funding Agency

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK063073-02
Application #
6690984
Study Section
Endocrinology Study Section (END)
Program Officer
Malozowski, Saul N
Project Start
2003-01-01
Project End
2007-12-31
Budget Start
2004-01-01
Budget End
2004-12-31
Support Year
2
Fiscal Year
2004
Total Cost
$265,760
Indirect Cost

  Institution

Name
Oregon Health and Science University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
096997515
City
Portland
State
OR
Country
United States
Zip Code
97239

  Publications

Varco-Merth, Benjamin; Feigerlová, Eva; Shinde, Ujwal et al. (2013) Severe growth deficiency is associated with STAT5b mutations that disrupt protein folding and activity. Mol Endocrinol 27:150-61
Mukherjee, Aditi; Rotwein, Peter (2009) Akt promotes BMP2-mediated osteoblast differentiation and bone development. J Cell Sci 122:716-26
Mukherjee, Aditi; Wilson, Elizabeth M; Rotwein, Peter (2008) Insulin-like growth factor (IGF) binding protein-5 blocks skeletal muscle differentiation by inhibiting IGF actions. Mol Endocrinol 22:206-15
Mukherjee, Aditi; Rotwein, Peter (2008) Insulin-like growth factor-binding protein-5 inhibits osteoblast differentiation and skeletal growth by blocking insulin-like growth factor actions. Mol Endocrinol 22:1238-50
Kuninger, David; Lundblad, James; Semirale, Anthony et al. (2007) A non-isotopic in vitro assay for histone acetylation. J Biotechnol 131:253-60
Mukherjee, Aditi; Rotwein, Peter (2007) Insulin-like growth factor binding protein-5 in osteogenesis: facilitator or inhibitor? Growth Horm IGF Res 17:179-85
Chia, Dennis J; Ono, Mitsuru; Woelfle, Joachim et al. (2006) Characterization of distinct Stat5b binding sites that mediate growth hormone-stimulated IGF-I gene transcription. J Biol Chem 281:3190-7
Chia, Dennis J; Subbian, Ezhilkani; Buck, Teresa M et al. (2006) Aberrant folding of a mutant Stat5b causes growth hormone insensitivity and proteasomal dysfunction. J Biol Chem 281:6552-8