Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Keith E. Fox"'
Autor:
Dwight J. Klemm, Jacob E. Friedman, Pernille Keller, Lillester A. Colton, Keith E. Fox, Ormond A. MacDougald, Hyuk C. Cha, Paul F. Erickson
Publikováno v:
Journal of Biological Chemistry. 283:35096-35105
Cyclin D1 expression is elevated and Wnt10b is repressed by cAMP during the first few hours of adipogenesis. cAMP-responsive element-binding protein (CREB) is a primary target for cAMP signaling, and we have shown that activation of CREB promotes adi
Autor:
Keith E. Fox, Joseph T. Crossno, Dwight J. Klemm, Paul F. Erickson, Susan M. Majka, Dana M. Fankell
Publikováno v:
Journal of Biological Chemistry. 281:40341-40353
The differentiation of preadipocytes to adipocytes is orchestrated by the expression of the "master adipogenic regulators," CCAAT/enhancer-binding protein (C/EBP) beta, peroxisome proliferator-activated receptor gamma (PPARgamma), and C/EBP alpha. In
Autor:
Keith E. Fox, Marileila Varella-Garcia, Alistaire S. Acosta, Brian T. Woessner, Rachel C. Janssen, John C. Psilas, Jacob E. Friedman, Susan M. Majka, Dwight J. Klemm, Theodore R. Shade, Christine R. Childs, Karen M. Helm
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 107(33)
It is generally assumed that white adipocytes arise from resident adipose tissue mesenchymal progenitor cells. We challenge this paradigm by defining a hematopoietic origin for both the de novo development of a subset of white adipocytes in adults an
Publikováno v:
American journal of physiology. Lung cellular and molecular physiology. 290(6)
Tight regulation of VEGF-A production and signaling is important for the maintenance of lung development and homeostasis. VEGF null mice have provided little insight into the role of VEGF during the later stages of lung morphogenesis. Therefore, we e
Publikováno v:
Developmental dynamics : an official publication of the American Association of Anatomists. 234(1)
Tenascin-C (TN-C) is a mesenchyme-derived extracellular matrix (ECM) glycoprotein required for fetal lung branching morphogenesis. Given that the low oxygen (O2) environment of the fetus is also essential for normal lung branching morphogenesis, we d