The Recombinant Protein Core was organized to meet the needs of the Research Projects for production, purification and characterization of proteins and antibodies that are unavailable elsewhere. In addition, the Core will generate new proteins and antibodies never before produced. The four basic science and translational Research Projects each will require growth factors, binding proteins, receptors, signaling cascade proteins, kinases, transcription factors, mutant forms thereof, and antibodies thereto. This core will be administered as a closed core due to its specialized nature. Priorities will be set by the International Advisory Committee in coordination with the Core Director. The centralization of production, purification and characterization of recombinant proteins and antibodies will prove highly cost effective. The duplication of effort, expertise and equipment necessary for each unit to produce, purify and characterize their own recombinant proteins and antibodies will be eliminated and the expertise and technology concentrated in the Core. The extensive experience of the Core Director will be brought to bear on the needs of each Research Project. In cases where the same proteins or antibodies need to be used by more than one Research Project, reliance on the uniformity and quality of the reagents will be particularly important. Providing these reagents to Research Projects 11-14 will greatly facilitate the advancement of the aims and in some cases will make key contributions without which some areas of investigation would not be possible.

Project Start
2001-04-01
Project End
2002-03-31
Budget Start
Budget End
Support Year
22
Fiscal Year
2001
Total Cost
$174,159
Indirect Cost
Name
University of California San Diego
Department
Type
DUNS #
077758407
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Fernandez, Marina O; Hsueh, Katherine; Park, Hyun Tae et al. (2017) Astrocyte-Specific Deletion of Peroxisome-Proliferator Activated Receptor-? Impairs Glucose Metabolism and Estrous Cycling in Female Mice. J Endocr Soc 1:1332-1350
Fernandez, Marina O; Sharma, Shweta; Kim, Sun et al. (2017) Obese Neuronal PPAR? Knockout Mice Are Leptin Sensitive but Show Impaired Glucose Tolerance and Fertility. Endocrinology 158:121-133
Yamada-Nomoto, Kaori; Yoshino, Osamu; Akiyama, Ikumi et al. (2017) PAI-1 in granulosa cells is suppressed directly by statin and indirectly by suppressing TGF-? and TNF-? in mononuclear cells by insulin-sensitizing drugs. Am J Reprod Immunol 78:
Takahashi, Nozomi; Harada, Miyuki; Hirota, Yasushi et al. (2017) Activation of Endoplasmic Reticulum Stress in Granulosa Cells from Patients with Polycystic Ovary Syndrome Contributes to Ovarian Fibrosis. Sci Rep 7:10824
Tang, Kechun; Pasqua, Teresa; Biswas, Angshuman et al. (2017) Muscle injury, impaired muscle function and insulin resistance in Chromogranin A-knockout mice. J Endocrinol 232:137-153
Homer, Michael V; Rosencrantz, Marcus A; Shayya, Rana F et al. (2017) The effect of estradiol on granulosa cell responses to FSH in women with polycystic ovary syndrome. Reprod Biol Endocrinol 15:13
Baeza-Raja, Bernat; Sachs, Benjamin D; Li, Pingping et al. (2016) p75 Neurotrophin Receptor Regulates Energy Balance in Obesity. Cell Rep 14:255-68
Hoffmann, Hanne M; Mellon, Pamela L (2016) A small population of hypothalamic neurons govern fertility: the critical role of VAX1 in GnRH neuron development and fertility maintenance. Neurosci Commun (Houst) 2:
Cho, Chang Gun; Pak, Kwang; Webster, Nicholas et al. (2016) Both canonical and non-canonical NF-?B activation contribute to the proliferative response of the middle ear mucosa during bacterial infection. Innate Immun 22:626-634
Stephens, Shannon B Z; Chahal, Navdeep; Munaganuru, Nagambika et al. (2016) Estrogen Stimulation of Kiss1 Expression in the Medial Amygdala Involves Estrogen Receptor-? But Not Estrogen Receptor-?. Endocrinology 157:4021-4031

Showing the most recent 10 out of 258 publications