Funding Agency

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM052092-02
Application #
2190986
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1995-07-01
Project End
1999-06-30
Budget Start
1996-07-01
Budget End
1997-06-30
Support Year
2
Fiscal Year
1996
Total Cost
Indirect Cost

  Institution

Name
University of Texas Health Science Center Houston
Department
Pharmacology
Type
Schools of Medicine
DUNS #
City
Houston
State
TX
Country
United States
Zip Code
77225

  Publications

Vida, Thomas A (2008) A cell-free system for reconstitution of transport between prevacuolar compartments and vacuoles in Saccharomyces cerevisiae. Methods Mol Biol 457:41-57
Yan, Qing; Hunt, Piper Reid; Frelin, Laurence et al. (2005) mVps24p functions in EGF receptor sorting/trafficking from the early endosome. Exp Cell Res 304:265-73
Yan, Qing; Sun, Wei; Kujala, Pekka et al. (2005) CART: an Hrs/actinin-4/BERP/myosin V protein complex required for efficient receptor recycling. Mol Biol Cell 16:2470-82
Sun, Wei; Yan, Qing; Vida, Thomas A et al. (2003) Hrs regulates early endosome fusion by inhibiting formation of an endosomal SNARE complex. J Cell Biol 162:125-37
Vida, Thomas; Wendland, Beverly (2002) Flow cytometry/cell sorting for isolating membrane trafficking mutants in yeast. Methods Enzymol 351:623-31
Vida, T; Gerhardt, B (1999) A cell-free assay allows reconstitution of Vps33p-dependent transport to the yeast vacuole/lysosome. J Cell Biol 146:85-98
Zheng, B; Wu, J N; Schober, W et al. (1998) Isolation of yeast mutants defective for localization of vacuolar vital dyes. Proc Natl Acad Sci U S A 95:11721-6
Gerhardt, B; Kordas, T J; Thompson, C M et al. (1998) The vesicle transport protein Vps33p is an ATP-binding protein that localizes to the cytosol in an energy-dependent manner. J Biol Chem 273:15818-29