Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
1R01CA070951-01
Application #
2114719
Study Section
Experimental Therapeutics Subcommittee 1 (ET)
Project Start
1996-06-01
Project End
1999-05-31
Budget Start
1996-06-01
Budget End
1997-05-31
Support Year
1
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
167204994
City
New York
State
NY
Country
United States
Zip Code
10032
Chan, Marion Man-Ying; Bulinski, J Chloe; Chang, Kwang-Poo et al. (2003) A microplate assay for Leishmania amazonensis promastigotes expressing multimeric green fluorescent protein. Parasitol Res 89:266-71
Bulinski, J C; Odde, D J; Howell, B J et al. (2001) Rapid dynamics of the microtubule binding of ensconsin in vivo. J Cell Sci 114:3885-97
Gruber, D; Faire, K; Bulinski, J C (2001) Abundant expression of the microtubule-associated protein, ensconsin (E-MAP-115), alters the cellular response to Taxol. Cell Motil Cytoskeleton 49:115-29
Nguyen, H L; Gruber, D; Bulinski, J C (1999) Microtubule-associated protein 4 (MAP4) regulates assembly, protomer-polymer partitioning and synthesis of tubulin in cultured cells. J Cell Sci 112 ( Pt 12):1813-24
Bulinski, J C; Gruber, D; Faire, K et al. (1999) GFP chimeras of E-MAP-115 (ensconsin) domains mimic behavior of the endogenous protein in vitro and in vivo. Cell Struct Funct 24:313-20
Faire, K; Waterman-Storer, C M; Gruber, D et al. (1999) E-MAP-115 (ensconsin) associates dynamically with microtubules in vivo and is not a physiological modulator of microtubule dynamics. J Cell Sci 112 ( Pt 23):4243-55
Waterman-Storer, C M; Desai, A; Bulinski, J C et al. (1998) Fluorescent speckle microscopy, a method to visualize the dynamics of protein assemblies in living cells. Curr Biol 8:1227-30