Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29NS028126-05
Application #
3477956
Study Section
Neurology C Study Section (NEUC)
Project Start
1990-01-01
Project End
1994-06-10
Budget Start
1994-01-01
Budget End
1994-06-10
Support Year
5
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Type
Schools of Medicine
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Zhan-Poe, X; Craft, C M (1999) Biochemical characterization of recombinant serotonin N-acetyltransferase. J Pineal Res 27:49-58
Craft, C M; Murage, J; Brown, B et al. (1999) Bovine arylalkylamine N-acetyltransferase activity correlated with mRNA expression in pineal and retina. Brain Res Mol Brain Res 65:44-51
Craft, C M; Xu, J; Slepak, V Z et al. (1998) PhLPs and PhLOPs in the phosducin family of G beta gamma binding proteins. Biochemistry 37:15758-72
Gauer, F; Craft, C M (1996) Circadian regulation of hydroxyindole-O-methyltransferase mRNA levels in rat pineal and retina. Brain Res 737:99-109
Craft, C M; Whitmore, D H (1995) The arrestin superfamily: cone arrestins are a fourth family. FEBS Lett 362:247-55
Gauer, F; Kedzierski, W; Craft, C M (1995) Identification of circadian gene expression in the rat pineal gland and retina by mRNA differential display. Neurosci Lett 187:69-73
Carcamo, B; Hurwitz, M Y; Craft, C M et al. (1995) The mammalian pineal expresses the cone but not the rod cyclic GMP phosphodiesterase. J Neurochem 65:1085-92
Craft, C M; Whitmore, D H; Wiechmann, A F (1994) Cone arrestin identified by targeting expression of a functional family. J Biol Chem 269:4613-9
Lolley, R N; Rong, H; Craft, C M (1994) Linkage of photoreceptor degeneration by apoptosis with inherited defect in phototransduction. Invest Ophthalmol Vis Sci 35:358-62
Yang, Y S; Hanke, J H; Carayannopoulos, L et al. (1993) NonO, a non-POU-domain-containing, octamer-binding protein, is the mammalian homolog of Drosophila nonAdiss. Mol Cell Biol 13:5593-603

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