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T

T. Michaeli

Researcher at Cold Spring Harbor Laboratory

Publications -  14
Citations -  1830

T. Michaeli is an academic researcher from Cold Spring Harbor Laboratory. The author has contributed to research in topics: Mutant & Saccharomyces cerevisiae. The author has an hindex of 11, co-authored 14 publications receiving 1796 citations.

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The S. cerevisiae CDC25 gene product regulates the RAS/adenylate cyclase pathway

TL;DR: It is proposed that CDC25 regulates adenylate cyclase by regulating the guanine nucleotide bound to RAS proteins, suggesting that normal RAS is dependent on CDC25 function.
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A family of human phosphodiesterases homologous to the dunce learning and memory gene product of Drosophila melanogaster are potential targets for antidepressant drugs

TL;DR: Four human genes (DPDE1 through DPDE4) closely related to the dnc learning and memory locus of Drosophila melanogaster are isolated and shown to encode cyclic AMP-specific phosphodiesterases.
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Cloning and characterization of CAP, the S. cerevisiae gene encoding the 70 kd adenylyl cyclase-associated protein

TL;DR: The results suggest that CAP is required for at least some aspects of the RAS-responsive signaling system, including the inability to grow on rich medium (YPD), temperature sensitivity on minimal medium, sensitivity to nitrogen starvation, and a swollen cell morphology.
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Isolation and characterization of a previously undetected human cAMP phosphodiesterase by complementation of cAMP phosphodiesterase-deficient Saccharomyces cerevisiae.

TL;DR: The biochemical and pharmacological properties of HCP1 suggest that it is a member of a previously undiscovered cyclic nucleotide PDE family, and northern blot analysis indicates that high levels of H CP1 mRNA are present in human skeletal muscle.
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Isolation and characterization of a mammalian gene encoding a high-affinity cAMP phosphodiesterase

TL;DR: It is shown that the DPD protein is a high-affinity cAMP-specific phosphodiesterase, a mutant form of the RAS2 gene analogous to an oncogenic mutant of the human HRAS gene.