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Christopher E. Heise

Researcher at Genentech

Publications -  28
Citations -  4350

Christopher E. Heise is an academic researcher from Genentech. The author has contributed to research in topics: Receptor & Kinase. The author has an hindex of 18, co-authored 28 publications receiving 4061 citations. Previous affiliations of Christopher E. Heise include University of Virginia.

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The immune modulator FTY720 targets sphingosine 1-phosphate receptors.

TL;DR: The results suggest that FTY720, after phosphorylation, acts through sphingosine 1-phosphate signaling pathways to modulate chemotactic responses and lymphocyte trafficking.
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Characterization of the human cysteinyl leukotriene 2 receptor.

TL;DR: The cloning and characterization of the second cysteinyl leukotriene receptor, CysLT2, a 346-amino acid protein with 38% amino acid identity to the Cys LT1 receptor is described and demonstrated high affinity binding and a rank order of potency for competition of LTC4 = LTD4 ≫ LTE4.
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Characterization of a novel sphingosine 1-phosphate receptor, Edg-8.

TL;DR: The cloned and characterized Edg-8 is a high affinity sphingosine 1-phosphate receptor that couples to Gi/oα proteins and is expressed predominantly by oligodendrocytes and/or fibrous astroCytes in the rat brain.
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Histone Deacetylase (HDAC) Inhibitor Kinetic Rate Constants Correlate with Cellular Histone Acetylation but Not Transcription and Cell Viability

TL;DR: Evaluating HDAC inhibitor properties using histone acetylation is not predictive of their function on cellular activity, and a panel of benzamide-containingHDACi are slow tight-binding inhibitors with long residence times unlike the hydroxamate-containing HDACi vorinostat and trichostatin-A.
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A Therapeutic Antibody Targeting BACE1 Inhibits Amyloid-β Production in Vivo

TL;DR: This elegant pair of papers demonstrates the therapeutic potential of an anti-BACE1 antibody for treating Alzheimer’s disease but also provides a strategy worthy of the ancient Greeks that could be applied to other therapeutic antibodies that require safe passage into the human brain.