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Hao Tang

Researcher at Washington University in St. Louis

Publications -  7
Citations -  1536

Hao Tang is an academic researcher from Washington University in St. Louis. The author has contributed to research in topics: Slit & Slit-Robo. The author has an hindex of 7, co-authored 7 publications receiving 1460 citations. Previous affiliations of Hao Tang include Vanderbilt University.

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Signal transduction in neuronal migration: roles of GTPase activating proteins and the small GTPase Cdc42 in the Slit-Robo pathway.

TL;DR: It is reported here that the intracellular domain of Robo interacts with a novel family of Rho GTPase activating proteins (GAPs) that are expressed in regions responsive to Slit and demonstrated important roles for GAPs and Cdc42 in neuronal migration.
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The neuronal repellent Slit inhibits leukocyte chemotaxis induced by chemotactic factors.

TL;DR: It is reported that Slit, a secreted protein previously known for its role of repulsion in axon guidance and neuronal migration, can also inhibit leukocyte chemotaxis induced by chemotactic factors, and a new therapeutic approach is proposed to treat diseases involving leukocytes andChemotactic Factors.
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Netrin requires focal adhesion kinase and Src family kinases for axon outgrowth and attraction

TL;DR: The results show the biochemical and functional links between netrin, a prototypical neuronal guidance cue, and FAK, a central player in intracellular signaling that is crucial for cell migration.
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Mutations in Tau Gene Exon 10 Associated with FTDP-17 Alter the Activity of an Exonic Splicing Enhancer to Interact with Tra2β*

TL;DR: The results implicate the human tau gene as a target gene for the alternative splicing regulator Tra2 β, suggesting that Tra2β may play a role in aberrant tau exon 10 alternativesplicing and in the pathogenesis of tauopathies.
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Neuronal Repellent Slit2 Inhibits Dendritic Cell Migration and the Development of Immune Responses

TL;DR: It is shown that Slit2, a neuronal repellent factor, is up-regulated in the skin by allergen sensitization and down-regulates the migration of Langerhans cells in a manner that results in suppression of contact hypersensitivity responses.