SARS-CoV-2 controlled kinase functions

Grant number: P 35159

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2021
    2024
  • Known Financial Commitments (USD)

    $475,969.07
  • Funder

    FWF
  • Principal Investigator

    N/A

  • Research Location

    Austria
  • Lead Research Institution

    Institut für Biochemie, Universität Innsbruck
  • Research Priority Alignment

    N/A
  • Research Category

    Clinical characterisation and management

  • Research Subcategory

    Disease pathogenesis

  • Special Interest Tags

    N/A

  • Study Type

    Unspecified

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

Publicationslinked via Europe PMC

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View all publications at Europe PMC

Phosphorylation of the compartmentalized PKA substrate TAF15 regulates RNA-protein interactions.

Direct comparison of SARS-CoV-2 variant specific neutralizing antibodies in human and hamster sera.

Characterizing SARS-CoV-2 neutralization profiles after bivalent boosting using antigenic cartography.

Disruptor: Computational identification of oncogenic mutants disrupting protein-protein and protein-DNA interactions.

Missense variant interaction scanning reveals a critical role of the FERM domain for tumor suppressor protein NF2 conformation and function.

Tracking and blocking interdependencies of cellular BRAF-MEK oncokinase activities.

BA.2 and BA.5 omicron differ immunologically from both BA.1 omicron and pre-omicron variants.

Kinase perturbations redirect mitochondrial function in cancer.

Physiological Cell Culture Media Tune Mitochondrial Bioenergetics and Drug Sensitivity in Cancer Cell Models.