Paula Grondona

ORCID: 0000-0002-2938-9975
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About
Contact & Profiles
Research Areas
  • NF-κB Signaling Pathways
  • Immune Response and Inflammation
  • Antimicrobial Peptides and Activities
  • Immune Cell Function and Interaction
  • Renal and related cancers
  • T-cell and Retrovirus Studies
  • Psoriasis: Treatment and Pathogenesis
  • Cytokine Signaling Pathways and Interactions
  • Signaling Pathways in Disease
  • CAR-T cell therapy research
  • CRISPR and Genetic Engineering
  • Lymphoma Diagnosis and Treatment
  • Dermatology and Skin Diseases
  • Pluripotent Stem Cells Research

University of Tübingen
2015-2020

Proinflammatory cytokine signaling in keratinocytes plays a crucial role the pathogenesis of psoriasis, skin disease characterized by hyperproliferation and abnormal differentiation infiltration inflammatory cells. Although IL-17A TNFα are effective therapeutic targets IL-36 has recently emerged as proinflammatory cytokine. However, little is known about its downstream transcriptional responses. Here, we found that exposure to induced expression IκBζ, an atypical IκB member specific...

10.1073/pnas.1801377115 article EN cc-by-nc-nd Proceedings of the National Academy of Sciences 2018-09-17

Pluripotent stem cells must strictly maintain genomic integrity to prevent transmission of mutations. In human induced pluripotent (iPSCs), we found that genome surveillance is achieved via two ways, namely, a hypersensitivity apoptosis and very low accumulation DNA lesions. The threshold was mediated by constitutive p53 expression marked upregulation proapoptotic target genes the BCL-2 family, ensuring efficient iPSC removal upon genotoxic insults. Intriguingly, despite elevated...

10.1016/j.stemcr.2015.04.004 article EN cc-by-nc-nd Stem Cell Reports 2015-05-01
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