Seoho Lee

ORCID: 0009-0009-6281-0985
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About
Contact & Profiles
Research Areas
  • Cytokine Signaling Pathways and Interactions
  • Retinoids in leukemia and cellular processes
  • Nuclear Receptors and Signaling
  • Epigenetics and DNA Methylation
  • Drug Transport and Resistance Mechanisms
  • Photochemistry and Electron Transfer Studies
  • Immune Cell Function and Interaction
  • Adenosine and Purinergic Signaling
  • Diversity and Career in Medicine
  • Dental Education, Practice, Research
  • Global Health Workforce Issues
  • Innovations in Medical Education
  • Surgical Simulation and Training
  • Neutrophil, Myeloperoxidase and Oxidative Mechanisms
  • Advanced Chemical Physics Studies
  • Simulation-Based Education in Healthcare
  • Mass Spectrometry Techniques and Applications

University of Chicago
2025

Lawrence Berkeley National Laboratory
2014

We present kinematically complete measurements of the photo-double-ionization ethylene (double CC bond) and acetylene (triple hydrocarbons just above double-ionization threshold. discuss results in terms coincident kinetic energy photoelectrons nuclear kinetic-energy release recoiling ions. have incorporated quantum chemistry calculations to interpret which electronic states dication been populated trace various subsequent fragmentation channels. suggest pathways that involve ground excited...

10.1103/physreva.89.013403 article EN Physical Review A 2014-01-13

Based on the notion that hypomorphic germline genetic variants are linked to autoimmune diseases, we reasoned novel targets for cancer immunotherapy might be identified through associated with greater T-cell infiltration into tumors. Here, report while investigating polymorphisms a tumor immune gene signature, PKCδ as candidate. Genetic deletion of in mice resulted improved endogenous antitumor immunity and increased efficacy anti-PD-L1. Single-cell RNA sequencing revealed myeloid cell...

10.1158/2326-6066.cir-23-0999 article EN Cancer Immunology Research 2025-01-14

<div>Abstract<p>Based on the notion that hypomorphic germline genetic variants are linked to autoimmune diseases, we reasoned novel targets for cancer immunotherapy might be identified through associated with greater T-cell infiltration into tumors. Here, report while investigating polymorphisms a tumor immune gene signature, protein kinase C delta (PKCδ) as candidate. Genetic deletion of <i>Prkcd</i> in mice resulted improved endogenous antitumor immunity and...

10.1158/2326-6066.c.7749848 preprint EN 2025-04-02

<p>Hematopoietic loss of PKCδ via Vav1-iCre delays tumor growth and alters inflammatory gene expression in alternative “2C1”Prkcdfl/fl founder.</p>

10.1158/2326-6066.28713791 preprint EN 2025-04-02

<p>Hematopoietic loss of PKCδ via Vav1-iCre delays tumor growth and alters inflammatory gene expression in “2B4”Prkcdfl/fl founder.</p>

10.1158/2326-6066.28713797 preprint EN 2025-04-02

<p>Loss of PKCδ in myeloid cells delays tumor growth and is further delayed with anti-PD-L1 therapy multiple Prkcdfl/fl founders.</p>

10.1158/2326-6066.28713788 preprint EN 2025-04-02
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