Yajie Yin

ORCID: 0000-0002-2220-005X
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About
Contact & Profiles
Research Areas
  • Single-cell and spatial transcriptomics
  • Cancer Immunotherapy and Biomarkers
  • Cancer Genomics and Diagnostics
  • Cancer, Lipids, and Metabolism
  • Cancer, Hypoxia, and Metabolism
  • Cancer-related Molecular Pathways
  • Immune Cell Function and Interaction
  • Ovarian cancer diagnosis and treatment
  • Metabolism, Diabetes, and Cancer
  • Cancer, Stress, Anesthesia, and Immune Response
  • RNA modifications and cancer
  • CAR-T cell therapy research
  • Estrogen and related hormone effects
  • Endometrial and Cervical Cancer Treatments
  • T-cell and B-cell Immunology
  • Lung Cancer Treatments and Mutations
  • PARP inhibition in cancer therapy
  • Fatty Acid Research and Health
  • Peroxisome Proliferator-Activated Receptors
  • Immunotherapy and Immune Responses
  • Phytochemical Studies and Bioactivities
  • Phytochemistry and Bioactive Compounds
  • Hormonal Regulation and Hypertension
  • Histone Deacetylase Inhibitors Research
  • PI3K/AKT/mTOR signaling in cancer

Daqing Normal University
2025

Stanford University
2021-2024

Gladstone Institutes
2022-2023

University of North Carolina at Chapel Hill
2017-2023

Wuhan Union Hospital
2023

Parker Institute for Cancer Immunotherapy
2023

Palo Alto University
2022

University of Jinan
2015-2017

Shandong Tumor Hospital
2016-2017

Shandong First Medical University
2015-2017

The autoimmune regulator (Aire), a well-defined transcriptional in the thymus, is also found extrathymic Aire-expressing cells (eTACs) secondary lymphoid organs. eTACs are hematopoietic antigen-presenting and inducers of immune tolerance, but their precise identity has remained unclear. Here, we use single-cell multiomics, transgenic murine models, functional approaches to define at transcriptional, genomic, proteomic level. We find that consist two similar cell types: CCR7+ migratory...

10.1126/sciimmunol.abl5053 article EN Science Immunology 2021-11-12

<div>Abstract<p>Low intratumor heterogeneity correlates with increased patient survival and immunotherapy response. However, even highly homogeneous tumors are variably aggressive, the immunologic factors impacting aggressiveness remain understudied. In this study, we analyzed mechanisms underlying immune escape in murine low heterogeneity. We used immunophenotyping single-cell RNA sequencing to compare temporal growth of <i>in vivo</i> transplanted, genetically...

10.1158/2159-8290.c.7700576 preprint EN 2025-03-03
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