H. Yee
Cell · with Dickins · 2008
A researcher in the Science corpus: 1 paper; trusts 1 researcher and is trusted by 2 researchers here, as inferred from the citation graph.
Whom H. Yee trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- M. Pinzani (in Hepatology)
Who trusts H. Yee
- J. Campisi (in Physiology)
- S. Friedman (in Immunology)
Papers from H. Yee's perspective
Ordered by how strongly the researchers H. Yee trusts endorse each paper. Same corpus, a different order for every researcher.
- Liver fibrosis (Springer Seminars in Immunopathology)
- Rb-mediated heterochromatin formation and silencing of E2F target genes during cellular senescence. (Cell)
- Tumour biology: Senescence in premalignant tumours (Nature)
- A senescence program controlled by p53 and p16INK4a contributes to the outcome of cancer therapy. (Cell)
- The DNA damage pathway regulates innate immune system ligands of the NKG2D receptor (Nature)
- Oncogene-induced senescence is a DNA damage response triggered by DNA hyper-replication (Nature)
- Natural killer cells ameliorate liver fibrosis by killing activated stellate cells in NKG2D-dependent and tumor necrosis factor-related apoptosis-inducing ligand-dependent manners. (Gastroenterology)
- Senescent fibroblasts promote epithelial cell growth and tumorigenesis: A link between cancer and aging (Proceedings of the National Academy of Sciences of the United States of America)
- Senescence and tumour clearance is triggered by p53 restoration in murine liver carcinomas (Nature)
- Oncogene-induced senescence is part of the tumorigenesis barrier imposed by DNA damage checkpoints (Nature)
Their papers
- Senescence of activated stellate cells limits liver fibrosis (2008) — 1,898 citations