Xiaoling Xu
Geriatrics and Gerontology · 2001–2010
A researcher in the Science corpus: 4 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Geriatrics and Gerontology — 9 citations into it
Whom Xiaoling Xu trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- L. Guarente (in Geriatrics and Gerontology)
Papers from Xiaoling Xu's perspective
Ordered by how strongly the researchers Xiaoling Xu trusts endorse each paper. Same corpus, a different order for every researcher.
- Tumor suppressor HIC1 directly regulates SIRT1 to modulate p53-dependent DNA-damage responses. (Cell)
- Sir2 links chromatin silencing, metabolism, and aging. (Genes & Development)
- Mammalian sirtuins--emerging roles in physiology, aging, and calorie restriction. (Genes & Development)
- The Sir2 family of protein deacetylases. (Annual Review of Biochemistry)
- The SIRT1 Deacetylase Suppresses Intestinal Tumorigenesis and Colon Cancer Growth (PLoS ONE)
- A New Mouse Liver-specific Gene, Encoding a Protein Homologous to Human Antimicrobial Peptide Hepcidin, Is Overexpressed during Iron Overload* (Journal of Biological Chemistry)
- Sirtuins: critical regulators at the crossroads between cancer and aging (Oncogene)
- IL-6 mediates hypoferremia of inflammation by inducing the synthesis of the iron regulatory hormone hepcidin. (Journal of Clinical Investigation)
- Small molecule activators of sirtuins extend Saccharomyces cerevisiae lifespan (Nature)
- Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis (Nature Genetics)
Their papers
- 53BP1 inhibits homologous recombination in Brca1-deficient cells by blocking resection of DNA breaks (2010) — 1,669 citations
- TGF-β/Smad3 Signals Repress Chondrocyte Hypertrophic Differentiation and Are Required for Maintaining Articular Cartilage (2001) — 676 citations
- Impaired DNA damage response, genome instability, and tumorigenesis in SIRT1 mutant mice (2008) — 804 citations
- A role of SMAD4 in iron metabolism through the positive regulation of hepcidin expression. (2005) — 650 citations