Jamie E. Hoberg
Cancer Research · 2004–2006
A researcher in the Science corpus: 2 papers; trusts 5 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Cancer Research — 35 citations into it
- Molecular Biology — 31 citations into it
- Immunology — 19 citations into it
- Oncology — 16 citations into it
Whom Jamie E. Hoberg trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Jamie E. Hoberg overall
Papers from Jamie E. Hoberg's perspective
Ordered by how strongly the researchers Jamie E. Hoberg trusts endorse each paper. Same corpus, a different order for every researcher.
- The Phosphorylation Status of Nuclear NF-ΚB Determines Its Association with CBP/p300 or HDAC-1
- Essential role of RelA Ser311 phosphorylation by ζPKC in NF‐κB transcriptional activation
- Post-activation Turn-off of NF-κB-dependent Transcription Is Regulated by Acetylation of p65* (Journal of Biological Chemistry)
- Acetylation of RelA at discrete sites regulates distinct nuclear functions of NF‐κB (EMBO Journal)
- Missing pieces in the NF-kappaB puzzle. (Cell)
- Transcriptional activation of the NF‐κB p65 subunit by mitogen‐ and stress‐activated protein kinase‐1 (MSK1) (EMBO Journal)
- Modulation of NF‐κB‐dependent transcription and cell survival by the SIRT1 deacetylase (EMBO Journal)
- Phylogenetic classification of prokaryotic and eukaryotic Sir2-like proteins. (Biochemical and Biophysical Research Communications - BBRC)
- Duration of Nuclear NF-κB Action Regulated by Reversible Acetylation (Science)
- NF-κB at the crossroads of life and death (Nature Immunology)
Their papers
- Modulation of NF‐κB‐dependent transcription and cell survival by the SIRT1 deacetylase (2004) — 2,787 citations
- IκB Kinase α-Mediated Derepression of SMRT Potentiates Acetylation of RelA/p65 by p300 (2006) — 175 citations