The N-Terminal Transactivation Domain Confers Target Gene Specificity of Hypoxia-inducible Factors HIF-1α and HIF-2α
By Cheng-Jun Hu, Aneesa Sataur, Liyi Wang, Hongqing Chen, M. C. Simon. 2007
325 citations recorded by the source corpus.
Subfields: Cancer Research, Molecular Biology, Oncology
View Paper: https://www.semanticscholar.org/paper/d9eec3ea3314f4977496ee2b2b1c9926286c41f0
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cancer Research
- G. Semenza
- P. Ratcliffe
- W. Kaelin
- N. Prabhakar
- J. Espinosa
- V. L. Dengler
- M. Galbraith
- Navdeep S. Chandel
In Molecular Biology
In Oncology
Citations in the corpus
- Hypoxia-Inducible Factor 1 (HIF-1) Pathway (2007, background): “Functional specificity for transactivation by HIF-1α and HIF-2α appears to reside in amino acid residues 415 to 659 and 418 to 619, respectively (21).”
- Oxygen sensing by metazoans: the central role of the HIF hydroxylase pathway. (2008, background): “Transcriptional selectivity is not mediated by selective DNA binding at HREs but involves sequences lying C terminal to DNA binding and dimerization domains (Hu et al., 2007; Lau et al., 2007).”
- Transcriptional Regulation by Hypoxia Inducible Factors (2013, background): “Instead, the N-TADs appear to contribute to target gene selectivity (Hu et al., 2007; Lau et al., 2007).”
- ADAPTIVE AND MALADAPTIVE CARDIORESPIRATORY RESPONSES TO CONTINUOUS AND INTERMITTENT HYPOXIA MEDIATED BY HYPOXIA-INDUCIBLE FACTORS 1 AND 2 (2012, background): “Interaction of HIF-2 with the ETS family transcription factor ELK-1 may be required for HIF-2-dependent transactivation of some target genes in some cell types (2, 122).”