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Bidirectional crosstalk between Hypoxia-Inducible Factor and glucocorticoid signalling in zebrafish larvae

https://doi.org/10.1101/748566
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/aja.1002030302openalex-snapshot
Stages of embryonic development of the zebrafish
inferredcites →https://doi.org/10.1002/hep.24655openalex-snapshot
Glucocorticoids Increase Interleukin–6–Dependent Gene Induction by Interfering With the Expression of the Suppressor of Cytokine Signaling 3 Feedback Inhibitor
inferredcites →https://doi.org/10.1002/jemt.1132openalex-snapshot
Dynamics and plasticity of peptidergic control centres in the retino‐brain‐pituitary system of Xenopus laevis
inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/82_2010_74openalex-snapshot
Hypoxia-Inducible Factors as Essential Regulators of Inflammation
inferredcites →https://doi.org/10.1007/s00424-005-1413-7openalex-snapshot
Hypoxia-responsive transcription factors
inferredcites →https://doi.org/10.1007/s101260000001openalex-snapshot
Overexpression of a Zebrafish ARNT2-like Factor Represses CYP1A Transcription in ZLE Cells
inferredcites →https://doi.org/10.1016/b978-0-08-046884-6.00214-1openalex-snapshot
ARNT: A Key bHLH/PAS Regulatory Protein Across Multiple Pathways
inferredcites →https://doi.org/10.1016/b978-0-12-381320-6.00007-2openalex-snapshot
A Zebrafish Model for VHL and Hypoxia Signaling
inferredcites →https://doi.org/10.1016/j.bbrc.2008.05.061openalex-snapshot
Dexamethasone impairs hypoxia-inducible factor-1 function
inferredcites →https://doi.org/10.1016/j.cbpa.2008.12.014openalex-snapshot
The zebrafish as a model system for glucocorticoid receptor research
inferredcites →https://doi.org/10.1016/j.cell.2012.01.021openalex-snapshot
Hypoxia-Inducible Factors in Physiology and Medicine
inferredcites →https://doi.org/10.1016/j.devcel.2018.06.003openalex-snapshot
A Rapid Method for Directed Gene Knockout for Screening in G0 Zebrafish
inferredcites →https://doi.org/10.1016/j.immuni.2014.09.008openalex-snapshot
HIF Transcription Factors, Inflammation, and Immunity
inferredcites →https://doi.org/10.1016/j.jaci.2013.09.007openalex-snapshot
The biology of the glucocorticoid receptor: New signaling mechanisms in health and disease
inferredcites →https://doi.org/10.1016/j.jsbmb.2013.01.003openalex-snapshot
Zebrafish and steroids: What do we know and what do we need to know?
inferredcites →https://doi.org/10.1016/j.lfs.2015.12.059openalex-snapshot
Down-regulation of GRα expression and inhibition of its nuclear translocation by hypoxia
inferredcites →https://doi.org/10.1016/j.mce.2017.02.036openalex-snapshot
Functional analysis reveals no transcriptional role for the glucocorticoid receptor β-isoform in zebrafish
inferredcites →https://doi.org/10.1016/j.molcel.2012.04.021openalex-snapshot
The Stat3/GR Interaction Code: Predictive Value of Direct/Indirect DNA Recruitment for Transcription Outcome
inferredcites →https://doi.org/10.1016/j.rdc.2015.08.002openalex-snapshot
Corticosteroids
inferredcites →https://doi.org/10.1016/j.tem.2012.11.005openalex-snapshot
The five Rs of glucocorticoid action during inflammation: ready, reinforce, repress, resolve, and restore
inferredcites →https://doi.org/10.1016/j.tips.2018.11.002openalex-snapshot
Non-genomic Effects of Glucocorticoids: An Updated View
inferredcites →https://doi.org/10.1016/j.ygcen.2008.09.011openalex-snapshot
The zebrafish stress axis: Molecular fallout from the teleost-specific genome duplication event
inferredcites →https://doi.org/10.1016/s0140-6736(09)60326-3openalex-snapshot
Glucocorticoid resistance in inflammatory diseases
inferredcites →https://doi.org/10.1016/s0278-2391(10)80207-1openalex-snapshot
The use of glucocorticosteroids to lessen the inflammatory sequelae following third molar surgery
inferredcites →https://doi.org/10.1038/mp.2012.64openalex-snapshot
An affective disorder in zebrafish with mutation of the glucocorticoid receptor
inferredcites →https://doi.org/10.1038/nrc2540openalex-snapshot
The impact of O2 availability on human cancer
inferredcites →https://doi.org/10.1038/s41598-017-04535-6openalex-snapshot
nr3c1 null mutant zebrafish are viable and reveal DNA-binding-independent activities of the glucocorticoid receptor
inferredcites →https://doi.org/10.1038/s41598-018-36681-wopenalex-snapshot
The mineralocorticoid receptor is essential for stress axis regulation in zebrafish larvae
inferredcites →https://doi.org/10.1042/bj20042121openalex-snapshot
Identification of a functional hypoxia-responsive element that regulates the expression of the egl nine homologue 3 (egln3/phd3) gene
inferredcites →https://doi.org/10.1056/nejmra0910283openalex-snapshot
Hypoxia and Inflammation
inferredcites →https://doi.org/10.1056/nejmra1011165openalex-snapshot
Oxygen Sensing, Homeostasis, and Disease
inferredcites →https://doi.org/10.1073/pnas.1705338114openalex-snapshot
Glucocorticoids promote Von Hippel Lindau degradation and Hif-1α stabilization
inferredcites →https://doi.org/10.1074/jbc.m302581200openalex-snapshot
Role of the Glucocorticoid Receptor for Regulation of Hypoxia-dependent Gene Expression
inferredcites →https://doi.org/10.1080/13684730412331302081openalex-snapshot
Molecular aspects of glucocorticoid hormone action in rheumatoid arthritis
inferredcites →https://doi.org/10.1089/zeb.2008.0536openalex-snapshot
Potential Roles of Arnt2 in Zebrafish Larval Development
inferredcites →https://doi.org/10.1093/embo-reports/kve130openalex-snapshot
Hypoxia‐inducible factor‐1α (HIF‐1α) escapes O2‐driven proteasomal degradation irrespective of its subcellular localization: nucleus or cytoplasm
inferredcites →https://doi.org/10.1093/nar/gku410openalex-snapshot
CHOPCHOP: a CRISPR/Cas9 and TALEN web tool for genome editing
inferredcites →https://doi.org/10.1093/nar/gkw398openalex-snapshot
CHOPCHOP v2: a web tool for the next generation of CRISPR genome engineering
inferredcites →https://doi.org/10.1111/gbb.12549openalex-snapshot
Novel zebrafish behavioral assay to identify modifiers of the rapid, nongenomic stress response
inferredcites →https://doi.org/10.1111/j.1365-4632.2009.04322.xopenalex-snapshot
Prevention and treatment of systemic glucocorticoid side effects
inferredcites →https://doi.org/10.1111/j.1476-5381.2010.01199.xopenalex-snapshot
Glucocorticosteroids: current and future directions
inferredcites →https://doi.org/10.1111/j.1755-148x.2008.00445.xopenalex-snapshot
Cyclical training enhances the melanophore responses of zebrafish to background colours
inferredcites →https://doi.org/10.1111/jne.12643openalex-snapshot
The role of the vagus nerve in appetite control: Implications for the pathogenesis of obesity
inferredcites →https://doi.org/10.1124/mol.105.016873openalex-snapshot
Identification of Zebrafish ARNT1 Homologs: 2,3,7,8-Tetrachlorodibenzo-p-dioxin Toxicity in the Developing Zebrafish Requires ARNT1
inferredcites →https://doi.org/10.1152/ajpregu.00671.2007openalex-snapshot
Development of the corticosteroid stress axis and receptor expression in zebrafish
inferredcites →https://doi.org/10.1158/0008-5472.can-11-3148openalex-snapshot
A Zebrafish Model to Study and Therapeutically Manipulate Hypoxia Signaling in Tumorigenesis
inferredcites →https://doi.org/10.1172/jci67230openalex-snapshot
HIF-1 mediates metabolic responses to intratumoral hypoxia and oncogenic mutations
inferredcites →https://doi.org/10.1177/1177625017713193openalex-snapshot
Overexpression and Knockdown of Hypoxia-Inducible Factor 1 Disrupt the Expression of Steroidogenic Enzyme Genes and Early Embryonic Development in Zebrafish
inferredcites →https://doi.org/10.1182/blood-2008-07-167890openalex-snapshot
Zebrafish mutants in the von Hippel-Lindau tumor suppressor display a hypoxic response and recapitulate key aspects of Chuvash polycythemia
inferredcites →https://doi.org/10.1186/1749-8104-4-22openalex-snapshot
Neuroendocrine transcriptional programs adapt dynamically to the supply and demand for neuropeptides as revealed in NSF mutant zebrafish
inferredcites →https://doi.org/10.1186/s12902-015-0017-2openalex-snapshot
Effects of hypoxia inducible factor-1α on apoptotic inhibition and glucocorticoid receptor downregulation by dexamethasone in AtT-20 cells
inferredcites →https://doi.org/10.1210/edrv-17-3-245openalex-snapshot
Molecular Determinants of Glucocorticoid Receptor Function and Tissue Sensitivity to Glucocorticoids
inferredcites →https://doi.org/10.1210/en.2014-1941openalex-snapshot
Transcriptional and Metabolic Effects of Glucocorticoid Receptor α and β Signaling in Zebrafish
inferredcites →https://doi.org/10.1210/en.2017-00549openalex-snapshot
Genetic Disruption of 21-Hydroxylase in Zebrafish Causes Interrenal Hyperplasia
inferredcites →https://doi.org/10.1242/dev.099085openalex-snapshot
Efficient CRISPR/Cas9 genome editing with low off-target effects in zebrafish
inferredcites →https://doi.org/10.1242/dev.134809openalex-snapshot
Maximizing mutagenesis with solubilized CRISPR-Cas9 ribonucleoprotein complexes.
inferredcites →https://doi.org/10.1242/dev.138305openalex-snapshot
Rx3 and Shh direct anisotropic growth and specification in the zebrafish tuberal/anterior hypothalamus
inferredcites →https://doi.org/10.1242/dmm.021865openalex-snapshot
Exploring the HIFs, buts and maybes of hypoxia signalling in disease: lessons from zebrafish models
inferredcites →https://doi.org/10.1242/dmm.037887openalex-snapshot
Glucocorticoids inhibit macrophage differentiation towards a pro-inflammatory phenotype upon wounding without affecting their migration
inferredcites →https://doi.org/10.1242/jeb.163709openalex-snapshot
Hypoxia-inducible transcription factors in fish: expression, function and interconnection with the circadian clock
inferredcites →https://doi.org/10.12968/joan.2012.1.4.198openalex-snapshot
Steroids: what are they and what is their mechanism of action?
inferredcites →https://doi.org/10.1371/journal.pbio.1001112openalex-snapshot
Hypoxia-Inducible Factor Directs POMC Gene to Mediate Hypothalamic Glucose Sensing and Energy Balance Regulation
inferredcites →https://doi.org/10.1371/journal.pone.0005077openalex-snapshot
Real-Time Imaging of HIF-1α Stabilization and Degradation
inferredcites →https://doi.org/10.1371/journal.pone.0077997openalex-snapshot
Glucocorticoid Receptor, but Not Mineralocorticoid Receptor, Mediates Cortisol Regulation of Epidermal Ionocyte Development and Ion Transport in Zebrafish (Danio Rerio)
inferredcites →https://doi.org/10.1371/journal.pone.0128938openalex-snapshot
Developmental Expression and Hypoxic Induction of Hypoxia Inducible Transcription Factors in the Zebrafish
inferredcites →https://doi.org/10.1530/joe-16-0661openalex-snapshot
30 YEARS OF THE MINERALOCORTICOID RECEPTOR: Evolution of the mineralocorticoid receptor: sequence, structure and function
inferredcites →https://doi.org/10.3389/fnbeh.2012.00068openalex-snapshot
A zebrafish model of glucocorticoid resistance shows serotonergic modulation of the stress response
inferredcites →https://doi.org/10.3389/fncir.2013.00145openalex-snapshot
Glucocorticoid receptor activity regulates light adaptation in the zebrafish retina
inferredcites →https://doi.org/10.4049/jimmunol.0903421openalex-snapshot
Macrophage Migration Inhibitory Factor Counterregulates Dexamethasone-Mediated Suppression of Hypoxia-Inducible Factor-1α Function and Differentially Influences Human CD4+ T Cell Proliferation under Hypoxia
inferredcites →https://doi.org/10.4049/jimmunol.174.4.2250openalex-snapshot
Potentiation of Glucocorticoid Activity in Hypoxia through Induction of the Glucocorticoid Receptor

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/s00018-020-03750-1openalex-snapshot
HIF1α is a direct regulator of steroidogenesis in the adrenal gland
inferred← citeshttps://doi.org/10.1101/2020.07.08.191783openalex-snapshot
HIF1α is an essential regulator of steroidogenesis in the adrenal gland
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