scholarly article | Q13442814 |
review article | Q7318358 |
P6179 | Dimensions Publication ID | 1017888042 |
P356 | DOI | 10.1203/PDR.0B013E31818FC83F |
P698 | PubMed publication ID | 18852690 |
P5875 | ResearchGate publication ID | 23317774 |
P50 | author | Ola Didrik Saugstad | Q47546644 |
P2093 | author name string | Emin Maltepe | |
P2860 | cites work | Archean Molecular Fossils and the Early Rise of Eukaryotes | Q22065553 |
HIFalpha targeted for VHL-mediated destruction by proline hydroxylation: implications for O2 sensing | Q24291102 | ||
C. elegans EGL-9 and mammalian homologs define a family of dioxygenases that regulate HIF by prolyl hydroxylation | Q24291783 | ||
A conserved family of prolyl-4-hydroxylases that modify HIF | Q24291794 | ||
Hypoxia-inducible factor 1 is a basic-helix-loop-helix-PAS heterodimer regulated by cellular O2 tension | Q24307473 | ||
The hypoxia-responsive transcription factor EPAS1 is essential for catecholamine homeostasis and protection against heart failure during embryonic development | Q24595910 | ||
Targeting of HIF-alpha to the von Hippel-Lindau ubiquitylation complex by O2-regulated prolyl hydroxylation | Q27860876 | ||
Cellular and developmental control of O2 homeostasis by hypoxia-inducible factor 1 alpha | Q28259513 | ||
HIF-1-mediated expression of pyruvate dehydrogenase kinase: a metabolic switch required for cellular adaptation to hypoxia | Q28300406 | ||
HIF-1 mediates adaptation to hypoxia by actively downregulating mitochondrial oxygen consumption | Q28300415 | ||
Lack of hypoxia-inducible factor-1 alpha impairs midbrain neural precursor cells involving vascular endothelial growth factor signaling | Q28506157 | ||
Placental but not heart defects are associated with elevated hypoxia-inducible factor alpha levels in mice lacking prolyl hydroxylase domain protein 2 | Q28508549 | ||
Loss of HIF-2alpha and inhibition of VEGF impair fetal lung maturation, whereas treatment with VEGF prevents fatal respiratory distress in premature mice | Q28508637 | ||
Defective brain development in mice lacking the Hif-1alpha gene in neural cells | Q28512300 | ||
HIF-1 alpha is required for solid tumor formation and embryonic vascularization. | Q28588778 | ||
VEGFA is necessary for chondrocyte survival during bone development | Q28590528 | ||
Multiple organ pathology, metabolic abnormalities and impaired homeostasis of reactive oxygen species in Epas1-/- mice | Q28594703 | ||
Purification and characterization of hypoxia-inducible factor 1 | Q28678375 | ||
Mitochondrial reactive oxygen species trigger hypoxia-induced transcription | Q29614203 | ||
Mitochondrial complex III is required for hypoxia-induced ROS production and cellular oxygen sensing | Q29615506 | ||
Hypoxia-mediated selection of cells with diminished apoptotic potential in solid tumours | Q29618396 | ||
Oxygen sensitivity severely limits the replicative lifespan of murine fibroblasts | Q29618748 | ||
Avoiding hyperoxia in infants 1250 g is associated with improved short- and long-term outcomes | Q30463931 | ||
Pulse oximetry, severe retinopathy, and outcome at one year in babies of less than 28 weeks gestation | Q30473664 | ||
Can Changes in Clinical Practice Decrease the Incidence of Severe Retinopathy of Prematurity in Very Low Birth Weight Infants? | Q30477134 | ||
Effects of oxygen toxicity on early development of mouse embryos | Q33432686 | ||
Deletion of Vhlh in chondrocytes reduces cell proliferation and increases matrix deposition during growth plate development. | Q47645076 | ||
HO-2 provides endogenous protection against oxidative stress and apoptosis caused by TNF-alpha in cerebral vascular endothelial cells | Q48478299 | ||
The developmental potential of the human oocyte is related to the dissolved oxygen content of follicular fluid: association with vascular endothelial growth factor levels and perifollicular blood flow characteristics | Q48958485 | ||
Factors affecting the developmental competence of mouse oocytes grown in vitro: oxygen concentration | Q49030684 | ||
Abnormal angiogenesis and responses to glucose and oxygen deprivation in mice lacking the protein ARNT. | Q52195684 | ||
Intracellular signaling by reactive oxygen species during hypoxia in cardiomyocytes. | Q52563106 | ||
Plasma Hypoxanthine Concentrations in Pigs | Q58144098 | ||
Hypoxanthine as a Measurement of Hypoxia | Q58144110 | ||
Maternal arterial connections to the placental intervillous space during the first trimester of human pregnancy: the Boyd collection revisited | Q33732595 | ||
Toxic effects of oxygen on human embryo development | Q34066138 | ||
HIF-1 and mechanisms of hypoxia sensing | Q34180645 | ||
Oxygen poisoning and x-irradiation: a mechanism in common | Q34235248 | ||
Biological defense mechanisms. The production by leukocytes of superoxide, a potential bactericidal agent | Q34501431 | ||
Carbon monoxide-induced suspended animation protects against hypoxic damage in Caenorhabditis elegans | Q34836826 | ||
Oxygen deprivation induced cell death: an update | Q34949087 | ||
Genetic models in applied physiology: invited review: effect of oxygen deprivation on cell cycle activity: a profile of delay and arrest | Q35101172 | ||
Mitochondrial dysfunction resulting from loss of cytochrome c impairs cellular oxygen sensing and hypoxic HIF-alpha activation | Q35120687 | ||
Multilineage embryonic hematopoiesis requires hypoxic ARNT activity | Q35207418 | ||
Placental cell fates are regulated in vivo by HIF-mediated hypoxia responses | Q35209175 | ||
Mitochondrial regulation of oxygen sensing | Q36250880 | ||
Oxygen deprivation causes suspended animation in the zebrafish embryo | Q36304805 | ||
Inhibition of NGF deprivation-induced death by low oxygen involves suppression of BIMEL and activation of HIF-1 | Q36321474 | ||
Free radicals, mitochondria, and hypoxia-ischemia in the developing brain | Q36380301 | ||
Defective placental vasculogenesis causes embryonic lethality in VHL-deficient mice | Q36551258 | ||
Culture of rabbit zygotes into blastocysts in protein-free medium with one to twenty per cent oxygen | Q36766323 | ||
Executive summary of the workshop on oxygen in neonatal therapies: controversies and opportunities for research | Q36778370 | ||
Optimal oxygenation at birth and in the neonatal period | Q36851888 | ||
Oxygen, the lead actor in the pathophysiologic drama: enactment of the trinity of normoxia, hypoxia, and hyperoxia in disease and therapy | Q36932714 | ||
Oxygen-reactive species and antioxidant responses during development: the metabolic paradox of cellular differentiation | Q37630871 | ||
Hypoxanthine as an indicator of hypoxia: its role in health and disease through free radical production | Q39634654 | ||
Oxygen radicals and pulmonary damage | Q39832951 | ||
A targeted antioxidant reveals the importance of mitochondrial reactive oxygen species in the hypoxic signaling of HIF-1alpha. | Q40429133 | ||
ERK activation upon hypoxia: involvement in HIF-1 activation | Q40898952 | ||
Maternal circulation in the first-trimester human placenta--myth or reality? | Q41392140 | ||
Expression of NADPH oxidases and enhanced H(2)O(2)-generating activity in human coronary artery endothelial cells upon induction with tumor necrosis factor-alpha | Q42439900 | ||
Suspended Animation in C. elegans Requires the Spindle Checkpoint | Q42612760 | ||
ARNT-deficient mice and placental differentiation | Q43703428 | ||
Intrauterine Oxygen Tension in the Rat During Progestation: Its Possible Relation to Carbohydrate Metabolism and the Regulation of Nidation | Q43978222 | ||
Hyperoxia-induced NAD(P)H oxidase activation and regulation by MAP kinases in human lung endothelial cells | Q44185726 | ||
HIF-1alpha controls extracellular matrix synthesis by epiphyseal chondrocytes | Q44383061 | ||
Tolerance to low O2: lessons from invertebrate genetic models | Q44825477 | ||
Life with oxygen | Q45345070 | ||
Reactive oxygen metabolites relax the lamb ductus arteriosus by stimulating prostaglandin production. | Q46040152 | ||
Hypoxia-inducible factor-dependent histone deacetylase activity determines stem cell fate in the placenta | Q46081787 | ||
To oxygenate or not to oxygenate--that is the question | Q46425704 | ||
Oxygen sensing requires mitochondrial ROS but not oxidative phosphorylation | Q46626427 | ||
Regulation of human placental development by oxygen tension | Q46733260 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | oxygen | Q629 |
P304 | page(s) | 261-268 | |
P577 | publication date | 2009-03-01 | |
P1433 | published in | Pediatric Research | Q7159215 |
P1476 | title | Oxygen in health and disease: regulation of oxygen homeostasis--clinical implications | |
P478 | volume | 65 |
Q46300078 | A Review of Oxygen Physiology and Appropriate Management of Oxygen Levels in Premature Neonates |
Q62397741 | A double-blind, randomized clinical trial of the effect of ω-3 fatty acids on the oxidative stress of preterm neonates fed through parenteral nutrition |
Q42875477 | A metabolomic approach in an experimental model of hypoxia-reoxygenation in newborn piglets: urine predicts outcome |
Q47142957 | Acute hypoxia-reoxygenation and vascular oxygen sensing in the chicken embryo. |
Q38201981 | Administration of 100% oxygen does not hasten resolution of symptomatic spontaneous pneumothorax in neonates |
Q39194532 | Analysis of lipid peroxidation biomarkers in extremely low gestational age neonate urines by UPLC-MS/MS. |
Q47871813 | Anti-oxidants correct disturbance of redox enzymes in the hearts of rat fetuses with congenital diaphragmatic hernia |
Q44062958 | Beyond pulmonary hypertension: sildenafil for chronic lung disease of prematurity |
Q47683682 | Bronchopulmonary dysplasia: A review of pathogenesis and pathophysiology |
Q26748643 | Can the preterm lung recover from perinatal stress? |
Q108395817 | Cell-Free Hemoglobin Does Not Attenuate the Effects of SARS-CoV-2 Spike Protein S1 Subunit in Pulmonary Endothelial Cells |
Q37406042 | Characterization of exosomal release in bovine endometrial intercaruncular stromal cells |
Q49713077 | Current Practices and Attitudes Regarding Use of Inhaled Nitric Oxide in the NICU: Results From a Survey of Members of the National Association of Neonatal Nurse Practitioners |
Q37763202 | Current and future therapeutic options for persistent pulmonary hypertension in the newborn |
Q44488466 | Delay in rat lung alveolarization after the combined exposure of maternal hyperglycemia and postnatal hyperoxia |
Q56543439 | Deleterious Effect of Hyperoxia at Birth on White Matter Damage in the Newborn Rat |
Q58999141 | Effective Single-Step Posttranscriptional Dynamics Allowing for a Direct Maximum Likelihood Estimation of Transcriptional Activity and the Quantification of Sources of Gene Expression Variability with an Illustration for the Hypoxia and TNFα Regulat |
Q38719362 | Effects of astaxanthin on oxidative stress induced by Cu2+ in prostate cells |
Q38842527 | Effects of targeting lower versus higher arterial oxygen saturations on death or disability in preterm infants. |
Q37577306 | Endoplasmic reticulum stress, inflammation, and perinatal brain damage |
Q47959386 | Follicular fluid lipid peroxidation levels in women with endometriosis during controlled ovarian hyperstimulation. |
Q37720165 | Gene expression profiles in preterm infants on continuous long‑term oxygen therapy suggest reduced oxidative stress‑dependent signaling during hypoxia |
Q31151332 | Glucose and Intermediary Metabolism and Astrocyte-Neuron Interactions Following Neonatal Hypoxia-Ischemia in Rat. |
Q33819143 | Glutathionylated γG and γA subunits of hemoglobin F: a novel post-translational modification found in extremely premature infants by LC-MS and nanoLC-MS/MS. |
Q55248750 | High-performance reoxygenation from PLGA-PEG/PFOB emulsions: a feedback relationship between ROS and HIF-1α. |
Q39109418 | Hyperbaric Environment: Oxygen and Cellular Damage versus Protection |
Q37992223 | Hyperoxia in the term newborn: more evidence is still needed for optimal oxygen therapy |
Q37769765 | Hypoxia-inducible factor (HIF) and HIF-stabilizing agents in neonatal care |
Q34757237 | Hypoxia-inducible vascular endothelial growth factor-engineered mesenchymal stem cells prevent myocardial ischemic injury |
Q64095662 | Mitochondrial superoxide anions induced by exogenous oxidative stress determine tumor cell fate: an individual cell-based study |
Q35157695 | N-methyl-D-aspartate receptor subtype 3A promotes apoptosis in developing mouse brain exposed to hyperoxia |
Q21133540 | Nuclear localization of the mitochondrial factor HIGD1A during metabolic stress |
Q44503420 | Omeprazole induces heme oxygenase-1 in fetal human pulmonary microvascular endothelial cells via hydrogen peroxide-independent Nrf2 signaling pathway |
Q60047016 | Oxidative Stress and Neonatal Respiratory Extracorporeal Membrane Oxygenation |
Q60954098 | Oxidative Stress in the Newborn Period: Useful Biomarkers in the Clinical Setting |
Q57053390 | Oxygen Regulation in Development: Lessons from Embryogenesis towards Tissue Engineering |
Q26752362 | Oxygen Supplementation to Stabilize Preterm Infants in the Fetal to Neonatal Transition: No Satisfactory Answer |
Q37784210 | Oxygen and oxidative stress in bronchopulmonary dysplasia |
Q33555704 | Oxygen and oxidative stress in the perinatal period. |
Q57300346 | Oxygen therapy of the newborn from molecular understanding to clinical practice |
Q36919904 | Quantifying hyperoxia-mediated damage to mammalian respiratory cilia-driven fluid flow using particle tracking velocimetry optical coherence tomography |
Q46966355 | Randomized clinical trial of new intravenous lipid (SMOFlipid 20%) versus medium-chain triglycerides/long-chain triglycerides in adult patients undergoing gastrointestinal surgery. |
Q42677471 | Rapid Generation and Detection of Biomimetic Oxygen Concentration Gradients In Vitro |
Q37438622 | Remodeling of the tight junction during recovery from exposure to hydrogen peroxide in kidney epithelial cells |
Q47318644 | SLC9B1 methylation predicts fetal intolerance of labor |
Q33452039 | Similarities and differences of hyperbaric oxygen and medical ozone applications |
Q90176437 | Technical Feasibility and Physiological Relevance of Hypoxic Cell Culture Models |
Q92349478 | The Effects of Hyperbaric Oxygen at Different Pressures on Oxidative Stress and Antioxidant Status in Rats |
Q34370825 | The role of genetic polymorphisms in antioxidant enzymes and potential antioxidant therapies in neonatal lung disease |
Q47284097 | The unveiling of the Warburg effect and the inscribed innovative approach to a radical non toxic anticancer therapy |
Q57235271 | Transcriptomic responses to darkness stress point to common coral bleaching mechanisms |