about
Neuroepithelial oxygen chemoreceptors of the zebrafish gillA confocal microscopic study of solitary pulmonary neuroendocrine cells in human airway epithelium.Post-transcriptional control of human maxiK potassium channel activity and acute oxygen sensitivity by chronic hypoxiaRedox control of oxygen sensing in the rabbit ductus arteriosusSerotonergic sensory-motor neurons mediate a behavioral response to hypoxia in pond snail embryos.Detecting acute changes in oxygen: will the real sensor please stand up?Selective gene expression analysis of the neuroepithelial body microenvironment in postnatal lungs with special interest for potential stem cell characteristics.Commitment and differentiation of lung cell lineages.Evolution of the hypoxia-sensitive cells involved in amniote respiratory reflexes.Neuroendocrine differentiation, neuropeptides, and neprilysin.The role of hypoxia and neurogenic genes (Mash-1 and Prox-1) in the developmental programming and maturation of pulmonary neuroendocrine cells in fetal mouse lungCellular oxygen sensing by mitochondria: old questions, new insight.Oxygen, gastrin-releasing Peptide, and pediatric lung disease: life in the balance.A mixture of carcinoid tumors, extensive neuroendocrine proliferation, and multiple pulmonary sclerosing hemangiomas.Ghrelin expression in human and rat fetal lungs and the effect of ghrelin administration in nitrofen-induced congenital diaphragmatic hernia.Moderate hypoxia influences potassium outward currents in adipose-derived stem cells.Molecular basis of hypoxia-induced pulmonary vasoconstriction: role of voltage-gated K+ channels.Branchial innervation.The mechanism(s) of hypoxic pulmonary vasoconstriction: potassium channels, redox O(2) sensors, and controversies.Airway chemotransduction: from oxygen sensor to cellular effector.Intraluminal volume homeostasis: A common sertonergic mechanism among diverse epitheliaHypoxia-inducible factor-1α regulates the expression of L-type voltage-dependent Ca(2+) channels in PC12 cells under hypoxia.Oxygen-sensing neurons in the central nervous system.The airway epithelium: structural and functional properties in health and disease.Regulation of oxygen sensing by ion channels.O2 sensing in the human ductus arteriosus: redox-sensitive K+ channels are regulated by mitochondria-derived hydrogen peroxide.Nicotinic alpha 7 receptor expression and modulation of the lung epithelial response to lipopolysaccharide.O2 sensing is preserved in mice lacking the gp91 phox subunit of NADPH oxidase.A mitochondrial redox oxygen sensor in the pulmonary vasculature and ductus arteriosusAMP-activated protein kinase and the regulation of Ca2+ signalling in O2-sensing cells.AMP-activated protein kinase underpins hypoxic pulmonary vasoconstriction and carotid body excitation by hypoxia in mammals.Biochemistry, physiology, and complications of blood doping: facts and speculation.Pulmonary neuroendocrine cell system in pediatric lung disease-recent advances.Nonhematopoietic NADPH oxidase regulation of lung eosinophilia and airway hyperresponsiveness in experimentally induced asthmaAre nicotine replacement therapy, varenicline or bupropion options for pregnant mothers to quit smoking? Effects on the respiratory system of the offspring.TRP channels as sensors of oxygen availability.Diphenylene iodonium inhibits the induction of erythropoietin and other mammalian genes by hypoxia. Implications for the mechanism of oxygen sensing.Oxygen sensing by the carotid body: mechanisms and role in adaptation to hypoxia.Oxygen Sensing in Early Life.Oxygen-sensing pathway for SK channels in the ovine adrenal medulla.
P2860
Q24676954-36977879-0938-42FA-9E65-376AC43F0B3DQ24814085-E2772157-ED63-4830-B69D-F778CF9B3504Q28206353-79E82428-DDCD-41C7-91C5-505A74E47BB1Q28365032-E22880E7-0F78-4C73-9676-37735B18A509Q30836467-E9B1C989-1007-49B1-A65B-539CAE49527DQ33251267-8463A34B-3D29-4916-9380-3418FB4F3D41Q33651475-42DE4842-4C09-44B0-BBE3-B92FEFC44D1AQ33678429-9B3794C3-56A3-4354-9C6C-39FDAD55E665Q33708212-630C517B-B012-43A1-B7FC-C4F5F8218C92Q33711153-0764D17F-BC0B-4FDE-AC3F-FDFEDBFB6C20Q33782802-8269D265-3635-49B2-9107-76D528D2680BQ33910357-52542B77-1004-484C-A1A0-B66D3223DA9AQ33918699-6A8DCFF1-8EC9-40E0-B6E0-08AA34B8968EQ33946857-39E43DD8-481F-4C04-96CC-838A5B974E02Q33994274-552971F8-4C41-42A0-B0FF-128EFE633EB3Q34035637-95FFD717-A2FF-4B0C-9C89-EAA8ED1E3C52Q34280464-EF4D6B90-1C83-40E0-A874-A9C02B2C707FQ34736941-C03B31AE-4BC3-4F07-B7A5-B7051DBEBBC9Q34756661-13A1A16D-9F19-4DA0-9095-EBE675A99383Q35019710-42F5E6E9-E3C6-4E6F-8E26-597132E07FA4Q35475673-72EA525E-8656-48CF-AAF2-C61842EBAA19Q35529017-DB930B0E-B196-43EA-885A-15C6A4138BB1Q35602028-3B7B2698-0AF8-4A88-A6FF-683E5E219C79Q35621610-AF2AD5F7-2854-444A-A2F0-C49BB5FFD606Q35651193-86CB7A60-A341-418C-9300-F1E8F1429342Q35768162-1305C2DF-1372-43F8-9888-FBE0F377EDACQ36338452-55C92896-C03D-4D78-A552-90E8D0D2975CQ36411174-7A0E8AE4-8EC5-4026-9AD8-EAA798DA2312Q36436833-0619A0F0-5480-44AD-B67D-DACF95C70983Q36482354-BC892B15-3C22-4295-9702-0D15AD1A57B2Q36494836-8C399BC5-AC97-4578-AB57-1CC66FD90295Q36504354-539A4C53-222E-4F9E-BAC4-75925EB12810Q37000667-2BC177DF-60E9-4D07-9D62-1BEBDB7244C3Q37260287-DDCEB605-9E29-410D-8C3B-063D23C1F50FQ37586662-B1B5A36B-E406-49B5-83D1-D68A64E4FE5EQ38082440-1B888CBD-2430-4E79-8CF0-7A7117F85596Q38289150-06B28839-E0DB-442E-A645-29CF434186B5Q38695841-BABA72DD-C7FC-4443-84AA-046D6493D03DQ38865984-E148C902-773E-4260-AC3B-DADADF58BB85Q40371017-4DC5D311-64CF-48A5-86E3-722AB5382969
P2860
description
article publié dans la revue scientifique Nature
@fr
scientific article published in Nature
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в Nature у вересні 1993
@uk
name
Oxygen sensing in airway chemoreceptors
@en
Oxygen sensing in airway chemoreceptors
@nl
type
label
Oxygen sensing in airway chemoreceptors
@en
Oxygen sensing in airway chemoreceptors
@nl
prefLabel
Oxygen sensing in airway chemoreceptors
@en
Oxygen sensing in airway chemoreceptors
@nl
P2093
P356
P1433
P1476
Oxygen sensing in airway chemoreceptors
@en
P2093
P2888
P304
P356
10.1038/365153A0
P407
P577
1993-09-01T00:00:00Z
P6179
1019066464