Glu496Ala polymorphism of human P2X7 receptor does not affect its electrophysiological phenotype.
about
Molecular and functional properties of P2X receptors--recent progress and persisting challengesInsights into the Molecular Mechanisms Underlying Mammalian P2X7 Receptor Functions and Contributions in Diseases, Revealed by Structural Modeling and Single Nucleotide PolymorphismsPoint mutation in the mouse P2X7 receptor affects intercellular calcium waves in astrocytesPannexin1 is part of the pore forming unit of the P2X(7) receptor death complexExpression of nitric oxide synthases and endogenous NO metabolism in bronchopulmonary dysplasiaNon-synonymous single nucleotide polymorphisms in the P2X receptor genes: association with diseases, impact on receptor functions and potential use as diagnosis biomarkersThe hyposensitive N187D P2X7 mutant promotes malignant progression in nude mice.Transcriptional control mechanisms associated with the nucleotide receptor P2X7, a critical regulator of immunologic, osteogenic, and neurologic functions.Kinetics of P2X7 receptor-operated single channels currents.Influence of extracellular monovalent cations on pore and gating properties of P2X7 receptor-operated single-channel currents.A truncated P2X7 receptor variant (P2X7-j) endogenously expressed in cervical cancer cells antagonizes the full-length P2X7 receptor through hetero-oligomerizationBlunted hypoxic pulmonary vasoconstriction in experimental neonatal chronic lung diseasePostnatal estradiol up-regulates lung nitric oxide synthases and improves lung function in bronchopulmonary dysplasiaExpression, signaling, and function of P2X7 receptors in bone.Inhaled nitric oxide effects on lung structure and function in chronically ventilated preterm lambsGenetics of the P2X7 receptor and human disease.P2X7-mediated chemoprevention of epithelial cancers.C terminus of the P2X7 receptor: treasure hunting.Heteromeric assembly of P2X subunits.Homodimeric anoctamin-1, but not homodimeric anoctamin-6, is activated by calcium increases mediated by the P2Y1 and P2X7 receptors.Identification and characterization of a novel variant of the human P2X(7) receptor resulting in gain of function.Are second messengers crucial for opening the pore associated with P2X7 receptor?The P2X(7) receptor mediates the uptake of organic cations in canine erythrocytes and mononuclear leukocytes: comparison to equivalent human cell types.Pulmonary hypertension in premature infants. Sharpening the tools of detection.Beyond pulmonary hypertension: sildenafil for chronic lung disease of prematurity.P2X7 and NRAMP1/SLC11 A1 gene polymorphisms in Mexican mestizo patients with pulmonary tuberculosis.Pulmonary and systemic nitric oxide metabolites in a baboon model of neonatal chronic lung disease.
P2860
Q24617046-01B4C85D-F774-4559-B6C7-7772D2112399Q27500422-A5ECA473-AFDD-4322-9632-37B1B51ED152Q30157211-EE2431D7-17FE-4EFA-8D10-420D5318399AQ30479449-1D53E455-1C51-4BE1-A923-4EB3A1D555C0Q33586455-C829EB7B-4914-49C5-B069-89D3148FDFE3Q34158330-B1F07ED2-7203-4882-80E4-9EA21298F416Q34285496-D0A4F283-52B8-4632-A684-9970056686E0Q35468810-E77A28A4-FEF1-4E9B-8159-8EEC7346AB7CQ35781225-858C6BBC-05BD-4731-8A6E-663D76BFFC64Q35878613-9A7E43A9-0983-489F-BC2B-513FCBEE495FQ36692683-038ED598-6DE4-439D-9C53-F466181AE70EQ36890004-386216E5-8140-48B6-8DB9-F42E4A1C85EFQ37126480-8E831B03-42EC-47A7-B9BB-76FBCA2A4A91Q37203211-4130228D-A0ED-4CFF-B03A-8C44C1F4D5D9Q37282588-15C38D44-491D-4BF3-A0F1-B9959C075C66Q37423180-CBBF9779-3712-412B-ADC2-6F77713E34F4Q37618815-BF5B87A5-847C-42A1-8DE8-115FCC18C799Q37864114-0B2CAAC6-F4A8-4AF6-B899-C29CF968E5ECQ38175966-0F31A2DD-DBC2-4923-AC38-7C4F07A55356Q38919495-EC947F6B-1FC5-49B3-A6E0-32232FA100A9Q39600810-13F07C49-40C9-4525-A128-C6A7FB4A6891Q40506943-0F3BDD4B-E3B8-4E3B-B809-B94E18D099A9Q42598769-91EDE827-B5B7-4457-B07F-B72736530807Q43111817-AD8098AE-3274-4580-B37C-60915642CB79Q44062958-F31A86B3-3724-4365-AE81-32FBB6461A8FQ46222139-396F4EAD-BC16-4EDF-A20A-ED68F5596D14Q46706481-67D45DEF-668D-4DB2-B79F-F8A78D59A0A3
P2860
Glu496Ala polymorphism of human P2X7 receptor does not affect its electrophysiological phenotype.
description
2002 nî lūn-bûn
@nan
2002 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Glu496Ala polymorphism of huma ...... lectrophysiological phenotype.
@ast
Glu496Ala polymorphism of huma ...... lectrophysiological phenotype.
@en
type
label
Glu496Ala polymorphism of huma ...... lectrophysiological phenotype.
@ast
Glu496Ala polymorphism of huma ...... lectrophysiological phenotype.
@en
prefLabel
Glu496Ala polymorphism of huma ...... lectrophysiological phenotype.
@ast
Glu496Ala polymorphism of huma ...... lectrophysiological phenotype.
@en
P2093
P1476
Glu496Ala polymorphism of huma ...... lectrophysiological phenotype.
@en
P2093
Cora Büttner
Fritz Markwardt
Günther Schmalzing
Manuela Klapperstück
Sven Sadtler
Wolfgang Boldt
P304
P356
10.1152/AJPCELL.00042.2002
P577
2002-11-13T00:00:00Z