about
Connexin and Pannexin hemichannels are regulated by redox potentialXLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencingDiseases associated with leaky hemichannelsSystemic inflammation disrupts oligodendrocyte gap junctions and induces ER stress in a model of CNS manifestations of X-linked Charcot-Marie-Tooth disease.Mild form of Charcot-Marie-Tooth type 1X disease caused by a novel Cys179Gly mutation in the GJB1/Cx32 gene.S-nitrosylation and permeation through connexin 43 hemichannels in astrocytes: induction by oxidant stress and reversal by reducing agents.Carbon monoxide (CO) is a novel inhibitor of connexin hemichannels.Atrial fibrillation-linked germline GJA5/connexin40 mutants showed an increased hemichannel functionConnexinopathies: a structural and functional glimpseCharacterization of the structure and intermolecular interactions between the connexin 32 carboxyl-terminal domain and the protein partners synapse-associated protein 97 and calmodulin.How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?The gap junction cellular internet: connexin hemichannels enter the signalling limelightMolecular genetics of X-linked Charcot-Marie-Tooth disease.Insights on the mechanisms of Ca(2+) regulation of connexin26 hemichannels revealed by human pathogenic mutations (D50N/Y).Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1).Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models.Do cell junction protein mutations cause an airway phenotype in mice or humans?Pathological hemichannels associated with human Cx26 mutations causing Keratitis-Ichthyosis-Deafness syndrome.Modulation of gap junction channels and hemichannels by growth factors.Demyelinating prenatal and infantile developmental neuropathies.Paracrine signaling through plasma membrane hemichannelsConnexin channel modulators and their mechanisms of action.Atrial fibrillation-linked GJA5/connexin40 mutants impaired gap junctions via different mechanisms.GJB1-associated X-linked Charcot-Marie-Tooth disease, a disorder affecting the central and peripheral nervous systems.Mechanisms linking connexin mutations to human diseases.Intraneural GJB1 gene delivery improves nerve pathology in a model of X-linked Charcot-Marie-Tooth disease.Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review.Secondary structural analysis of the carboxyl-terminal domain from different connexin isoforms.Intracellular cysteine 346 is essentially involved in regulating Panx1 channel activity.Charcot-marie-tooth disease type 1X in women: Electrodiagnostic findings.Pelizaeus-Merzbacher-like disease is caused not only by a loss of connexin47 function but also by a hemichannel dysfunction.Modulation of membrane channel currents by gap junction protein mimetic peptides: size matters.Cx32 hemichannel opening by cytosolic Ca2+ is inhibited by the R220X mutation that causes Charcot-Marie-Tooth disease.Mitochondrial Cx43 hemichannels contribute to mitochondrial calcium entry and cell death in the heart.Functional characterization of oculodentodigital dysplasia-associated Cx43 mutants.What's the Function of Connexin 32 in the Peripheral Nervous System?
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh-hant
name
Severe neuropathy with leaky connexin32 hemichannels.
@en
Severe neuropathy with leaky connexin32 hemichannels.
@nl
type
label
Severe neuropathy with leaky connexin32 hemichannels.
@en
Severe neuropathy with leaky connexin32 hemichannels.
@nl
prefLabel
Severe neuropathy with leaky connexin32 hemichannels.
@en
Severe neuropathy with leaky connexin32 hemichannels.
@nl
P2093
P356
P1433
P1476
Severe neuropathy with leaky connexin32 hemichannels.
@en
P2093
Grace S Lin Liang
Jonathan D Glass
Juan M Gómez-Hernández
Kenneth H Fischbeck
Luis C Barrio
Mark Mintz
Marta de Miguel
Steven S Scherer
P304
P356
10.1002/ANA.20459
P577
2005-05-01T00:00:00Z