Selenoprotein N is required for ryanodine receptor calcium release channel activity in human and zebrafish muscle
about
Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathyStac3 is a component of the excitation-contraction coupling machinery and mutated in Native American myopathySelenoprotein K knockout mice exhibit deficient calcium flux in immune cells and impaired immune responsesThe human selenoproteome: recent insights into functions and regulationHadp1, a newly identified pleckstrin homology domain protein, is required for cardiac contractility in zebrafishCongenital myopathies: an updateSelenoproteins in nervous system development and functionSwimming into prominence: the zebrafish as a valuable tool for studying human myopathies and muscular dystrophies.Loss of myotubularin function results in T-tubule disorganization in zebrafish and human myotubular myopathyStructure-function relations, physiological roles, and evolution of mammalian ER-resident selenoproteins.Pathophysiological concepts in the congenital myopathies: blurring the boundaries, sharpening the focusCongenital muscular dystrophies: a brief reviewMinding the calcium store: Ryanodine receptor activation as a convergent mechanism of PCB toxicityTriclosan impairs swimming behavior and alters expression of excitation-contraction coupling proteins in fathead minnow (Pimephales promelas).Selenoprotein N deficiency in mice is associated with abnormal lung developmentSEPN1, an endoplasmic reticulum-localized selenoprotein linked to skeletal muscle pathology, counteracts hyperoxidation by means of redox-regulating SERCA2 pump activitySatellite cell loss and impaired muscle regeneration in selenoprotein N deficiencyZebrafish MTMR14 is required for excitation-contraction coupling, developmental motor function and the regulation of autophagy.Cross-tissue and cross-species analysis of gene expression in skeletal muscle and electric organ of African weakly-electric fish (Teleostei; Mormyridae).Diagnostic approach to the congenital muscular dystrophies.Selenoprotein N is dynamically expressed during mouse development and detected early in muscle precursors.Selenoproteins: molecular pathways and physiological roles.Transcriptional activation of antioxidants may compensate for selenoprotein deficiencies in Amblyomma maculatum (Acari: Ixodidae) injected with selK- or selM-dsRNA.Regulation and function of selenoproteins in human diseaseRyanodine receptors, a family of intracellular calcium ion channels, are expressed throughout early vertebrate development.SHIP2, a factor associated with diet-induced obesity and insulin sensitivity, attenuates FGF signaling in vivo.Simple methods for generating and detecting locus-specific mutations induced with TALENs in the zebrafish genome.Regulation of Ryanodine Receptor Ion Channels Through Posttranslational Modifications.Selenium. Role of the essential metalloid in healthTriadopathies: an emerging class of skeletal muscle diseases.Oxidative stress and successful antioxidant treatment in models of RYR1-related myopathyDietary Selenium Levels Affect Selenoprotein Expression and Support the Interferon-γ and IL-6 Immune Response Pathways in Mice.Understanding selenoprotein function and regulation through the use of rodent models.Comparative Transcriptomic Study of Muscle Provides New Insights into the Growth Superiority of a Novel Grouper Hybrid.Dietary selenium and selenoprotein function.Precise Editing of the Zebrafish Genome Made Simple and Efficient.Gene expression of endoplasmic reticulum resident selenoproteins correlates with apoptosis in various muscles of se-deficient chicks.Structure-activity relationship of selected meta- and para-hydroxylated non-dioxin like polychlorinated biphenyls: from single RyR1 channels to muscle dysfunction.Dietary selenium augments sarcoplasmic calcium release and mechanical performance in mice.The power of the zebrafish for disease analysis.
P2860
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P2860
Selenoprotein N is required for ryanodine receptor calcium release channel activity in human and zebrafish muscle
description
2008 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
article publié dans les Procee ...... f the United States of America
@fr
artículu científicu espublizáu en 2008
@ast
im August 2008 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2008/08/26)
@sk
vědecký článek publikovaný v roce 2008
@cs
wetenschappelijk artikel (gepubliceerd op 2008/08/26)
@nl
наукова стаття, опублікована в серпні 2008
@uk
name
Selenoprotein N is required fo ...... in human and zebrafish muscle
@ast
Selenoprotein N is required fo ...... in human and zebrafish muscle
@en
Selenoprotein N is required fo ...... in human and zebrafish muscle
@nl
type
label
Selenoprotein N is required fo ...... in human and zebrafish muscle
@ast
Selenoprotein N is required fo ...... in human and zebrafish muscle
@en
Selenoprotein N is required fo ...... in human and zebrafish muscle
@nl
prefLabel
Selenoprotein N is required fo ...... in human and zebrafish muscle
@ast
Selenoprotein N is required fo ...... in human and zebrafish muscle
@en
Selenoprotein N is required fo ...... in human and zebrafish muscle
@nl
P2093
P2860
P50
P921
P356
P1476
Selenoprotein N is required fo ...... in human and zebrafish muscle
@en
P2093
David Jonah Grunwald
Derrick Gunther
Jonathan J Abramson
Michael J Jurynec
Michael T Howard
Thomas Crawford
P2860
P304
12485-12490
P356
10.1073/PNAS.0806015105
P407
P577
2008-08-19T00:00:00Z