ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating
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Cardiomyopathy classification: ongoing debate in the genomics eraGenetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathyDual role of K ATP channel C-terminal motif in membrane targeting and metabolic regulationA novel custom resequencing array for dilated cardiomyopathyAdenylate kinase and AMP signaling networks: metabolic monitoring, signal communication and body energy sensingA mutation (R826W) in nucleotide-binding domain 1 of ABCC8 reduces ATPase activity and causes transient neonatal diabetesGenetics of Human and Canine Dilated CardiomyopathyKATP channels and cardiovascular disease: suddenly a syndromeDystrophin is required for the normal function of the cardio-protective K(ATP) channel in cardiomyocytesA heterozygous activating mutation in the sulphonylurea receptor SUR1 (ABCC8) causes neonatal diabetes.Genetic Variations Leading to Familial Dilated CardiomyopathyCoding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathyKv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillationSodium channel mutations and susceptibility to heart failure and atrial fibrillationTetrameric structure of SUR2B revealed by electron microscopy of oriented single particlesABC Transport Proteins in Cardiovascular Disease-A Brief Summary.Imaging phenotype vs genotype in nonhypertrophic heritable cardiomyopathies: dilated cardiomyopathy and arrhythmogenic right ventricular cardiomyopathyDirect observation of individual KCNQ1 potassium channels reveals their distinctive diffusive behavior.The ATP-sensitive K(+)-channel (K(ATP)) controls early left-right patterning in Xenopus and chick embryos.Multifaceted roles of miR-1s in repressing the fetal gene program in the heartPolony multiplex analysis of gene expression (PMAGE) in mouse hypertrophic cardiomyopathy.Canine candidate genes for dilated cardiomyopathy: annotation of and polymorphic markers for 14 genes.Quaternary structure of KATP channel SUR2A nucleotide binding domains resolved by synchrotron radiation X-ray scattering.ATP-sensitive K+ channel knockout induces cardiac proteome remodeling predictive of heart disease susceptibility.Genetic causes of human heart failure.Hematopoietic stem cells exhibit a specific ABC transporter gene expression profile clearly distinct from other stem cells.Abcc9 is required for the transition to oxidative metabolism in the newborn heart.Disruption of sarcolemmal ATP-sensitive potassium channel activity impairs the cardiac response to systolic overload.ATP-sensitive potassium channelopathies: focus on insulin secretionHuman K(ATP) channelopathies: diseases of metabolic homeostasis.Association of 25 bp deletion in MYBPC3 gene with left ventricle dysfunction in coronary artery disease patients.Targeted ablation of the abcc6 gene results in ectopic mineralization of connective tissuesThe role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.Essential role of the zinc finger transcription factor Casz1 for mammalian cardiac morphogenesis and developmentRelating diseases by integrating gene associations and information flow through protein interaction networkK(ATP) channel-dependent metaboproteome decoded: systems approaches to heart failure prediction, diagnosis, and therapy.Interstitial 12p deletion involving more than 40 genes in a patient with postnatal microcephaly, psychomotor delay, optic nerve atrophy, and facial dysmorphism.Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.Exercise-induced expression of cardiac ATP-sensitive potassium channels promotes action potential shortening and energy conservation.Cardiomyopathy, familial dilated.
P2860
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P2860
ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating
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2004 nî lūn-bûn
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2004 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2004年の論文
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2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
ABCC9 mutations identified in ...... catalytic KATP channel gating
@ast
ABCC9 mutations identified in ...... catalytic KATP channel gating
@en
ABCC9 mutations identified in ...... catalytic KATP channel gating
@nl
type
label
ABCC9 mutations identified in ...... catalytic KATP channel gating
@ast
ABCC9 mutations identified in ...... catalytic KATP channel gating
@en
ABCC9 mutations identified in ...... catalytic KATP channel gating
@nl
prefLabel
ABCC9 mutations identified in ...... catalytic KATP channel gating
@ast
ABCC9 mutations identified in ...... catalytic KATP channel gating
@en
ABCC9 mutations identified in ...... catalytic KATP channel gating
@nl
P2093
P2860
P3181
P356
P1433
P1476
ABCC9 mutations identified in ...... catalytic KATP channel gating
@en
P2093
Alexey E Alekseev
Andre Terzic
Denice M Hodgson
Eva C Kathmann
Fearghas O'Cochlain
Jeffrey D Ballew
Leonid V Zingman
Martin Bienengraeber
Timothy M Olson
P2860
P2888
P3181
P356
10.1038/NG1329
P407
P577
2004-04-01T00:00:00Z
P5875
P6179
1007322782