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Xiaolin Zhang et al.
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Parisha P. Shah et al.
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Sten Anslan et al.
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Hao Su et al.
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Hua Li et al.
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Ruth Jinfen Chai et al.
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Zhu-Jun Cai et al.
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Melissa J. Landrum et al.
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Maria Chatzifrangkeskou et al.
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Silvia Crasto et al.
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Gaelle Auguste et al.
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Sherif M. Shoieb et al.
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Nazish Sayed et al.
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Stephen P. Evanko et al.
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Protease-activated receptor 2 deficiency mediates cardiac fibrosis and diastolic dysfunction
Julian Friebel et al.
EUROPEAN HEART JOURNAL (2019)
Metascape provides a biologist-oriented resource for the analysis of systems-level datasets
Yingyao Zhou et al.
NATURE COMMUNICATIONS (2019)
Transgenic expression of carbonic anhydrase III in cardiac muscle demonstrates a mechanism to tolerate acidosis
Han-Zhong Feng et al.
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TRRUST v2: an expanded reference database of human and mouse transcriptional regulatory interactions
Heonjong Han et al.
NUCLEIC ACIDS RESEARCH (2018)
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Shannon M. Jones et al.
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Erik Laurini et al.
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Sherif M. Shoieb et al.
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Rasha A. Al-Saaidi et al.
EUROPEAN JOURNAL OF HEART FAILURE (2018)
miRWalk: An online resource for prediction of microRNA binding sites
Carsten Sticht et al.
PLOS ONE (2018)
Dhcr24 activates the PI3K/Akt/HKII pathway and protects against dilated cardiomyopathy in mice
Wei Dong et al.
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Partial microduplication in the histone acetyltransferase complex member KANSL1 is associated with congenital heart defects in 22q11.2 microdeletion syndrome patients
Luis E. Leon et al.
SCIENTIFIC REPORTS (2017)
Fibromodulin: A regulatory molecule maintaining cellular architecture for normal cellular function
Arif Tasleem Jan et al.
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2016)
A targeted metabolomics assay for cardiac metabolism and demonstration using a mouse model of dilated cardiomyopathy
James A. West et al.
METABOLOMICS (2016)
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Rasha Al-Saaidi et al.
CHROMOSOMA (2015)
'State-of-the-heart' of cardiac laminopathies
Marie-Elodie Cattin et al.
CURRENT OPINION IN CARDIOLOGY (2013)
Implantable cardioverter-defibrillators in lamin A/C mutation carriers with cardiac conduction disorders
Frédéric Anselme et al.
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Wei Wu et al.
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Ligand docking and binding site analysis with PyMOL and Autodock/Vina
Daniel Seeliger et al.
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Michele Pasotti et al.
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Cytochrome P450 and arachidonic acid metabolites:: Role in myocardial ischemia/reperfusion injury revisited
GJ Gross et al.
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Natural history of dilated cardiomyopathy due to lamin A/C gene mutations
MRG Taylor et al.
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Cytoscape: A software environment for integrated models of biomolecular interaction networks
P Shannon et al.
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Structure of the globular tail of nuclear lamin
S Dhe-Paganon et al.
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Autosomal dominant dilated cardiomyopathy with atrioventricular block: A lamin A/C defect-related disease
E Arbustini et al.
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