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MARIAN, ALI

One or more keywords matched the following items that are connected to MARIAN, ALI

Item Type	Name
Academic Article	On predictors of sudden cardiac death in hypertrophic cardiomyopathy.
Academic Article	Can an energy-deficient heart grow bigger and stronger?
Academic Article	Resolution of established cardiac hypertrophy and fibrosis and prevention of systolic dysfunction in a transgenic rabbit model of human cardiomyopathy through thiol-sensitive mechanisms.
Academic Article	Genetic fate mapping identifies second heart field progenitor cells as a source of adipocytes in arrhythmogenic right ventricular cardiomyopathy.
Academic Article	Update on hypertrophic cardiomyopathy.
Academic Article	Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy.
Academic Article	Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathy.
Academic Article	Enhanced transmural fiber rotation and connexin 43 heterogeneity are associated with an increased upper limit of vulnerability in a transgenic rabbit model of human hypertrophic cardiomyopathy.
Academic Article	Differential interactions of thin filament proteins in two cardiac troponin T mouse models of hypertrophic and dilated cardiomyopathies.
Academic Article	Contemporary treatment of hypertrophic cardiomyopathy.
Academic Article	Arrhythmogenic right ventricular cardiomyopathy is a disease of cardiac stem cells.
Academic Article	Metabolomic distinction and insights into the pathogenesis of human primary dilated cardiomyopathy.
Academic Article	Hypertrophic cardiomyopathy: from genetics to treatment.
Academic Article	Experimental therapies in hypertrophic cardiomyopathy.
Academic Article	Atorvastatin and cardiac hypertrophy and function in hypertrophic cardiomyopathy: a pilot study.
Academic Article	Human molecular genetic and functional studies identify TRIM63, encoding Muscle RING Finger Protein 1, as a novel gene for human hypertrophic cardiomyopathy.
Academic Article	Pathogenesis of hypertrophic cardiomyopathy caused by myozenin 2 mutations is independent of calcineurin activity.
Academic Article	Antifibrotic effects of antioxidant N-acetylcysteine in a mouse model of human hypertrophic cardiomyopathy mutation.
Academic Article	Suppression of canonical Wnt/beta-catenin signaling by nuclear plakoglobin recapitulates phenotype of arrhythmogenic right ventricular cardiomyopathy.
Academic Article	Phenotypic plasticity of sarcomeric protein mutations.
Academic Article	Molecular genetic and functional characterization implicate muscle-restricted coiled-coil gene (MURC) as a causal gene for familial dilated cardiomyopathy.
Concept	Cardiomyopathy, Hypertrophic
Concept	Cardiomyopathy, Restrictive
Concept	Cardiomyopathies
Concept	Cardiomyopathy, Dilated
Academic Article	On the diagnostic utility of junction plakoglobin in arrhythmogenic right ventricular cardiomyopathy.
Academic Article	Causality in genetics: the gradient of genetic effects and back to Koch's postulates of causality.
Academic Article	Ali J. Marian: life and science are one.
Academic Article	Arrhythmogenic cardiomyopathy in a patient with a rare loss-of-function KCNQ1 mutation.
Academic Article	Cardiac Fibro-Adipocyte Progenitors Express Desmosome Proteins and Preferentially Differentiate to Adipocytes Upon Deletion of the Desmoplakin Gene.
Academic Article	Challenges in the Diagnosis of Anderson-Fabry Disease: A Deceptively Simple and Yet Complicated Genetic Disease.
Academic Article	Genetics and Genomics of Single-Gene Cardiovascular Diseases: Common Hereditary Cardiomyopathies as Prototypes of?Single-Gene Disorders.
Academic Article	A Potential Oligogenic Etiology of Hypertrophic Cardiomyopathy: A Classic Single-Gene Disorder.
Academic Article	Identification of established arrhythmogenic right ventricular cardiomyopathy mutation in a patient with the contrasting phenotype of hypertrophic cardiomyopathy.
Academic Article	Hypertrophy Regression With N-Acetylcysteine in Hypertrophic Cardiomyopathy (HALT-HCM): A Randomized, Placebo-Controlled, Double-Blind Pilot Study.
Academic Article	Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy.
Academic Article	Distinct Cellular Basis for Early Cardiac Arrhythmias, the Cardinal Manifestation of Arrhythmogenic Cardiomyopathy, and the Skin Phenotype of Cardiocutaneous Syndromes.
Academic Article	Genomic Reorganization of Lamin-Associated Domains in Cardiac Myocytes Is Associated With Differential Gene Expression and DNA Methylation in Human Dilated Cardiomyopathy.
Academic Article	DNA Damage Response/TP53 Pathway Is Activated and Contributes to the Pathogenesis of Dilated Cardiomyopathy Associated With LMNA (Lamin A/C) Mutations.
Grant	Hypertrophy Regression with N-Acetylcysteine in Hypertrophic Cardiomyopathy
Grant	Cardiovascular Ultrasonography Unit
Grant	Canonical Wnt Signaling in Pathogenesis and Rescue of ARVC
Grant	Mechanisms and Therapeutic Targeting of DNA Damage in Dilated Cardiomyopathy Caused by LMNA Mutations
Grant	Modifier Genes of Familial Hypertrophic Cardiomyopathy
Academic Article	Exercise restores dysregulated gene expression in a mouse model of arrhythmogenic cardiomyopathy.
Academic Article	Role of the Extracellular Matrix in?the?Pathogenesis of Hypertrophic?Cardiomyopathy.
Academic Article	RNA sequencing-based transcriptome profiling of cardiac tissue implicates novel putative disease mechanisms in FLNC-associated arrhythmogenic cardiomyopathy.
Grant	Cell type-Specific Therapeutic Targeting of canonical WNT Pathway in Arrhythmogenic Cardiomyopathy
Academic Article	Genetic basis and molecular biology of cardiac arrhythmias in cardiomyopathies.
Academic Article	Evaluation of Mavacamten in Symptomatic Patients With Nonobstructive Hypertrophic Cardiomyopathy.
Academic Article	BET bromodomain inhibition attenuates cardiac phenotype in myocyte-specific lamin A/C-deficient mice.
Academic Article	Haploinsufficiency of Tmem43 in cardiac myocytes activates the DNA damage response pathway leading to a late-onset senescence-associated pro-fibrotic cardiomyopathy.
Academic Article	Single-Cell RNA Sequencing Uncovers Paracrine Functions of the Epicardial-Derived Cells in Arrhythmogenic Cardiomyopathy.
Academic Article	The EP300/TP53 pathway, a suppressor of the Hippo and canonical WNT pathways, is activated in human hearts with arrhythmogenic cardiomyopathy in the absence of overt heart failure.
Academic Article	Deletion of the Lmna gene in fibroblasts causes senescence-associated dilated cardiomyopathy by activating the double-stranded DNA damage response and induction of senescence-associated secretory phenotype.
Academic Article	Genetic Ablation of the DNA Damage Response Pathway Attenuates Lamin-Associated Dilated Cardiomyopathy in Mice.
Academic Article	Sporadic dilated cardiomyopathy is often familial.
Academic Article	A combinatorial oligogenic basis for the phenotypic plasticity between late-onset dilated and arrhythmogenic cardiomyopathy in a single family.
Academic Article	PANoptosis is a prominent feature of desmoplakin cardiomyopathy.
Academic Article	Pharmacological suppression of the WNT signaling pathway attenuates age-dependent expression of the phenotype in a mouse model of arrhythmogenic cardiomyopathy.
Academic Article	Clinical Significance of Variants in the TTN Gene in a Large Cohort of Patients With Sporadic Dilated Cardiomyopathy.
Academic Article	Oligogenic cardiomyopathy.
Academic Article	Shared Genetic Etiology of Primary Dilated Cardiomyopathy and Ischemic Dilated Cardiomyopathy.
Academic Article	Cytosolic DNA sensing protein pathway is activated in human hearts with dilated cardiomyopathy.
Academic Article	Genetic inactivation of ?-catenin is salubrious, whereas its activation is deleterious in desmoplakin cardiomyopathy.
Academic Article	A human mitofusin 2 mutation can cause mitophagic cardiomyopathy.
Academic Article	DNA double-stranded breaks, a hallmark of aging, defined at the nucleotide resolution, are increased and associated with transcription in the cardiac myocytes in LMNA-cardiomyopathy.

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Cardiomyopathies