PLEKHM2mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompaction

The role of the autophagy in myocardial ischemia/reperfusion injury

(2015) Sai Ma et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

Isolated Noncompaction of the Left Ventricle in Adults

(2015) Ayman Hussein et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Cardiac fibroblasts as sentinel cells in cardiac tissue: Receptors, signaling pathways and cellular functions

(2015) G. Díaz-Araya et al.   PHARMACOLOGICAL RESEARCH

The PI3K/AKT/mTOR pathway is a potential predictor of distinct invasive and migratory capacities in human ovarian cancer cell lines

(2015) Huimin Bai et al.   Oncotarget

Autophagy and SQSTM1 on the RHOA(d) again

(2014) Amine Belaid et al.   Autophagy

Left Ventricular Noncompaction

(2014) Eloisa Arbustini et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Regulation of cell proliferation and migration by p62 through stabilization of Twist1

(2014) L. Qiang et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Molecular mechanism of ventricular trabeculation/compaction and the pathogenesis of the left ventricular noncompaction cardiomyopathy (LVNC)

(2013) Wenjun Zhang et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Signalphagy

(2013) Amine Belaid et al.   Autophagy

Autophagy Plays a Critical Role in the Degradation of Active RHOA, the Control of Cell Cytokinesis, and Genomic Stability

(2013) A. Belaid et al.   CANCER RESEARCH

2013 ACCF/AHA Guideline for the Management of Heart Failure

(2013) Clyde W. Yancy et al.   CIRCULATION

Congenital myopathy is caused by mutation of HACD1

(2013) Emad Muhammad et al.   HUMAN MOLECULAR GENETICS

The role of membrane-trafficking small GTPases in the regulation of autophagy

(2013) C. F. Bento et al.   JOURNAL OF CELL SCIENCE

Genetic mutations and mechanisms in dilated cardiomyopathy

(2013) Elizabeth M. McNally et al.   JOURNAL OF CLINICAL INVESTIGATION

Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy

(2013) Guillermo Luxán et al.   NATURE MEDICINE

Guidelines for the use and interpretation of assays for monitoring autophagy

(2012) Daniel J. Klionsky et al.   Autophagy

Left Ventricular Noncompaction

(2012) Timothy E. Paterick et al.   CIRCULATION JOURNAL

Genetics of Hypertrophic and Dilated Cardiomyopathy

(2012) Felix W. Friedrich et al.   CURRENT PHARMACEUTICAL BIOTECHNOLOGY

ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure 2012

(2012) et al.   EUROPEAN JOURNAL OF HEART FAILURE

Where Genome Meets Phenome: Rationale for Integrating Genetic and Protein Biomarkers in the Diagnosis and Management of Dilated Cardiomyopathy and Heart Failure

(2012) Sanaz Piran et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Review and Metaanalysis of the Frequency of Familial Dilated Cardiomyopathy

(2011) Mario Petretta et al.   AMERICAN JOURNAL OF CARDIOLOGY

Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy

(2011) Nadine Norton et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genome-wide Investigation of the Rab Binding Activity of RUN Domains: Development of a Novel Tool that Specifically Traps GTP-Rab35

(2011) Mitsunori Fukuda et al.   CELL STRUCTURE AND FUNCTION

BAG3-related myofibrillar myopathy in a Chinese family

(2011) HC Lee et al.   CLINICAL GENETICS

Tuning flux: autophagy as a target of heart disease therapy

(2011) Min Xie et al.   CURRENT OPINION IN CARDIOLOGY

Arl8 and SKIP Act Together to Link Lysosomes to Kinesin-1

(2011) Cláudia Rosa-Ferreira et al.   DEVELOPMENTAL CELL

A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy

(2011) Eric Villard et al.   EUROPEAN HEART JOURNAL

Dilated cardiomyopathy-associatedBAG3mutations impair Z-disc assembly and enhance sensitivity to apoptosis in cardiomyocytes

(2011) Takuro Arimura et al.   HUMAN MUTATION

Tafazzin knockdown causes hypertrophy of neonatal ventricular myocytes

(2010) Quan He   AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY

Inhibition of autophagy in the heart induces age-related cardiomyopathy

(2010) Manabu Taneike et al.   Autophagy

Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase

(2010) Aviva Levitas et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

SKIP, the Host Target of the Salmonella Virulence Factor SifA, Promotes Kinesin-1-Dependent Vacuolar Membrane Exchanges

(2010) Audrey Dumont et al.   TRAFFIC

Left Ventricular Noncompaction: A New Form of Heart Failure

(2010) Jeffrey A. Towbin   Heart Failure Clinics

Autophagy in Ischemic Heart Disease

(2009) Åsa B. Gustafsson et al.   CIRCULATION RESEARCH

Cardiogenetics, Neurogenetics, and Pathogenetics of Left Ventricular Hypertrabeculation/Noncompaction

(2009) Josef Finsterer   PEDIATRIC CARDIOLOGY

Analysis of Ventricular Hypertrabeculation and Noncompaction Using Genetically Engineered Mouse Models

(2009) Hanying Chen et al.   PEDIATRIC CARDIOLOGY

Mutation in BAG3 causes severe dominant childhood muscular dystrophy

(2008) Duygu Selcen et al.   ANNALS OF NEUROLOGY

Autophagy in the Pathogenesis of Disease

(2008) Beth Levine et al.   CELL

Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction

(2008) Sabine Klaassen et al.   CIRCULATION

The Salmonella virulence protein SifA is a G protein antagonist

(2008) L. K. Jackson et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Genetic Heterogeneity of Left-ventricular Noncompaction Cardiomyopathy

(2007) Ewa Moric-Janiszewska et al.   CLINICAL CARDIOLOGY

Supraventricular arrhythmias in noncompaction of left ventricle: Is this a frequent complication?

(2007) Giovanni Fazio et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY