JCM | Free Full-Text | Molecular Diagnosis of Hypertrophic Cardiomyopathy (HCM): In the Heart of Cardiac Disease
Genetics and Genomics of Single-Gene Cardiovascular Diseases: Common Hereditary Cardiomyopathies as Prototypes of Single-Gene Disorders - ScienceDirect
Methods and Procedures in Adipose Stem Cells: State of the Art and Perspective for Translation Medicine - Nicoletti - 2015 - Journal of Cellular Physiology - Wiley Online Library
Vascular Expression of Lamin A/C (A) Lamin A/C expression in the... | Download Scientific Diagram
Nuclear Shape, Mechanics, and Mechanotransduction | Circulation Research
The Case of “Missing Causal Genes” and the Practice of Medicine | Circulation Research
IJMS | Free Full-Text | The Time Has Come to Explore Plasma Biomarkers in Genetic Cardiomyopathies
Natural history of dilated cardiomyopathy due to lamin A/C gene mutations | Journal of the American College of Cardiology
Frontiers | Characterization of cardiac involvement in children with LMNA-related muscular dystrophy
The Natural Antiangiogenic Compound AD0157 Induces Caspase-Dependent Apoptosis in Human Myeloid Leukemia Cells - Frontiers
Cardiac myosin-binding protein C in hypertrophic cardiomyopathy: Mechanisms and therapeutic opportunities - Journal of Molecular and Cellular Cardiology
Natural history of dilated cardiomyopathy due to lamin A/C gene mutations - ScienceDirect
Imunofluorescence staining of lamin A/C in young cardiomyocytes (A) vs... | Download Scientific Diagram
NPM1 (mutant) Polyclonal Antibody (PA1-46356)
Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: Demand for strategies in the management of presymptomatic lamin A/C mutant carriers - Perrot - 2006 - European Journal of Heart
IJMS | Free Full-Text | Nuclear Lipid Microdomains Regulate Daunorubicin Resistance in Hepatoma Cells
Phenotype and Course of Hutchinson–Gilford Progeria Syndrome | NEJM
IJMS | Free Full-Text | The Role of Z-disc Proteins in Myopathy and Cardiomyopathy
Natural history of dilated cardiomyopathy due to lamin A/C gene mutations - ScienceDirect
Cardiac Phenotypes, Genetics, and Risks in Familial Noncompaction Cardiomyopathy | Journal of the American College of Cardiology
Efficient Correction of a Hypertrophic Cardiomyopathy Mutation by ABEmax-NG | Circulation Research
Natural history of dilated cardiomyopathy due to lamin A/C gene mutations - ScienceDirect
Frontiers | The grand challenge of discovering new cardiovascular drugs
Biomedicines | Free Full-Text | Biological Effects of BET Inhibition by OTX015 (MK-8628) and JQ1 in NPM1-Mutated (NPM1c) Acute Myeloid Leukemia (AML)
IJMS | Free Full-Text | Molecular Mechanisms Underlying the Progression of Aortic Valve Stenosis: Bioinformatic Analysis of Signal Pathways and Hub Genes
