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LMNA
Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth
ARVC-Variants.Pdf
Genetic Mutations and Mechanisms in Dilated Cardiomyopathy
Nuclear Titin Interacts with A- and B-Type Lamins in Vitro and in Vivo
Lamin A/C Cardiomyopathy: Implications for Treatment
Hippocampal LMNA Gene Expression Is Increased in Late-Stage Alzheimer’S Disease
Deficiencies in Lamin B1 and Lamin B2 Cause Neurodevelopmental Defects and Distinct Nuclear Shape Abnormalities in Neurons
Doubly Heterozygous LMNA and TTN Mutations Revealed by Exome Sequencing in a Severe Form of Dilated Cardiomyopathy
Supplementary Table 1
Mechanosensing Defects and YAP-Signaling in LMNA-Related Congenital Muscular Dystrophy
Kif1b Rab7a Lmna
Human Induced Pluripotent Stem Cell–Derived Podocytes Mature Into Vascularized Glomeruli Upon Experimental Transplantation
LMNA-Related Disorders
Dominant LMNA Mutations Can Cause Combined Muscular Dystrophy and Peripheral Neuropathy
Myosin Contraction During Apoptosis Release Damage-Associated Molecular Pattern Proteins Before Secondary Necrosis Occurs
Disease Modeling with Human Neurons Reveals LMNB1 Dysregulation Underlying DYT1 Dystonia
Roles of ERK1/2 Signaling in LMNA-Cardiomyopathy
Fibroblasts Lacking Nuclear Lamins Do Not Have Nuclear Blebs Or Protrusions but Nevertheless Have Frequent Nuclear Membrane Ruptures
Top View
Cytoskeletal Proteins in Neurological Disorders
Clinical and Genetic Issues in Dilated Cardiomyopathy: a Review for Genetics Professionals Ray E
Ankyrin G Overexpression in Hutchinson-Gilford Progeria Syndrome fibroblasts Identified Through Biological filtering of Expression Profiles
Role of the Nuclear Lamina in Age-Associated Nuclear Reorganization and Inflammation
Expanding the Phenotype of LMNA Mutations in Dilated Cardiomyopathy and Functional Consequences of These Mutations
Consequences of Lmna Exon 4 Mutations in Myoblast Function
Dilated Cardiomyopathy (CMD)
RNA Mis-Splicing in Disease
Gene Expression Profiling of Fibroblasts in a Family with LMNA-Related Cardiomyopathy Reveals Molecular Pathways Implicated in Disease Pathogenesis
Lamin B1 Regulates Somatic Mutations and Progression of B-Cell Malignancies
Mechanosensing by the Lamina Protects Against Nuclear Rupture, DNA Damage, and Cell Cycle Arrest
Review LAMINOPATHIES
Lamin A/C Dysregulation Contributes to Cardiac Pathology in a Mouse Model of Severe Spinal Muscular Atrophy
Disrupting the LINC Complex by AAV Mediated Gene Transduction Prevents Progression of Lamin Induced Cardiomyopathy
Pipis NRN CMT Review for UCL RPS Supplem.Pdf
Mono- and Bi-Allelic Protein Truncating Variants in Alpha-Actinin 2 Cause Cardiomyopathy Through Distinct Mechanisms
Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
The Broad Spectrum of LMNA Cardiac Diseases: from Molecular Mechanisms to Clinical Phenotype
Dilated Cardiomyopathy and Arrhythmogenic Left Ventricular
Independent Functions for A-Type Lamins
The Nuclear Lamina: Protein Accumulation and Disease
Roles of ERK1/2 Signaling in LMNA-Cardiomyopathy Maria Chatzifrangkeskou
Heart Failure Arrhythmogenic Cardiomyopathy
Neuronal Lamin Regulates Motor Circuit Integrity and Controls Motor Function and Lifespan Lisa J
Novel LMNA Mutations in Patients with Emery-Dreifuss Muscular
Nuclear Lamins A/C and B1 Provide a Structural Framework That
Widespread Remodeling of Proteome Solubility in Response to Different Protein Homeostasis Stresses
Genetics of Inherited Cardiocutaneous Syndromes: a Review
S13148-020-00996-1.Pdf
Biomarkers of Tumor Invasiveness in Proteomics (Review)
Nonsense Mutations in Alpha-II Spectrin in Three Families
Lamin B1 and Lamin B2 Are Long-Lived Proteins with Distinct Functions in Retinal Development
M2072: Genetic Testing for Diagnosis of Inherited Peripheral Neuropathies
Exploring the Crosstalk Between LMNA and Splicing Machinery Gene Mutations in Dilated Cardiomyopathy
Distinct Myocardial Transcriptomic Profiles of Cardiomyopathies
Increased Lamin B1 Levels Promote Cell Migration by Altering Perinuclear Actin Organization
LMNA Gene Lamin A/C
A Genome-First Approach to Aggregating Rare Genetic Variants in LMNA for Association with Electronic Health Record Phenotypes
Skeletal and Cardiac Muscle Disorders Caused by Mutations in Genes Encoding Intermediate Filament Proteins
LMNA – Associated Dilated Cardiomyopathy
Investigating LMNA-Related Dilated Cardiomyopathy Using Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
Modeling of LMNA-Related Dilated Cardiomyopathy Using Human Induced Pluripotent Stem Cells
Targeted Regulation of Nuclear Lamins by Ubiquitin and Ubiquitin-Like Modifiers
Natural History of Dilated Cardiomyopathy Due to Lamin A/C Gene Mutations Matthew R
Protein Profiling Reveals Energy Metabolism and Cytoskeletal Protein