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IJMS | Free Full-Text | Lamin A/C and the Immune System: One Intermediate  Filament, Many Faces | HTML
IJMS | Free Full-Text | Lamin A/C and the Immune System: One Intermediate Filament, Many Faces | HTML

Clinical and Functional Characterization of a Novel Mutation in Lamin A/C  Gene in a Multigenerational Family with Arrhythmogenic Cardiac Laminopathy  | PLOS ONE
Clinical and Functional Characterization of a Novel Mutation in Lamin A/C Gene in a Multigenerational Family with Arrhythmogenic Cardiac Laminopathy | PLOS ONE

Lamin A/C-Related Cardiac Disease | Circulation: Cardiovascular Genetics
Lamin A/C-Related Cardiac Disease | Circulation: Cardiovascular Genetics

Cureus | Lamin A/C Cardiomyopathy with E203K Pathogenic Mutation
Cureus | Lamin A/C Cardiomyopathy with E203K Pathogenic Mutation

A typical laminopathy ECG, showing first-degree atrioventricular block... |  Download Scientific Diagram
A typical laminopathy ECG, showing first-degree atrioventricular block... | Download Scientific Diagram

Localization of the R189W mutation in lamin A/C gene and lamin A/C... |  Download Scientific Diagram
Localization of the R189W mutation in lamin A/C gene and lamin A/C... | Download Scientific Diagram

Refractory ventricular arrhythmia in a patient with Lamin A/C (LMNA)  cardiomyopathy successfully treated with thoracic bilateral stellate  ganglionectomy - HeartRhythm Case Reports
Refractory ventricular arrhythmia in a patient with Lamin A/C (LMNA) cardiomyopathy successfully treated with thoracic bilateral stellate ganglionectomy - HeartRhythm Case Reports

Direct Synthesis of Lamin A, Bypassing Prelamin A Processing, Causes  Misshapen Nuclei in Fibroblasts but No Detectable Pathology in Mice* -  Journal of Biological Chemistry
Direct Synthesis of Lamin A, Bypassing Prelamin A Processing, Causes Misshapen Nuclei in Fibroblasts but No Detectable Pathology in Mice* - Journal of Biological Chemistry

Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin  A/C defect-related disease - ScienceDirect
Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease - ScienceDirect

MedShare | Facebook
MedShare | Facebook

Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in  Mechanophenotype
Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype

Structural basis for lamin assembly at the molecular level | Nature  Communications
Structural basis for lamin assembly at the molecular level | Nature Communications

Frontiers | Effect of Occurrence of Lamin A/C (LMNA) Genetic Variants in a  Cohort of 101 Consecutive Apparent “Lone AF” Patients: Results and Insights
Frontiers | Effect of Occurrence of Lamin A/C (LMNA) Genetic Variants in a Cohort of 101 Consecutive Apparent “Lone AF” Patients: Results and Insights

Electropherogram of the lamin A/C gene. Electropherograms of control... |  Download Scientific Diagram
Electropherogram of the lamin A/C gene. Electropherograms of control... | Download Scientific Diagram

Phosphorylated Lamin A/C in the nuclear interior binds active enhancers  associated with abnormal transcription in progeria | bioRxiv
Phosphorylated Lamin A/C in the nuclear interior binds active enhancers associated with abnormal transcription in progeria | bioRxiv

Anti-Lamin A + C Antibody (A12573) | Antibodies.com
Anti-Lamin A + C Antibody (A12573) | Antibodies.com

Lamin A/C (4C11) Mouse mAb | Cell Signaling Technology
Lamin A/C (4C11) Mouse mAb | Cell Signaling Technology

PE Anti-Lamin A + Lamin C antibody [EPR4100] (ab210433) | Abcam
PE Anti-Lamin A + Lamin C antibody [EPR4100] (ab210433) | Abcam

Pulmonary vein isolation treats symptomatic AF in a patient with Lamin A/C  mutation: case report and review of the literature | SpringerLink
Pulmonary vein isolation treats symptomatic AF in a patient with Lamin A/C mutation: case report and review of the literature | SpringerLink

Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between  Brugada Syndrome and Laminopathies | Circulation: Genomic and Precision  Medicine
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies | Circulation: Genomic and Precision Medicine

Lamin A/C mutation is independently associated with an increased risk of  arterial and venous thromboembolic complications - International Journal of  Cardiology
Lamin A/C mutation is independently associated with an increased risk of arterial and venous thromboembolic complications - International Journal of Cardiology

Cardiovascular Medicine - Lamin A/C cardiomyopathy: case report and review  of the literature
Cardiovascular Medicine - Lamin A/C cardiomyopathy: case report and review of the literature

Phosphorylated Lamin A/C in the nuclear interior binds active enhancers  associated with abnormal transcription in progeria | bioRxiv
Phosphorylated Lamin A/C in the nuclear interior binds active enhancers associated with abnormal transcription in progeria | bioRxiv

Role of nuclear Lamin A/C in cardiomyocyte functions - Carmosino - 2014 -  Biology of the Cell - Wiley Online Library
Role of nuclear Lamin A/C in cardiomyocyte functions - Carmosino - 2014 - Biology of the Cell - Wiley Online Library

Cardiovascular Medicine - Lamin A/C cardiomyopathy: case report and review  of the literature
Cardiovascular Medicine - Lamin A/C cardiomyopathy: case report and review of the literature

A novel mutation in LAMIN A/C is associated with isolated early-onset  atrial fibrillation and progressive atrioventricular block followed by  cardiomyopathy and sudden cardiac death - Heart Rhythm
A novel mutation in LAMIN A/C is associated with isolated early-onset atrial fibrillation and progressive atrioventricular block followed by cardiomyopathy and sudden cardiac death - Heart Rhythm