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Retuşare Accidental Facultate lamin a c av block Simpatic din nou tâlhar

Phosphorylation of Lamin A/C at serine 22 modulates Nav1.5 function -  Olaopa - 2021 - Physiological Reports - Wiley Online Library
Phosphorylation of Lamin A/C at serine 22 modulates Nav1.5 function - Olaopa - 2021 - Physiological Reports - Wiley Online Library

Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation  Carriers: A European Cohort Study - ScienceDirect
Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers: A European Cohort Study - ScienceDirect

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

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

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

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

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

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

Modeling of lamin A/C mutation premature cardiac aging using  patient-specific induced pluripotent stem cells | Aging
Modeling of lamin A/C mutation premature cardiac aging using patient-specific induced pluripotent stem cells | Aging

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

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

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

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

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

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

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

Familial lamin A/C mutation cardiomyopathy with arrhythmia substrate  detected by cardiac magnetic resonance imaging and electroanatomical  mapping - International Journal of Cardiology
Familial lamin A/C mutation cardiomyopathy with arrhythmia substrate detected by cardiac magnetic resonance imaging and electroanatomical mapping - International Journal of Cardiology

Structure of the asymmetric unit of the human lamin A/C fragment. a... |  Download Scientific Diagram
Structure of the asymmetric unit of the human lamin A/C fragment. a... | Download Scientific Diagram

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

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

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

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

Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers  Associated with Abnormal Transcription in Progeria - ScienceDirect
Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers Associated with Abnormal Transcription in Progeria - ScienceDirect

p53 induces senescence through Lamin A/C stabilization-mediated nuclear  deformation | Cell Death & Disease
p53 induces senescence through Lamin A/C stabilization-mediated nuclear deformation | Cell Death & Disease