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Activation of PDGFRA signaling contributes to filamin C–related  arrhythmogenic cardiomyopathy | Science Advances
Activation of PDGFRA signaling contributes to filamin C–related arrhythmogenic cardiomyopathy | Science Advances

Truncating FLNC Mutations Are Associated With High-Risk Dilated and  Arrhythmogenic Cardiomyopathies - ScienceDirect
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies - ScienceDirect

A mutation update for the FLNC gene in myopathies and cardiomyopathies -  Verdonschot - 2020 - Human Mutation - Wiley Online Library
A mutation update for the FLNC gene in myopathies and cardiomyopathies - Verdonschot - 2020 - Human Mutation - Wiley Online Library

Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive  Cardiomyopathy | Semantic Scholar
Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy | Semantic Scholar

American Journal of Case Reports | Cardiomyopathy, Proximal Myopathy,  Camptocormia, and Novel Filamin C (FLNC) Variant: A Case Report - Article  abstract #932648
American Journal of Case Reports | Cardiomyopathy, Proximal Myopathy, Camptocormia, and Novel Filamin C (FLNC) Variant: A Case Report - Article abstract #932648

Screening of the Filamin C Gene in a Large Cohort of Hypertrophic  Cardiomyopathy Patients | Circulation: Cardiovascular Genetics
Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients | Circulation: Cardiovascular Genetics

Force-Dependent Structural Changes of Filamin C Rod Domains Regulated by  Filamin C Dimer | Journal of the American Chemical Society
Force-Dependent Structural Changes of Filamin C Rod Domains Regulated by Filamin C Dimer | Journal of the American Chemical Society

Myocardial Disease : mutations in filamin C cause a new form of familial  hypertrophic cardiomyopathy
Myocardial Disease : mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

FLNC variants identified in patients of the Belgian FTD cohort. a... |  Download Scientific Diagram
FLNC variants identified in patients of the Belgian FTD cohort. a... | Download Scientific Diagram

Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation |  Circulation Research
Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation | Circulation Research

A map of how disease-related FLNC mutations are distributed on FLNC... |  Download Scientific Diagram
A map of how disease-related FLNC mutations are distributed on FLNC... | Download Scientific Diagram

Missense Mutations in the FLNC Gene Causing Familial Restrictive  Cardiomyopathy | Circulation: Genomic and Precision Medicine
Missense Mutations in the FLNC Gene Causing Familial Restrictive Cardiomyopathy | Circulation: Genomic and Precision Medicine

Schematic representation of Filamin C shown as a dimer with missense... |  Download Scientific Diagram
Schematic representation of Filamin C shown as a dimer with missense... | Download Scientific Diagram

In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in  a family with myofibrillar myopathy | European Journal of Human Genetics
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy | European Journal of Human Genetics

Cells | Free Full-Text | Novel Filamin C Myofibrillar Myopathy Variants  Cause Different Pathomechanisms and Alterations in Protein Quality Systems
Cells | Free Full-Text | Novel Filamin C Myofibrillar Myopathy Variants Cause Different Pathomechanisms and Alterations in Protein Quality Systems

FLNC and MYLK2 gene mutations in a Chinese family with different phenotypes  of cardiomyopathy | medRxiv
FLNC and MYLK2 gene mutations in a Chinese family with different phenotypes of cardiomyopathy | medRxiv

IJMS | Free Full-Text | Structure and Function of Filamin C in the Muscle  Z-Disc
IJMS | Free Full-Text | Structure and Function of Filamin C in the Muscle Z-Disc

JCM | Free Full-Text | Cardiac Filaminopathies: Illuminating the Divergent  Role of Filamin C Mutations in Human Cardiomyopathy
JCM | Free Full-Text | Cardiac Filaminopathies: Illuminating the Divergent Role of Filamin C Mutations in Human Cardiomyopathy

FLNC Gene - GeneCards | FLNC Protein | FLNC Antibody
FLNC Gene - GeneCards | FLNC Protein | FLNC Antibody

FLNC Gene - GeneCards | FLNC Protein | FLNC Antibody
FLNC Gene - GeneCards | FLNC Protein | FLNC Antibody

Activation of PDGFRA signaling contributes to filamin C–related  arrhythmogenic cardiomyopathy | Science Advances
Activation of PDGFRA signaling contributes to filamin C–related arrhythmogenic cardiomyopathy | Science Advances

A mutation update for the FLNC gene in myopathies and cardiomyopathies -  Verdonschot - 2020 - Human Mutation - Wiley Online Library
A mutation update for the FLNC gene in myopathies and cardiomyopathies - Verdonschot - 2020 - Human Mutation - Wiley Online Library

Structure of the FLNC gene and filamin C protein. (a) Within the human... |  Download Scientific Diagram
Structure of the FLNC gene and filamin C protein. (a) Within the human... | Download Scientific Diagram