Pages that link to "Q28139053"

The following pages link to Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease (Q28139053):

Displaying 50 items.

• dilated cardiomyopathy (Q283656) (← links)
• The nuclear envelopathies and human diseases (Q21284427) (← links)
• Cardiomyopathy classification: ongoing debate in the genomics era (Q21284968) (← links)
• Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy (Q24288778) (← links)
• Isolation of novel heart-specific genes using the BodyMap database (Q24291261) (← links)
• Titin mutations as the molecular basis for dilated cardiomyopathy (Q24292301) (← links)
• The inner nuclear membrane protein emerin regulates beta-catenin activity by restricting its accumulation in the nucleus (Q24297804) (← links)
• TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy (Q24299150) (← links)
• Nesprin-1alpha self-associates and binds directly to emerin and lamin A in vitro (Q24303760) (← links)
• Sumoylation regulates lamin A function and is lost in lamin A mutants associated with familial cardiomyopathies (Q24310688) (← links)
• A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16 (Q24535586) (← links)
• Many roads lead to a broken heart: the genetics of dilated cardiomyopathy (Q24535744) (← links)
• Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy. (Q24539152) (← links)
• Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy (Q24604161) (← links)
• Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C (Q24612380) (← links)
• A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome (Q24627210) (← links)
• Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse (Q24632769) (← links)
• Altered protein dynamics of disease-associated lamin A mutants (Q24791233) (← links)
• Expression and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation (Q24798448) (← links)
• Skeletal Muscle Laminopathies: A Review of Clinical and Molecular Features (Q26741163) (← links)
• Genetics of Human and Canine Dilated Cardiomyopathy (Q26798712) (← links)
• Role of Imaging in the Evaluation of Patients at Risk for Sudden Cardiac Death: Genotype-Phenotype Intersection (Q26800070) (← links)
• Charcot-Marie-Tooth disease and intracellular traffic (Q26824841) (← links)
• When lamins go bad: nuclear structure and disease (Q26827624) (← links)
• The nuclear lamina is mechano-responsive to ECM elasticity in mature tissue (Q26859120) (← links)
• The nuclear envelope: an intriguing focal point for neurogenetic disease (Q27006719) (← links)
• Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy (Q27310698) (← links)
• Linker of nucleoskeleton and cytoskeleton (LINC) complex-mediated actin-dependent nuclear positioning orients centrosomes in migrating myoblasts (Q27311126) (← links)
• Cardiomyocyte-specific expression of lamin a improves cardiac function in Lmna-/- mice (Q27324330) (← links)
• Cytoskeletal tension induces the polarized architecture of the nucleus (Q27330134) (← links)
• Structure of the globular tail of nuclear lamin (Q27638385) (← links)
• Genetics and disease of ventricular muscle (Q27691994) (← links)
• Genetic Variations Leading to Familial Dilated Cardiomyopathy (Q28067043) (← links)
• Inherited bradyarrhythmia: A diverse genetic background (Q28071683) (← links)
• Clinical and Mechanistic Insights Into the Genetics of Cardiomyopathy (Q28075470) (← links)
• Recent advances in animal and human pluripotent stem cell modeling of cardiac laminopathy (Q28077171) (← links)
• The cardiac conduction system (Q28116242) (← links)
• Emery-Dreifuss muscular dystrophy - a 40 year retrospective (Q28145710) (← links)
• Mutational analysis of the beta- and delta-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathy (Q28177723) (← links)
• Functional consequences of an LMNA mutation associated with a new cardiac and non-cardiac phenotype (Q28188458) (← links)
• The nuclear envelope in muscular dystrophy and cardiovascular diseases (Q28189195) (← links)
• LMNA mutations in atypical Werner's syndrome (Q28202570) (← links)
• The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms (Q28203734) (← links)
• Mutations in the muscle LIM protein and α-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis (Q28211195) (← links)
• Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly) (Q28214680) (← links)
• A nuclear lamin is required for cytoplasmic organization and egg polarity in Drosophila (Q28215100) (← links)
• Emery-Dreifuss muscular dystrophy (Q28215723) (← links)
• Life at the edge: the nuclear envelope and human disease (Q28216767) (← links)
• Inherited conduction system abnormalities--one group of diseases, many genes (Q28236888) (← links)
• Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy (Q28243560) (← links)