Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy - Test2 - elhamkhani - TriplyDB

Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

http://www.wikidata.org/entity/Q24604161

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Cardiomyopathy classification: ongoing debate in the genomics era Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16 Many roads lead to a broken heart: the genetics of dilated cardiomyopathy.A novel custom resequencing array for dilated cardiomyopathy Heart Disease in Disorders of Muscle, Neuromuscular Transmission, and the Nerves Genetics of Human and Canine Dilated Cardiomyopathy Genetic Variations Leading to Familial Dilated Cardiomyopathy Muscle fatigue, nNOS and muscle fiber atrophy in limb girdle muscular dystrophy Mutational analysis of the beta- and delta-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathy Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy Sarcoglycan, the heart, and skeletal muscles: new treatment, old drug?Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex Disruption of integrin function in the murine myocardium leads to perinatal lethality, fibrosis, and abnormal cardiac performance Imaging phenotype vs genotype in nonhypertrophic heritable cardiomyopathies: dilated cardiomyopathy and arrhythmogenic right ventricular cardiomyopathy Drosophila as a model for the identification of genes causing adult human heart disease.Serial examination of an inducible and reversible dilated cardiomyopathy in individual adult Drosophila.Whole-exome sequencing identifies SGCD and ACVRL1 mutations associated with total anomalous pulmonary venous return (TAPVR) in Chinese population.Rescue of hereditary form of dilated cardiomyopathy by rAAV-mediated somatic gene therapy: amelioration of morphological findings, sarcolemmal permeability, cardiac performances, and the prognosis of TO-2 hamsters.Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy.Translocation and cleavage of myocardial dystrophin as a common pathway to advanced heart failure: a scheme for the progression of cardiac dysfunction Worsening of cardiomyopathy using deflazacort in an animal model rescued by gene therapy.Dilated cardiomyopathy in mice deficient for the lysosomal cysteine peptidase cathepsin L.A Cypher/ZASP mutation associated with dilated cardiomyopathy alters the binding affinity to protein kinase C.Does delta-sarcoglycan-associated autosomal-dominant cardiomyopathy exist?The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.Genes and their polymorphisms in mono- and multifactorial cardiomyopathies: towards pharmacogenomics in heart failure.Molecular mechanisms of inherited cardiomyopathies.Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionals Secondary coronary artery vasospasm promotes cardiomyopathy progression.Sarcolemma instability during mechanical activity in Largemyd cardiac myocytes with loss of dystroglycan extracellular matrix receptor function Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.Progression of familial and non-familial dilated cardiomyopathy: long term follow up.Mice deleted for heart-type cytochrome c oxidase subunit 7a1 develop dilated cardiomyopathy.Dysferlin-mediated membrane repair protects the heart from stress-induced left ventricular injury.A Haplotype of Two Novel Polymorphisms in δ-Sarcoglycan Gene Increases Risk of Dilated Cardiomyopathy in Mongoloid Population Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era.Mutation of delta-sarcoglycan is associated with Ca(2+) -dependent vascular remodeling in the Syrian hamster.Cardiac-specific deletion of the microtubule-binding protein CENP-F causes dilated cardiomyopathy

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P2860

Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

http://www.wikidata.org/entity/Q24604161

description

2000 nî lūn-bûn

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2000 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2000年の論文

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2000年論文

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2000年論文

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Mutations in the human delta-s ...... poradic dilated cardiomyopathy

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Mutations in the human delta-s ...... poradic dilated cardiomyopathy

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Mutations in the human delta-s ...... poradic dilated cardiomyopathy

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Mutations in the human delta-s ...... poradic dilated cardiomyopathy

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Mutations in the human delta-s ...... poradic dilated cardiomyopathy

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Mutations in the human delta-s ...... poradic dilated cardiomyopathy

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Mutations in the human delta-s ...... poradic dilated cardiomyopathy

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Mutations in the human delta-s ...... poradic dilated cardiomyopathy

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Mutations in the human delta-s ...... poradic dilated cardiomyopathy

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Mutations in the human delta-s ...... poradic dilated cardiomyopathy

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P2860

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein

A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies.

Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy.

Analysis of the accuracy and implications of simple methods for predicting the secondary structure of globular proteins

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2)

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