Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy
about
Cardiomyopathy classification: ongoing debate in the genomics eraGenetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathyA new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16Many roads lead to a broken heart: the genetics of dilated cardiomyopathy.A novel custom resequencing array for dilated cardiomyopathyHeart Disease in Disorders of Muscle, Neuromuscular Transmission, and the NervesGenetics of Human and Canine Dilated CardiomyopathyGenetic Variations Leading to Familial Dilated CardiomyopathyMuscle fatigue, nNOS and muscle fiber atrophy in limb girdle muscular dystrophyMutational analysis of the beta- and delta-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathyCoding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathySarcoglycan, the heart, and skeletal muscles: new treatment, old drug?Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complexDisruption of integrin function in the murine myocardium leads to perinatal lethality, fibrosis, and abnormal cardiac performanceImaging phenotype vs genotype in nonhypertrophic heritable cardiomyopathies: dilated cardiomyopathy and arrhythmogenic right ventricular cardiomyopathyDrosophila 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 dysfunctionWorsening 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 professionalsSecondary coronary artery vasospasm promotes cardiomyopathy progression.Sarcolemma instability during mechanical activity in Largemyd cardiac myocytes with loss of dystroglycan extracellular matrix receptor functionExpanding 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 PopulationEvaluating 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
P2860
Q21284968-D06F42B7-C0B0-44FA-A12E-EC10104B28F5Q24288778-3283BE43-324C-4A68-A106-847A254DDB5FQ24535586-FA4083F9-64A9-4574-BA3A-30DB41F0F65BQ24535744-DF40D422-CD37-4C40-9371-9DAF4B32A6A0Q24602132-DE4CFFE8-894B-442B-BAEF-16913E532824Q26750958-7B8171D7-D583-482B-B1C0-47F16F5067D1Q26798712-57BDF6A2-DDC8-4288-B4B4-9440F97ACC54Q28067043-C3EA65CC-B489-41D8-AC2D-AB1A8D49141EQ28083989-97650586-A787-47CB-B380-3A3D1EC5AE56Q28177723-48DDBF85-5911-4924-BAEB-B741947B86A4Q28243560-9AF3FB67-0E66-4388-B705-156FB7656AEAQ28346521-CB30EB53-8A8F-436E-B348-329C5C9928DEQ28346540-4536F3B4-EE0A-4433-B3AA-89E39D9F7360Q28359740-27E5C805-CBF4-489D-B548-1F33FD978884Q30473247-CF060D9B-382F-45F6-A83D-6BA3A129934EQ30476715-EE00E8B4-E496-44DE-84BE-268254F2314CQ33505660-587E1373-416D-47B5-9EA7-F6D9DBFEFAB0Q33709450-E46158FA-581B-47C8-9D15-46C978D1655BQ33894636-5E897764-ADE9-40A5-B26B-823D4B3A57AFQ33894656-4352268D-8653-4DC5-9791-E356FB8AE1AFQ33905340-34EBE0C7-035F-47A1-8CB1-B9A7C4B97979Q34023992-358F39FF-5C06-4135-AA99-2AE515690C4BQ34028619-FE671973-C9A6-4F26-8324-2A3AF7249B91Q34281800-68277F24-0938-4FB2-AFB8-AA41B23EBF1AQ34327042-8EED1500-A03F-4A08-ABF1-CAFCDD7F92D2Q34327150-E31C101A-5C07-4472-B185-E0AE307AE5DAQ34673385-8FAA4BCA-D824-4045-8D84-22F6F8B33867Q34882653-82E68822-EC3E-4837-8263-5C31D72EF237Q34930971-203A0569-47AA-4620-8E94-5519EDA305B8Q35054950-2A1B1E6F-D141-4CB4-BEB3-A0CD1060B7E5Q35096094-F856FF44-89F6-4139-ACE8-280524079C6CQ35155971-EED2CD2F-466B-41D6-8E26-044B33ECB80FQ35443492-A628F759-CCF7-46E8-B0DA-6214F3D80962Q35581284-2745E859-BACB-41BC-AF55-AB9BEAE28E95Q35822926-DD998470-417B-4BE7-AAB2-F2FE313AB2BDQ35865366-01C36310-62E6-41A7-909B-CE1827322A6FQ35882721-1BB886F6-DD14-4007-AA29-85DD51E537D4Q35903638-630D725A-2DB8-46FA-992E-741ABB9DCBFDQ35928235-3B752509-FB14-4468-B92B-445F5E4D785EQ36051051-D5E4A7A3-8823-4AE3-974E-05CC3699A1E0
P2860
Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy
description
2000 nî lūn-bûn
@nan
2000 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Mutations in the human delta-s ...... poradic dilated cardiomyopathy
@ast
Mutations in the human delta-s ...... poradic dilated cardiomyopathy
@en
Mutations in the human delta-s ...... poradic dilated cardiomyopathy
@nl
type
label
Mutations in the human delta-s ...... poradic dilated cardiomyopathy
@ast
Mutations in the human delta-s ...... poradic dilated cardiomyopathy
@en
Mutations in the human delta-s ...... poradic dilated cardiomyopathy
@nl
prefLabel
Mutations in the human delta-s ...... poradic dilated cardiomyopathy
@ast
Mutations in the human delta-s ...... poradic dilated cardiomyopathy
@en
Mutations in the human delta-s ...... poradic dilated cardiomyopathy
@nl
P2093
P2860
P3181
P356
P1476
Mutations in the human delta-s ...... poradic dilated cardiomyopathy
@en
P2093
J A Towbin
K R Bowles
N E Bowles
P2860
P304
P3181
P356
10.1172/JCI9224
P407
P577
2000-09-01T00:00:00Z