Large-scale mutation screening in patients with dilated or hypertrophic cardiomyopathy: a pilot study using DGGE (Q83821167)

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28 January 2020

title

Large-scale mutation screening in patients with dilated or hypertrophic cardiomyopathy: a pilot study using DGGE (English)

1 reference

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hypertrophic cardiomyopathy

28 January 2020

main subject

1 reference

8

Hugo A Katus

1 reference

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28 January 2020

6

Andrew Remppis

1 reference

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28 January 2020

author name string

Raphael Zeller

1

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28 January 2020

Boris T Ivandic

2

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28 January 2020

Philipp Ehlermann

3

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28 January 2020

Oliver Mücke

4

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28 January 2020

Christian Zugck

5

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28 January 2020

Evangelos Giannitsis

7

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28 January 2020

Dieter Weichenhan

9

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28 January 2020

publication date

20 May 2006

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Journal of Molecular Medicine

28 January 2020

published in

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28 January 2020

volume

84

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28 January 2020

issue

8

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28 January 2020

page(s)

682-691

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Global gene expression profiling of end-stage dilated cardiomyopathy using a human cardiovascular-based cDNA microarray

28 January 2020

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00109-006-0056-2

Molecular mechanisms of inherited cardiomyopathies

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00109-006-0056-2

Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

21 January 2018

1 reference

12 December 2020

A novel missense mutation in the myosin binding protein-C gene is responsible for hypertrophic cardiomyopathy with left ventricular dysfunction and dilation in elderly patients

1 reference

12 December 2020

Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy.

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12 December 2020

Sarcomeric genotyping in hypertrophic cardiomyopathy

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12 December 2020

Optimal temperature selection for mutation detection by denaturing HPLC and comparison to single-stranded conformation polymorphism and heteroduplex analysis

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12 December 2020

Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy

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12 December 2020

Methods for detection of point mutations: performance and quality assessment. IFCC Scientific Division, Committee on Molecular Biology Techniques

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12 December 2020

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

1 reference

12 December 2020

Frequency and phenotypes of familial dilated cardiomyopathy

1 reference

12 December 2020

Genomic organization and single-nucleotide polymorphism map of desmuslin, a novel intermediate filament protein on chromosome 15q26.3

1 reference

12 December 2020

Spectrum of clinical phenotypes and gene variants in cardiac myosin-binding protein C mutation carriers with hypertrophic cardiomyopathy.

1 reference

12 December 2020

Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy

1 reference

12 December 2020

Patterns of inheritance in hypertrophic cardiomyopathy: assessment by M-mode and two-dimensional echocardiography.

1 reference

12 December 2020

Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy

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12 December 2020

Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy

1 reference

12 December 2020

Comprehensive detection of single base changes in human genomic DNA using denaturing gradient gel electrophoresis and a GC clamp

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12 December 2020

The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

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12 December 2020

A comparison of fluorescent SSCP and denaturing HPLC for high throughput mutation scanning.

1 reference

12 December 2020

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

1 reference

12 December 2020

Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland

1 reference

12 December 2020

Novel mutations in sarcomeric protein genes in dilated cardiomyopathy.

1 reference

12 December 2020

Denaturing high-performance liquid chromatography: A review

1 reference

12 December 2020

American College of Cardiology/European Society of Cardiology Clinical Expert Consensus Document on Hypertrophic Cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the Europ

1 reference

12 December 2020

VEGF-PLCgamma1 pathway controls cardiac contractility in the embryonic heart

1 reference

12 December 2020

The sarcomeric Z-disc: a nodal point in signalling and disease

1 reference

12 December 2020

Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy

1 reference

12 December 2020

Cardiac hypertrophy: the good, the bad, and the ugly

1 reference

12 December 2020

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

1 reference

12 December 2020

Genome sequencing in microfabricated high-density picolitre reactors

1 reference

12 December 2020

Improved mutation detection in GC-rich DNA fragments by combined DGGE and CDGE.

1 reference

12 December 2020

Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization Of cardiac transcript and protein

1 reference

12 December 2020

Desmuslin, an intermediate filament protein that interacts with alpha -dystrobrevin and desmin

1 reference

12 December 2020

The Genetic Basis for Cardiomyopathy

1 reference

12 December 2020