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A new approach for the identification of modifier genes in heart failure

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title

A new approach for the identification of modifier genes in heart failure (English)

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P Charron

2

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Michel Komajda

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M Komajda

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publication date

25 May 2004

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published in

The Pharmacogenomics Journal

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volume

4

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issue

4

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page(s)

221-223

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exact match

https://scigraph.springernature.com/pub.10.1038/sj.tpj.6500257

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Finding genes that underlie complex traits

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Modifier genes in mice and humans

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Genes and their polymorphisms in mono- and multifactorial cardiomyopathies: towards pharmacogenomics in heart failure

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Synergistic polymorphisms of beta1- and alpha2C-adrenergic receptors and the risk of congestive heart failure

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Expression profiling of human idiopathic dilated cardiomyopathy

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Genomics, proteomics and bioinformatics of human heart failure

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21 January 2018

From mouse to man: understanding heart failure through genetically altered mouse models

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

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Multiple quantitative trait loci modify the heart failure phenotype in murine cardiomyopathy.

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Cardiac beta ARK1 inhibition prolongs survival and augments beta blocker therapy in a mouse model of severe heart failure

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Complexities in the genetic dissection of quantitative trait loci

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7 January 2021

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Effect of the Asp298 variant of endothelial nitric oxide synthase on survival for patients with congestive heart failure

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7 January 2021

based on heuristic

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Genetic modifier loci affecting survival and cardiac function in murine dilated cardiomyopathy

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Genetic analysis of inherited hypertension in the rat.

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Identifiers

DOI

10.1038/SJ.TPJ.6500257

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PubMed publication ID

15159767

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(Q57907328)

A new approach for the identification of modifier genes in heart failure

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