(Q24308001)

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Dilated cardiomyopathy mutant tropomyosin mice develop cardiac dysfunction with significantly decreased fractional shortening and myofilament calcium sensitivity

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Dilated cardiomyopathy mutant tropomyosin mice develop cardiac dysfunction with significantly decreased fractional shortening and myofilament calcium sensitivity (English)

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1 reference

GOA release 2020-03-11

positive regulation of heart rate by epinephrine

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GOA release 2020-03-11

Tropomyosin 1, alpha

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GOA release 2020-03-11

dilated cardiomyopathy

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based on heuristic

inferred from title

author name string

Sudarsan Rajan

1

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Rafeeq P H Ahmed

2

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Ganapathy Jagatheesan

3

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Natalia Petrashevskaya

4

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Greg P Boivin

5

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Dalia Urboniene

6

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Grace M Arteaga

7

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Beata M Wolska

8

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R John Solaro

9

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Stephen B Liggett

10

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David F Wieczorek

11

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language of work or name

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publication date

20 July 2007

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Circulation Research

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101

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2

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205-14

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Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy

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https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

A familial hypertrophic cardiomyopathy alpha-tropomyosin mutation causes severe cardiac hypertrophy and death in mice

1 reference

https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure

1 reference

https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

Local destabilization of the tropomyosin coiled coil gives the molecular flexibility required for actin binding

1 reference

https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

A mouse model of familial hypertrophic cardiomyopathy caused by a alpha-tropomyosin mutation

1 reference

https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

Phospholamban: a crucial regulator of cardiac contractility

1 reference

https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

Desmin-related cardiomyopathy in transgenic mice: a cardiac amyloidosis

1 reference

https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function.

1 reference

https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

Deciphering the design of the tropomyosin molecule

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https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

Cardiomyopathic tropomyosin mutations that increase thin filament Ca2+ sensitivity and tropomyosin N-domain flexibility

1 reference

https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype

1 reference

https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

Functional consequences of hypertrophic and dilated cardiomyopathy-causing mutations in alpha-tropomyosin.

1 reference

https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

The effect of mutations in alpha-tropomyosin (E40K and E54K) that cause familial dilated cardiomyopathy on the regulatory mechanism of cardiac muscle thin filaments.

1 reference

https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

Rescue of tropomyosin-induced familial hypertrophic cardiomyopathy mice by transgenesis

1 reference

https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

Microarray analysis of gene expression during early stages of mild and severe cardiac hypertrophy

1 reference

https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

Myofibril degeneration caused by tropomodulin overexpression leads to dilated cardiomyopathy in juvenile mice

1 reference

https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

Complexity in simplicity: monogenic disorders and complex cardiomyopathies

1 reference

https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice

1 reference

https://api.crossref.org/works/10.1161%2FCIRCRESAHA.107.148379

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1161/CIRCRESAHA.107.148379

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