(Q57279219)

6

0 references

William McKenna

object named as

William J. McKenna

5

0 references

Jens Mogensen

object named as

Jens Mogensen

4

0 references

author name string

Laura C. Preston

1

0 references

Simon Lipscomb

2

0 references

Paul Robinson

3

0 references

Chris C. Ashley

7

0 references

Charles S. Redwood

https://scigraph.springernature.com/pub.10.1007/s00424-006-0161-7

8

0 references

publication date

26 September 2006

0 references

published in

Pfluegers Archiv

0 references

volume

453

0 references

issue

6

0 references

page(s)

771-776

0 references

exact match

0 references

cites work

Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

The role of the four Ca2+ binding sites of troponin C in the regulation of skeletal muscle contraction

1 reference

12 December 2020

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

1 reference

12 December 2020

Nitrophenyl-EGTA, a photolabile chelator that selectively binds Ca2+ with high affinity and releases it rapidly upon photolysis

1 reference

12 December 2020

Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy.

1 reference

12 December 2020

Ca2+ and activation mechanisms in skeletal muscle

1 reference

12 December 2020

Different functional properties of troponin T mutants that cause dilated cardiomyopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial dilated cardiomyopathy: cardiac abnormalities are common in asymptomatic relatives and may represent early disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy

1 reference

12 December 2020

Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T-tropomyosin interaction and causes a Ca2+ desensitization

1 reference

12 December 2020

Occurrence and significance of progressive left ventricular wall thinning and relative cavity dilatation in hypertrophic cardiomyopathy

1 reference

12 December 2020

Activation kinetics of skinned cardiac muscle by laser photolysis of nitrophenyl-EGTA.

1 reference

12 December 2020

Effects of troponin C isoform on the action of the cardiotonic agent EMD 57033.

1 reference

12 December 2020

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

1 reference

12 December 2020

The effects of the inotropic agent EMD 57033 on activation and relaxation kinetics in frog skinned skeletal muscle

1 reference

12 December 2020

Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy.

1 reference

12 December 2020

Invited Review: pathophysiology of cardiac muscle contraction and relaxation as a result of alterations in thin filament regulation

1 reference

12 December 2020

The Genetic Basis for Cardiomyopathy

1 reference

12 December 2020