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Parvalbumin isoforms for enhancing cardiac diastolic function
Wang Wang
,
Joseph M. Metzger
Integrative Biology and Physiology
Cellular Mechanisms of Cancer
Lillehei Heart Institute
Research output
:
Contribution to journal
›
Review article
›
peer-review
10
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Scopus citations
Overview
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Keyphrases
Diastolic Heart Failure
100%
Parvalbumin
100%
Cardiac Diastolic Function
100%
Ca2+
40%
Myocytes
40%
Diastolic Dysfunction
40%
Myocardial Relaxation
40%
Ca2+-binding Protein
40%
Heart Failure Patients
20%
Heart Failure
20%
Gene Transfer
20%
Skeletal muscle
20%
Therapeutic Use
20%
Sequestration
20%
Potential Therapeutics
20%
Genetic Manipulation
20%
Diastole
20%
Contractile Function
20%
Ectopic Expression
20%
Divergent Effects
20%
Intracellular Calcium
20%
Systolic Performance
20%
Ca2+ Handling
20%
Relaxed Performance
20%
Ventricular Filling
20%
Ca2+ Transient
20%
Parvalbumin Gene
20%
Impaired Relaxation
20%
Transfer Approach
20%
Medicine and Dentistry
Calcium Ion
100%
Diastolic Function
100%
Parvalbumin
100%
Diastolic Heart Failure
100%
Congestive Heart Failure
40%
Diastolic Dysfunction
40%
Cardiac Muscle Cell
40%
In Vitro
20%
Buffer
20%
Gene Transfer
20%
Intracellular Calcium
20%
Contractile Function
20%
Calcium-Binding Protein
20%
Ectopic Expression
20%
Skeletal Muscle
20%
Biochemistry, Genetics and Molecular Biology
Isoform
100%
Parvalbumin
100%
Cardiac Muscle Cell
40%
Ectopic Expression
20%
Genetic Manipulation
20%
Skeletal Muscle
20%
Calcium Cell Level
20%
Calcium-Binding Protein
20%