Molecular Approaches to Heart Failure Therapy
Editat de G. Hasenfuss, E. Marbanen Limba Engleză Paperback – 14 oct 2012
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Specificații
ISBN-13: 9783642633324
ISBN-10: 3642633323
Pagini: 357
Ilustrații: X, 357 p.
Dimensiuni: 155 x 235 x 22 mm
Greutate: 0.52 kg
Ediția:Softcover reprint of the original 1st ed. 2000
Editura: Steinkopff
Colecția Steinkopff
Locul publicării:Heidelberg, Germany
ISBN-10: 3642633323
Pagini: 357
Ilustrații: X, 357 p.
Dimensiuni: 155 x 235 x 22 mm
Greutate: 0.52 kg
Ediția:Softcover reprint of the original 1st ed. 2000
Editura: Steinkopff
Colecția Steinkopff
Locul publicării:Heidelberg, Germany
Public țintă
Professional/practitionerCuprins
1 Alterations in excitation-contraction coupling and potential gene therapy targets in failing human hearts.- 2 Cardiac overexpression of fl-adrenergic receptors.- 3 Genetic approaches to elucidate the regulatory role of phospholamban in the heart.- 4 Manipulation of SERCA2a in the heart by gene transfer.- 5 Changing the cardiac calcium transient: SERCA2 overexpression versus phospholamban inhibition.- 6 Adenovirus-mediated gene transfer of SERCA isoforms.- 7 Overexpression of FKBP12.6 to influence SR function.- 8 Adenovirus-mediated myocardial gene therapy.- 9 Adenovirus-mediated transfection of multicellular cardiac preparations.- 10 Myocardial-specific gene delivery.- 11 Transfection studies using a new cardiac 3D gel system.- 12 Cellular mechanisms of cardiac arrhythmias — do they play a role in heart failure?.- 13 Potassium channel overexpression.- 14 Mechanisms and relevance of apoptosis.- 15 Strategies to prevent apoptosis.- 16 Neurohumoral modulation of metalloproteinases in cardiac failure:impact on remodeling.- 17 Oxidative stress in heart failure.- 18 Modulation of cardiac function by essential myosin light chains in health and disease.- 19 Myocardial infarction, infarct repair, and strategies for muscle regeneration.- 20 Cardiomyocytes can induce rhythmic contraction of skeletal muscle cells. Potential use for infarct repair.- 21 Strategies to identify cardiomyocyte cell cycle regulatory genes.