Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Andre Klaassen Kamdar"'
Autor:
Christine S. Moravec, Kayla Mislick, Andre Klaassen Kamdar, Srinivasa T. Reddy, David J. Kennedy, Xi Wang, Brendan Agatisa-Boyle, Rommel Morales, Malory E. Weber, Diana M. Shih, Zhili Shao, Wei Li, W.H. Wilson Tang, Kathryn Kiefer
Publikováno v:
Free Radical Biology and Medicine. 121:117-126
Background Mitochondrial oxidation is a major source of reactive oxygen species (ROS) and mitochondrial dysfunction plays a central role in development of heart failure (HF). Paraoxonase 2 deficient (PON2-def) mitochondria are impaired in function. I
Publikováno v:
Food Control. 60:621-628
In recent years, high protein food bars (HPFB) are a rapidly growing market. One major problem for commercial HPFB is that they become harder over time without moisture loss, making the product unacceptable to consumers. In this study, the effect of
Autor:
James M. Ervasti, Timothy J. Kamp, Forum Kamdar, Jianyi Zhang, Daniel J. Garry, Satyabrata Das, DeWayne Townsend, Mary G. Garry, Wuming Gong, Tatyana A. Meyers, Pruthvi Shah, Joseph C. Wu, Andre Klaassen Kamdar
Publikováno v:
J Am Coll Cardiol
Background Although cardiomyopathy has emerged as a leading cause of death in Duchenne muscular dystrophy (DMD), limited studies and therapies have emerged for dystrophic heart failure. Objectives The purpose of this study was to model DMD cardiomyop
Publikováno v:
Critical Reviews in Food Science and Nutrition. 56:1169-1192
In recent years, mainly due to the specific health benefits associated with (1) the discovery of bioactive peptides in protein hydrolysates, (2) the reduction of protein allergenicity by protein hydrolysis, and (3) the improved protein digestibility
Autor:
Andre Klaassen Kamdar, Daniel J. Garry, Christopher S. Chapman, Forum Kamdar, Timothy J. Kamp, Naoko Koyano-Nakagawa, Joseph C. Wu
Publikováno v:
Circulation. 132
Introduction: DMD is the most common muscular dystrophy and is characterized by the absence of dystrophin. Cardiomyopathy and associated arrhythmias have emerged as a leading cause of death in DMD. Hypothesis: We hypothesized that the pathophysiology
Publikováno v:
Journal of cardiac failure. 21(9)
Inherited cardiomyopathies including hypertrophic cardiomyopathy (HCM), dilated cardiomyopathies (DCM), arrythmogenic right ventricular cardiomyopathy (ARVC), and other inherited forms of heart failure represent a unique set of genetically defined ca
Autor:
Daniel J. Garry, Andre Klaassen Kamdar, Christopher S. Chapman, Naoko Koyano Nakagawa, Forum Kamdar
Publikováno v:
Journal of the American College of Cardiology. (10):A2149
DMD is the most common muscular dystrophy characterized by absence of dystrophin. A significant cardiomyopathic phenotype has emerged as a leading cause of death in DMD. There is limited knowledge about DMD cardiomyopathy due to limited access to hum