Author: "Kamdar, Forum" / Publisher: churchill livingstone - Searchworks@Jio Institute Digital Library Search Results

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Start Over Author "Kamdar, Forum" Publisher churchill livingstone

Author: Kamdar F and Randhawa VK
Subjects: Humans, Heart, Proteomics, Thorax, Heart Failure diagnosis, Heart Failure therapy
Abstract: Competing Interests: Disclosures None.
Published: 2023
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Author: Jedeon Z, Masotti M, Schultz J, Vest AR, Alexy T, Pritzker M, Maharaj V, Kamdar F, Knopper R, Shaffer A, John R, and Cogswell R
Subjects: Humans, Creatinine, Glomerular Filtration Rate, Kidney physiology, Heart Failure diagnosis, Heart Failure epidemiology
Published: 2023
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Author: Garry DJ, Kamdar F, and Alexy T
Subjects: Humans, Cardiomyopathies diagnosis, Heart Failure, Muscular Dystrophies diagnosis
Published: 2022
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Author: Garry DJ, Kamdar F, and Alexy T
Subjects: Humans, Cardiomyopathies diagnosis, Cardiomyopathies epidemiology, Cardiomyopathies therapy, Heart Failure, Muscular Dystrophy, Duchenne
Abstract: Competing Interests: Conflicts of Interest None.
Published: 2022
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Author: Bellam N, Denfeld QE, Kamdar F, Alexy T, Breathett K, Patel PA, Faulkenberg K, Moyer B, Psotka MA, and Ginwalla M
Subjects: COVID-19 therapy, Career Mobility, Heart Failure therapy, Humans, Telemedicine methods, COVID-19 epidemiology, Career Choice, Health Personnel trends, Heart Failure epidemiology, Telemedicine trends
Published: 2021
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Author: Kamdar F, Klaassen Kamdar A, Koyano-Nakagawa N, Garry MG, and Garry DJ
Subjects: Animals, Humans, Cardiomyopathies congenital, Cardiomyopathies genetics, Cardiomyopathies pathology, Induced Pluripotent Stem Cells cytology, Models, Cardiovascular, Myocytes, Cardiac pathology
Abstract: Inherited cardiomyopathies, including hypertrophic cardiomyopathy, dilated cardiomyopathies, arrythmogenic right ventricular cardiomyopathy, and other inherited forms of heart failure, represent a unique set of genetically defined cardiovascular disease processes. Unraveling the molecular mechanisms of these deadly forms of human heart disease has been challenging, but recent groundbreaking scientific advances in stem cell technology have allowed for the generation of patient-specific human inducible stem cell (hiPSC)-derived cardiomyocytes (CMs). hiPSC-derived CMs retain the genetic blueprint of the patient, they can be maintained in culture, and they recapitulate the phenotypic characteristics of the disease in vitro, thus serving as a disease in a dish. This review provides an overview of in vitro modeling of inherited cardiomyopathies with the use of patient-specific hiPSC-derived CMs., (Copyright © 2015. Published by Elsevier Inc.)
Published: 2015
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