Drosophila as a model for the identification of genes causing adult human heart disease. - Test2 - elhamkhani - TriplyDB

Drosophila as a model for the identification of genes causing adult human heart disease.

Drosophila as a model for the identification of genes causing adult human heart disease.

http://www.wikidata.org/entity/Q30476715

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KCNQ potassium channel mutations cause cardiac arrhythmias in Drosophila that mimic the effects of aging.Drosophila tools and assays for the study of human diseases Methods to assess Drosophila heart development, function and aging Drosophila comet assay: insights, uses, and future perspectives Animal and in silico models for the study of sarcomeric cardiomyopathies Comparative approaches to the study of physiology: Drosophila as a physiological tool.Genetic variation for cardiac dysfunction in Drosophila Arrhythmia caused by a Drosophila tropomyosin mutation is revealed using a novel optical coherence tomography instrument A Circadian Clock Gene, Cry, Affects Heart Morphogenesis and Function in Drosophila as Revealed by Optical Coherence Microscopy PGC-1/Spargel Counteracts High-Fat-Diet-Induced Obesity and Cardiac Lipotoxicity Downstream of TOR and Brummer ATGL Lipase.Fermitins, the orthologs of mammalian Kindlins, regulate the development of a functional cardiac syncytium in Drosophila melanogaster Complex genetic architecture of cardiac disease in a wild type inbred strain of Drosophila melanogaster Vinculin network-mediated cytoskeletal remodeling regulates contractile function in the aging heart The UNC-45 chaperone is critical for establishing myosin-based myofibrillar organization and cardiac contractility in the Drosophila heart model Optogenetic pacing in Drosophila melanogaster Cardiac hypertrophy involves both myocyte hypertrophy and hyperplasia in anemic zebrafish A mighty small heart: the cardiac proteome of adult Drosophila melanogaster Obesity-associated cardiac dysfunction in starvation-selected Drosophila melanogaster Myosin transducer mutations differentially affect motor function, myofibril structure, and the performance of skeletal and cardiac muscles Dystrophin deficiency in Drosophila reduces lifespan and causes a dilated cardiomyopathy phenotype.A new method for detection and quantification of heartbeat parameters in Drosophila, zebrafish, and embryonic mouse hearts SMAD signaling drives heart and muscle dysfunction in a Drosophila model of muscular dystrophy Physiological homology between Drosophila melanogaster and vertebrate cardiovascular systems.A Drosophila melanogaster model of diastolic dysfunction and cardiomyopathy based on impaired troponin-T function.Distinct effects of tafazzin deletion in differentiated and undifferentiated mitochondria.Strong dietary restrictions protect Drosophila against anoxia/reoxygenation injuries Serial examination of an inducible and reversible dilated cardiomyopathy in individual adult Drosophila.Affecting Rhomboid-3 function causes a dilated heart in adult Drosophila.Age-dependent electrical and morphological remodeling of the Drosophila heart caused by hERG/seizure mutations.Aging and CaMKII alter intracellular Ca2+ transients and heart rhythm in Drosophila melanogaster.Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet-Biedl syndrome Cardiac copper deficiency activates a systemic signaling mechanism that communicates with the copper acquisition and storage organs.Drosophila, genetic screens, and cardiac function In vivo effects of traditional Ayurvedic formulations in Drosophila melanogaster model relate with therapeutic applications Galactokinase is a novel modifier of calcineurin-induced cardiomyopathy in Drosophila.Heart wall velocimetry and exogenous contrast-based cardiac flow imaging in Drosophila melanogaster using Doppler optical coherence tomography.Orthologs of human disease associated genes and RNAi analysis of silencing insulin receptor gene in Bombyx mori.Big, bad hearts: from flies to man The NADPH metabolic network regulates human αB-crystallin cardiomyopathy and reductive stress in Drosophila melanogaster Sizing up models of heart failure: Proteomics from flies to humans.

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Drosophila as a model for the identification of genes causing adult human heart disease.

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Drosophila as a model for the identification of genes causing adult human heart disease.

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Drosophila as a model for the identification of genes causing adult human heart disease.

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Drosophila as a model for the identification of genes causing adult human heart disease.

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Drosophila as a model for the identification of genes causing adult human heart disease.

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Drosophila as a model for the identification of genes causing adult human heart disease.

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Drosophila as a model for the identification of genes causing adult human heart disease.

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Proceedings of the National Academy of Sciences of the United States of America

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Drosophila as a model for the identification of genes causing adult human heart disease.

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Howard A Rockman

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Hubert Amrein

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Joseph A Izatt

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Mary C Reedy

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Matthew J Wolf

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Michael A Choma

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P2860

Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

A systematic analysis of human disease-associated gene sequences in Drosophila melanogaster

Targeted gene expression as a means of altering cell fates and generating dominant phenotypes

Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy

The gene tinman is required for specification of the heart and visceral muscles in Drosophila

Mutations affecting segment number and polarity in Drosophila

A Drosophila model of Parkinson's disease

Optical coherence tomography

Muscle abnormalities in Drosophila melanogaster heldup mutants are caused by missing or aberrant troponin-I isoforms

Intersecting signalling and transcriptional pathways in Drosophila heart specification.

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