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Our laboratory investigates a range of focus areas, all of which center on understanding the molecular mechanisms of heart and skeletal muscle disease. Toward this end we study the basic machinery that underlies cell death, with a special interest in mitochondrial-dependent mechanisms of nonapoptotic death (such as cellular necrosis). Prominent diseases of both heart and skeletal muscle are affected by cellular necrosis, so identifying the genes that control this process could have a substantial effect on our treatment of these types of diseases.
We are also interested in characterizing the intracellular signaling pathways that control cellular growth, differentiation and replication in cardiac and skeletal muscle. A better understanding of the signaling pathways that control these processes, coupled with the identification of novel genes, could suggest new treatment strategies for human diseases. Similarly, we are examining the transcriptional regulatory factors and epigenetic mechanisms that regulate cardiac and skeletal muscle differentiation, growth, death and replication, in order to suggest additional targets for treating human disease.
Our laboratory is also actively engaged in identifying novel secreted protein factors in the heart (cytokines, growth factors, chemokines) that might control disease responsiveness. We study the cardiac fibroblast and how it functions during disease to alter the extracellular matrix, which affects heart remodeling. And we are investigating the basic mechanisms of intracellular calcium handling in cardiac and skeletal muscle to further understand the paradigms of excitation-transcription coupling and excitation-signaling coupling.
The Jeffery Molkentin Lab is investigating the molecular mechanisms that underlie cell death, and are exploring the potential medical benefits that might arise from inhibition of death in certain disease states.
The Jeffery Molkentin Lab researches the molecular events that underlie the cardiac growth response, both developmentally and in the adult heart in response to pathologic stimuli.
The laboratory is interested in cardiac regeneration after myocardial infarction.
The laboratory is interested in understanding how fibroblasts convert into myofibroblasts during disease stimulation to help mediate tissue remodeling.
The Jeffery Molkentin Lab is interested in defining basic mechanisms of gene expression regulation in mammalian cells through alterations in transcription factor potency as mediated by phosphorylation or by alterations in subcellular localization.
The Jeffery Molkentin Lab is investigating the molecular mechanisms that underlie skeletal muscle degeneration in muscular dystrophy (MD).
The Jeffery Molkentin Lab is investigating the regulatory mechanisms that control skeletal muscle hypertrophy and fiber-type switching between the fast (glycolytic) and the slow (oxidative) programs.
Jeffery D. Molkentin, PhD
Professor, Howard Hughes Medical Institute
Member, Molecular Cardiovascular Biology, Cincinnati Children's Hospital Medical Center
Mailing Address:240 Albert Sabin WayMLC 7020Cincinnati, OH 45229-3039
Phone: 513-636-3557Email: firstname.lastname@example.org
Learn more about the faculty, staff and student members of our research team.
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