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mitochondrial diseases — a diverse group of mainly multisystemic and maternally inherited disorders caused by mutations of mitochondrial DNA; some are sporadic and tissue specific. They affect tissues having a high rate of oxidative metabolism, including the brain and… … Medical dictionary
Mitochondrial disease — Classification and external resources Micrograph showing ragged red fibres, a finding seen in mitochondrial diseases. Muscle biopsy. Gomori trichrome stain … Wikipedia
Mitochondrial myopathy — Classification and external resources Simplified structure of a typical mitochondrion ICD 10 G … Wikipedia
Mitochondrial neurogastrointestinal encephalopathy syndrome — Classification and external resources ICD 9 277.87 OMIM 603041 … Wikipedia
Mitochondrial membrane transport protein — Mitochondrial membrane transport proteins are proteins which exist in the membranes of mitochondria and which serve to transport[1] molecules and other factors such as ions into or out of the organelles. Examples Examples of mitochondrial… … Wikipedia
Mitochondrial encephalomyopathy — Classification and external resources ICD 9 277.87 MeSH D017237 A Mitochondr … Wikipedia
Mitochondrial DNA — Human mitochondrial DNA … Wikipedia
Mitochondrial permeability transition pore — The Mitochondrial Permeability Transition, or MPT, is defined as an increase in the permeability of the mitochondrial membranes to molecules of less than 1500 Daltons in molecular weight. MPT results from the opening of a mitochondrial… … Wikipedia
Mitochondrial genome — The mitochondrial genome is the genetic material of the mitochondria. The mitochondria are organelles that reproduce themselves semi autonomously within eukaryotic cells.The genetic material forming the mitochondrial genome is similar in… … Wikipedia
Mitochondrial carrier — Mitochondrial ADP/ATP carrier Identifiers Symbol Mito carr Pfam … Wikipedia
