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A list of all pages that have property "Has abstract" with value "The Tim23 protein is the key component of the mitochondrial import machinery. It locates to the inner mitochondrial membrane and its own import is dependent on the DDP1/TIM13 complex. Mutations in human DDP1 cause the Mohr-Tranebjaerg syndrome (MTS/DFN-1; OMIM #304700), which is one of the two known human diseases of the mitochondrial protein import machinery. We created a ''Tim23'' knockout mouse from a gene trap embryonic stem cell clone. Homozygous Tim23 mice were not viable. Heterozygous F1 mutants showed a 50% reduction of Tim23 protein in Western blot, a ''neurological phenotype'' and a markedly reduced life span. Haploinsufficiency of the ''Tim23'' mutation underlines the critical role of the mitochondrial import machinery for maintaining mitochondrial function.". Since there have been only a few results, also nearby values are displayed.

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    • Ahting 2009 Biochim Biophys Acta  + (The Tim23 protein is the key component of The Tim23 protein is the key component of the mitochondrial import machinery. It locates to the inner mitochondrial membrane and its own import is dependent on the DDP1/TIM13 complex. Mutations in human DDP1 cause the Mohr-Tranebjaerg syndrome (MTS/DFN-1; OMIM #304700), which is one of the two known human diseases of the mitochondrial protein import machinery. We created a ''Tim23'' knockout mouse from a gene trap embryonic stem cell clone. Homozygous Tim23 mice were not viable. Heterozygous F1 mutants showed a 50% reduction of Tim23 protein in Western blot, a ''neurological phenotype'' and a markedly reduced life span. Haploinsufficiency of the ''Tim23'' mutation underlines the critical role of the mitochondrial import machinery for maintaining mitochondrial function.ry for maintaining mitochondrial function.)