Pages that link to "Q34458260"
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The following pages link to Defects of intergenomic communication: autosomal disorders that cause multiple deletions and depletion of mitochondrial DNA. (Q34458260):
Displaying 41 items.
- The conserved translocase Tim17 prevents mitochondrial DNA loss (Q27931436) (← links)
- Structure-function defects of human mitochondrial DNA polymerase in autosomal dominant progressive external ophthalmoplegia (Q28272479) (← links)
- Thymidine kinase 2 (H126N) knockin mice show the essential role of balanced deoxynucleotide pools for mitochondrial DNA maintenance. (Q28504546) (← links)
- Mitochondrial respiratory rates and activities of respiratory chain complexes correlate linearly with heteroplasmy of deleted mtDNA without threshold and independently of deletion size (Q30320769) (← links)
- Mitochondrial encephalopathy (Q30890554) (← links)
- Encephalomyopathies caused by abnormal nuclear-mitochondrial intergenomic cross-talk (Q33810387) (← links)
- Defects of mitochondrial DNA replication. (Q34098312) (← links)
- Deoxypyrimidine monophosphate bypass therapy for thymidine kinase 2 deficiency. (Q34131169) (← links)
- Defects in mitochondrial DNA replication and human disease (Q34241192) (← links)
- Modeling pathogenic mutations of human twinkle in Drosophila suggests an apoptosis role in response to mitochondrial defects (Q34405895) (← links)
- MPV17 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA Deletions (Q34410634) (← links)
- Inherited mitochondrial diseases of DNA replication (Q34692482) (← links)
- Site-specific somatic mitochondrial DNA point mutations in patients with thymidine phosphorylase deficiency (Q35095598) (← links)
- Nuclear genes in mitochondrial disorders. (Q35145869) (← links)
- Alteration of nucleotide metabolism: a new mechanism for mitochondrial disorders. (Q35206509) (← links)
- Antiretroviral nucleosides, deoxynucleotide carrier and mitochondrial DNA: evidence supporting the DNA pol gamma hypothesis. (Q35606742) (← links)
- POS5 gene of Saccharomyces cerevisiae encodes a mitochondrial NADH kinase required for stability of mitochondrial DNA. (Q35613347) (← links)
- Mitochondriopathies (Q35685889) (← links)
- Decreased mtDNA, oxidative stress, cardiomyopathy, and death from transgenic cardiac targeted human mutant polymerase gamma. (Q35695170) (← links)
- Targeted transgenic overexpression of mitochondrial thymidine kinase (TK2) alters mitochondrial DNA (mtDNA) and mitochondrial polypeptide abundance: transgenic TK2, mtDNA, and antiretrovirals (Q35781380) (← links)
- Mitochondrial diseases: a nosological update. (Q36765849) (← links)
- Removal of oxidative DNA damage via FEN1-dependent long-patch base excision repair in human cell mitochondria (Q36845992) (← links)
- Inhibition of DNA synthesis facilitates expansion of low-complexity repeats: is strand slippage stimulated by transient local depletion of specific dNTPs? (Q37149212) (← links)
- Human mitochondrial DNA replication machinery and disease (Q37322422) (← links)
- Syndromes associated with mitochondrial DNA depletion. (Q37701180) (← links)
- Infantile-onset disorders of mitochondrial replication and protein synthesis (Q37875602) (← links)
- MELAS syndrome and cardiomyopathy: linking mitochondrial function to heart failure pathogenesis (Q38681881) (← links)
- Mitochondrial Neurogastrointestinal Encephalomyopathy Caused by Thymidine Phosphorylase Enzyme Deficiency: From Pathogenesis to Emerging Therapeutic Options (Q38750535) (← links)
- Role of the mitochondrial DNA replication machinery in mitochondrial DNA mutagenesis, aging and age-related diseases (Q38824997) (← links)
- Human mitochondrial pyrophosphatase: cDNA cloning and analysis of the gene in patients with mtDNA depletion syndromes. (Q40348949) (← links)
- The common A467T mutation in the human mitochondrial DNA polymerase (POLG) compromises catalytic efficiency and interaction with the accessory subunit. (Q40396587) (← links)
- Thymidine phosphorylase deficiency causes MNGIE: an autosomal recessive mitochondrial disorder. (Q40464447) (← links)
- Increased mitochondrial respiratory chain enzyme activities correlate with minor extent of liver damage in mice suffering from erythropoietic protoporphyria. (Q40468676) (← links)
- Kinetic properties of mutant human thymidine kinase 2 suggest a mechanism for mitochondrial DNA depletion myopathy (Q44257239) (← links)
- Huntington's disease and mitochondrial DNA deletions: event or regular mechanism for mutant huntingtin protein and CAG repeats expansion?! (Q45306758) (← links)
- A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement Disorder. (Q48502216) (← links)
- Inter-individual variation in adaptations to endurance and resistance exercise training: genetic approaches towards understanding a complex phenotype. (Q52391007) (← links)
- Proteomic analysis of cancer-cell mitochondria (Q54687587) (← links)
- The use of lymphocytes to screen for oxidative phosphorylation disorders (Q57086168) (← links)
- Energetic depression caused by mitochondrial dysfunction (Q76377719) (← links)
- Nucleoside supplementation modulates mitochondrial DNA copy number in the dguok -/- zebrafish (Q93072760) (← links)