MIP1/YOR330C Literature Guide Help

Other names published for MIP1: mitochondrial DNA polymerase catalytic subunit, YOR330C

MIP1 - Disease Gene Related (11)

ReferenceOther Genes Addressed
Baruffini E, et al.  (2011) Predicting the contribution of novel POLG mutations to human disease through analysis in yeast model. Mitochondrion 11(1):182-90
Euro L, et al.  (2011) Clustering of Alpers disease mutations and catalytic defects in biochemical variants reveal new features of molecular mechanism of the human mitochondrial replicase, Pol ?. Nucleic Acids Res 39(21):9072-84
Rinaldi T, et al.  (2010) Mitochondrial diseases and the role of the yeast models. FEMS Yeast Res 10(8):1006-22
Stewart JD, et al.  (2010) Polymerase ? gene POLG determines the risk of sodium valproate-induced liver toxicity. Hepatology 52(5):1791-6
Stumpf JD, et al.  (2010) mip1 Containing mutations associated with mitochondrial disease causes mutagenesis and depletion of mtDNA in Saccharomyces cerevisiae. Hum Mol Genet 19(11):2123-33
Szczepanowska K and Foury F  (2010) A cluster of pathogenic mutations in the 3'-5' exonuclease domain of DNA polymerase gamma defines a novel module coupling DNA synthesis and degradation. Hum Mol Genet 19(18):3516-29
Fontanesi F, et al.  (2009) Evaluation of the mitochondrial respiratory chain and oxidative phosphorylation system using yeast models of OXPHOS deficiencies. Curr Protoc Hum Genet Chapter 19:Unit19.5
Baruffini E, et al.  (2007) Mitochondrial DNA defects in Saccharomyces cerevisiae caused by functional interactions between DNA polymerase gamma mutations associated with disease in human. Biochim Biophys Acta 1772(11-12):1225-35
Baruffini E, et al.  (2006) Genetic and chemical rescue of the Saccharomyces cerevisiae phenotype induced by mitochondrial DNA polymerase mutations associated with progressive external ophthalmoplegia in humans. Hum Mol Genet 15(19):2846-55
Stuart GR, et al.  (2006) Mitochondrial and nuclear DNA defects in Saccharomyces cerevisiae with mutations in DNA polymerase gamma associated with progressive external ophthalmoplegia. Hum Mol Genet 15(2):363-74
Steinmetz LM, et al.  (2002) Systematic screen for human disease genes in yeast. Nat Genet 31(4):400-4