Ing-nucleotide composition on single nucleotide polymorphisms (SNPs) in the mouse genome
Ing-nucleotide composition on single nucleotide polymorphisms (SNPs) in the mouse genome and its comparison with human SNPs. Genomics 2004, 84:785?95. Giulivi C, Boveris A, Cadenas E: Hydroxyl radical generation during mitochondrial electron transfer and the formation of 8hydroxydesoxyguanosine in mitochondrial DNA. Arch Biochem Biophys 1995, 316:909?16. Loft S, Poulsen HE: Markers of oxidative damage to DNA: antioxidants and molecular damage. Methods Enzymol 1999, 300:166?84. Wong TS, Rajagopalan S, Townsley FM, Freund SM, Petrovich M, Loakes D, Fersht AR: Physical and functional interactions between human mitochondrial single-stranded DNA-binding protein and tumour suppressor p53. Nucleic Acids Res 2009, 37:568?81. Le Page F, Guy A, Cadet J, Sarasin A, Gentil A: Repair and mutagenic potency of 8-oxoG:A and 8-oxoG:C base pairs in mammalian cells. Nucleic Acids Res 1998, 26:1276?281. Shibutani S, Takeshita M, Grollman AP: Insertion of specific bases during DNA synthesis past the oxidation-damaged base 8-oxodG. Nature 1991, 349:431?34. Wood ML, Dizdaroglu M, Gajewski E, Essigmann JM: Mechanistic studies of ionizing radiation and oxidative mutagenesis: genetic effects of a single 8-hydroxyguanine (7-hydro-8-oxoguanine) residue inserted at a unique site in a viral genome. Biochemistry 1990, 29:7024?032. Pinz KG, Shibutani S, Bogenhagen DF: Necrostatin-1 site Action of mitochondrial DNA polymerase gamma at sites of base loss or oxidative damage. J Biol Chem 1995, 270:9202?206. Marcelino LA, Thilly WG: Mitochondrial mutagenesis in human cells and tissues. PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/25681438 Mutat Res 1999, 434:177?03. Marcelino LA, Andre PC, Khrapko K, Coller HA, Griffith J, Thilly WG: Chemically induced mutations in mitochondrial DNA of human cells: mutational spectrum of N-methyl-N’-nitro-N-nitrosoguanidine. Cancer Res 1998, 58:2857?862. Holt IJ, Harding AE, Cooper JM, Schapira AH, Toscano A, Clark JB, MorganHughes JA: Mitochondrial myopathies: clinical and biochemical featuresNapoli et al. Molecular Autism 2013, 4:2 http://www.molecularautism.com/content/4/1/Page 8 of48.49.50.51.52.53.54.55.56.57.58.59.60.61.62.63.64.65.66.of 30 patients with major deletions of muscle mitochondrial DNA. Ann Neurol 1989, 26:699?08. Cortopassi GA, Shibata D, Soong NW, Arnheim N: A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues. Proc Natl Acad Sci USA 1992, 89:7370?374. Shelton JF, Hertz-Picciotto I, Pessah IN: Tipping the balance of autism risk: potential mechanisms linking pesticides and autism. Environ Health Perspect 2012, 120:944?51. Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, et al: Functional impact of global rare copy number variation in autism spectrum disorders. Nature 2010, 466:368?72. Shanks N, Windle RJ, Perks PA, Harbuz MS, Jessop DS, Ingram CD, Lightman SL: Early-life exposure to endotoxin alters hypothalamic-pituitary-adrenal function and predisposition to inflammation. Proc Natl Acad Sci USA 2000, 97:5645?650. Boisse L, Mouihate A, Ellis S, Pittman QJ: Long-term alterations in neuroimmune responses after neonatal exposure to lipopolysaccharide. J Neurosci 2004, 24:4928?934. Ellis S, Mouihate A, Pittman QJ: Early life immune challenge alters innate immune responses to lipopolysaccharide: implications for host defense as adults. FASEB J 2005, 19:1519?521. Spencer SJ, Heida JG, Pittman QJ: Early life immune challenge ffects on behavioural indices of adult rat fear and anxiety. Behav Brain Res.
