Analysis of phylogenetically reconstructed mutational spectra in human mitochondrial DNA control region
暂无分享,去创建一个
[1] S. Benzer,et al. ON THE TOPOGRAPHY OF THE GENETIC FINE STRUCTURE. , 1961, Proceedings of the National Academy of Sciences of the United States of America.
[2] Philip J. Farabaugh,et al. Molecular basis of base substitution hotspots in Escherichia coli , 1978, Nature.
[3] H. Cann,et al. Maternal inheritance of human mitochondrial DNA. , 1980, Proceedings of the National Academy of Sciences of the United States of America.
[4] W. Brown. Polymorphism in mitochondrial DNA of humans as revealed by restriction endonuclease analysis. , 1980, Proceedings of the National Academy of Sciences of the United States of America.
[5] L. Gold,et al. rII cistrons of bacteriophage T4. DNA sequence around the intercistronic divide and positions of genetic landmarks. , 1981, Journal of molecular biology.
[6] F. Sanger,et al. Sequence and organization of the human mitochondrial genome , 1981, Nature.
[7] T. Kunkel,et al. The mutational specificity of DNA polymerase-beta during in vitro DNA synthesis. Production of frameshift, base substitution, and deletion mutations. , 1985, The Journal of biological chemistry.
[8] T. Kunkel,et al. Mutagenesis by transient misalignment. , 1988, The Journal of biological chemistry.
[9] B. Ames,et al. Normal oxidative damage to mitochondrial and nuclear DNA is extensive. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[10] James E. Hixson,et al. Comparisons of ape and human sequences that regulate mitochondrial DNA transcription and D-loop DNA synthesis , 1988, Nucleic Acids Res..
[11] B W Glickman,et al. Mutational specificity of alkylating agents and the influence of DNA repair , 1990, Environmental and molecular mutagenesis.
[12] K. Hawkes,et al. African populations and the evolution of human mitochondrial DNA. , 1991, Science.
[13] N A Kolchanov,et al. Somatic hypermutagenesis in immunoglobulin genes. II. Influence of neighbouring base sequences on mutagenesis. , 1992, Biochimica et biophysica acta.
[14] L. Loeb,et al. 8-Hydroxyguanine, an abundant form of oxidative DNA damage, causes G----T and A----C substitutions. , 1992, The Journal of biological chemistry.
[15] N F Cariello,et al. Software for the analysis of mutations at the human hprt gene. , 1994, Mutation research.
[16] B. Sykes,et al. Length heteroplasmy in the first hypervariable segment of the human mtDNA control region. , 1995, American journal of human genetics.
[17] D. Wallace,et al. 1994 William Allan Award Address. Mitochondrial DNA variation in human evolution, degenerative disease, and aging. , 1995, American journal of human genetics.
[18] A. Torroni,et al. Classification of European mtDNAs from an analysis of three European populations. , 1996, Genetics.
[19] D. Mackey,et al. How rapidly does the human mitochondrial genome evolve? , 1996, American journal of human genetics.
[20] D. Zorov,et al. Mitochondrial damage as a source of diseases and aging: a strategy of how to fight these. , 1996, Biochimica et biophysica acta.
[21] J. Poulton,et al. Do sequence variants in the major non-coding region of the mitochondrial genome influence mitochondrial mutations associated with disease? , 1996, Human molecular genetics.
[22] Luciano Milanesi,et al. The subclass approach for mutational spectrum analysis: application of the SEM algorithm. , 1998, Journal of theoretical biology.
[23] B. Sykes,et al. Phylogeography of mitochondrial DNA in western Europe , 1998, Annals of human genetics.
[24] Location and frequency of polymorphic positions in the mtDNA control region of individuals from Germany , 1998, International Journal of Legal Medicine.
[25] M Krawczak,et al. Neighboring-nucleotide effects on the rates of germ-line single-base-pair substitution in human genes. , 1998, American journal of human genetics.
[26] A. von Haeseler,et al. Pattern of nucleotide substitution and rate heterogeneity in the hypervariable regions I and II of human mtDNA. , 1999, Genetics.
[27] A. Torroni,et al. The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs. , 1999, American journal of human genetics.
[28] L. Excoffier,et al. Substitution rate variation among sites in mitochondrial hypervariable region I of humans and chimpanzees. , 1999, Molecular biology and evolution.
[29] Igor B. Rogozin,et al. Regression trees for analysis of mutational spectra in nucleotide sequences , 1999, Bioinform..
[30] A. Eyre-Walker,et al. How clonal are human mitochondria? , 1999, Proceedings of the Royal Society of London. Series B: Biological Sciences.
[31] M. Holland,et al. Mitochondrial DNA regions HVI and HVII population data. , 1999, Forensic science international.
[32] R. Sukernik,et al. Mitochondrial DNA variation in Koryaks and Itel'men: population replacement in the Okhotsk Sea-Bering Sea region during the Neolithic. , 1999, American journal of physical anthropology.
[33] Molecular instability of the mitochondrial haplogroup T sequences at nucleotide positions 16292 and 16296. , 1999, Annals of human genetics.
[34] D. Wallace,et al. Mitochondrial DNA variation in human evolution and disease. , 1999, Gene.
[35] H. Bandelt,et al. Median networks: speedy construction and greedy reduction, one simulation, and two case studies from human mtDNA. , 2000, Molecular phylogenetics and evolution.
[36] J. Gulcher,et al. mtDNA and the origin of the Icelanders: deciphering signals of recent population history. , 2000, American journal of human genetics.
[37] A. Di Rienzo,et al. Tracing European founder lineages in the Near Eastern mtDNA pool. , 2000, American journal of human genetics.
[38] M. Gurven. How can we distinguish between mutational "hot spots" and "old sites" in human mtDNA samples? , 2000, Human biology.
[39] M. Nei,et al. Molecular Evolution and Phylogenetics , 2000 .
[40] H. Bandelt,et al. The ancestry of Brazilian mtDNA lineages. , 2000, American journal of human genetics.
[41] M. Stoneking. Hypervariable sites in the mtDNA control region are mutational hotspots. , 2000, American journal of human genetics.
[42] D. Wallace,et al. mtDNA variation in the South African Kung and Khwe-and their genetic relationships to other African populations. , 2000, American journal of human genetics.
[43] On the estimation of the rate of nucleotide substitution for the control region of human mitochondrial DNA. , 2000, Gene.
[44] N. Howell,et al. Persistent heteroplasmy of a mutation in the human mtDNA control region: hypermutation as an apparent consequence of simple-repeat expansion/contraction. , 2000, American journal of human genetics.
[45] C. Broeckhoven,et al. Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions , 2001, Nature Genetics.
[46] N. Maca-Meyer,et al. Major genomic mitochondrial lineages delineate early human expansions , 2001, BMC Genetics.
[47] G. Glazko,et al. Use of mutation spectra analysis software , 2001, Human mutation.
[48] T. Kunkel,et al. The Fidelity of Human DNA Polymerase γ with and without Exonucleolytic Proofreading and the p55 Accessory Subunit* , 2001, The Journal of Biological Chemistry.
[49] D. Labuda,et al. Phylogenetic and familial estimates of mitochondrial substitution rates: study of control region mutations in deep-rooting pedigrees. , 2001, American journal of human genetics.
[50] M. Lehtonen,et al. Phylogenetic network for European mtDNA. , 2001, American journal of human genetics.
[51] T B Kepler,et al. Statistical inference of sequence-dependent mutation rates. , 2001, Current opinion in genetics & development.
[52] T. Kunkel,et al. Active Site Mutation in DNA Polymerase γ Associated with Progressive External Ophthalmoplegia Causes Error-prone DNA Synthesis* , 2002, The Journal of Biological Chemistry.
[53] Vladimir B. Berikov. An approach to the evaluation of the performance of a discrete classifier , 2002, Pattern Recognit. Lett..
[54] B. Malyarchuk,et al. Variation of Human Mitochondrial DNA: Distribution of Hot Spots in Hypervariable Segment I of the Major Noncoding Region , 2001, Russian Journal of Genetics.
[55] S. Hess,et al. The influence of nearest neighbors on the rate and pattern of spontaneous point mutations , 1992, Journal of Molecular Evolution.
[56] David N. Cooper,et al. The CpG dinucleotide and human genetic disease , 1988, Human Genetics.
[57] M. Hasegawa,et al. Toward a more accurate time scale for the human mitochondrial DNA tree , 1993, Journal of Molecular Evolution.
[58] J. Wakeley. Substitution rate variation among sites in hypervariable region 1 of human mitochondrial DNA , 1993, Journal of Molecular Evolution.