Is mammalian chromosomal evolution driven by regions of genome fragility?
暂无分享,去创建一个
Jose Castresana | J. Castresana | T. Robinson | A. Ruiz-Herrera | Aurora Ruiz-Herrera | Terence J Robinson | Jose Castresana | Aurora Ruiz-Herrera | Terence J Robinson | Terence J Robinson
[1] T. J. Robinson,et al. Dissecting the mammalian genome--new insights into chromosomal evolution. , 2006, Trends in genetics : TIG.
[2] M. Z. Limongi,et al. Characterization of the human common fragile site FRA2G. , 2003, Genomics.
[3] J. Egozcue,et al. High‐resolution chromosome banding studies in Cebus apella, Cebus albifrons, and Lagothrix lagothricha: Comparison with the human karyotype , 1987, American journal of primatology.
[4] T. Shaikh,et al. Alu-mediated PCR artifacts and the constitutional t(11;22) breakpoint. , 2000, Human Molecular Genetics.
[5] T. Boby,et al. TRbase: a database relating tandem repeats to disease genes for the human genome , 2005, Bioinform..
[6] D. Beer,et al. The murine Fhit gene is highly similar to its human orthologue and maps to a common fragile site region. , 1998, Cancer research.
[7] M. Cáceres,et al. Generation of a widespread Drosophila inversion by a transposable element. , 1999, Science.
[8] S. Müller,et al. The evolutionary history of human chromosome , 2004 .
[9] A. Ruiz-Herrera,et al. Evolutionary breakpoints are co-localized with fragile sites and intrachromosomal telomeric sequences in primates , 2004, Cytogenetic and Genome Research.
[10] L. Pérez-Jurado,et al. Evolutionary mechanisms shaping the genomic structure of the Williams-Beuren syndrome chromosomal region at human 7q11.23. , 2005, Genome research.
[11] P. Pevzner,et al. Human and mouse genomic sequences reveal extensive breakpoint reuse in mammalian evolution , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[12] J. Egozcue,et al. Chromosome evolution in the cercopithecidae and its relationship to human fragile sites and neoplasia , 1990, International Journal of Primatology.
[13] B. Emanuel,et al. Genetic Variation Affects de Novo Translocation Frequency , 2006, Science.
[14] Fengtang Yang,et al. Genomic structure and paralogous regions of the inversion breakpoint occurring between human chromosome 3p12.3 and orangutan chromosome 2 , 2004, Cytogenetic and Genome Research.
[15] L. Shaffer,et al. Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE , 1994, Nature Genetics.
[16] T. Haaf,et al. Segmental duplication associated with evolutionary instability of human chromosome 3p25.1 , 2006, Cytogenetic and Genome Research.
[17] R I Richards,et al. FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis. , 1998, Molecular cell.
[18] P. Pevzner,et al. Dynamics of Mammalian Chromosome Evolution Inferred from Multispecies Comparative Maps , 2005, Science.
[19] G. Benson,et al. Tandem repeats finder: a program to analyze DNA sequences. , 1999, Nucleic acids research.
[20] A. Ruiz-Herrera,et al. Fragile Sites in Human and Macaca Fascicularis Chromosomes are Breakpoints in Chromosome Evolution , 2004, Chromosome Research.
[21] G. Sutherland. Heritable fragile sites on human chromosomes , 2004, Human Genetics.
[22] H. Hameister,et al. Breakpoint analysis of the pericentric inversion between chimpanzee chromosome 10 and the homologous chromosome 12 in humans , 2004, Cytogenetic and Genome Research.
[23] T. Glover,et al. FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites. , 1996, Human molecular genetics.
[24] K. Davies,et al. Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation , 1993, Cell.
[25] F. Apiou,et al. Characterization of a conserved aphidicolin-sensitive common fragile site at human 4q22 and mouse 6C1: possible association with an inherited disease and cancer , 2004, Oncogene.
[26] U. Francke,et al. A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK. , 1998, Human molecular genetics.
[27] D. Paslier,et al. Human Chromosomal Fragile Site FRA16B Is an Amplified AT-Rich Minisatellite Repeat , 1997, Cell.
[28] M. Rønne. Putative fragile sites in the horse karyotype. , 2008, Hereditas.
[29] P. Stankiewicz,et al. Serial segmental duplications during primate evolution result in complex human genome architecture. , 2004, Genome research.
[30] T. Glover,et al. ATR Regulates Fragile Site Stability , 2002, Cell.
[31] Sutherland Gr. Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture. , 1979 .
[32] J. Wienberg,et al. The evolutionary history of human chromosome 7. , 2004, Genomics.
[33] David I. Smith,et al. Characterization of FRA6E and its potential role in autosomal recessive juvenile parkinsonism and ovarian cancer , 2003, Genes, chromosomes & cancer.
[34] S. Scherer,et al. Murine segmental duplications are hot spots for chromosome and gene evolution. , 2005, Genomics.
[35] A. Ruiz-Herrera,et al. Conservation of aphidicolin-induced fragile sites in Papionini (Primates) species and humans , 2004, Chromosome Research.
[36] K. Sato,et al. Novel putative fragile sites observed in feline fibroblasts treated with aphidicolin and fluorodeoxyuridine. , 1998, The Journal of veterinary medical science.
[37] B. Roe,et al. Refinement of a chimpanzee pericentric inversion breakpoint to a segmental duplication cluster , 2003, Genome Biology.
[38] M. Schwab,et al. The neurobeachin gene spans the common fragile site FRA13A , 2005, Human Genetics.
[39] J. Gécz,et al. Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein. , 2004, Genomics.
[40] M. Schwab,et al. FRA1E common fragile site breaks map within a 370kilobase pair region and disrupt the dihydropyrimidine dehydrogenase gene (DPYD). , 2007, Cancer letters.
[41] C. Fuster,et al. Fragile sites, chromosome evolution, and human neoplasia , 1987, Human Genetics.
[42] T. Robinson,et al. Multiple common fragile sites are expressed in the genome of the laboratory rat , 2004, Chromosoma.
[43] M. Adams,et al. Recent Segmental Duplications in the Human Genome , 2002, Science.
[44] David I. Smith,et al. Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors , 2002, Oncogene.
[45] W. Chung,et al. Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints. , 2000, Genome research.
[46] L. Froenicke,et al. Origins of primate chromosomes – as delineated by Zoo-FISH and alignments of human and mouse draft genome sequences , 2004, Cytogenetic and Genome Research.
[47] D. Le Paslier,et al. Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis. , 1994, Science.
[48] S. Scherer,et al. Molecular Basis for Expression of Common and Rare Fragile Sites , 2003, Molecular and Cellular Biology.
[49] D. Smeets,et al. Common fragile sites in man and three closely related primate species. , 1990, Cytogenetics and cell genetics.
[50] Pavel A Pevzner,et al. The Fragile Breakage versus Random Breakage Models of Chromosome Evolution , 2006, PLoS Comput. Biol..
[51] R. Richards,et al. Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3. , 1994, Human molecular genetics.
[52] D. Haussler,et al. Hotspots of mammalian chromosomal evolution , 2004, Genome Biology.
[53] Fengtang Yang,et al. Comparative cytogenetics of human chromosome 3q21.3 reveals a hot spot for ectopic recombination in hominoid evolution. , 2005, Genomics.
[54] Niclas Jareborg,et al. Genome-wide prediction of human VNTRs. , 2005, Genomics.
[55] D. Beer,et al. Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells , 2002, Genes, chromosomes & cancer.
[56] S. Scherer,et al. Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[57] B. Kerem,et al. The molecular basis of common and rare fragile sites. , 2006, Cancer letters.
[58] M. Mar Albà,et al. Clustering of Genes Coding for DNA Binding Proteins in a Regionof Atypical Evolution of the Human Genome , 2004, Journal of Molecular Evolution.
[59] A. Ruiz-Herrera,et al. Evolutionary conserved chromosomal segments in the human karyotype are bounded by unstable chromosome bands , 2004, Cytogenetic and Genome Research.
[60] Matthias Platzer,et al. Molecular characterization of the pericentric inversion that causes differences between chimpanzee chromosome 19 and human chromosome 17. , 2002, American journal of human genetics.
[61] J. Castresana. Genes on human chromosome 19 show extreme divergence from the mouse orthologs and a high GC content. , 2002, Nucleic acids research.
[62] David I. Smith,et al. Characterization of the common fragile site FRA9E and its potential role in ovarian cancer , 2003, Oncogene.
[63] David I. Smith,et al. A role for common fragile site induction in amplification of human oncogenes. , 2002, Cancer cell.
[64] R. Richards,et al. Fragile sites-cytogenetic similarity with molecular diversity. , 1999, American journal of human genetics.
[65] L. Roberts,et al. The characterization of the common fragile site FRA16D and its involvement in multiple myeloma translocations. , 2000, Genomics.
[66] R. Sudbrak,et al. Plasticity of human chromosome 3 during primate evolution. , 2004, Genomics.
[67] E. Green,et al. Isolation and analysis of candidate myeloid tumor suppressor genes from a commonly deleted segment of 7q22. , 2005, Genomics.
[68] G. Sutherland. Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture. , 1979, American journal of human genetics.
[69] B. Trask,et al. Genomic structure and evolution of the ancestral chromosome fusion site in 2q13-2q14.1 and paralogous regions on other human chromosomes. , 2002, Genome research.
[70] A. Delcher,et al. Human, mouse, and rat genome large-scale rearrangements: stability versus speciation. , 2004, Genome research.
[71] Matthias Platzer,et al. Breakpoint analysis of the pericentric inversion distinguishing human chromosome 4 from the homologous chromosome in the chimpanzee (Pan troglodytes) , 2005, Human mutation.
[72] J. Nadeau,et al. Lengths of chromosomal segments conserved since divergence of man and mouse. , 1984, Proceedings of the National Academy of Sciences of the United States of America.
[73] G. Rincón,et al. Localisation of aphidicolin-induced break points in Holstein-Friesian cattle (Bos taurus) using RBG-banding , 2002, Genetics Selection Evolution.
[74] D. Stone,et al. Bromodeoxyuridine induces chromosomal fragile sites in the canine genome. , 1993, American journal of medical genetics.
[75] E. Eichler,et al. Structural Dynamics of Eukaryotic Chromosome Evolution , 2003, Science.
[76] R I Richards,et al. Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n , 1991, Science.