Is mammalian chromosomal evolution driven by regions of genome fragility? - Wikidata - awgldk - TriplyDB

Is mammalian chromosomal evolution driven by regions of genome fragility?

Is mammalian chromosomal evolution driven by regions of genome fragility?

http://www.wikidata.org/entity/Q35629768

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The genome diversity and karyotype evolution of mammals Breaking Good: Accounting for Fragility of Genomic Regions in Rearrangement Distance Estimation.Chromosome fragile sites in Arabidopsis harbor matrix attachment regions that may be associated with ancestral chromosome rearrangement events Comprehensive characterization of evolutionary conserved breakpoints in four New World Monkey karyotypes compared to Chlorocebus aethiops and Homo sapiens SNP microarray analyses reveal copy number alterations and progressive genome reorganization during tumor development in SVT/t driven mice breast cancer Molecular cytogenetic and genomic insights into chromosomal evolution Assessing the role of tandem repeats in shaping the genomic architecture of great apes Gene synteny comparisons between different vertebrates provide new insights into breakage and fusion events during mammalian karyotype evolution Chromosomal instability in Afrotheria: fragile sites, evolutionary breakpoints and phylogenetic inference from genome sequence assemblies Hemiplasy and homoplasy in the karyotypic phylogenies of mammals Reduced FHIT expression is associated with mismatch repair deficient and high CpG island methylator phenotype colorectal cancer.Are there rearrangement hotspots in the human genome?Distinct retroelement classes define evolutionary breakpoints demarcating sites of evolutionary novelty The where and wherefore of evolutionary breakpoints.Long-range regulation is a major driving force in maintaining genome integrity Variability in the incidence of miRNAs and genes in fragile sites and the role of repeats and CpG islands in the distribution of genetic material.Unraveling the effect of genomic structural changes in the rhesus macaque - implications for the adaptive role of inversions.Fragile regions and not functional constraints predominate in shaping gene organization in the genus Drosophila.An update of the goat genome assembly using dense radiation hybrid maps allows detailed analysis of evolutionary rearrangements in Bovidae.Association between simple sequence repeat-rich chromosome regions and intergenomic translocation breakpoints in natural populations of allopolyploid wild wheats Females and males contribute in opposite ways to the evolution of gene order in Drosophila.Late replication domains are evolutionary conserved in the Drosophila genome.Sequencing and characterisation of rearrangements in three S. pastorianus strains reveals the presence of chimeric genes and gives evidence of breakpoint reuse FRA2A is a CGG repeat expansion associated with silencing of AFF3 Genome-wide association study (GWAS) for growth rate and age at sexual maturation in Atlantic salmon (Salmo salar)A genome-wide analysis of common fragile sites: what features determine chromosomal instability in the human genome?Comparative analysis of chicken chromosome 28 provides new clues to the evolutionary fragility of gene-rich vertebrate regions.Chromosomal Speciation in the Genomics Era: Disentangling Phylogenetic Evolution of Rock-wallabies.Genomic instability within centromeres of interspecific marsupial hybrids.Genome-wide mapping and characterization of hypomethylated sites in human tissues and breast cancer cell lines.Recombination rates and genomic shuffling in human and chimpanzee--a new twist in the chromosomal speciation theory.Molecular parameters of genome instability: roles of fragile genes at common fragile sites.Breakpoint regions and homologous synteny blocks in chromosomes have different evolutionary histories The biological effects of simple tandem repeats: lessons from the repeat expansion diseases.Uncovering the functional constraints underlying the genomic organization of the odorant-binding protein genes.First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae)WWOX gene and gene product: tumor suppression through specific protein interactions.Making a long story short: noncoding RNAs and chromosome change.Non-Sciuromorph rodent karyotypes in evolution.Chromosomal polymorphism in mammals: an evolutionary perspective.

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P2860

Is mammalian chromosomal evolution driven by regions of genome fragility?

http://www.wikidata.org/entity/Q35629768

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2006 nî lūn-bûn

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2006年论文

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Is mammalian chromosomal evolution driven by regions of genome fragility?

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Is mammalian chromosomal evolution driven by regions of genome fragility?

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Is mammalian chromosomal evolution driven by regions of genome fragility?

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Is mammalian chromosomal evolution driven by regions of genome fragility?

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Is mammalian chromosomal evolution driven by regions of genome fragility?

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Is mammalian chromosomal evolution driven by regions of genome fragility?

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Aurora Ruiz-Herrera

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Jose Castresana

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Terence J Robinson

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P2860

Molecular basis for expression of common and rare fragile sites

Hotspots of mammalian chromosomal evolution

Refinement of a chimpanzee pericentric inversion breakpoint to a segmental duplication cluster

The fragile breakage versus random breakage models of chromosome evolution

Tandem repeats finder: a program to analyze DNA sequences

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

The molecular basis of common and rare fragile sites

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

Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat

Evolutionary mechanisms shaping the genomic structure of the Williams-Beuren syndrome chromosomal region at human 7q11.23

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gb-2006-7-12-r115

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10.1186/GB-2006-7-12-R115

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