Processes of de novo duplication of human alpha-globin genes.
about
Mechanisms of change in gene copy numberMechanisms underlying structural variant formation in genomic disordersCNVs: harbingers of a rare variant revolution in psychiatric geneticsGeneration of tandem direct duplications by reversed-ends transposition of maize ac elementsCharacterizing complex structural variation in germline and somatic genomesDynamics and processes of copy number instability in human gamma-globin genes.Copy number variation in human health, disease, and evolution.Identification of copy number variation hotspots in human populations.High spontaneous rate of gene duplication in Caenorhabditis elegansGenome destabilization by homologous recombination in the germ lineEvolution of new functions de novo and from preexisting genes.CNVs into the wild: screening the genomes of conifer trees (Picea spp.) reveals fewer gene copy number variations in hybrids and links to adaptation.Replicative mechanisms of CNV formation preferentially occur as intrachromosomal events: evidence from Potocki-Lupski duplication syndrome.Mechanisms for human genomic rearrangementsAllelic recombination between distinct genomic locations generates copy number diversity in human beta-defensins.Tandem duplication PCR: an ultrasensitive assay for the detection of internal tandem duplications of the FLT3 gene.Rapid repetitive element-mediated expansion of piRNA clusters in mammalian evolution.Genomic disorders ten years on.Mutations in the paralogous human alpha-globin genes yielding identical hemoglobin variantsNew genes originated via multiple recombinational pathways in the beta-globin gene family of rodentsCopy-number changes in evolution: rates, fitness effects and adaptive significance.Different molecular mechanisms causing 9p21 deletions in acute lymphoblastic leukemia of childhood.Evidence of differential selection for the -α(3.7) and -α(4.2) single-α-globin gene deletions within the same population.The -(α)(5.2) Deletion Detected in a Uruguayan Family: First Case Report in the Americas.Evidence of Selection for the α-Globin Gene Deletions and Triplications in a Southern Chinese Population.The molecular basis of α-thalassemia.Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder.Analysis of crossover breakpoints yields new insights into the nature of the gene conversion events associated with large NF1 deletions mediated by nonallelic homologous recombination.Selection and mutation for α Thalassemia in nonmalarial and malarial environments.
P2860
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P2860
Processes of de novo duplication of human alpha-globin genes.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Processes of de novo duplication of human alpha-globin genes.
@ast
Processes of de novo duplication of human alpha-globin genes.
@en
type
label
Processes of de novo duplication of human alpha-globin genes.
@ast
Processes of de novo duplication of human alpha-globin genes.
@en
prefLabel
Processes of de novo duplication of human alpha-globin genes.
@ast
Processes of de novo duplication of human alpha-globin genes.
@en
P2860
P356
P1476
Processes of de novo duplication of human alpha-globin genes
@en
P2093
Alec J Jeffreys
P2860
P304
10950-10955
P356
10.1073/PNAS.0703856104
P407
P577
2007-06-15T00:00:00Z