One short well conserved region of Alu-sequences is involved in human gene rearrangements and has homology with prokaryotic chi.
about
Accelerated evolution of the ASPM gene controlling brain size begins prior to human brain expansionMolecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndromeA spectrum of ABCC6 mutations is responsible for pseudoxanthoma elasticumComparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome geneCharacterisation of a novel minisatellite that provides multiple splice donor sites in an interferon-induced transcriptX-linked hyper IgM (HIGM1) in an African kindred: the first report from South AfricaTissue distribution of a plasmid DNA encoding Hsp65 gene is dependent on the dose administered through intramuscular delivery.Uncommon deletions of the Smith-Magenis syndrome region can be recurrent when alternate low-copy repeats act as homologous recombination substratesTransposable elements and the dynamic somatic genomeAlu-mediated 100-kb deletion in the primate genome: the loss of the agouti signaling protein gene in the lesser apesAlu-associated interstitial deletions and chromosomal re-arrangement in 2 human multidrug-resistant cell lines.Genomic characterization of five deletions in the LDL receptor gene in Danish Familial Hypercholesterolemic subjects.Alu recombination-mediated structural deletions in the chimpanzee genome.Molecular emergence of acute myeloid leukemia during treatment for acute lymphoblastic leukemiaCharacterization of the human and mouse genes for the alpha subunit of type II prolyl 4-hydroxylase. Identification of a previously unknown alternatively spliced exon and its expression in various tissues.Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination.Cloning, sequencing, and analysis of inv8 chromosome breakpoints associated with recombinant 8 syndromeQuantitative analysis of survival motor neuron copies: identification of subtle SMN1 mutations in patients with spinal muscular atrophy, genotype-phenotype correlation, and implications for genetic counselingHuman Rad51 protein displays enhanced homologous pairing of DNA sequences resembling those at genetically unstable lociHuman genomic deletions mediated by recombination between Alu elements.Delineation of large deletions of the MECP2 gene in Rett syndrome patients, including a familial case with a male proband.The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors.Alu elements in ANRIL non-coding RNA at chromosome 9p21 modulate atherogenic cell functions through trans-regulation of gene networks.Double-strand break repair by interchromosomal recombination: an in vivo repair mechanism utilized by multiple somatic tissues in mammals.Tandem repeats and G-rich sequences are enriched at human CNV breakpointsOrigins of chromosome translocations in childhood leukaemia.On the sequence-directed nature of human gene mutation: the role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease.The contribution of alu elements to mutagenic DNA double-strand break repair.Inviting instability: Transposable elements, double-strand breaks, and the maintenance of genome integrity.Molecular characterization of the pericentric inversion that causes differences between chimpanzee chromosome 19 and human chromosome 17Molecular cloning of a rat chromosome putative recombinogenic sequence homologous to the hepatitis B virus encapsidation signal.Large duplications at reciprocal translocation breakpoints that might be the counterpart of large deletions and could arise from stalled replication bubbles.Progress in the molecular biology of ewing tumors.Involvement of hepatitis B virus X gene (HBx) integration in hepatocarcinogenesis via a recombination of HBx/Alu core sequence/subtelomeric DNA.High Frequency of Pathogenic Rearrangements in SPG11 and Extensive Contribution of Mutational Hotspots and Founder Alleles.Gene targeting with a replication-defective adenovirus vector.A recurrent large Alu-mediated deletion in the hypoxanthine phosphoribosyltransferase (HPRT1) gene associated with Lesch-Nyhan syndrome.Molecular characterization of a myelodysplasia-associated chromosome 7 inversion.Maple syrup urine disease in the Austronesian aboriginal tribe Paiwan of Taiwan: a novel DBT (E2) gene 4.7 kb founder deletion caused by a nonhomologous recombination between LINE-1 and Alu and the carrier-frequency determination.The efficacy, biodistribution and safety of an inhibin DNA vaccine delivered by attenuated Salmonella choleraesuis.
P2860
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P2860
One short well conserved region of Alu-sequences is involved in human gene rearrangements and has homology with prokaryotic chi.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
1995年學術文章
@zh
1995年學術文章
@zh-hant
name
One short well conserved regio ...... homology with prokaryotic chi.
@en
type
label
One short well conserved regio ...... homology with prokaryotic chi.
@en
prefLabel
One short well conserved regio ...... homology with prokaryotic chi.
@en
P2093
P2860
P356
P1476
One short well conserved regio ...... homology with prokaryotic chi.
@en
P2093
Gregersen N
Kielland-Brandt MC
Rüdiger NS
P2860
P304
P356
10.1093/NAR/23.2.256
P577
1995-01-01T00:00:00Z