Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene.
about
Ku regulates the non-homologous end joining pathway choice of DNA double-strand break repair in human somatic cellsMucopolysaccharidosis type IVA. N-acetylgalactosamine-6-sulfate sulfatase exonic point mutations in classical Morquio and mild casesSequence variation in the Fanconi anemia gene FAAX-linked hyper IgM (HIGM1) in an African kindred: the first report from South AfricaPol32, a subunit of Saccharomyces cerevisiae DNA polymerase delta, suppresses genomic deletions and is involved in the mutagenic bypass pathway.MMEJ repair of double-strand breaks (director's cut): deleted sequences and alternative endingsA microhomology-mediated break-induced replication model for the origin of human copy number variation.Identification of a 428-kb homozygously deleted region disrupting the SEZ6L gene at 22q12.1 in a lung cancer cell line.Molecular defect in siblings with prolidase deficiency and absence or presence of clinical symptoms. A 0.8-kb deletion with breakpoints at the short, direct repeat in the PEPD gene and synthesis of abnormal messenger RNA and inactive polypeptideRole of the retinoblastoma gene in the initiation and progression of human cancerDeletions at short direct repeats and base substitutions are characteristic mutations for bleomycin-induced double- and single-strand breaks, respectively, in a human shuttle vector system.Organization of the human CD40L gene: implications for molecular defects in X chromosome-linked hyper-IgM syndrome and prenatal diagnosis.Parental somatic and germ-line mosaicism for a multiexon deletion with unusual endpoints in a type III collagen (COL3A1) allele produces Ehlers-Danlos syndrome type IV in the heterozygous offspring.Molecular and genetic analysis of a compound heterozygote for dysprothrombinemia of prothrombin Tokushima and hypoprothrombinemia.Somatic mosaicism in a patient with bilateral retinoblastoma.Deletion of RB exons 24 and 25 causes low-penetrance retinoblastomaDNA damage response factors from diverse pathways, including DNA crosslink repair, mediate alternative end joining.Identification of three novel RB1 mutations in Brazilian patients with retinoblastoma by "exon by exon" PCR mediated SSCP analysisApparent and real recombination frequencies in multicopy plasmids: the need for a novel approach in frequency determinationDirect sequencing of PCR-amplified junction fragments from tandemly repeated transgenes.Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.Mechanisms of oncogenesis in patients with familial retinoblastoma.Formation of large deletions by illegitimate recombination in the HPRT gene of primary human fibroblasts.How do retinoblastoma tumours form?DNA polymerases δ and λ cooperate in repairing double-strand breaks by microhomology-mediated end-joining in Saccharomyces cerevisiaeFine-resolution analysis of products of intrachromosomal homeologous recombination in mammalian cells.A novel, plasmid-based system for studying gene rearrangements in mammalian cellsPerspective on genes and mutations causing retinitis pigmentosa.Structural analysis of a carcinogen-induced genomic rearrangement event.The retinoblastoma gene: its role in human malignancies.Spi(-) selection: An efficient method to detect gamma-ray-induced deletions in transgenic mice.Mutator phenotype induced by aberrant replicationA mechanism for deletion formation in DNA by human cell extracts: the involvement of short sequence repeats.Partial aldolase B gene deletions in hereditary fructose intoleranceThe role of mitotic recombination in carcinogenesis.Detailed characterization of a homozygously deleted region corresponding to a candidate tumor suppressor locus at distal 17p13.3 in human lung cancer.Correlations between long inverted repeat (LIR) features, deletion size and distance from breakpoint in human gross gene deletions.Constitutively methylated CpG dinucleotides as mutation hot spots in the retinoblastoma gene (RB1).The rates and patterns of deletions in the human factor IX gene.Retinoblastoma cell lines Y79, RB355 and WERI-Rb27 are genetically related.
P2860
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P2860
Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene.
description
1989 nî lūn-bûn
@nan
1989 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene.
@ast
Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene.
@en
Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene.
@nl
type
label
Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene.
@ast
Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene.
@en
Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene.
@nl
prefLabel
Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene.
@ast
Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene.
@en
Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene.
@nl
P2860
P356
P1476
Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene.
@en
P2093
P2860
P304
P356
10.1073/PNAS.86.13.5044
P407
P577
1989-07-01T00:00:00Z