Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations - Wikidata - wikimedia - TriplyDB

Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations

Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations

http://www.wikidata.org/entity/Q33608638

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New approaches to the analysis of palindromic sequences from the human genome: evolution and polymorphism of an intronic site at the NF1 locus Palindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal Rearrangements Chromosomal translocations and palindromic AT-rich repeats ATP-dependent RecG helicase is required for the transcriptional regulator OxyR function in Pseudomonas species A palindrome-driven complex rearrangement of 22q11.2 and 8q24.1 elucidated using novel technologies A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer.Age has no effect on de novo constitutional t(11;22) translocation frequency in sperm.Palindrome-mediated chromosomal translocations in humans.Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm.Protein switches identified from diverse insertion libraries created using S1 nuclease digestion of supercoiled-form plasmid DNA Cruciform structures are a common DNA feature important for regulating biological processes.Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndrome.Paternal origin of the de novo constitutional t(11;22)(q23;q11).Self-catalyzed site-specific depurination of guanine residues within gene sequences A perfect palindrome in the Escherichia coli chromosome forms DNA hairpins on both leading- and lagging-strands.Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22)Prophage-mediated dynamics of 'Candidatus Liberibacter asiaticus' populations, the destructive bacterial pathogens of citrus huanglongbing.The consensus sequence for self-catalyzed site-specific G residue depurination in DNA.DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation.Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats.Complexity of a small non-protein coding sequence in chromosomal region 22q11.2: presence of specialized DNA secondary structures and RNA exon/intron motifs.The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements.DNA palindromes with a modest arm length of greater, similar 20 base pairs are a significant target for recombinant adeno-associated virus vector integration in the liver, muscles, and heart in mice.Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?Molecular analysis of a deletion hotspot in the NRXN1 region reveals the involvement of short inverted repeats in deletion CNVs.Very small mobile repeated elements in cyanobacterial genomes.De novo-generated small palindromes are characteristic of amplicon boundary junction of double minutes.The apolipoprotein CIII enhancer regulates both extensive histone modification and intergenic transcription of human apolipoprotein AI/CIII/AIV genes but not apolipoprotein AV.Methods to determine DNA structural alterations and genetic instability.Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells.ATM and ATR protect the genome against two different types of tandem repeat instability in Fragile X premutation mice.SIRT1 gene expression upon genotoxic damage is regulated by APE1 through nCaRE-promoter elements.How does DNA break during chromosomal translocations?Mechanisms of oncogenic chromosomal translocations.Impact of alternative DNA structures on DNA damage, DNA repair, and genetic instability Non-B DNA Secondary Structures and Their Resolution by RecQ Helicases.Self-catalyzed site-specific depurination of G residues mediated by cruciform extrusion in closed circular DNA plasmids.A novel mode of nuclease action is revealed by the bacterial Mre11/Rad50 complex.Recognition of Local DNA Structures by p53 Protein.Effects of Replication and Transcription on DNA Structure-Related Genetic Instability

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Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations

http://www.wikidata.org/entity/Q33608638

description

2004 nî lūn-bûn

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2004 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2004 թվականի հունիսին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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name

Cruciform DNA structure underl ...... man chromosomal translocations

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Cruciform DNA structure underl ...... man chromosomal translocations

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type

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Cruciform DNA structure underl ...... man chromosomal translocations

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Cruciform DNA structure underl ...... man chromosomal translocations

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Cruciform DNA structure underl ...... man chromosomal translocations

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Cruciform DNA structure underl ...... man chromosomal translocations

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Journal of Biological Chemistry

P1476

Cruciform DNA structure underl ...... man chromosomal translocations

@en

P2093

Beverly S Emanuel

http://www.w3.org/2001/XMLSchema#string

Hidehito Inagaki

http://www.w3.org/2001/XMLSchema#string

Hiroki Kurahashi

http://www.w3.org/2001/XMLSchema#string

Kouji Yamada

http://www.w3.org/2001/XMLSchema#string

Mariko Taniguchi

http://www.w3.org/2001/XMLSchema#string

Tamae Ohye

http://www.w3.org/2001/XMLSchema#string

Tatsushi Toda

http://www.w3.org/2001/XMLSchema#string

P2860

The DNA sequence of human chromosome 22

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers.

A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2.

The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeats.

Generation of superhelical torsion by ATP-dependent chromatin remodeling activities.

AT-rich palindromes mediate the constitutional t(11;22) translocation.

Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).

Segmental duplications: an 'expanding' role in genomic instability and disease.

Cruciform-extruding regulatory element controls cell-specific activity of the tyrosine hydroxylase gene promoter

P304

35377-35383

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scholarly article

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10.1074/JBC.M400354200

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P433

34

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279

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15208332

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2810964

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