Palindrome-mediated chromosomal translocations in humans. - sprookjes - yvandenbroek - TriplyDB

Palindrome-mediated chromosomal translocations in humans.

Palindrome-mediated chromosomal translocations in humans.

http://www.wikidata.org/entity/Q33668703

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The Hypocrea jecorina (Trichoderma reesei) hypercellulolytic mutant RUT C30 lacks a 85 kb (29 gene-encoding) region of the wild-type genome The mechanism of double-strand DNA break repair by the nonhomologous DNA end-joining pathway Replication stalling at unstable inverted repeats: interplay between DNA hairpins and fork stabilizing proteins Chromosomal translocations and palindromic AT-rich repeats The hidden side of unstable DNA repeats: Mutagenesis at a distance Copy-number gains of HUWE1 due to replication- and recombination-based rearrangements Gene conversion causing human inherited disease: evidence for involvement of non-B-DNA-forming sequences and recombination-promoting motifs in DNA breakage and repair.Mechanisms of chromosomal rearrangement in the human genome Genomic basis of aromatase excess syndrome: recombination- and replication-mediated rearrangements leading to CYP19A1 overexpression GAP-Seq: a method for identification of DNA palindromes.Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm.Analysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocation.A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21).Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocations.Non-B DNA structure-induced genetic instability and evolution.Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation.Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.X-linked congenital hypertrichosis syndrome is associated with interchromosomal insertions mediated by a human-specific palindrome near SOX3 Genome-wide screen reveals replication pathway for quasi-palindrome fragility dependent on homologous recombination.DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation.Assessment of palindromes as platforms for DNA amplification in breast cancer Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats.E. coli SbcCD and RecA control chromosomal rearrangement induced by an interrupted palindrome.The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements.Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3.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.Unexpected complexity at breakpoint junctions in phenotypically normal individuals and mechanisms involved in generating balanced translocations t(1;22)(p36;q13)DNA secondary structures: stability and function of G-quadruplex structures.Translocation and deletion breakpoints in cancer genomes are associated with potential non-B DNA-forming sequences The tumor suppressor gene TRC8/RNF139 is disrupted by a constitutional balanced translocation t(8;22)(q24.13;q11.21) in a young girl with dysgerminoma.Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells.Competitive superhelical transitions involving cruciform extrusion Chromosome aberrations resulting from double-strand DNA breaks at a naturally occurring yeast fragile site composed of inverted ty elements are independent of Mre11p and Sae2p.DNA polymerases ζ and Rev1 mediate error-prone bypass of non-B DNA structures.Checkpoint responses to unusual structures formed by DNA repeats.How does DNA break during chromosomal translocations?The yin and yang of repair mechanisms in DNA structure-induced genetic instability.Mechanisms of oncogenic chromosomal translocations.Impact of alternative DNA structures on DNA damage, DNA repair, and genetic instability Effects of Replication and Transcription on DNA Structure-Related Genetic Instability

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P2860

Palindrome-mediated chromosomal translocations in humans.

http://www.wikidata.org/entity/Q33668703

description

2006 nî lūn-bûn

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2006 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2006 թվականի հուլիսին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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name

Palindrome-mediated chromosomal translocations in humans.

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Palindrome-mediated chromosomal translocations in humans.

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type

label

Palindrome-mediated chromosomal translocations in humans.

@ast

Palindrome-mediated chromosomal translocations in humans.

@en

prefLabel

Palindrome-mediated chromosomal translocations in humans.

@ast

Palindrome-mediated chromosomal translocations in humans.

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J.DNAREP.2006.05.035

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P1476

Palindrome-mediated chromosomal translocations in humans.

@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

Hiroshi Kogo

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

Takema Kato

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

Tamae Ohye

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

P2860

Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction

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

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

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.

The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats

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).

Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families

A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation.

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1136-1145

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scholarly article

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10.1016/J.DNAREP.2006.05.035

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9-10

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5

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2006-07-10T00:00:00Z

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6956604

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16829213

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2824556

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