A novel gene, Translin, encodes a recombination hotspot binding protein associated with chromosomal translocations
about
RP58 associates with condensed chromatin and mediates a sequence-specific transcriptional repressionThe kinesin KIF17b and RNA-binding protein TB-RBP transport specific cAMP-responsive element modulator-regulated mRNAs in male germ cellsDiversity of genomic breakpoints in TFG-ALK translocations in anaplastic large cell lymphomas: identification of a new TFG-ALK(XL) chimeric gene with transforming activityChromosome translocation based on illegitimate recombination in human tumorsCloning and characterization of the Schizosaccharomyces pombe homologs of the human protein Translin and the Translin-associated protein TRAXSystematic discovery of new recognition peptides mediating protein interaction networksC1D family proteins in coordinating RNA processing, chromosome condensation and DNA damage responseCrystal structures of Drosophila mutant translin and characterization of translin variants reveal the structural plasticity of translin proteinsStructure of C3PO and mechanism of human RISC activationMultimeric assembly and biochemical characterization of the Trax–translin endonuclease complexLow-resolution structure ofDrosophilatranslinStructural basis for single-stranded RNA recognition and cleavage by C3POTranslin binds to the sequences adjacent to the breakpoints of the TLS and CHOP genes in liposarcomas with translocation t(12;6)Structure of the MLT gene and molecular characterization of the genomic breakpoint junctions in the t(11;18)(q21;q21) of marginal zone B-cell lymphomas of MALT typeInteraction between hepatitis C virus core protein and translin protein--a possible molecular mechanism for hepatocellular carcinoma and lymphoma caused by hepatitis C virusTrax (translin-associated factor X), a primarily cytoplasmic protein, inhibits the binding of TB-RBP (translin) to RNAThe translin ring specifically recognizes DNA ends at recombination hot spots in the human genomeThe Translin/Trax RNA binding complex: clues to function in the nervous systemGene conversion causing human inherited disease: evidence for involvement of non-B-DNA-forming sequences and recombination-promoting motifs in DNA breakage and repair.Co-expressed recombinant human Translin-Trax complex binds DNA.Exploring the link between MORF4L1 and risk of breast cancer.Altering the GTP binding site of the DNA/RNA-binding protein, Translin/TB-RBP, decreases RNA binding and may create a dominant negative phenotypeMalaria severity and human nitric oxide synthase type 2 (NOS2) promoter haplotypesIdentification of nucleic acid binding sites on translin-associated factor X (TRAX) protein.Multifunctional regulatory proteins that control gene expression in both the nucleus and the cytoplasm.A novel selection system for chromosome translocations in Saccharomyces cerevisiae.The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors.The pathological phenotypes of human TDP-43 transgenic mouse models are independent of downregulation of mouse Tdp-43Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.The t(14;21)(q11.2;q22) chromosomal translocation associated with T-cell acute lymphoblastic leukemia activates the BHLHB1 geneFunctional characterization of Drosophila Translin and TraxMice deficient for testis-brain RNA-binding protein exhibit a coordinate loss of TRAX, reduced fertility, altered gene expression in the brain, and behavioral changesThe translin-TRAX complex (C3PO) is a ribonuclease in tRNA processingThe RNA-binding protein, TB-RBP, is the mouse homologue of translin, a recombination protein associated with chromosomal translocationsAltered protamine expression and diminished spermatogenesis: what is the link?Unexpected complexity at breakpoint junctions in phenotypically normal individuals and mechanisms involved in generating balanced translocations t(1;22)(p36;q13)Sequencing human-gibbon breakpoints of synteny reveals mosaic new insertions at rearrangement sites.High-resolution patterns of meiotic recombination across the human major histocompatibility complex.Molecular characterization of the pericentric inversion that causes differences between chimpanzee chromosome 19 and human chromosome 17Noncoding RNAs of the mammalian testis: the meiotic transcripts Nct1 and Nct2 encode piRNAs.
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P2860
A novel gene, Translin, encodes a recombination hotspot binding protein associated with chromosomal translocations
description
1995 nî lūn-bûn
@nan
1995 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
A novel gene, Translin, encode ...... ith chromosomal translocations
@ast
A novel gene, Translin, encode ...... ith chromosomal translocations
@en
A novel gene, Translin, encode ...... ith chromosomal translocations
@en-gb
A novel gene, Translin, encode ...... ith chromosomal translocations
@nl
type
label
A novel gene, Translin, encode ...... ith chromosomal translocations
@ast
A novel gene, Translin, encode ...... ith chromosomal translocations
@en
A novel gene, Translin, encode ...... ith chromosomal translocations
@en-gb
A novel gene, Translin, encode ...... ith chromosomal translocations
@nl
prefLabel
A novel gene, Translin, encode ...... ith chromosomal translocations
@ast
A novel gene, Translin, encode ...... ith chromosomal translocations
@en
A novel gene, Translin, encode ...... ith chromosomal translocations
@en-gb
A novel gene, Translin, encode ...... ith chromosomal translocations
@nl
P2093
P2860
P3181
P356
P1433
P1476
A novel gene, Translin, encode ...... ith chromosomal translocations
@en
P2093
K Nakahara
P2860
P2888
P304
P3181
P356
10.1038/NG0695-167
P407
P577
1995-06-01T00:00:00Z
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P6179
1012769965