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Chromosomal instability at common fragile sites in Seckel syndromeSequence conservation at human and mouse orthologous common fragile regions, FRA3B/FHIT and Fra14A2/FhitCommon fragile sites: genomic hotspots of DNA damage and carcinogenesisJacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.ATR preferentially interacts with common fragile site FRA3B and the binding requires its kinase activity in response to aphidicolin treatment.ATR suppresses telomere fragility and recombination but is dispensable for elongation of short telomeres by telomerase.DNA breaks at fragile sites generate oncogenic RET/PTC rearrangements in human thyroid cells.Identifying Mazama gouazoubira (Artiodactyla; Cervidae) chromosomes involved in rearrangements induced by doxorubicinSecondary structure formation and DNA instability at fragile site FRA16BAnalysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocation.DNA instability at chromosomal fragile sites in cancerMonozygotic twins with discordant karyotypes following preimplantation genetic screening and single embryo transfer: case report.Fragile site orthologs FHIT/FRA3B and Fhit/Fra14A2: evolutionarily conserved but highly recombinogenicCommon fragile site tumor suppressor genes and corresponding mouse models of cancer.CGG repeats associated with DNA instability and chromosome fragility form structures that block DNA synthesis in vitro.The F-box protein Dia2 overcomes replication impedance to promote genome stability in Saccharomyces cerevisiae.Loss of heterozygosity of the BRCA1 and FHIT genes in patients with sporadic breast cancer from Southern Brazil.Cancer-specific chromosome alterations in the constitutive fragile region FRA3B.Replication stress induces tumor-like microdeletions in FHIT/FRA3BPositional cloning of the hereditary renal carcinoma 3;8 chromosome translocation breakpointA TRF1-controlled common fragile site containing interstitial telomeric sequences.The role of human papillomavirus type 16 and the fragile histidine triad gene in the outcome of cervical neoplastic lesionsGeneration of a new adenovirus type 12-inducible fragile site by insertion of an artificial U2 locus in the human genome.Sequence of the FRA3B common fragile region: implications for the mechanism of FHIT deletion.Integration of HIV in the Human Genome: Which Sites Are Preferential? A Genetic and Statistical Assessment.The expression of folate sensitive fragile sites in patients with bipolar disorder.Recombinogenic conditions influence partner choice in spontaneous mitotic recombination.Karyological evidence for diversification of Italian slow worm populations (Squamata, Anguidae)Fhit tumor suppressor: guardian of the preneoplastic genome.Preferential integration of marker DNA into the chromosomal fragile site at 3p14: an approach to cloning fragile sites.Genome organization, instabilities, stem cells, and cancer.Repeat expansion in the budding yeast ribosomal DNA can occur independently of the canonical homologous recombination machinery.Infection with retroviral vectors leads to perturbed DNA replication increasing vector integrations into fragile sitesFragile sites in cancer: more than meets the eye.Human DNA Helicase B as a Candidate for Unwinding Secondary CGG Repeat Structures at the Fragile X Mental Retardation Gene.
P2860
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P2860
description
1988 nî lūn-bûn
@nan
1988 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Chromosome breakage and recombination at fragile sites
@ast
Chromosome breakage and recombination at fragile sites
@en
type
label
Chromosome breakage and recombination at fragile sites
@ast
Chromosome breakage and recombination at fragile sites
@en
prefLabel
Chromosome breakage and recombination at fragile sites
@ast
Chromosome breakage and recombination at fragile sites
@en
P2860
P1476
Chromosome breakage and recombination at fragile sites
@en
P2093
P2860
P304
P407
P577
1988-09-01T00:00:00Z