Pages that link to "Q43167080"
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The following pages link to Conformational variants of duplex DNA correlated with cytosine-rich chromosomal fragile sites. (Q43167080):
Displaying 24 items.
- The mechanism of double-strand DNA break repair by the nonhomologous DNA end-joining pathway (Q22065419) (← links)
- Common fragile sites: genomic hotspots of DNA damage and carcinogenesis (Q26825040) (← links)
- A Rare Nucleotide Base Tautomer in the Structure of an Asymmetric DNA Junction (Q27646475) (← links)
- Base damage within single-strand DNA underlies in vivo hypermutability induced by a ubiquitous environmental agent (Q28484339) (← links)
- Mechanisms of chromosomal rearrangement in the human genome (Q33531510) (← links)
- AID-induced decrease in topoisomerase 1 induces DNA structural alteration and DNA cleavage for class switch recombination (Q33563951) (← links)
- Nonhomologous DNA end joining (NHEJ) and chromosomal translocations in humans (Q34813549) (← links)
- Human lymphoid translocation fragile zones are hypomethylated and have accessible chromatin (Q35165170) (← links)
- Polynucleotide kinase and aprataxin-like forkhead-associated protein (PALF) acts as both a single-stranded DNA endonuclease and a single-stranded DNA 3' exonuclease and can participate in DNA end joining in a biochemical system (Q35379148) (← links)
- Unifying the DNA end-processing roles of the artemis nuclease: Ku-dependent artemis resection at blunt DNA ends (Q36115770) (← links)
- G clustering is important for the initiation of transcription-induced R-loops in vitro, whereas high G density without clustering is sufficient thereafter (Q37192001) (← links)
- Preventing AID, a physiological mutator, from deleterious activation: regulation of the genomic instability that is associated with antibody diversity (Q37704005) (← links)
- How does DNA break during chromosomal translocations? (Q37865973) (← links)
- Sequence and structural basis for chromosomal fragility during translocations in cancer (Q38048886) (← links)
- RNA Polymerase Collision versus DNA Structural Distortion: Twists and Turns Can Cause Break Failure (Q38827679) (← links)
- Both CpG methylation and activation-induced deaminase are required for the fragility of the human bcl-2 major breakpoint region: implications for the timing of the breaks in the t(14;18) translocation (Q39221479) (← links)
- Monitoring the reversible B to A-like transition of DNA in eukaryotic cells using Fourier transform infrared spectroscopy. (Q39568704) (← links)
- Formation of a G-quadruplex at the BCL2 major breakpoint region of the t(14;18) translocation in follicular lymphoma (Q41903712) (← links)
- AID and Reactive Oxygen Species Can Induce DNA Breaks within Human Chromosomal Translocation Fragile Zones (Q46105139) (← links)
- Structure-specific nuclease activity of RAGs is modulated by sequence, length and phase position of flanking double-stranded DNA. (Q53010435) (← links)
- Differential Reaction Kinetics, Cleavage Complex Formation, and Nonamer Binding Domain Dependence Dictate the Structure-Specific and Sequence-Specific Nuclease Activity of RAGs (Q53202899) (← links)
- Concept of DNA Lesion Longevity and Chromosomal Translocations (Q88863901) (← links)
- Current insights into the mechanism of mammalian immunoglobulin class switch recombination (Q90057553) (← links)
- Concerted dynamics of metallo-base pairs in an A/B-form helical transition (Q90910802) (← links)