Structure-specific nuclease activity of RAGs is modulated by sequence, length and phase position of flanking double-stranded DNA.
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Snaps and mends: DNA breaks and chromosomal translocationsMicrohomology-mediated end joining is the principal mediator of double-strand break repair during mitochondrial DNA lesionsHIV integrase inhibitor, Elvitegravir, impairs RAG functions and inhibits V(D)J recombination.Biochemical Characterization of Nonamer Binding Domain of RAG1 Reveals its Thymine Preference with Respect to Length and Position.
P2860
Structure-specific nuclease activity of RAGs is modulated by sequence, length and phase position of flanking double-stranded DNA.
description
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name
Structure-specific nuclease ac ...... flanking double-stranded DNA.
@en
Structure-specific nuclease ac ...... flanking double-stranded DNA.
@nl
type
label
Structure-specific nuclease ac ...... flanking double-stranded DNA.
@en
Structure-specific nuclease ac ...... flanking double-stranded DNA.
@nl
prefLabel
Structure-specific nuclease ac ...... flanking double-stranded DNA.
@en
Structure-specific nuclease ac ...... flanking double-stranded DNA.
@nl
P2860
P356
P1433
P1476
Structure-specific nuclease ac ...... flanking double-stranded DNA.
@en
P2093
Rupa Kumari
Sathees C Raghavan
P2860
P356
10.1111/FEBS.13121
P407
P577
2014-11-14T00:00:00Z