In vivo formation of double-stranded T-DNA molecules by T-strand priming.
about
Transfer of DNA from Bacteria to EukaryotesThe non-homologous end-joining pathway is involved in stable transformation in riceDNA repair genes RAD52 and SRS2, a cell wall synthesis regulator gene SMI1, and the membrane sterol synthesis scaffold gene ERG28 are important in efficient Agrobacterium-mediated yeast transformation with chromosomal T-DNA.Blocking single-stranded transferred DNA conversion to double-stranded intermediates by overexpression of yeast DNA REPLICATION FACTOR A.Enhanced targeted integration mediated by translocated I-SceI during the Agrobacterium mediated transformation of yeast.Involvement of Rad52 in T-DNA circle formation during Agrobacterium tumefaciens-mediated transformation of Saccharomyces cerevisiae.
P2860
In vivo formation of double-stranded T-DNA molecules by T-strand priming.
description
2013 nî lūn-bûn
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name
In vivo formation of double-stranded T-DNA molecules by T-strand priming.
@en
In vivo formation of double-stranded T-DNA molecules by T-strand priming.
@nl
type
label
In vivo formation of double-stranded T-DNA molecules by T-strand priming.
@en
In vivo formation of double-stranded T-DNA molecules by T-strand priming.
@nl
prefLabel
In vivo formation of double-stranded T-DNA molecules by T-strand priming.
@en
In vivo formation of double-stranded T-DNA molecules by T-strand priming.
@nl
P2860
P356
P1476
In vivo formation of double-stranded T-DNA molecules by T-strand priming.
@en
P2093
Tzvi Tzfira
Zhuobin Liang
P2860
P2888
P356
10.1038/NCOMMS3253
P407
P577
2013-01-01T00:00:00Z