An improved method for photofootprinting yeast genes in vivo using Taq polymerase.
about
Proline-independent binding of PUT3 transcriptional activator protein detected by footprinting in vivo.Cell cycle dependent topological changes of chromosomal replication origins in Saccharomyces cerevisiae.Genomic footprinting of the yeast zinc finger protein Rme1p and its roles in repression of the meiotic activator IME1.Amino termini of histones H3 and H4 are required for a1-alpha2 repression in yeast.Nucleosome structure and positioning modulate nucleotide excision repair in the non-transcribed strand of an active geneGenomic footprinting in mammalian cells with ultraviolet lightBinding to the yeast SwI4,6-dependent cell cycle box, CACGAAA, is cell cycle regulated in vivo.Taq DNA polymerase blockage at pyrimidine dimersLocal supercoil-stabilized DNA structures.DNA-protein interactions at the S.cerevisiae alpha 2 operator in vivo.The transcriptionally-active MMTV promoter is depleted of histone H1.Fine-mapping of DNA damage and repair in specific genomic segments.Nucleosomes are positioned with base pair precision adjacent to the alpha 2 operator in Saccharomyces cerevisiae.Accessibility of alpha 2-repressed promoters to the activator Gal4.The yeast SWI-SNF complex facilitates binding of a transcriptional activator to nucleosomal sites in vivoA transcriptionally active tRNA gene interferes with nucleosome positioning in vivo.Interferon induction of gene transcription analyzed by in vivo footprintingChromosomal organization of Xenopus laevis oocyte and somatic 5S rRNA genes in vivoCrosslinking of progesterone receptor to DNA using tuneable nanosecond, picosecond and femtosecond UV laser pulses.Binding of transcription factors creates hot spots for UV photoproducts in vivo.Transcription-coupled and global genome repair in the Saccharomyces cerevisiae RPB2 gene at nucleotide resolutionRNA polymerase III transcription complexes on chromosomal 5S rRNA genes in vivo: TFIIIB occupancy and promoter opening.Assessment of DNA damage and repair in specific genomic regions by quantitative immuno-coupled PCR.Analysis of DNA damage and repair in murine leukemia L1210 cells using a quantitative polymerase chain reaction assayDestabilization of nucleosomes by an unusual DNA conformation adopted by poly(dA) small middle dotpoly(dT) tracts in vivo.A simplified method for in vivo footprinting using DMS.Incomplete primer extension during in vitro DNA amplification catalyzed by Taq polymerase; exploitation for DNA sequencing.Excess histone levels mediate cytotoxicity via multiple mechanisms.Cell type-specific chromatin organization of the region that governs directionality of yeast mating type switchingThe ability of a variety of polymerases to synthesize past site-specific cis-syn, trans-syn-II, (6-4), and Dewar photoproducts of thymidylyl-(3'-->5')-thymidine.
P2860
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P2860
An improved method for photofootprinting yeast genes in vivo using Taq polymerase.
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
1989年论文
@zh
1989年论文
@zh-cn
name
An improved method for photofootprinting yeast genes in vivo using Taq polymerase.
@ast
An improved method for photofootprinting yeast genes in vivo using Taq polymerase.
@en
type
label
An improved method for photofootprinting yeast genes in vivo using Taq polymerase.
@ast
An improved method for photofootprinting yeast genes in vivo using Taq polymerase.
@en
prefLabel
An improved method for photofootprinting yeast genes in vivo using Taq polymerase.
@ast
An improved method for photofootprinting yeast genes in vivo using Taq polymerase.
@en
P2860
P356
P1476
An improved method for photofootprinting yeast genes in vivo using Taq polymerase.
@en
P2093
P2860
P304
P356
10.1093/NAR/17.1.171
P407
P577
1989-01-01T00:00:00Z