(+)-CC-1065 as a structural probe of mu transposase-induced bending of DNA: Overcoming limitations of hydroxyl-radical footprinting

Z. M. Ding; R. M. Harshey; L. H. Hurley

doi:10.1093/nar/22.2.256

(+)-CC-1065 as a structural probe of mu transposase-induced bending of DNA: Overcoming limitations of hydroxyl-radical footprinting

Z. M. Ding, R. M. Harshey, L. H. Hurley

Research output: Contribution to journal › Comment/debate › peer-review

Abstract

The publishers wish to apologize for a typographical error which occurred within this paper. MPEβFe was incorrectly translated and should read MPEFe throughout this paper.

Original language	English (US)
Pages (from-to)	256
Number of pages	1
Journal	Nucleic acids research
Volume	22
Issue number	2
DOIs	https://doi.org/10.1093/nar/22.2.256
State	Published - Jan 25 1994
Externally published	Yes

ASJC Scopus subject areas

Genetics

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title = "(+)-CC-1065 as a structural probe of mu transposase-induced bending of DNA: Overcoming limitations of hydroxyl-radical footprinting",

abstract = "The publishers wish to apologize for a typographical error which occurred within this paper. MPEβFe was incorrectly translated and should read MPEFe throughout this paper.",

author = "Ding, \{Z. M.\} and Harshey, \{R. M.\} and Hurley, \{L. H.\}",

year = "1994",

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doi = "10.1093/nar/22.2.256",

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AU - Ding, Z. M.

AU - Harshey, R. M.

AU - Hurley, L. H.

PY - 1994/1/25

Y1 - 1994/1/25

N2 - The publishers wish to apologize for a typographical error which occurred within this paper. MPEβFe was incorrectly translated and should read MPEFe throughout this paper.

AB - The publishers wish to apologize for a typographical error which occurred within this paper. MPEβFe was incorrectly translated and should read MPEFe throughout this paper.

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U2 - 10.1093/nar/22.2.256

DO - 10.1093/nar/22.2.256

M3 - Comment/debate

AN - SCOPUS:0028352082

SN - 0305-1048

VL - 22

SP - 256

JO - Nucleic acids research

JF - Nucleic acids research

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ER -

(+)-CC-1065 as a structural probe of mu transposase-induced bending of DNA: Overcoming limitations of hydroxyl-radical footprinting

Abstract

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