ICR-191

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1967-2018
024619672018

Papers overview

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2008
2008
We have investigated the ability of chlorophyllin (CHL) to interact with acridine mutagen ICR-191 (2-methoxy-6-chloro-9-(3-(2… (More)
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2003
2003
Previous studies performed by others indicated that apart from its other biological effects, caffeine (CAF) may have a role in… (More)
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1994
1994
Human TK6 lymphoblasts were treated with the acridine derivative ICR-191, and mutants at the hprt locus were isolated. Mutant… (More)
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1991
1991
As the most nucleophilic site in DNA, the guanine N7 atom is a major site of adduction by a large number of alkylating mutagens… (More)
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1990
1990
We describe a method to identify and enumerate mutants at the nucleotide level in complex cell populations. Several thousand… (More)
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1982
1982
A thymidine kinase heterozygote was isolated from a diploid human lymphoblast line which forms colonies with high efficiency in… (More)
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1982
1982
We have analyzed forward-mutation specificity in S49 mouse T lymphoma cells. Our criteria of specificity were based upon relative… (More)
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1980
1980
The toxic and mutagenic effects of the alkylating agents methylnitrosourea (MNU) and methylnitronitrosoguanidine (MNNG) and of… (More)
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1977
1977
Concentration-dependent mutagenicity of ICR-191 has been measured in Salmonella typhimurium strain TA98 and in a diploid human… (More)
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1971
1971
ICR-191, an acridine half-mustard known to cause frameshift mutations in bacteria, was used to induce Lac(-) mutations revertible… (More)
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