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Transversion Mutation
Known as:
Mutation, Transversion
, Nucleotide Transversion Abnormality
, Transversion
A relatively less common point mutation in which a purine is exchanged for a pyrimidine or a pyrimidine is exchanged for a purine.
National Institutes of Health
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Related topics
Related topics
14 relations
CYP1A2*1 Allele
CYP2C8*2 Allele
CYP2C8*4 Allele
CYP2C9*18 Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2005
Highly Cited
2005
Detecting Site-Specific Physicochemical Selective Pressures: Applications to the Class I HLA of the Human Major Histocompatibility Complex and the SRK of the Plant Sporophytic Self-Incompatibility…
R. Sainudiin
,
Wendy S. W. Wong
,
Krithika Yogeeswaran
,
J. Nasrallah
,
Ziheng Yang
,
R. Nielsen
Journal of Molecular Evolution
2005
Corpus ID: 3124798
Models of codon substitution are developed that incorporate physicochemical properties of amino acids. When amino acid sites are…
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Highly Cited
1992
Highly Cited
1992
In vitro DNA replication implicates O2-ethyldeoxythymidine in transversion mutagenesis by ethylating agents.
O. Bhanot
,
P. C. Grevatt
,
Jean M. Donahue
,
Christine N. Gabrielides
,
Jerome J. Solomon
Nucleic Acids Research
1992
Corpus ID: 13562486
A 36-nucleotide oligomer containing a single O2-ethyldeoxythymidine (O2-Et-dT) adduct at a specific site was synthesized. The…
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Highly Cited
1992
Highly Cited
1992
Nucleotide sequence variation in the mitochondrial 12S rRNA gene and the phylogeny of African mole-rats (Rodentia: Bathyergidae).
M. Allard
,
R. Honeycutt
Molecular biology and evolution
1992
Corpus ID: 8407209
Mitochondrial DNA (mtDNA) sequence variation was examined in eight taxa of the African rodent family Bathyergidae, as well as in…
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Highly Cited
1991
Highly Cited
1991
Point mutation in the human dystrophin gene: identification through western blot analysis.
D. Bulman
,
S. Gangopadhyay
,
Karen G. Bebchuck
,
R. Worton
,
P. Ray
Genomics
1991
Corpus ID: 31110794
Highly Cited
1991
Highly Cited
1991
Ocular findings associated with a rhodopsin gene codon 58 transversion mutation in autosomal dominant retinitis pigmentosa.
G. Fishman
,
E. Stone
,
L. D. Gilbert
,
P. Kenna
,
V. Sheffield
A M A Archives of Ophthalmology
1991
Corpus ID: 34660103
Eight members of a family with autosomal dominant retinitis pigmentosa were found to have a cytosine-to-guanine (C-to-G…
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Highly Cited
1991
Highly Cited
1991
Assessing the Reliability of 5S rRNA Sequence Data for Phylogenetic Analysis in Green Plants
K. Steele
,
K. Holsinger
,
R. Jansen
,
D. W. Taylor
1991
Corpus ID: 17340402
Elimination of compensating substitutions in portions of 5S rRNA sequences that exhibit secondary structure and scoring of common…
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Highly Cited
1991
Highly Cited
1991
Activating mutations at codon 61 of the c-Ha-ras gene in thin-tissue sections of tumors induced by aristolochic acid in rats and mice.
H. Schmeiser
,
H. Scherf
,
M. Wiessler
Cancer Letters
1991
Corpus ID: 2214659
Highly Cited
1985
Highly Cited
1985
DNA binding and mutation spectra of the carcinogen N-2-aminofluorene in Escherichia coli. A correlation between the conformation of the premutagenic lesion and the mutation specificity.
M. Bichara
,
R. Fuchs
Journal of Molecular Biology
1985
Corpus ID: 6671549
Highly Cited
1984
Highly Cited
1984
Coordinate increase in major transcripts from the high pI alpha-amylase multigene family in barley aleurone cells stimulated with gibberellic acid.
J. Rogers
,
C. Milliman
Journal of Biological Chemistry
1984
Corpus ID: 25084728
The purpose of this study was to identify specifically genes and transcripts for the high pI isozyme of barley alpha-amylase…
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Highly Cited
1974
Highly Cited
1974
Specificity and frequency of ultraviolet-induced reversion of an iso-1-cytochrome c ochre mutant in radiation-sensitive strains of yeast.
C. Lawrence
,
J. Stewart
,
F. Sherman
,
R. Christensen
Journal of Molecular Biology
1974
Corpus ID: 35285676
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