Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Carrie R. Valentine"'
Autor:
Joseph G. Shaddock, Jessica M. Farrell, Robert R. Delongchamp, Vasily N. Dobrovolsky, Heather F. Rainey, Carrie R. Valentine
Publikováno v:
Mutagenesis. 23:383-397
A perceived disadvantage of transgenic rodent mutation assays is that spontaneous mutant frequencies are high compared to those of endogenous genes and may consequently reduce sensitivity to induced mutation. We have previously argued that unrepaired
Autor:
Jessica M. Farrell, Bruce S. Hass, Paul C. Howard, Heather F. Rainey, Carrie R. Valentine, Robert R. Delongchamp
Publikováno v:
Genes and Environment. 29:38-53
Autor:
Jessica L. Raney, Joseph G. Shaddock, Carrie R. Valentine, Robert R. Delongchamp, Vasily N. Dobrovolsky
Publikováno v:
Environmental and Molecular Mutagenesis. 44:128-150
Single-burst analysis was applied to a forward assay for gene A mutation in splenic lymphocytes of phiX174 transgenic mice for the purpose of optimizing analytical parameters for identifying in vivo mutations. The effect of varying the cutoff value f
Publikováno v:
Environmental and Molecular Mutagenesis. 42:258-273
Transgenic systems for measuring mammalian mutagenesis often use recoverable viral vectors. We hypothesize that mutations in these transgenic systems can arise from three different origins of DNA damage and replication errors and that these three ori
Autor:
Robert R. Delongchamp, Beverly Montgomery, Scott G. Miller, Bentley A. Fane, Heinrich V. Malling, Carrie R. Valentine
Publikováno v:
Environmental and Molecular Mutagenesis. 39:55-68
The sensitivity of in vivo transgenic mutation assays benefits from the sequencing of mutations, although the large number of possible mutations hinders high throughput sequencing. A forward mutational assay exists for ΦX174 that requires an altered
Publikováno v:
Environmental and Molecular Mutagenesis. 37:356-360
In mutation assays using transgenic mice, with recoverable vectors such as PhiX174 am3, cs70, mutations originate from two sources: (1) in vivo mutations, that is, mutations that were fixed in the mouse, or (2) ex vivo mutations, that is, mutations t
Publikováno v:
Mutation Research/Mutation Research Genomics. 432:15-32
Exon skipping that accompanies exonic mutation might be caused by an effect of the mutation on pre-mRNA secondary structure. Previous attempts to associate predicted secondary structure of pre-mRNA with exon skipping have been hindered by either a sm
Autor:
Carrie R. Valentine
Publikováno v:
Mutation Research/Reviews in Mutation Research. 411:87-117
Some genes that contain premature nonsense codons express alternatively-spliced mRNA that has skipped the exon containing the nonsense codon. This paradoxical association of translation signals (nonsense codons) and RNA splicing has inspired numerous
Publikováno v:
Plasmid. 32:222-227
The restriction enzyme and genetic map of the antibiotic-resistance region of plasmid pSa is related to Tn21 integrons by the insertion of 5.4 kb containing a chloramphenicol resistance gene (catII) and a 1.1-kb direct repeat. We report here the nucl
Autor:
Heinrich V. Malling, Heather F. Rainey, Robert R. Delongchamp, Mason G. Pearce, Vasily N. Dobrovolsky, Carrie R. Valentine, Robert H. Heflich
Publikováno v:
Mutation research. 705(3)
The ΦX174 transgenic mouse was first developed as an in vivo Ames test, detecting base pair substitution (bps) at a single bp in a reversion assay. A forward mutational assay was also developed, which is a gain of function assay that also detects bp