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mismatches(passive) are caused byBase substitution mutations
Qcausesbase substitution mutations
mitochondrial polymerase(passive) caused bybase - substitution mutations
realignment of the primer / template strandsleadsto a base substitution mutation
the mutagen(passive) caused bythe base substitution mutations
Some analogs might be incorporated into nucleic acids in place of the standard baseoften leadingto a base substitution mutation
Some analogs may be incorporated into nucleic acids in place of the normal baseoften resultingin a base substitution mutation
replicationwould causebase substitution mutations
that the primary role of BER is correcting base damagepreventingbase substitution mutations
substituting DNA 46 Gene Regulation Genes(passive) caused bySubstitution - mutation
that does not affect NF-1 binding ( 29 ) but abolishes the formation of the novel complex(passive) was createdA two - base substitution mutation
base tautomerismresultingin base substitution mutation
e.g. , sickle cell anemiaresultingfrom base substitution mutation
8-oxoguanine in DNA(passive) caused bybase substitution mutations
because phenotypic reversion has not been demonstrated conclusivelyto result exclusivelyfrom a specific base substitution mutation
As endogenous DNA adducts are knownto causebase substitution mutations
in exon 8(passive) was discoveredA single base substitution mutation
Cas9(passive) caused bysubstitution mutation
when one base is substituted for anotherresultswhen one base is substituted for another
from “ wobble ” pairingcan resultfrom “ wobble ” pairing
in the alteration of a single amino acidresultsin the alteration of a single amino acid
to abolish MAPK sites within the SMRT sequencedesignedto abolish MAPK sites within the SMRT sequence
the replacement of single base nucleotide with another nucleotidecausesthe replacement of single base nucleotide with another nucleotide
in a translational stopresultingin a translational stop
in an amino acid substitutionresultingin an amino acid substitution
in an alternate codonresultingin an alternate codon
to nonsense codonsleadingto nonsense codons
to alter local stem - loop structureswere designedto alter local stem - loop structures
primarily from base misincorporation or biochemical alterationoriginateprimarily from base misincorporation or biochemical alteration
in a STOP codon and thus stops translation of the sequence into a proteinresultsin a STOP codon and thus stops translation of the sequence into a protein
Multidrug Resistance(passive) Caused byMultidrug Resistance
in codon changeresultedin codon change
the same amino acid to be inserted as was found in wild - typecausesthe same amino acid to be inserted as was found in wild - type
a missense mutation in one of the polypeptide chains of hemoglobincausesa missense mutation in one of the polypeptide chains of hemoglobin
cell and tissue dysfunction with agecausecell and tissue dysfunction with age
to a C - C mismatch in the hDNA and palindromic - insertion mutationsledto a C - C mismatch in the hDNA and palindromic - insertion mutations
from induction of the SOS systemresultingfrom induction of the SOS system
in a reduced shattering phenotyperesultsin a reduced shattering phenotype
sickle cell anemia a.causingsickle cell anemia a.
the codon GAG to become GUGcausesthe codon GAG to become GUG
or abolishes the recognition site of a restriction enzymecreatesor abolishes the recognition site of a restriction enzyme
premature stop , exon 17causespremature stop , exon 17
it to code for a much shorter proteincausesit to code for a much shorter protein
in a stop codon or Mutationresultedin a stop codon or Mutation
in a stop - codon or a different amino acidresultedin a stop - codon or a different amino acid
Another disease(passive) caused byAnother disease