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Research demonstratedresultedfrom one insertion mutation
Analysis revealedresultedfrom one insertion mutation
Deletion or insertion of three or a multiple of three base pairs inside coding sequencesdoes ... causeframeshift mutation
a novel deleterious homozygous four - nucleotide deletioncausingframeshift mutation
by insertion or deletion(passive) caused byframeshift mutation
Genetic analysis demonstratedresultedfrom a single insertion mutation
Genetic analysis revealedresultedfrom a single insertion mutation
exon 6causesframeshift mutation
Research demonstratedresultedfrom a single insertion mutation
that may insert between bases in DNAcausingframeshift mutation
INT-407 cellsresultingfrom an insertion mutation of cj1461
a variety of agents known as mutagens which may be chemical compounds(passive) may be caused byPoint mutation
a mutagencausesframeshift mutation
The breakcausesframeshift mutation
This mechanismcould causeframeshift mutation
likely(passive) would ... be causedI368N mutation
DNA mismatch repair deficiency is observed in about 15 % of human colorectal , gastric , and endometrial tumors and in lower frequencies in a minority of other tumorscausinginsertion / deletion mutations
the potentialto causeinsertion mutations in oncogenes
Abou Jamra R.leadsMAN1B1 mutation
DNAcan causeinsertion mutations
the probability of this sequence occurring ... DNAcan causeinsertion mutations
mobile genetic elementscauseinsertion mutations
A build - up of DNA adductscausesinsertion mutations
a potentialto causeinsertion mutations
All the above splice defect andresultedinsertion mutations
All deletions ( except the deletion in intron 5 ) andcausedinsertion mutations
Virusescan causeinsertion mutations
A T - DNA and adjacent flanking sequences containing the gene of interest could be inserted into a second locuscausingan insertion mutation
transposition(passive) caused byinsertion mutations
Mechanisms by which SCN5Acausesmutation N1325S
by inserting DNA that should not be there(passive) caused byInsertion - mutation
inserting into a segment of genomic DNAthereby causingan insertion mutation
the first diseasecausinggermline mutation
Another benefit that they have ... the host cellcould leadto insertion mutation
reverse slippagewill resultin an insertion mutation
a novel Leigh syndromecausingNDUFS3 mutation
insertion of new genetic material into a normal gene , particularly of retroviruses into chromosomal DNA(passive) caused bymutation
A mousewill causeMecp2-null mutation
A mousecausesMecp2-null mutation
A. A mousecausesMecp2-null mutation
the Dna to get longerwill causethe Dna to get longer
a frame shift and a premature termination of protein synthesiscausea frame shift and a premature termination of protein synthesis
to a frame shift in the coding sequenceleadsto a frame shift in the coding sequence
severe defectscausedsevere defects
defects in gliding motilitycauseddefects in gliding motility
Which disease(passive) can be caused byWhich disease
a shift of the open reading frame and formed a termination codon early at Amino Acid Positioncauseda shift of the open reading frame and formed a termination codon early at Amino Acid Position
in reduced activity of the protein encoded by the genemay resultin reduced activity of the protein encoded by the gene
in a frame shift that caused a stop codon to appear 18 amino acid residues downstream from the insertionresultedin a frame shift that caused a stop codon to appear 18 amino acid residues downstream from the insertion
premature truncation of the proteincausingpremature truncation of the protein
to the development of a number of inherited diseaseshave ledto the development of a number of inherited diseases
in potential polar effects on downstream genesresultingin potential polar effects on downstream genes
a shift in the reading framecausea shift in the reading frame
the gene to code for protein so long that it can not fold properlymay causethe gene to code for protein so long that it can not fold properly
in the production of the wrong amino acidsresultin the production of the wrong amino acids
to cancerleadto cancer
in a null phenotyperesultin a null phenotype
a frameshiftCausesa frameshift
a complete change of the first transmembrane domaincauseda complete change of the first transmembrane domain
in the addition of extra DNAresultin the addition of extra DNA
in the addition of extra DNAresultin the addition of extra DNA
a frameshift mutationWill ... causea frameshift mutation
with a premature stop codonresultingwith a premature stop codon
in a premature stop codonresultsin a premature stop codon
1 or more amino acids to be added to a proteincauses1 or more amino acids to be added to a protein
in shorter proteins being formedresultin shorter proteins being formed
complete loss or severe reduction in the level of full lengthcausescomplete loss or severe reduction in the level of full length
more defects ... than a point mutationdoes ... causemore defects ... than a point mutation
a frame shiftcausesa frame shift
a complete change of the first transmembrane domain ... and deletion of the remaining six transmembrane domains ( Figure 3causeda complete change of the first transmembrane domain ... and deletion of the remaining six transmembrane domains ( Figure 3
from a duplication mutationhad resultedfrom a duplication mutation
neural differentiation or cause cancerinfluenceneural differentiation or cause cancer
in some nucleotides being gainedresultin some nucleotides being gained
usually ... than point mutationcausesusually ... than point mutation
the amino acid change from ser ( Serine ) to glu ( Glutamatecausesthe amino acid change from ser ( Serine ) to glu ( Glutamate
to a frameshiftleadingto a frameshift
usuallycausesusually
the 6 bp larger band(passive) caused bythe 6 bp larger band
to Li - Fraumeni syndromeleadsto Li - Fraumeni syndrome
conformational disturbance(passive) caused byconformational disturbance