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Smart Reasoning:

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Qaagi - Book of Why

Causes

Effects

SOAPsnp little insertion / deletion ( InDels(passive) had been discovered byOne nucleotide polymorphisms ( SNPs

interactions and has been shownto influenceHsp90 nucleotide binding.[120][121

has been shownto influenceHsp90 nucleotide binding.[120][121

of : Phosphate group Deoxyribose sugar Nitrogen base Cytosine(passive) is composedNucleotide in DNA

has been shownto influencenucleotide binding.[119][120

has been shownto influencenucleotide binding.[120][121

allelic differences from pooling multiple individuals for sequencing(passive) caused byreal nucleotide polymorphisms

of a pentose sugar , a nitrogenous base , and a phosphate group(passive) are composednucleotide Nucleotides

has been shownto influencenucleotide binding.[123][124

by mutation , which could be substitution , deletion , insertion or frame shift mutation(passive) caused bynucleotide sequence

genes on chromosomes DNAis composedof nucleotides A Nucleotide

for each gene(passive) were designednucleotide sequences

chemical synthesis errors(passive) were probably caused byNucleotide deletions

by the polymorphism(passive) caused bynucleotide sequences

by research teams(passive) contributed bynucleotide sequences

to replace most wild - type codons with codons from highly expressed human being genes(passive) were designedNucleotide sequences

with the prefix TM and GM(passive) were designedNucleotide sequences

by SEQ ID No . 9 , SEQ ID No . 11 and SEQ ID No . 13 ; or ii(passive) composed bynucleotide sequences

polymerase interactions with the [ [ DNA minor groove ... the active siteinfluencenucleotide selectivity

the active siteinfluencenucleotide selectivity

of a phosphate group and a nitrogenous base , which are attached to a pentose sugar(passive) is composedNucleotide

of a sugar , a phosphate group , and a nitrogen containing molecule called a base(passive) is composedNucleotide

of pentose sugar , nitrogenous base & phosphate group(passive) is composedNucleotide

of a nitrogenous base , deoxyribose ( 5-carbon sugar ) , and a phosphate group(passive) are composedNucleotide

of a nitrogenous base , sugar and a phosphate group(passive) is composedNucleotide

of a nitrogenous base , pentose sugar and phosphate(passive) is composedNucleotide

Interestingly , A3 G decreased the fidelity of RTcausingmisincorporation of nucleotides

of a sugar , phosphate , and nitrogenous base Nitrogenous base ( A(passive) is composednucleotide

Resistance to azoles has been shownto resultfrom nucleotide polymorphisms

of three units : an organic base , a sugar , and a phosphate(passive) is composednucleotide

The catabolism ofresultsadenine nucleotides

of : Sugar Base Phosphate(passive) is composednucleotide

UVA lightmainly causesthymine - thymine dimers

of base , pentose , and phosphate(passive) is composedNucleotide

of a nucleobase ( nitrogenous base ) and a five - carbon(passive) is composedNucleotide A nucleotide

by the fusion protein(passive) to have been caused byAdenine methylation

of a nucleobase ( nitrogenous base(passive) is composedNucleotide A nucleotide

of : _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ group _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ base _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _(passive) is composedNucleotide in _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _

of : a. One deoxyribose sugar(passive) is composedNucleotide

of a nitrogenous base(passive) is composedNucleotide

patient outcome such as drug response and toxicity after drug interventioncan ... influencepatient outcome such as drug response and toxicity after drug intervention

forth in < 400>20 or an amino acid sequence being at least about 60 % similar theretois setforth in < 400>20 or an amino acid sequence being at least about 60 % similar thereto

forth in < 400>26 or an amino acid sequence being at least about 60 % similar theretois setforth in < 400>26 or an amino acid sequence being at least about 60 % similar thereto

in the addition of one or more amino acid or nucleotide residues ... respectivelyhas resultedin the addition of one or more amino acid or nucleotide residues ... respectively

from the transcription of the genomic DNA to mRNAresultingfrom the transcription of the genomic DNA to mRNA

replication stress(passive) caused byreplication stress

to sequestration of replication proteinleadsto sequestration of replication protein

in conservative amino acid substitutionsresultingin conservative amino acid substitutions

to the changeleadingto the change

alsoinfluencesalso

in amino - acid sequence changesresultedin amino - acid sequence changes

defective homologouscausesdefective homologous

in amino - acid substitutionsresultin amino - acid substitutions

a disease phenotype in contrast to an epigenetic disease , which can be defined as an aberration in epigenotype ( stable / heritable change in gene expression ) causing a disease phenotype in the absence of nucleotide sequence aberrationcausinga disease phenotype in contrast to an epigenetic disease , which can be defined as an aberration in epigenotype ( stable / heritable change in gene expression ) causing a disease phenotype in the absence of nucleotide sequence aberration

to stalled replication forksleadsto stalled replication forks

to stalling of replication forksleadingto stalling of replication forks

in SEQ ID NOSset forthin SEQ ID NOS

upper bounds for the rates , which are then further modulated by the partitioning between ATP and ADP bindingsetsupper bounds for the rates , which are then further modulated by the partitioning between ATP and ADP binding

to amino acid substitutions in the lanosterol demethylase gene ( cyp51Aleadingto amino acid substitutions in the lanosterol demethylase gene ( cyp51A

differences in Ehd1 expressionmay causedifferences in Ehd1 expression

in aa variationsresultingin aa variations

feline geneticcausingfeline genetic

frame shiftcauseframe shift

that the termini have an overlapping sequence of about 20 basesbeing designedthat the termini have an overlapping sequence of about 20 bases

SNPsleadSNPs

differential gene expression and single feature polymorphisms ( SFP )(passive) caused bydifferential gene expression and single feature polymorphisms ( SFP )

to the first gene to be completely sequencedleadingto the first gene to be completely sequenced

to the first gene to be completely sequencedeventually leadingto the first gene to be completely sequenced

feline genetic diseasescausingfeline genetic diseases

the virusdiscoveredthe virus

to the implementation of marker - assisted and genomic selectionare ... contributingto the implementation of marker - assisted and genomic selection

mutationsmay causemutations

to stalled replication forks , which progressively become inactivated and require two different RAD51-mediated pathways for restart and repairleadsto stalled replication forks , which progressively become inactivated and require two different RAD51-mediated pathways for restart and repair

the termination of the polymerase reactioncausingthe termination of the polymerase reaction

of a phosphate group , sugar , and nitrogenous base connected by a phosphodiester bondcomposedof a phosphate group , sugar , and nitrogenous base connected by a phosphodiester bond

to Thrleadingto Thr

familial glucocorticoid deficiencycausefamilial glucocorticoid deficiency

1contribute1

to transition mutationsleadto transition mutations

to the identification of novel candidate molecules with AC activity such as F - box and TIR proteinscan contributeto the identification of novel candidate molecules with AC activity such as F - box and TIR proteins

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Smart Reasoning:

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