Loading ...

Blob

Smart Reasoning:

C&E

See more*

Qaagi - Book of Why

Causes

Effects

radiation , viruses , transposons , and mutagenic chemicals(passive) are caused byMutation Mutations

copying errors in the genetic material during cell division , by exposure to ultraviolet or ionizing radiation , chemical mutagens , or viruses(passive) can be caused byMutation Mutations

copying errors in the genetic material during cell division , by exposure to ultraviolet or ionizing radiation , chemical mutagens , or viruses(passive) can be caused by Mutation Mutations

mutagen : environmental factorcausesmutations mutation

environmental factorcausesmutations mutation

Abou Jamra R.leadsMAN1B1 mutation

by the NRTIs(passive) caused byreplication mutations

the NRTIs(passive) caused byreplication mutations

this insertion mutationhad resultedfrom a duplication mutation

Each bandcausesdistinct mutations

Although compositions haw alter undramatically withinfamilies , specic phenotypess be givento be discoveredwithcertain mutations

in autism , schizophrenia , ADHD , etc .(passive) are discoveredIRSp53 mutations

a techniqueto discoverredundant mutations

Mechanisms by which SCN5Acausesmutation N1325S

to be 1 of 300 in the US with her diseasecausingCRB1 mutation

by the deletion or insertion one or more bases into the DNA molecule(passive) caused bymutation - 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. A mousecausesMecp2-null mutation

A mousewill causeMecp2-null mutation

A mousecausesMecp2-null mutation

Insertions or deletion mutations of one or more nucleotidescan causemutation

Exposing an organism to a certain chemical can change nucleotide bases in a genecausingmutation

harsh environmentscausenonrandom mutations

2 disease ... and no normal copies of the gene ( for referencecausingmutation

by the substitution of a one or more DNA bases(passive) caused by Mutation

by the addition of one or more adjacent base pairs to a gene(passive) caused bymutation

the diseasecausingF508del mutation

by the addition or deletion of one or more bases in DNA 18 Genetic Code(passive) caused byMutation A mutation

spontaneous and induced and the result of a change in the gene or chromosome(passive) may be caused byMutation

an addition or deletion of a base that changes the length of the sequence(passive) is caused bymutation

only the one known diseasecausingmutation

A common cancer - associated DNA polymerasecauses mutation

the first disease ... that has been identified in the human CCT subunit genescausingmutation

by a change in a gene or a chromosome(passive) caused bymutation

the X - Gene in the mutants ' DNA(passive) is caused byMutation Mutation

the rate and types of mutation ... radiationcausemutation

by A ) substitution B ) insertion C(passive) caused bymutation

only one nucleotide changecan causemutation

a very rare but known ' diseasecausingmutation

in loss of functionresultin loss of function

to diseaseleadsto disease

new genescan causenew genes

to improvements while rare can cause evolutionleadto improvements while rare can cause evolution

to Fragile X Syndromecan leadto Fragile X Syndrome

the diseasecausethe disease

in reduced levels of and/or dysfunctional blood plateletsmay thereby resultin reduced levels of and/or dysfunctional blood platelets

nonsense mutations(passive) caused bynonsense mutations

DNA and promoter binding to RNA polymerasecould influenceDNA and promoter binding to RNA polymerase

from the countryoriginatingfrom the country

to the formation of both organs at the same timeledto the formation of both organs at the same time

ocular albinism type 1causesocular albinism type 1

to the formation of both organsledto the formation of both organs

lethalitywould causelethality

rapid progressioncausesrapid progression

late floweringcausedlate flowering

to an increase of 130 %will leadto an increase of 130 %

in male sterilityresultedin male sterility

an 80 % impairment in folic acid metabolismcausesan 80 % impairment in folic acid metabolism

new genescan causenew genes

to disrupt binding of isoprenoiddesignedto disrupt binding of isoprenoid

in malignant transformation leading to tumour formation by clonal expansioncan resultin malignant transformation leading to tumour formation by clonal expansion

Duchenne muscular dystrophy(passive) caused byDuchenne muscular dystrophy

individuals affected by PMD(passive) caused byindividuals affected by PMD

duplication of this genecausesduplication of this gene

to increased informationleadingto increased information

cataractscausescataracts

the disorders(passive) can be caused bythe disorders

Type 1A , the commonest form(passive) is caused byType 1A , the commonest form

DMD(passive) caused byDMD

to developmental delays and other abnormalitiesleadsto developmental delays and other abnormalities

in developmental delays and other abnormalitiesresultsin developmental delays and other abnormalities

to developmental delays and other abnormalitiescontributesto developmental delays and other abnormalities

to the accumulation of fat droplets in the livers of S193D mice at very early ages ( days 1 and 3 after birthleadsto the accumulation of fat droplets in the livers of S193D mice at very early ages ( days 1 and 3 after birth

any benefit to an organismcauseany benefit to an organism

Charcot - Marie - Tooth disease type 1A ( CMT1A(passive) is caused byCharcot - Marie - Tooth disease type 1A ( CMT1A

Pathology Charcot - Marie - Tooth disease type 1A ( CMT1A(passive) is caused byPathology Charcot - Marie - Tooth disease type 1A ( CMT1A

mitochondria dysfunction ... leading to heart abnormalities and progressive liver diseasecausesmitochondria dysfunction ... leading to heart abnormalities and progressive liver disease

primary ciliary dyskinesia with normal ultrastructure and hyperkinetic ciliacausesprimary ciliary dyskinesia with normal ultrastructure and hyperkinetic cilia

alsocausealso

Blob

Smart Reasoning:

C&E

See more*