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The CSF3RcausesT618I mutation
the ability of different mutagensto causereverse mutations
by radiation(passive) caused byreverse mutations
radiationcausingreverse mutations
At that concentrationdid ... causereverse mutations
Abou Jamra R.leadsMAN1B1 mutation
their abilityto causereverse mutation
the diseasecausingIVS1 mutation
A casesresultfrom an inversion mutation
by UV damage(passive) caused byreversing mutations
the first diseasecausinggermline mutation
to be 1 of 300 in the US with her diseasecausingCRB1 mutation
a novel Leigh syndromecausingNDUFS3 mutation
In case of DNA viruses , DNA strand of virus insert directly into one chromosomecausingmutation
insertion of new genetic material into a normal gene , particularly of retroviruses into chromosomal DNA(passive) caused bymutation
Insertions or deletion mutations of one or more nucleotidescan causemutation
by addition or deletion of base pair in DNA(passive) caused byMutation
Exposing an organism to a certain chemical can change nucleotide bases in a genecausingmutation
the conditionscausedpalatal mutation
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
by irradiation(passive) caused bygermline mutation
spontaneous and induced and the result of a change in the gene or chromosome(passive) may be caused byMutation
environmental factors(passive) caused bysomatic mutation
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 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
spontaneous and induced and the result of a change in the gene or chromosomes or change in the cytoplasmic genes(passive) may be caused byMutation
the addition or deletion of the base pair(passive) can also be caused byMutation
The sequence of bases and consequently gene sequence is sometimes alteredcausingmutation
Insertion into a functional genecausesmutation
one disease ... 20causingmutation
one cf diseasecausingmutation
Petit Basset Griffon Vendeen Type(passive) is caused byPetit Basset Griffon Vendeen Type
in a functional defect of the properly localized ABCA3resultingin a functional defect of the properly localized ABCA3
to altered nuclear localization of the protein ... and upregulation of the IFN - beta /STAT1 pathway , which plays a critical role in the maintenance of bone homeostasisleadsto altered nuclear localization of the protein ... and upregulation of the IFN - beta /STAT1 pathway , which plays a critical role in the maintenance of bone homeostasis
in resistanceresultingin resistance
in the individualscausingin the individuals
in increased virulencewould ... resultin increased virulence
to Li - Fraumeni syndromeleadsto Li - Fraumeni syndrome
in resistance to 5-fluoroorotic acid ( FOAresultingin resistance to 5-fluoroorotic acid ( FOA
to increased colorectal cancer riskleadingto increased colorectal cancer risk
to independent cytokine signaling and clonal proliferation of hematopoietic cells in MPNsleadsto independent cytokine signaling and clonal proliferation of hematopoietic cells in MPNs
to familial retinoblastomaleadsto familial retinoblastoma
in familial Rbresultsin familial Rb
hypertrichosis lanuginosa Congenital(passive) may be caused byhypertrichosis lanuginosa Congenital
increased risk to an individual over a lifetimecausingincreased risk to an individual over a lifetime
HNPCC(passive) is caused byHNPCC
Bilateral retinoblastoma(passive) is often caused byBilateral retinoblastoma
in the more widespread skin disorderresultingin the more widespread skin disorder
idiopathic pulmonary arterial hypertensioncausesidiopathic pulmonary arterial hypertension
15 % of unilateral retinoblastoma(passive) are caused by15 % of unilateral retinoblastoma
primary ciliary dyskinesia with normal ultrastructure and hyperkinetic ciliacausesprimary ciliary dyskinesia with normal ultrastructure and hyperkinetic cilia
Leber hereditary optic neuropathy and dystoniacausingLeber hereditary optic neuropathy and dystonia
HLA)-identical siblings with HLA - A*0201(passive) are influenced byHLA)-identical siblings with HLA - A*0201
to loss of the phylogenetic signal over the time frame of several hundred yearsleadingto loss of the phylogenetic signal over the time frame of several hundred years
to citrullinemia I inleadingto citrullinemia I in
Cyclophilin interactions with incoming human HLA - A*0201(passive) are influenced byCyclophilin interactions with incoming human HLA - A*0201
pontocerebellar hypoplasia type 4causingpontocerebellar hypoplasia type 4
congenital ichthyosis and recurrent eczemacausingcongenital ichthyosis and recurrent eczema
to postnatal lethality due to constitutive Nrf2 activationleadsto postnatal lethality due to constitutive Nrf2 activation
to citrullinemia I in a Chinese Han familyleadingto citrullinemia I in a Chinese Han family
a severe form of pontocerebellar hypoplasia type 1 in a familycausesa severe form of pontocerebellar hypoplasia type 1 in a family
to genomic instability in prostate cancerleadsto genomic instability in prostate cancer
early?onsetcausingearly?onset
in the more widespread skin disorder epidermolytic ichthyosis ( EI ) , which affects the whole bodyresultingin the more widespread skin disorder epidermolytic ichthyosis ( EI ) , which affects the whole body
type 1 polysaccharide storage myopathy in continental European draught horse breedscausingtype 1 polysaccharide storage myopathy in continental European draught horse breeds
type 1 polysaccharide storage myopathy in continental European draught horse breeds causingtype 1 polysaccharide storage myopathy in continental European draught horse breeds