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the conditionscan causechromosome breakage
that indicatemay causechromosome breakage
That LSDcauseschromosome breakage
DNA double - strand breaks produced by ionising radiation are often misrejoinedto causechromosome exchange aberrations
The dicentric chromosomes generated by telomere fusionscan causechromosome breakage
Ozonecauseschromosome aberration
the Philadelphia chromosome or the fused BCR - ABL generesultsfrom the chromosome translocation
using radiationto causechromosome breakages
cells ... clastogenic agentscausechromosome breakages
Chromosome breakagecan resultin CHROMOSOME TRANSLOCATION
the mechanismscausingchromosome aberrations in
by radiation(passive) caused bychromosome aberrations
RET rearrangement is the commonest oncogenic alterations in Chernobyl - related PTC ; nearly all to RET / PTC1 or RET / PTC3resultingfrom paracentric inversion of chromosome 10
Such telomere damagecould causechromosome aberrations
by ionising radiation(passive) caused bychromosome aberrations
DNA damageleadsto chromosome translocation
humanscausingchromosome aberrations
clastogeniccausingchromosome aberrations
Ionizing radiation ... the initiating factors of CMLleadsto chromosome translocation
by X - ray irradiation(passive) caused bychromosome aberrations
and to what extentcausedchromosome aberrations
acute ATR inhibitioninfluenceschromosome translocation
clastogenic ( ... ) compounds [ 4causingchromosome aberrations
power - frequency fieldscould causechromosome aberrations
the mechanismscauseaberrant chromosome /
the underlying molecular mechanismsresultingin chromosome aberrations
as free radicals are emitted in the process of breaking downalso resultingin chromosome aberrations
anti - tumor preparations(passive) caused bychromosome aberrations
High concentrations have been reportedto causechromosome damage606
This combinationresultsfrom chromosome inversion
by two particular chromosomes joining together(passive) caused bychromosome rearrangement
Spatial orientationinfluenceschromosome ' switching
when there are two breaks in one chromosome and(passive) is causedA chromosomal inversion
when there are two breaks in one chromosome and the area between the breaks(passive) is causedA chromosomal inversion
mutationscausingmycobacteria chromosome
by three breaks in the same chromosome(passive) caused byA chromosomal inversion
any drugcausingFOETAL CHROMOSOME
BBS - associated ligasesleadchromosome progenitors
by three breaks(passive) caused byA chromosomal inversion
It may reattach back to the original chromosome , but in reverse orientationcausingchromosomal inversion
to a fusion geneleadsto a fusion gene
in a fusion generesultsin a fusion gene
to a fusion with the echinoderm microtubule - associated protein like 4 ( EML4 ) gene , which results in the abnormal expression and activation of this tyrosine kinase in the cytoplasm of cancer cellsleadingto a fusion with the echinoderm microtubule - associated protein like 4 ( EML4 ) gene , which results in the abnormal expression and activation of this tyrosine kinase in the cytoplasm of cancer cells
miscarriage in 30 % of the cases ... but 1can causemiscarriage in 30 % of the cases ... but 1
to disruption of the hlcs geneleadingto disruption of the hlcs gene
to the over expression of the MALT1 gene , trisomy 3 , trisomy 18 , and deletions at position 23 on the long arm of chromosome 6leadsto the over expression of the MALT1 gene , trisomy 3 , trisomy 18 , and deletions at position 23 on the long arm of chromosome 6
in Alpha - TFEB gene fusion [ PMID11395386resultingin Alpha - TFEB gene fusion [ PMID11395386
to the adaptation of An . gambiae ( s.s . ... to arid conditions [ 6 , 9 , 15contributesto the adaptation of An . gambiae ( s.s . ... to arid conditions [ 6 , 9 , 15
First Down Syndrome(passive) is caused byFirst Down Syndrome
to loss of genetic information , aberrant rearrangements of chromosomesleadingto loss of genetic information , aberrant rearrangements of chromosomes
to loss of genetic information , aberrant rearrangements of chromosomes , and genomic instabilityleadingto loss of genetic information , aberrant rearrangements of chromosomes , and genomic instability
to this diseasecan leadto this disease
The condition(passive) is caused byThe condition
the deletion in the child 's chromosome via a non - allelic homologous recombination ( NAHR ) mechanisminfluencesthe deletion in the child 's chromosome via a non - allelic homologous recombination ( NAHR ) mechanism
in chromosome disordersmay resultin chromosome disorders
in CHROMOSOME DISORDERS.may resultin CHROMOSOME DISORDERS.
in exchange of genetic material between the chromosomesresultsin exchange of genetic material between the chromosomes
to cancer and/orleadto cancer and/or
in CHROMOSOME DISORDERS.Radiation Injuriesmay resultin CHROMOSOME DISORDERS.Radiation Injuries
microdeletion syndromecausesmicrodeletion syndrome
from double - strand DNA breaks at a naturally occurring yeast fragile site composed of inverted ty elementsresultingfrom double - strand DNA breaks at a naturally occurring yeast fragile site composed of inverted ty elements
to the fusion of the anaplastic lymphoma kinase ( ALK ) gene with the echinoderm microtubule - associated protein - like 4leadingto the fusion of the anaplastic lymphoma kinase ( ALK ) gene with the echinoderm microtubule - associated protein - like 4
> Edwards syndrome(passive) is caused by> Edwards syndrome
to dominant expression of a second S layer proteinleadingto dominant expression of a second S layer protein
to retrocerebellar CSF spacecan leadto retrocerebellar CSF space
both Activation of a proto - oncogenecausingboth Activation of a proto - oncogene
disruption of replication(passive) caused bydisruption of replication
these discrepancies appear(passive) to have been caused bythese discrepancies appear
to cancerledto cancer
to our issuesis contributingto our issues
replication(passive) caused byreplication
According to the marker order in the genetic maps of these two chromosomes ( see Additional file 1 ) , these discrepancies appear(passive) to have been caused byAccording to the marker order in the genetic maps of these two chromosomes ( see Additional file 1 ) , these discrepancies appear
meiotic drivecan causemeiotic drive
to the identification of the Neuregulin-1 gene ( NRG1 ) as a potential genetic risk factorledto the identification of the Neuregulin-1 gene ( NRG1 ) as a potential genetic risk factor
tumorigenesis and breast cancer developmentalso influencetumorigenesis and breast cancer development
to genome heterozygosity of the two closely related haploid strains ... and the meiotic recombination between the two homoeologous chromosomes generates both inviable and viable SAN progenyleadsto genome heterozygosity of the two closely related haploid strains ... and the meiotic recombination between the two homoeologous chromosomes generates both inviable and viable SAN progeny
almost 50 % of the cases of severe Factor VIII deficiencycausesalmost 50 % of the cases of severe Factor VIII deficiency