「Chromosome」の共起表現(1語右で並び替え)

Weblio 辞書 > 英和辞典・和英辞典 > Chromosomeの意味・解説 > Chromosomeに関連した共起表現

意味

例文

類語

共起表現

「Chromosome」の共起表現一覧(1語右で並び替え)

該当件数 : 186件

n gene with the BCR gene in the Philadelphia	chromosome, a characteristic abnormality in chronic mye
B47 is linked to (close to on the	chromosome) a gene that causes adrenal deficiency.
ions such as cancer and birth defects due to	chromosome aberrations.
	Chromosome abnormalities can be numerical, as in the pr
Suspicion of a	chromosome abnormality is typically raised due to the p
ntifiable Mendelian (single-gene) condition,	chromosome abnormality, or other genetic syndrome, and
w the specific structure of that region of a	chromosome affect expression levels and function.
usly transcribed tetratricopeptide repeat, X	chromosome, also known as UTX, is a protein which in hu
etrasomy 18p is typically made via a routine	chromosome analysis from a blood sample.
During her graduate studies she worked on	chromosome analysis, comparing chimpanzee and human chr
e piece is matched to a strand of the intact	chromosome and that strand is used to form a D-loop at
nheritance rather than being linked to the X	chromosome, and (4) prolonged bleeding times by the Duk
ion causing the disorder is located on the X	chromosome, and while two copies of the mutated gene mu
, a protein crystal growth experiment, and a	chromosome and plant cell division experiment.
This gene maps to a GC-rich region of the X	chromosome and was identified by its proximity to a CpG
istinct gene (TAF9B) has been found on the X	chromosome and a pseudogene has been identified on chro
genome consists of a large (4 Mb), multicopy	chromosome and several megaplasmids.
amilies should always discuss the results of	chromosome and FISH studies with a genetic counselor or
ted on two chromosomes; Ci-Hox1 to 10 on one	chromosome and Ci-Hox12 and 13 on another.
to the direction of the DNA template in the	chromosome and is used to distinguish between the two u
more ambitious plan would be to remove one X	chromosome and add a Y chromosome from another still-ex
1876, long before the genetic roles of the X	chromosome and Y chromosome and the social components o
MSL complex was unable to localize on the X	chromosome and mislocalize to the heterochromatic chrom
Two markers on a	chromosome are one centimorgan apart if they have a 1%
amete; trisomies, in which three copies of a	chromosome are present instead of the usual two, are co
h population maintaining a single artificial	chromosome, are stored in various laboratories around t
which segments of DNA along the length of a	chromosome are duplicated.
The multiple Ter sites in the	chromosome are oriented such that the two oppositely mo
cuckoos, which like all male birds have no W	chromosome, are able to mate with females of any gens,
The P1-derived artificial	chromosome are DNA constructs that are derived from the
complex repeated DNAs at centromeres and on	chromosome arms (LINES) and their organization in inter
requently have aneuploidy of chromosomes and	chromosome arms, although a cause and effect relationsh
BAC (Bacterial Artificial	Chromosome) arrays were historically the first microarr
e PHEX gene sequence, located on the human X	chromosome at location Xp22.2-p22.1.
ene is located on the short (p) arm of the X	chromosome at position 22.
s between men and women, starting with the X	chromosome, autoimmunity in women, fetal mouth movement
was likely located on the long arm of the X	chromosome between positions Xq22.2-q28.
	Chromosome biology (chromosome structure, translocation
rganization of genes; mechanism of repair of	chromosome breaks and molecular changes in the Notch ge
ed adjacent to the original gene on the same	chromosome), but not in the case of chromosome duplicat
50 percent chance of inheriting the X-linked	chromosome but usually are not severely affected by the
y Nomura and colleagues in 1994, mapped to a	chromosome by Taguchi and colleagues in 1996.
n, nuclear divisions begin, and a break in a	chromosome can have drastic effects on the viability of
ochromatin organization and formation of the	chromosome centromeres, resulting in slow or stalled an
of Ran requires the presence of regulator of	chromosome condensation 1 (RCC1).
s, but virtually at every mitosis when the Y	chromosome condenses, because it doesn't require pairin
In both organisms, the	chromosome consists of seven exons and six introns and
In 2002, the Y	chromosome consortium published a widely used proposal
No	chromosome count has yet been reported for the species
Based on the reported	chromosome counts, Alvordia includes both diploid and p
ops from the genus Gamolepis on the basis of	chromosome counts.
38-76 times at a single genomic locus on cat	chromosome D2.
sion of the experiment (March 1989) revealed	chromosome damage in root tip cells but no damage to co
ild hemorrhagic tendency associated with 11q	chromosome deletion.
mming, and Edouard van Beneden he elucidated	chromosome distribution during cell division.
showed that a suspected hybrid had undergone	chromosome doubling in the course of evolution, one of
neracy associated with the lack of a partner	chromosome during meiosis.
The hla gene on the S. aureus	chromosome encodes the 293 residue protein monomer, whi
prevents constant loss of important DNA from	chromosome ends.
lted in exceptionally low diversity in the Y	chromosome, estimated to reflect the survival of just t
Since the gene is on the X	chromosome, females are primarily carriers while males
origins open up to duplicate a segment of a	chromosome, followed some time later by another group o
ective of using DNA-sequencing of the male Y	chromosome for indicating kinship between members of ha
upplement the genetic narrative (e.g., the Y	chromosome for describing the history of the male linea
Xq28 is a genetic marker on the X	chromosome found by Dean Hamer and others in 1993.
The	chromosome found to be carrying the gene encoding for N
First, D. radiodurans reconnects some	chromosome fragments through a process called single-st
tance where a child inherits two copies of a	chromosome from one parent, as opposed to one copy from
world seem to leave the men they obtain the	chromosome from with a strange virus that overtakes bot
genes to offspring, there must be a matching	chromosome from the other partner, so at least right aw
phism; the variability occurs as a result of	chromosome fusions or disassociations.
Haplogroup Q1a3a1 is one of only two Y	Chromosome haplogroup strictly associated with the indi
Y	chromosome haplogroups are a frequent topic of discussi
Y	Chromosome Haplogroups all form "family trees" or "phyl
The distribution of Y	chromosome haplotypes within Finland is consistent with
or them arises where two adjacent genes on a	chromosome have very different transcription patterns,
ly across the genome (different regions of a	chromosome have different propensities towards crossove
Males are normally hemizygous for the X	chromosome, having only one copy.
This makes use of the intact	chromosome homologous to the broken one as a template t
uce roughly how far apart two genes are on a	chromosome if they know the frequency of the crossovers
d movement during anaphase of one homologous	chromosome in meiosis or of one chromatid in mitosis.
The extra	chromosome in people with idic(15) can be easily detect
His lab mapped the human Y	chromosome in 1992.
sed a range of insects, she identified the Y	chromosome in the mealworm Tenebrio.
re situated very close to one another on the	chromosome in groups or clusters.
real world in order to obtain a supply of Y	chromosome in the form of semen to keep them alive.
For example, the pattern of X	chromosome inactivation is affected by placental status
ns or features, but may demonstrate skewed X	chromosome inactivation.
They are used in top-down mapping to cut a	chromosome into chunks of these sizes on average.
one copy of a gene, provided by the balancer	chromosome, is often enough to rescue a mutant phenotyp
As the X	chromosome is one of the sex chromosomes (the other bei
The result is that the lagging	chromosome is not incorporated into the nucleus of one
Interestingly, the order of the genes on the	chromosome is the same as the expression of the genes i
complementary DNA strand or in a homologous	chromosome, is available for copying.
The G + C content for the major	chromosome is 64.0%
As a result, every time the	chromosome is copied only 100-200 nucleotides are lost,
drome type 2 occurs when the long arm of the	chromosome is affected (18q).
n region found that, although similar, the X	chromosome is larger than that of samples of M. savii f
In most cases, the abnormal	chromosome is generated in the mother's germ cells; ooc
	Chromosome jumping is a tool of molecular biology that
	Chromosome jumping is used to bypass regions difficult
In	chromosome jumping, the DNA of interest is identified,
le nucleotide polymorphism mutation on the Y	chromosome known as "M168".
means of generating genetic diversity, named	chromosome length polymorphisms (contraction/expansion
and gastrointestinal cancers (Lez), the 8q24	chromosome link to prostate and colon cancer (Haiman, H
The mutation is from G to T. The	chromosome location is 15170096.
n recently discovered from which the somatic	chromosome number and detailed chromosome morphology ha
The	chromosome number is 12, 24 or 36.
It has a	chromosome number of 46, 54 or 108.
r caused by having three copies (trisomy) of	chromosome number 9. It can appear with or without mosa
mber contributed by the female and the human	chromosome number must be 48.
The	chromosome number (karyotype) of Chilocorus stigma vari
m, but is unique within the genus because of	chromosome number and other signatures, including the i
c properties are sex-linked and lie on the W	chromosome of the female.
genes of interest from one organism into the	chromosome of another.
boxB is found twice in the lambda	chromosome, once in each of the two early operons.
In males (who have only one X	chromosome), one altered copy of the gene in each cell
NA can move from position to position on the	chromosome or plasmid by cut-and-paste transposition (a
y may be located on different locations on a	chromosome, or on different chromosomes altogether.
participate in many aspects of higher-order	chromosome organization and dynamics.
l reproducing eukaryotes in which homologous	chromosome pairing, synapse and recombination are uniqu
Identical	chromosome pairs are separated into two different cells
to be born alive with an extra copy of this	chromosome present in all cells (called Full Trisomy 16
A study of haplotypes of the Y	chromosome, published in 2000, addressed the paternal o
teins that the larva requires, and it causes	chromosome puffs (sites of high expression) to form.
Originally, it was held that	chromosome rearrangement would play an important role.
re are four generally accepted states of the	chromosome region involved in Fragile X syndrome which
ction of the total genetic variation in that	chromosome region.
probability of recombination in the proximal	chromosome regions, and thus the introduction of the tr
study of the protein complexes which enable	chromosome replication when living cells divide.
For the	chromosome, see balancer chromosome.
arch focuses on mechanisms and regulation of	chromosome segregation during mitotic cell division.
budding yeast cells exit from mitosis after	chromosome segregation is the removal of the mitotic de
The special	chromosome separation in meiosis, homologous chromosome
propose the expression Genom for the haploid	chromosome set, which, together with the pertinent prot
pecies has a record of the entire kingdom of	chromosome set.
homologous with any member of the normal (A)	chromosome set; morphologically and structurally differ
capable of polyploidy - where more than two	chromosome sets are inherited from the parents.
sues, blood or bone marrow smears, metaphase	chromosome spreads, and fixed cells.
small organisms, histological sections, and	chromosome squashes.
x-loop-helix protein family, is required for	chromosome stability and methionine prototrophy", Cell
The filament searches for the homologous	chromosome, strand invasion occurs where the new chromo
Histone acetylation/deacetylation alters	chromosome structure and affects transcription factor a
Eukaryotic	chromosome structure refers to the levels of packaging
organism and two bi-allelic loci on the same	chromosome such as single-nucleotide polymorphisms (SNP
He then went on to do research on	chromosome synapsis and crossing-over in higher plants,
These maps confirm the presence of	chromosome territories and the spatial proximity of sma
descend in a direct paternal line for the Y	chromosome testing, or a maternal line for the Mitochon
A Y	chromosome that has the YAP mutation is called YAP-posi
he mother carries the affected gene on the X	chromosome that determines the child's gender and passe
ich are the two different copies of the same	chromosome that diploid organisms (like humans) inherit
earch in 2007 suggests another gene on the X	chromosome, that lies close to the androgen receptor ge
ltiple origins of replication on each linear	chromosome that initiate at different times (replicatio
ound in lampbrush chromosomes (see Lampbrush	chromosome) that are characterisitc for the female germ
When the F genes become integrated into the	chromosome, the cell is said to be Hfr (high frequency
In 1961 she described inactivation of the X	chromosome, the Lyon hypothesis explaining how X chromo
This would involve adding a completely new	chromosome to the forty-six others that we already have
tion involves the transfer of genes from one	chromosome to another, nonhomologous chromosome.
mes changed their position, jumping from one	chromosome to another.
Having registered "one	chromosome too many", she failed an early form of the c
evaluate gene amplification, gene deletion,	chromosome translocation, and chromosome number.
cleave DNA at its own site on the homologous	chromosome, triggering the DNA double-stranded break re
During early prophase the broken	chromosome undergoes normal replication, but during met
ently in males as they have a single X and Y	chromosome, unlike females, whose genetics are characte
NRPS genes from three different sites in the	chromosome, using ermEp* for expression of two genes fr
	Chromosome walking can be used from the new jump positi
Thus, sequences not reachable by	chromosome walking can be sequenced.
e used to sequence entire chromosomes (thus,	chromosome walking).
r tools used for the same purpose, including	chromosome walking.
that expresses it, and X-arrestin, after the	chromosome where its gene resides.
gene that codes for PIGA is located on the X	chromosome, which means that only one active copy of th
a set of differences, or markers, on their Y	chromosome, which distinguish them from men in other ha
a mutation in the MEFV gene on the sixteenth	chromosome, which codes for a protein called pyrin or m
entical copies of DNA making up a duplicated	chromosome, which are joined at their centromeres, for
Furthermore all ten men who carry the	chromosome with mutation A are the direct male line des
Genetic males (has one X and one Y	chromosome) with androgen insensitivity syndrome is res
value are announced to represent a part of a	chromosome with an anomaly (an abnormal copy number sta
of a daughter receiving two copies of the X	chromosome with the defective gene is 50%, since daught
This gene maps to the candidate region on	chromosome X for incontinentia pigmenti.
sed by mutations in the ALA synthase gene on	chromosome X, whereas no diseases are known to be cause
he red blood cell form is coded by a gene on	chromosome x, whereas the other form is coded by a gene
proximity to another family member, TLR7, on	chromosome X.
ity to another family member, TLR8, on human	chromosome X.
In humans, gene CLCN5 is located on	chromosome Xp11.22 and has a 2238-bp coding sequence th
It is mapped to	chromosome Xq28 in a cluster of genes encoding alpha 3,
The human gene for IKBKG is located on	chromosome Xq28.

共起表現

「Chromosome」の共起表現(1語右で並び替え) - Weblio英語共起表現検索

「Chromosome」の共起表現一覧(1語右で並び替え)