「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. |
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