「Pore」の共起表現一覧(1語右で並び替え)
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uble, and the oviducts open by a median ventral | pore about the middle of the body; in this region th |
s are identifiably pseudophyllid as the genital | pore and uterine pore are located on the mid-ventral |
The α subunit forms the ion conduction | pore and the β subunit contributes to channel gating |
Its interior is close-packed with no central | pore and contains both hydrophobic residues and char |
ppermost permafrost layers and mainly comprises | pore and segregated ice in Earth material. |
e Soccer in 2011, along with Steve Cronin, Ryan | Pore and Eddie Johnson. |
ervated, and sensory endings around the genital | pore are more plentiful than other areas. |
Richard Le | Pore as Staff Sergeant Kemler, boom operator on KC-1 |
s well as magnesium ions, that plug the channel | pore at positive potentials, resulting in a decrease |
lin D is thought to regulate the opening of the | pore because cyclosporin A (CsA), which binds to CyP |
decreases over subsequent cycles as a result of | pore blockages and damage to adsorption sites by the |
Most likely, apamin acts as a | pore blocker, although residues both inside and outs |
ng nucleoporins and is localized to the nuclear | pore central plug. |
Main article: Nuclear | pore complex |
eoporins are the main components of the nuclear | pore complex in eukaryotic cells. |
PIC1/SUMO-1, which are associated with nuclear | pore complex also associate with nuclear dots. |
eads to its trafficking from cytosol to nuclear | pore complex . |
The nuclear | pore complex is a massive structure that extends acr |
Aladin is a component of the nuclear | pore complex. |
ocation of RNA and proteins through the nuclear | pore complex. |
er eukaryotic proteins that make up the nuclear | pore complex. |
portin heterodimer-bound protein to the nuclear | pore complex. |
The nuclear | pore complexes are embedded in the nuclear lamina. |
The presence of several million | pore complexes in the oocyte nuclear membrane and th |
is depleted p62 fails to assemble with nuclear | pore complexes. |
he cytosol into the nucleus through the nuclear | pore complexes. |
hibit different functional properties including | pore conductance, size selectivity, charge selectivi |
S is introduced, in cement mixtures control air | pore content and prevent agglomeration of powders du |
The somatal | pore controls the diffusion of CO2 into the leaves t |
d is the average, or effective | pore diameter [length]. |
brane can also be classified according to their | pore diameter. |
The resultant size of the | pore directly affects what molecules are able to pas |
A K+ channel | pore domain (S5, selectivity filter, and S6). |
Inward rectifiers also differ from tandem | pore domain potassium channels, which are largely re |
and c) that form part of the proton-conducting | pore, each containing a buried glutamic acid residue |
Basins with different | pore fluid chemistry will have differing hydrostatic |
rals at grain-to-grain contacts into an aqueous | pore fluid in areas of relatively high stress and ei |
urce rock are first expelled , along with other | pore fluids, due to the effects of internal source r |
nds to gp41 preventing the creation of an entry | pore for the capsid of the virus, keeping it out of |
ently, however, researchers found evidence that | pore formation is not necessarily linked to cell dea |
(IPR005639) involved in membrane insertion and | pore formation; a beta-sheet central domain involved |
s aureus and the first identified member of the | pore forming beta-barrel toxin family. |
nting the mitochondrial permeability transition | pore from opening, thus inhibiting cytochrome c rele |
aland Gasteromycetes (puffballs), Polyporaceae ( | pore fungi), Thelephoraceae (crust fungi), and Uredi |
They are dehiscent through the large basal | pore, green to brownish purple [to magenta], spheric |
transmembrane alpha helices, numbered S1-S6, a | pore helix situated between S5 and S6, and cytoplasm |
e longest piece is entitled ‘A complaint of the | pore husbandmen in meter.' |
al assembly into cyclical hexamers with a small | pore in the center. |
tide sequence, which allows for the size of the | pore in the protein to differ between aquaporins. |
large and kidney-shaped, reaching form the male | pore in segment X into segment XI. |
he conformational change that opens the channel | pore in response to a displacement in membrane poten |
first general description of the K+ ion channel | pore, including the fundamental ideas of a selectivi |
es are micro-organisms that can live within the | pore interstices of sedimentary and even igneous (if |
ne-spanning alpha helixes (M1, M2, M3, M4), the | pore is primarily formed by M2 of the two alpha subu |
ding site) compared to where the ion conduction | pore is located. |
Inflated in the middle of each | pore, it is quite crispy yet spongy. |
he Australian C. nicolli, which has the genital | pore located further to the front. |
acellular loop (known as 'the turret') and 'the | pore loop', which begins and ends extracellularly bu |
intermediate region of the receptor, within the | pore lumen, valine and leucine residues (Val 255 and |
hat activated Bax and/or Bak form an oligomeric | pore, MAC in the outer membrane. |
innamon brown, smooth and ellipsoid with a germ | pore, measuring 8 x 5 micrometers. |
Aerating water by means of fine | pore membrane diffuser |
a protein which is only slightly smaller than a | pore might enter the pore but does not easily leave |
The | pore of sodium channels contains a selectivity filte |
It induces mitochondrial permeability | pore opening and inhibits respiration by interfering |
The | pore opening raises the permeability of the mitochon |
These conformational changes could also lead to | pore opening. |
to a functional disorder, so the opening of the | pore plays an important role in cell death. |
As with all matters relating to | pore pressure analysis, the method cannot be applied |
nge in applied stress (effective stress - σe or | pore pressure - p) per unit volume. |
y dc-exponent plots by examining multiple other | pore pressure indicators. |
y suddenly) becomes less than the formation, or | pore, pressure in a permeable section downhole, and |
he dam site, and the possibility that the added | pore pressure of the deeper water could reactivate t |
t-range interaction with the negatively charged | pore region of potassium-channels leading to channel |
C287Y and G293R are both located in the | pore region of domain 1 and are present in a single |
ning segments and a predicted calcium-selective | pore region. |
However, research has shown that the MPT | pore remains closed during ischemia, but opens once |
Aplysina fulva, a scattered | pore rope sponge |
For the mitochondrial | pore, see mitochondrial permeability transition. |
by | pore Shakerlaye. |
Correctly used, wheel filters with at least | pore size 0.5 µm (e.g. |
The nominal | pore size of the membrane is typically about 1 nanom |
A typical microfiltration membrane | pore size range is 0.1 to 10 micrometres (µm). |
nd only a few inches above the water table when | pore size is large. |
Pore size is controlled by controlling the concentra | |
pores provide greater surface area while larger | pore size has better kinetics, especially for larger |
If | pore size is small and relatively uniform, it is pos |
e from 5 to 2,000 kiloDalton due to the uniform | pore size provided by the polyacrylamide gel. |
The bag has a characteristic | pore size that allows small particles, like water or |
the material which is smaller than the membrane | pore size passes through the membrane as permeate or |
ng to IUPAC, there are three different types of | pore size classifications: microporous (dp < 2 nm), |
But the variable | pore size of the agarose causes a potential upper si |
ple is drawn through a membrane filter (0.45 µm | pore size) through the use of a vacuum pump. |
ious factors including membrane sizes, membrane | pore size, temperature, operating pressure and membr |
In soils with a wide range in | pore size, the unsaturated zone can be several times |
They do not have a uniform | pore size, but are optimal for electrophoresis of pr |
illary rise because of the presence of a mix in | pore size. |
It indicates the | pore space within the rock structure. |
etimes, under the right conditions, some of the | pore space in the rock is occupied by other liquids |
is not a direct or physical measurement of the | pore space but rather an extrapolation from other dr |
ontains an open framework of particles with the | pore space being usually filled with water. |
njected into a bituminous coal bed would occupy | pore space and also adsorb onto the carbon in the co |
3.6 trillion cubic feet of gas filled a lot of | pore space in the source rocks - the field was part |
ere there is gas instead of water or oil in the | pore space, the two porosity logs separate, to form |
The oil and gas resides within this | pore space. |
t coloured areas new mineral growth has reduced | pore space. |
Above a capillary fringe, | pore spaces have air in them too. |
Blue epoxy fills | pore spaces. |
lying horizons, forming tiny quartz crystals in | pore spaces. |
8 x 7-10 µm, elliptical, smooth, with an apical | pore, spore print black. |
either by macromolecular adsorption to internal | pore structure of membrane, or aggregation of protei |
As these fruiting bodies age, the | pore surface turns from yellow to greenish yellow, t |
r more across with a characteristic pale yellow | pore surface. |
ations flow into a more constricted part of the | pore that is 0.3 by 0.5 nm wide, which is just large |
osed of five subunits arranged around a central | pore that opens to allow ions to pass through. |
ts depends on the chemistry of the water in the | pore, the surrounding mineralogy, and the temperatur |
opening, the electrical conductance of the ion | pore, the activation voltage, and the activation dur |
e visible and a truncate apex with a broad germ | pore, thick walled, and dingy yellow brown. |
in a geologic model incorporate an estimate of | pore throat size, the densities of the fluids, and t |
It is a doughnut shaped | pore through the membrane with 3 major subunits (het |
nit has 24 transmembrane segments and forms the | pore through which ions pass into the cell. |
others of this class, the α1 subunit forms the | pore through which calcium enters the cell and deter |
arranged in such a way that there is a central | pore through which ions can travel down their electr |
ge-dependent and has four subunits which form a | pore through which ions flow, carrying type-A potass |
ntical alpha subunits, which form the channel's | pore through the plasma membrane. |
its fit together and form a ring with a central | pore through which cell contents leak and which acts |
The dimer was thought to be a gated | pore through which ADP and ATP were exchanged betwee |
nit that acts as the channel gate, blocking the | pore until the channel is bound by ligand. |
The | pore velocity (v) is related to the Darcy flux (q) b |
The | pore velocity would be the velocity a conservative t |
channel pore-forming α-subunit by blocking the | pore via a bimolecular reaction. |
f its highly porous structure, large accessible | pore volume with fully exposed edges and faces of th |
The location of the ionic | pore was identified, made up of the second transmemb |
ive theory is that basal till, weakened by high | pore water pressure, deformed upwards into parallel |
e top of the salt when the halite is removed by | pore waters. |
l the nucleocapsids make their way to a nuclear | pore where the virus genome is released and transloc |
ptate and have a pronounced sigmoid germination | pore, which enables their use in paleoecology as a p |
altered but simply shift position, opening up a | pore which acts as the conductive pathway through th |
Pore wing ochreous white irrorated with red-brown, t | |
Pore wing: narrow subbasal and outer cellular transv | |
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