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「ca 2」の共起表現一覧(1語右で並び替え)

該当件数 : 120



TsTx-IV blocks Ca2+ activated K+ channels of high conductance.
-Ca2+ activated K+ Channel affecting peptides: TsTX-
ied by compound screening to be an activator of Ca2+ activated Cl- channels (CaCCs), thus a potentia
potassium channels: the voltage-activated, the Ca2+- activated and the inward-rectifier potassium c
Its hormone binds to a receptor, and Ca2+ activates a protein, calmodulin, and the comple
This protein has a Ca2+ affinity 20- to 100-fold higher than the other
Hard water has high concentrations of Ca2+ and Mg2+ ions.
The hormone participates in calcium ( Ca2+) and phosphorus metabolism.
most important ions in the 5th group are Ba2+, Ca2+, and Sr2+.
release (exocytosis) is dependent upon calcium Ca2+ and is a presynaptic response.
ranes in response to physiological increases in Ca2+ and selectively hydrolyses arachidonyl phosphol
the annexin family of evolutionarily conserved Ca2+ and phospholipid binding proteins.
Furthermore, the KCa1 family is both Ca2+ and voltage activated, further complicating the
, for the most part, activated by intracellular Ca2+ and contains 8 members.
inorganic salts (mostly Na+, Cl-, K+, Mg2+, and Ca2+), and organic compounds (mostly carbohydrates,
IPA interaction with the BK channel enhances Ca2+ and / or voltage sensitivity of the α subunit o
t known formation constant for the complexation Ca2+ and Gd3+ ions.
tivation of TRPC6 induces the entry of calcium ( Ca2+) and sodium (Na+) into the cell, which results
e humite series Mg2+ is replaced by Fe2+, Mn2+, Ca2+ and Zn2+ in that order of abundance, though Mg2
selective for Mn2+, somewhat less selective for Ca2+ and Mg2+, much less selective for Sr2+, and eve
with divalent metallic cations such as calcium ( Ca2+) and iron(II) (Fe2+) to form crystals of the co
ished: the stoichiometry of exchange is 3 Na+:1 Ca2+ and the exchanger is electrogenic and voltage-s
Chelators for Ca2+ are well established, have high affinity for th
of the calcium, and ionic solutions of calcium ( Ca2+) are colorless as well.
ex is made up of tissue factor, factor VII, and Ca2+ as an activating ion.
lar biochemistry of granins includes binding of Ca2+, ATP and catecholamines (epinephrine, norepinep
Plasma membrane Ca2+ ATPase (PMCA)
Sarcoplasmic reticulum Ca2+ ATPase (SERCA)
The plasma membrane Ca2+ ATPase (PMCA) is a transport protein in the pla
which stands for sarco / endoplasmic reticulum Ca2+ ATPase.
Beauvericin ( Ca2+, Ba2+)
of Ca2+-mediated events occur when the released Ca2+ binds to and activates the regulatory protein c
k to this surface through their Gla domain with Ca2+ bridges.
(R3, R4), Rodalies Barcelona line R7, Ca1, Ca2, Ca3, Ca4, Ca6, R42)
Ca2+, calcium is a component of bones and teeth.
Constitutively high levels of mitochondrial Ca2+ cause inappropriate MPTP opening leading to a d
ashout could only moderately reverse the R-type Ca2+ channel inhibition after treatment with 200 nM
is stimulatory to adenylyl cyclase, acts on the Ca2+ channel directly as an effector.
R) is a membrane glycoprotein complex acting as Ca2+ channel activated by inositol trisphosphate (In
fer into rabbit erythrocytes (red blood cells), Ca2+ channel antagonistic action, α1 adrenergic bloc
ha1E, R-type) channel (strong affinity), L-type Ca2+ channel, P/Q type Ca2+ channel, Na+ channel .
asmic reticulum and mitochondria, help open the Ca2+ channel.
s direct gating has also been found in specific Ca2+ channels in the heart and skeletal muscle T tub
own that it can also inhibit L-type or P/Q type Ca2+ channels and incompletely block Na+ channels.
g mobilization of calcium ions through specific Ca2+ channels into the cytosol.
es and associated sarcolemmal vesicles in which Ca2+ channels are able to survive and function in th
n cAMP in the cell, inhibition of voltage-gated Ca2+ channels, and efflux of K+, in general, leading
strong voltage reverses the blocking of R-type Ca2+ channels.
Fluo-4 is used to measure calcium ( Ca2+) concentrations inside living cells, and is oft
cation is primarily controlled by the change in Ca2+ concentrations, causing excitability within the
e together the main regulators of intracellular Ca2+ concentrations.
leased is referred to as Ca2+-release-activated Ca2+ current (ICRAC).
SNX-482 inhibits native R-type Ca2+ currents at weak nanomolar concentrations in ra
However, it does not influence R-type Ca2+ currents at concentrations of 200-500 nM in sev
If a cell has Na+ or Ca2+ currents at rest, then inhibition of those curr
synaptotagmin, among others, in the presence of Ca2+, displaces complexin allowing the SNARE protein
large transmembrane electrochemical gradient of Ca2+ driving the entry of the ion into cells, yet it
ium from the endoplasmic reticulum will lead to Ca2+ entry from outside the cell by activation of "S
l loop, diuretics cause an increase in Mg2+ and Ca2+ excretion.
vated by voltage, while others are activated by Ca2+, extracellular ligands, and pH among other modu
he addition of another required factor, such as Ca2+ for the photoprotein aequorin.
tually it contains only divalent ions, Mg2+ and Ca2+ for cation exchange resins, and SO42- for anion
this is because of a biological requirement for Ca2+ for the protein to fold into the correct form.
In fact, the PMCA is involved in removing Ca2+ from all eukaryotic cells.
nant second messenger leading to the release of Ca2+ from intracellular store sites.
gradient generated by the Na+-K+ pump to remove Ca2+ from the intracellular space, slowing down the
ology, two photon laser scanning microscopy and Ca2+ imaging have been used to study activity at the
ditionally, honokiol increases free cytoplasmic Ca2+ in rat cortical neurons.
The Ca2+ in turn activates chloride channels, causing ef
It increases the level of calcium ( Ca2+) in the blood by (1) increasing the uptake of c
IP3 is one of the most effective inducer of Ca2+ increase from cytoplasmic pools and from outsid
bited by Rhoa and Rho kinase, components of the Ca2+ independent pathway for maintaining muscle cont
gonists reversibly block NMDA receptor-mediated Ca2+ influx and thus may inhibit excitotoxicity.
nerves to their terminals where they initiate a Ca2+ influx and the release of acetylcholine (ACh).
Since it transports Ca2+ into the extracellular space, the PMCA is also
y a key role in the modulation of intracellular Ca2+ involved in presynaptic neurotransmitter releas
leads to the closure of cGMP-regulated Na+ and Ca2+ ion channels and a hyperpolarized membrane pote
ginate forms an adhesive gel in the presence of Ca2+ ion.
Ca2+ ions are a key component to muscle contraction.
The increase in intracellular Ca2+ ions induces the RYR to release even more Ca2+
is opening allows for an influx of both Na+ and Ca2+ ions into the cell, thus depolarizing it.
channels are activated and cause the influx of Ca2+ ions over the membrane and to the release of ca
lectroneutrality requires that the transport of Ca2+ ions catalyzed by the intestinal epithelial cel
Ca2+ ions can damage cells if they enter in excessiv
nlike most TRP channels, TRPV6 is selective for Ca2+ ions, similarly to its close homologue, TRPV5,
nges of electric field, pH, or concentration of Ca2+ ions.
inlet for the action potential near a source of Ca2+ ions.
(6290) 1985 CA2 is a main-belt minor planet.
For GnRH, TRH and GHRH the increase in Ca2+ is achieved by the releasing hormone coupling a
Since Ca2+ is actively reabsorbed in the distal convoluted
Calcium ( Ca2+) is often considered part of the BMP, though, b
The effects of Ca2+ is also remarkable: it cooperates with DAG in a
is dye to cell types where the resting level of Ca2+ is < 1 μM and does not vary with the experiment
d cations, to cation selective allowing passage Ca2+, K+ and Na+, a highly selective K+ channels.
used in laboratories to increase intracellular Ca2+ levels in intact cells.
result of the process is increased cytoplasmic Ca2+ levels via the direct pathway described above a
higher concentrations of divalent ions (SO42-, Ca2+, Mg2+) and lower Na+ and Cl- than the surroundi
obscures the part of the molecule that chelates Ca2+, Mg2+, Zn2+ and other ions.
ls, which play critical roles in proliferation, Ca2+ mobilization and cell differentiation.
It is involved in B-cell receptor induced Ca2+ mobilization from intracellular stores and prom
in part through the regulation of intracellular Ca2+ mobilization.
OX2 receptor activation, such as intracellular Ca2+ mobilization.
t each of the 3 positions have an impact on the Ca2+ permeability of the channel
Rendered image of the Ca2+ pump
connections to R1 and R2 Rodalies trains and to Ca2 regional trains.
he sarcoplasmic reticulum may cause spontaneous Ca2+ release during repolarization, causing the rele
se) the intracellular concentration of calcium ( Ca2+), resulting in vesicle fusion of the respective
by synaptobrevin, syntaxin and SNAP-25) and the Ca2+ sensor synaptotagmin.
ell as increasing the overall complexity of the Ca2+ signaling mechanism.
conversion of external stimuli to intracellular Ca2+ signals characterized by complex patterns relat
and affect the flow of potassium (K+), calcium ( Ca2+), sodium (Na+), and chloride (Cl-) across the p
c inhibitor of Ca2+-ATPase in the intracellular Ca2+ storage sites.
he positions of the ions are reversed: calcium ( Ca2+) take the oxide (O2−) positions and nitride ion
nts for the sustained transport of ions such as Ca2+ that controls T lymphocyte (T cell) proliferati
Na+ through Na+ channels, or Ca2+ through Ca2+ channels.
Na+ through Na+ channels or Ca2+ through Ca2+ channels, inhibits hyperpolarizati
r disease state by increasing the intracellular Ca2+ to increase the contractility cycling rates.
ns as a positive regulator of the transcellular Ca2+ transport pathway, and it plays a role in the i
For example, Ca2+ waves and oscillations.
It is vital for regulating the amount of Ca2+ within cells.
                                                                                                    


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