コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 activation of SERCA (sarcoplasmic reticulum calcium ATPase).
2 mban, and sarcoplasmic/endoplasmic reticulum calcium ATPase).
3 ban in regulating the sarcoplasmic reticulum calcium ATPase.
4 um pump isoform 1 (PMCA1), a plasma membrane calcium ATPase.
5 (+)-ATPase, but failed to have any effect on calcium ATPase.
6 ole as a regulator of sarcoplasmic reticulum calcium ATPase.
7 e) and stimulation of sarcoplasmic reticulum calcium ATPase.
8 itor of the endoplasmic reticulum-associated calcium-ATPase.
9 ilin and the Ca(2+) ATPase secretory pathway calcium ATPase 1 (SPCA1) in the sorting of soluble secre
10 ATP-powered calcium pump (secretory pathway calcium ATPase 1 [SPCA1]) encoded by the ATP2C1 gene in
12 nsitivity to pain stimuli in plasma membrane calcium ATPase 2 (PMCA2) heterozygous mice: a possible m
14 elevated sarcoplasmic/endoplasmic reticulum calcium ATPase 2 (SERCA2a) expression, and faster lusitr
15 , whereas sarcoplasmic endoplasmic reticular calcium ATPase 2 abundance and sarcoplasmic reticulum Ca
18 ncreased SERCA2 (Sarco/Endoplasmic Reticulum Calcium ATPase 2) expression, which correlated with a le
20 e, as was sarcoplasmic endoplasmic reticular calcium ATPase 2/phospholamban protein ratio (45% reduce
22 he expression of sarco/endoplasmic reticulum calcium ATPase-2 (SERCA2), a protein that transports cal
23 izes with sarcoplasmic/endoplasmic reticulum calcium/ATPase-2 and calreticulin at membrane-bound cyto
24 ting the cardiac sarco/endoplasmic reticulum calcium ATPase 2a (SERCA2a) in the regulation of overall
26 ptor 2, Ca(V)1.2, and sarcoplasmic reticulum calcium ATPase 2a, by attenuating transverse aortic cons
27 horylates sarcoplasmic/endoplasmic reticulum calcium-ATPase 2a (SERCA2a) and accelerates calcium re-u
28 creases in homogenate sarcoplasmic reticulum calcium ATPase-2a (SERCA2a) activity, protein density, a
29 fibrosis, normalized sarcoplasmic reticulum calcium ATPase-2a activity and expression of UCP-2 and U
30 nterstitial fibrosis, sarcoplasmic reticulum calcium ATPase-2a activity, expression of mitochondria u
31 s novel RyR2/PLN/sarco/endoplasmic reticulum calcium ATPase-2a complex was also identified in human a
33 eostasis through preserving sarcoplasmic/EnR calcium ATPase 2b (SERCA2b) function in AI-resistant cel
35 oach, we discovered that the plasma membrane calcium ATPase 4 (PMCA4) is required for TNF-induced cel
36 form of the Ca(2+)-extruding plasma membrane calcium ATPase 4 (PMCA4) pump in Jurkat T cells unexpect
38 explored the role played by plasma membrane calcium ATPase-4 (PMCA4) and its alternative splice vari
39 e NADPH oxidase RBOHD, ABC-transporter PEN3, calcium-ATPase ACA8, noncanonical Galpha protein XLG2 an
42 RS and the decrease of Na(+)-K(+)-ATPase and calcium ATPase activities in retinas of diabetic animals
45 e calcium channel/sarcoendoplasmic reticulum calcium-ATPase activity and cardiac tissue fibrosis.
47 +) channels, N-methyl-d-aspartate receptors, calcium ATPase, adenomatous polyposis coli, and PTEN tum
49 SERCA2a (sarcoplasmic-endoplasmic reticulum calcium ATPase), along with an increased BNIP3 expressio
51 of an intracellular calcium gradient by the calcium ATPase and processing within the Golgi compartme
52 e to mitochondria and sarcoplasmic reticulum calcium ATPase and restored mitochondrial and cardiac fu
55 tectable abundance of sarcoplasmic reticulum calcium-ATPase and sodium calcium exchanger were greater
56 ion of SERCA1a [sarco(endo)plasmic reticulum calcium ATPase] and SERCA2a calcium pump isoforms by pho
58 estrated by the preferential localization of calcium ATPases at one cell pole, in a ring pattern, fac
60 nce ryanodine and sarcoendoplasmic reticulum calcium-ATPase blockers altered the time course and magn
61 and cardiac muscle, where it inhibits SERCA (calcium ATPase) by lowering its apparent Ca2+ affinity i
64 of the sarcoplasmic or endoplasmic reticulum calcium ATPase family that pumps Ca(2+) into the ER, res
66 ) vector carrying the sarcoplasmic reticulum calcium ATPase gene (AAV1/SERCA2a) in patients with adva
67 The sodium-calcium exchanger and sarcolemmal calcium ATPase had a lower activity and the exchanger wa
68 idue integral membrane protein that inhibits calcium ATPase in the cardiac sarcoplasmic reticulum.
69 etes-induced reductions in Na+-K+-ATPase and calcium ATPase in the retina are mediated in large part
70 oding beta1- and beta2-adrenergic receptors, calcium ATPase in the sarcoplasmic reticulum, and alpha-
72 gargin, a sarcoplasmic/endoplasmic reticulum calcium ATPase inhibitor that induces ER stress, underwe
73 IP3), the sarcoplasmic-endoplasmic reticulum calcium ATPase inhibitor, thapsigargin, and the calcium
74 s were induced to undergo apoptosis with the calcium ATPase inhibitor, thapsigargin, or the glucocort
75 with the sarcoplasmic-endoplasmic reticulum calcium ATPase inhibitor, thapsigargin, was completely b
76 channel release activator (caffeine) and SR calcium-ATPase inhibitor (cyclopiazonic acid), consisten
79 a decrease in the levels of plasma membrane calcium ATPase isoform 2 (PMCA2), a major pump extruding
80 l as an activation of sarcoplasmic reticulum calcium ATPase isoform 2 and citrate synthase, was evide
81 ntified the calcium exporter plasma membrane calcium ATPase isoform 4 (PMCA4) as the interaction part
82 gin-resistant activity was a plasma membrane calcium ATPase isoform in transit to the plasma membrane
85 Inhibition of sarco-endoplasmic reticulum calcium ATPase led to store depletion and dramatic redis
86 ession of sarcoplasmic/endoplasmic reticular calcium ATPase, less stored calcium, smaller calcium tra
87 ionophore, and thapsigargin, an inhibitor of calcium ATPase, mimicked the ET-1-stimulated PGHS-2 mRNA
88 se had an increase in sarcoplasmic-reticulum calcium ATPase mRNA and alpha-myosin heavy chain mRNA an
90 malarial exerts its activity by inhibiting a calcium ATPase (PfATP6) that is most similar to sarcopla
91 ntly described by our group, plasma membrane calcium ATPase (PMCA) activity can be regulated by the a
93 H+ uptake by the ubiquitous plasma membrane calcium ATPase (PMCA) has not been measured in any neuro
97 lar calcium ([Ca2+](i)), the plasma-membrane calcium-ATPase (PMCA) may actively contribute to the gen
98 hibition of isoform 4 of the plasma membrane calcium ATPase (PMCA4) prevents chronic remodelling and
100 ) extrusion by high-affinity plasma membrane calcium ATPases (PMCAs) is a principal mechanism for the
105 inhibitor of the Sarco/Endoplasmic Reticulum Calcium ATPase pump (SERCA), but unlike thapsigargin, ar
106 2 trial targeting the sarcoplasmic reticulum calcium ATPase pump (SERCA2a), along with the start of m
108 bling the sarcoplasmic/endoplasmic reticulum calcium ATPase pump-leak system and suggest that it is i
113 /l of the SERCA (sarco/endoplasmic reticulum calcium ATPase) pump inhibitor thapsigargin and reduced
114 ceptors, and calcium reuptake and efflux via calcium-ATPase pumps and sodium-calcium exchangers.
116 tions of regulatory membrane proteins of the calcium ATPase SERCA, namely sarcolipin and phospholamba
118 ion of CLNX with sarco endoplasmic reticulum calcium ATPase (SERCA) 2b results in inhibition of intra
119 sequence of sarco endoplasmic reticulum (ER) calcium ATPase (SERCA) 2b to inhibit Ca2+ oscillations.
120 tightly regulated, and the sarco-endoplasmic calcium ATPase (SERCA) actively pumps calcium from the c
122 ver, high sarcoplasmic/endoplasmic reticulum calcium ATPase (SERCA) activity can also decrease local
123 used by impaired sarco/endoplasmic reticulum calcium ATPase (SERCA) activity due to altered phospholi
126 plasmic reticulum (ER) Ca(2+) pump sarco-/ER calcium ATPase (SERCA) and the single transmembrane-solu
127 structure, and sarco(endo)plasmic reticulum calcium ATPase (SERCA) binding were quantified by fluore
129 The cardiac sarco/endoplasmic reticulum calcium ATPase (SERCA) establishes the intracellular cal
130 hat a decline in sarco/endoplasmic reticulum calcium ATPase (SERCA) function occurs with advancing ag
131 ose, a blocker of sarcoendoplasmic reticulum calcium ATPase (SERCA) had little effect on OCR despite
132 activity of the sarco(endo)plasmic reticulum calcium ATPase (SERCA) in cardiac myocytes is modulated
137 ncreasing sarcoplasmic/endoplasmic reticulum calcium ATPase (SERCA) pump activity enhances sarcoplasm
138 te a role for the sarcoendoplasmic reticulum calcium ATPase (SERCA) pump in the regulation of endopla
140 sP(3)R)], sarcoplasmic/endoplasmic reticulum calcium ATPase (SERCA) pumps, bradykinin receptors, and
142 ibitor of sarcoplasmic endoplasmic reticulum calcium ATPase (SERCA)) while 1-EBIO (300 microM, an IKC
143 uding the sarcoplasmic/endoplasmic reticulum calcium ATPase (SERCA), calreticulin, and calsequestrin,
144 onists of sarcoplasmic/endoplasmic reticulum calcium ATPase (SERCA), cyclopiazonic acid, and thapsiga
147 ylation activates the sarcoplasmic reticulum calcium ATPase (SERCA), which reduces cytoplasmic Ca(2+)
155 Reduced expression of sarcoplasmic reticulum calcium ATPase (SERCA)2 and other genes in the adult car
156 hibitors of sarco- and endoplasmic reticulum calcium-ATPase (SERCA) have important therapeutic value
157 symmetric distributions of RyRs and sarco/ER calcium-ATPase (SERCA) pumps that we predict using a com
158 ed mild ER stress and inhibition of sarco/ER calcium-ATPase (SERCA) without significant increase in s
161 skeletal muscle sarco(endo)plasmic reticulum calcium ATPase (SERCA1) gene is transactivated as early
163 The stimulation of sarcoplasmic reticulum calcium ATPase SERCA2a emerged as a novel therapeutic st
164 own-regulation of the sarcoplasmic reticulum calcium ATPase (SERCA2a) by GSK-3beta, acting at the lev
165 ession of the cardiac sarcoplasmic reticulum calcium ATPase (SERCA2a), a critical pump regulating cal
169 or actin and P-type ATPase secretory pathway calcium ATPase (SPCA)-dependent sorting of secretory pro
170 ltiazem), ryanodine and inhibitors of the SR calcium ATPase (thapsigargin, cyclopiazonic acid) were w
171 f IRS-1 and the sarco(endo)plasmic reticulum calcium ATPase, the calcium pump of the endoplasmic reti
172 ine changes in expression of plasma membrane calcium ATPase type 2 (PMCA2), a high-affinity calcium e
174 revealed that PDE3A associates with both SR calcium ATPase type 2a and phospholamban in a complex th
177 calcium channel, sarco/endoplasmic reticulum calcium-ATPase type 2a, Kv1.4, and Kv4.3 were downregula
180 nto contact with the PLB binding site on the calcium ATPase, while the presence of twisting motions a
181 s similar to that for phosphorylation of the calcium ATPase with and without initial incubation with
182 nhibiting sarcoplasmic/endoplasmic reticulum calcium ATPase with cyclopiazonic acid or thapsigargin),