ライフサイエンスコーパス: calcium

1 in which activates CaMKII in the presence of calcium.

2 ANXA2), with high affinity at high levels of calcium.

3 f small foci of intracranial hemorrhage from calcium.

4 rupting the mutant thin filament response to calcium.

5 milarly tightened by buffering intracellular calcium.

6 Moreover, the 22q11DS calcium abnormality could also be restored by applicatio

7 Vitamin D has a key role in stimulating calcium absorption from the gut and promoting skeletal h

8 shots of ryanodine receptor type 1 (RyR1), a calcium-activated calcium channel engaged in the binding

9 Purkinje-cell-specific knockout (KO) of the calcium-activated K+ channel SK2 (L7-SK2) show intact ve

10 nucleotide-gated (HCN) and small conductance calcium-activated potassium (SK) channels.

11 Among the altered genes, an increase of the calcium-activated potassium channel Kcnn2 in the motor c

12 Population calcium activity of dorsomedial iMSNs was disrupted in m

13 Calcium alone or in combination with vitamin D may reduc

14 f the neck because of its ability to resolve calcium and create multiplanar reconstructions.

15 g two-photon microscopy to monitor astrocyte calcium and electrocorticogram to record neuronal networ

16 justing for potential confounders, including calcium and fiber intake (P for trend = 0.03), and were

17 association between admission serum ionized calcium and in-hospital AKI, with nadir in-hospital AKI

18 any synaptic modification in 1.3 and 1.5 mM calcium and lead to depression in 1.8 mM.

19 of reactive oxygen species on mitochondrial calcium and mitochondria-dependent apoptosis in cardiac

20 /cholinergic/dopaminergic synaptic function, calcium and PI3K-AKT signaling.

21 t is widely hypothesized that an increase in calcium and reactive oxygen species activate a large con

22 ulate metabolism and ATP production, such as calcium and reactive oxygen species, are also key regula

23 ns, micro- and macronutrients, milk contains calcium and the insulin-like growth factor-1 that are of

24 No interactions between calcium and vitamin D in relation to all-cause mortality

25 In order to study the bioavailability of calcium and vitamin D(3), the W/O/W double emulsions wer

26 lcified segment length was 47.9 +/- 18.8 mm, calcium angle was 292.5 +/- 76.5 degrees , and calcium t

27 odulation of signaling cascades that rely on calcium as a transduction mechanism.

28 the environment because it precipitates with calcium as low-solubility apatite minerals.

29 ing oil core mode particles contained, e.g., calcium as well as agglomerated soot mode particles.

30 activity of the sarco(endo)plasmic reticulum calcium ATPase (SERCA) in cardiac myocytes is modulated

31 ATP-powered calcium pump (secretory pathway calcium ATPase 1 [SPCA1]) encoded by the ATP2C1 gene in

32 horylates sarcoplasmic/endoplasmic reticulum calcium-ATPase 2a (SERCA2a) and accelerates calcium re-u

33 imulations, we demonstrate that cbEGF domain calcium binding decreases under mechanical stress (i.e.

34 response to environmental stresses, in their calcium binding properties, and in their conformational

35 evelopmental stages of other markers such as calcium binding proteins and neuropeptides, helped the i

36 Secretagogin (SCGN) is a recently discovered calcium-binding protein belonging to the group of EF-han

37 The S100 calcium-binding proteins A8 (S100A8) and A9 (S100A9) eme

38 ng genes for calcium management (calmodulin, calcium-binding proteins), pH regulation (V-type proton

39 ng protein belonging to the group of EF-hand calcium-binding proteins.

40 receptor signaling, while mutagenesis of the calcium-binding site abolishes Gpr126 function in vivo.

41 stretch-elicited X-ROS primes intracellular calcium (Ca(2+) ) channels for synchronized activation i

42 ted insulin secretion (GSIS) is regulated by calcium (Ca(2+) ) entry into pancreatic beta-cells throu

43 Calcium (Ca(2+) ) transients were measured in isolated c

44 these granules is dependent on intracellular calcium (Ca(2+)) signals.

45 nisms that control mobilization of cytosolic calcium [Ca(2+)](i) are key for regulation of numerous e

46 For example, a change in calcium (Ca2+) concentration in a cell in the present ex

47 ther, these results show that the binding of calcium-calmodulin to the C-terminus has long-range allo

48 estigations, we show that in the presence of calcium-calmodulin, the distance across the two GluN1 su

49 The calcium-calmodulin-dependent protein kinase kinase-2 (Ca

50 mut(PG1)JPH2 overexpressing myocytes caused calcium/calmodulin-dependent kinase II activation and al

51 pgef2 allele with a cre mouse line driven by calcium/calmodulin-dependent kinase IIalpha promoter als

52 The model predicted new crosstalks between calcium/calmodulin-dependent pathways and upstream signa

53 Calcium/calmodulin-dependent protein kinase II (CaMKII)

54 Using Raman microspectroscopy, amorphous calcium carbonate (ACC) was observed first in the drops,

55 calcium oxalate crystals (CaOx) or amorphous calcium carbonate cystoliths are spread among most photo

56 Porous PLA film, was fabricated using calcium carbonate nanoparticles to enhance film porosity

57 microbial activity leads to the formation of calcium carbonate precipitates.

58 One example is microbially induced calcium carbonate precipitation (MICP) in which microbia

59 in we report our full investigation into the calcium catalyzed generation and trapping of N-acylimini

60 In the pancreas, excessive intracellular calcium causes mitochondrial dysfunction, premature zymo

61 These calcium changes correlate with increased cell mobility i

62 ial (AP) prolongation (~50%), reduced L-type calcium channel (LCC) current (~33%), reduced outward po

63 We previously proposed that T-type calcium channel (TTCC) expression may serve as a biomark

64 Calcium channel blockers (CCB) improve TB treatment outc

65 , either beta-blockers or nondihydropyridine calcium channel blockers are reasonable drugs in patient

66 beta-Blockers, calcium channel blockers, and mineralocorticoid receptor

67 m as it did not replicate for beta-blockers, calcium channel blockers, or diuretics.

68 receptor type 1 (RyR1), a calcium-activated calcium channel engaged in the binding of ligands.

69 d this process is dependent on the lysosomal calcium channel TRPML1.

70 otal firing and the ictal increase of T-type calcium channel-mediated burst firing of thalamocortical

71 Studies suggest that dihydropyridine calcium-channel blockers may be associated with reduced

72 For example, presynaptic voltage-gated calcium channels (VGCCs) and postsynaptic ligand-gated i

73 ions in the significant set of voltage-gated calcium channels among CNVs called from both exome seque

74 at the alpha2delta2 subunit of voltage-gated calcium channels negatively regulates axon growth and re

75 e of TRPV4 channels, which are transmembrane calcium channels that can regulate vascular tone, in mod

76 at the calyx synapse in coupling presynaptic calcium channels to release sites.

77 ergic augmentation of Ca(V)1.2 voltage-gated calcium channels(1-4).

78 CaMKII were previously shown to bind L-type calcium channels, and we show here that Shank3 also bind

79 P, an auxiliary subunit of voltage-dependent calcium channels, promoted alpha6beta4 surface expressio

80 including glutamate receptors, voltage-gated calcium channels, the dopamine D2 receptor, and compleme

81 icity, and increased selectivity for Mn over calcium compared with two established Mn ionophores, cal

82 he H(2)O(2)-stimulated rise in mitochondrial calcium concentration was attenuated by 40%.

83 Caco-2 cells treated with the chelate at calcium concentrations of 0-10 mM exhibited enhanced abs

84 cium-sensing receptor (CaSR) regulates serum calcium concentrations.

85 oft X-ray microscopy we imaged intracellular calcium-containing particles in the PMCs and acquired Ca

86 in apo state (lacking calcium), whereas in a calcium-containing solution it is stuck in an intermedia

87 cells expressing the C674S mutant, basal SR calcium content was decreased by 31% and the H(2)O(2)-st

88 ed, and powdered bones yielded 31.4 +/- 0.6% calcium content.

89 ked AF-type [Ca(2+)](Nuc) changes and L-type calcium current decreases versus 1-Hz-paced cardiomyocyt

90 Voltage-gated calcium currents were unchanged between the genotypes.

91 ellar glia and granule cells and fired large calcium currents, measured with the genetically encoded

92 c function that is mediated by regulation of calcium cycling via 12,13-diHOME and NOS1.

93 Calcium dependent protein kinase 1 (CDPK1) is an essenti

94 s of the receptor that may contribute to the calcium-dependent inactivation.

95 irments on autophagy flux and apoptosis in a calcium-dependent manner.

96 tivation in the axonal bouton by PKC-induced calcium-dependent phosphorylation at Ser-41 (pGAP-43).

97 Here, we report that the Arabidopsis calcium-dependent protein kinase CPK3 is a key regulator

98 2)R activation, and downstream intracellular calcium-dependent signal transduction.

99 ER calcium depletion robustly activates the unfolded protei

100 ficantly increased tissue mineralization and calcium deposition at the tissue-implant interface in re

101 ose of P(i) led to a significantly increased calcium deposition, phenotypic change and sEV secretion

102 rary of 645,000 compounds using a cell-based calcium detection system.

103 Recording population calcium dynamics by fiber photometry, we observe that th

104 ned by calcium-sensing proteins that trigger calcium dynamics in response to calcium fluctuations.

105 r measuring contractile forces and cytosolic calcium dynamics of single muscle fibers.

106 ysosome contacts in regulating mitochondrial calcium dynamics through the lysosomal calcium efflux ch

107 The synaptic calcium dysregulation is due to a loss of dendritic inhi

108 drial calcium dynamics through the lysosomal calcium efflux channel, transient receptor potential muc

109 s and is controlled, in part, by non-uniform calcium elevation across the AZ.

110 Both imaging of glutamate-induced calcium elevations and Western blots reveal ionotropic g

111 Performance was similarly poor for calcium-enhanced broth microdilution.

112 rall categorical and essential agreement for calcium-enhanced gradient agar diffusion were 73.7% and

113 hese results support a scenario in which the calcium-enriched oyster environment triggers IamP-mediat

114 Store-operated calcium entry (SOCE) is important in the maintenance of

115 uired Ca(2+) flux through the store-operated calcium entry (SOCE) pathway and accompanied plasma memb

116 that CFTR dysfunction in platelets increased calcium entry though the transient receptor potential ca

117 rapidly due to lipid peroxidation, allowing calcium entry to initiate lysosome fusion.

118 and protect the endothelial barrier against calcium entry-induced disruption.

119 (K(+)) currents (~30%), and increased sodium/calcium exchanger (NCX) activity (~52%).

120 tes cardiomyocyte contractility via a sodium-calcium exchanger (NCX) mediated pathway.

121 between bioelectric ion channel activity and calcium, finding that cell hyperpolarization and depolar

122 granule neurons, along with bioluminescence, calcium FLIPR, and short hairpin RNA-based gene-silencin

123 signalling network underlying the cytosolic calcium fluctuations are hitherto not fully understood.

124 that trigger calcium dynamics in response to calcium fluctuations.

125 ptor signaling, but mediated by an increased calcium flux and calcineurin-mediated dephosphorylation

126 We find that intra-axonal calcium flux is accompanied by actin-Rho dependent growt

127 hanosensitive (as demonstrated by changes in calcium flux under applied luminal flow).

128 actant synthesis is triggered by a sustained calcium flux upon contact with necrotic tissue that requ

129 el 6 (TRPC6) reduced platelet activation and calcium flux, and reduced lung injury in CF mice after i

130 ctivities including protein quality control, calcium flux, and sterol homeostasis.

131 xin-1 (CCL11)-mediated eosinophil migration, calcium flux, cell polarization, and ERK1/2 activation,

132 evolution of intracellular and extracellular calcium fluxes during a single beat which is away from h

133 formatics drug repurposing analyses, such as calcium folinate and betulin.

134 Vitamin D and calcium for the prevention of fracture: a systematic rev

135 OCT demonstrated multiplane and longitudinal calcium fractures after IVL in 67.4% of lesions.

136 eedback through the activation of associated calcium-gated potassium channels.

137 Because sarcoplasmic reticulum (SR) calcium has been shown to play a critical role in mediat

138 ry (SOCE) is important in the maintenance of calcium homeostasis and alterations in this mechanism ar

139 suggests that dysregulation of mitochondrial calcium homeostasis is also related to tau and other ris

140 vement of endoplasmic reticulum-mitochondria calcium homeostasis with hepatic HAX-1 inactivation sugg

141 ients, which restores lysosomal proteolysis, calcium homeostasis, and normal autophagy flux.

142 zo1-dependent control of shear flow sensing, calcium homeostasis, cytoskeletal dynamics and pressure-

143 Essential for calcium homeostasis, TRPV5 and TRPV6 are calcium-selecti

144 tein that plays a key role in the control of calcium homeostasis.

145 Dental materials to date including calcium hydroxide paste, mineral trioxide aggregate, and

146 neurons of the lateral OFC using two-photon calcium imaging and investigated how OFC dynamically int

147 Applying 2-photon calcium imaging and optogenetic manipulation of anatomic

148 r and flow in individual brain microvessels, calcium imaging and optogenetics allow the investigation

149 application of optogenetics, chemogenetics, calcium imaging and related approaches.

150 vation was evaluated by c-Fos expression and calcium imaging at one minute after the anesthetic admin

151 Using in vivo multiphoton calcium imaging from transgenic PUb-GCaMP6s mosquitoes,

152 Using cellular calcium imaging in a virtual reality (VR)-based locomoti

153 We develop methods for stable hindbrain calcium imaging in free-moving mice, which show that per

154 Using longitudinal in vivo calcium imaging in un-anesthetized mouse pups, we show t

155 We applied the technology to calcium imaging of entire dendritic spans of neurons as

156 d natural scene representation, we performed calcium imaging of excitatory neurons in the primary vis

157 uperior capacity of BPI for optogenetics and calcium imaging of human neurons.

158 In vivo calcium imaging revealed that different GA drugs activat

159 In vivo calcium imaging revealed that T4 and T5 neurons encode t

160 Projection-specific labeling and calcium imaging showed that the great majority of STN-pr

161 of visual cortical areas, we used two-photon calcium imaging to characterize the effects of juvenile

162 combine adaptive optics ophthalmoscopy with calcium imaging to optically record optogenetically rest

163 question by combining whole-brain volumetric calcium imaging using light-field microscopy and an oper

164 Using a dexterity task, calcium imaging, optogenetic perturbations, and behavior

165 Using genetic labeling and calcium imaging, we show that npvf-expressing neurons in

166 By utilizing optical calcium imaging, which records calcium ion flux indicati

167 ellular activity in the DMS astrocytes using calcium imaging.

168 sible to significantly increase the level of calcium in plant matrice.

169 e ion channels that exhibit a preference for calcium in response to mechanical stimuli.

170 Carbon-calcium inclusions (CCaI) either as calcium oxalate crys

171 rents, measured with the genetically encoded calcium indicator jRGECO1a.

172 l (Cav1.2) antagonist that directly inhibits calcium influx and smooth muscle contractility, leading

173 Glucose metabolism and calcium influx are involved in primiR-199a2 expression b

174 A decrease in the L-type calcium influx is observed in both glutamatergic neurons

175 during associative conditioning to integrate calcium influx resulting from acetylcholine stimulation

176 r by measuring inhibition of the ATP-induced calcium influx.

177 d reactive oxidative species (ROS)-regulated calcium influx.

178 Mean baseline calcium intake ranged from 562 to 1333 mg/d.

179 Near-infrared (NIR) genetically encoded calcium ion (Ca2+) indicators (GECIs) can provide advant

180 A native calcium ion channel has been identified in bacteria for

181 izing optical calcium imaging, which records calcium ion flux indicating occurrence of an action pote

182 Results indicated that PLA2 required calcium ion for both the hydrolyzing activity and the an

183 Herein, we used the biologically relevant calcium ion to investigate the conformation of monomeric

184 With high initial ratio of calcium ion to phosphate, periodic precipitation was obt

185 e treated these podocytes temporarily with a Calcium Ionophore and facultatively with Latrunculin A,

186 zed by hydroxyl ligands and charge balancing calcium ions in the interlayer space.

187 During scale formation, calcium is frequently bound to the Pb(II) phosphate crys

188 ying and characterizing novel solid forms of calcium l-lactate.

189 Luminal calcium levels are determined by calcium-sensing protein

190 s for improving fruit firmness, but elevated calcium levels in grape cells were shown to reduce total

191 al and S6 phosphorylation and enhanced basal calcium levels in human CLL cells.

192 e persistent static elevation of cytoplasmic calcium levels that fade over developmental time.

193 ogical response and a normalization of serum calcium levels, confirming the hypothesis of a calcitrio

194 rombin and histamine, increase intracellular calcium levels.

195 say to quantify the plant-available pools of calcium, magnesium and potassium and trace the soil phas

196 entral to calcification, including genes for calcium management (calmodulin, calcium-binding proteins

197 family have been reported to be involved in calcium, manganese, and pH homeostases.

198 e introduce rsCaMPARI, a genetically encoded calcium marker engineered from a reversibly switchable f

199 th long-term follow-up after coronary artery calcium measurement.

200 The combination of hard (titanium) and soft (calcium) metals in the heterometallic nodes of MUV-10(Ca

201 ly assessed mAChR-A to monitor intracellular calcium mobilization upon receptor activation.

202 tion of BCR signaling results in a decreased calcium mobilization.

203 itrous acid, which is generated in situ from calcium nitrite that is added to the concrete.

204 h nadir in-hospital AKI was in serum ionized calcium of 5.00-5.19 mg/dL.

205 ch is linked to an increase in intracellular calcium oscillation mediated by ryanodine receptor (RyR)

206 Carbon-calcium inclusions (CCaI) either as calcium oxalate crystals (CaOx) or amorphous calcium car

207 of gut microbial communities and early-onset calcium oxalate kidney stone disease is unknown.

208 h as otters, dolphins and ferrets, that form calcium oxalate, struvite, uric acid, cystine and other

209 udied Zn(2+) inhibition of AMPARs by varying calcium permeability, auxiliary subunits, and activation

210 gous mutations in the gene encoding TRPM3, a calcium permeable ion channel, were identified as the ca

211 pecifically, we hybridized the cryogels with calcium peroxide microparticles to controllably produce

212 ine (MCT), monophosphoryl lipid A (MPLA) and calcium phosphate (CaP) used less frequently.

213 ube induced microstructural phase changes of calcium phosphate (CP) leading to the formation of brush

214 of 3D scaffolds using magnetic levitation of calcium phosphate particles.

215 defects in sheep using 3D-printed customized calcium phosphate scaffolds with or without surgical vas

216 Crucially, calcium plays a fundamental role in stabilizing cbEGF do

217 Moreover, comparable calcium propagation also promotes apical extrusion of ap

218 host Golgi compartment-resident ATP-powered calcium pump (secretory pathway calcium ATPase 1 [SPCA1]

219 acutely stimulate the sarcoplasmic reticulum calcium pump (SERCA) by relieving its inhibition by PLN.

220 calcium-ATPase 2a (SERCA2a) and accelerates calcium re-uptake into the SR.

221 These include calcium, reactive oxygen species (ROS), hydraulic and el

222 lacking sperm-specific calcineurin (PP2B), a calcium regulated phosphatase, in testis and sperm, are

223 Moreover, expression of the c-di-GMP and calcium-regulated, biofilm-promoting brp exopolysacchari

224 reveal distinct differences in intracellular calcium regulation and excitation-contraction (EC) coupl

225 The transform between neural activity and calcium-related fluorescence involves nonlinearities and

226 al duration, Ca2+ alternans, and spontaneous calcium release (SCR) incidence were determined.

227 0% (P<0.001, n=18), and promoted spontaneous calcium release activity (n=14, P<0.013) in human cardia

228 to impaired Pitx2 by preventing spontaneous calcium release and increasing wavelength.

229 hionine oxidation on CaM's regulation of the calcium release channel, ryanodine receptor (RyR).

230 ms that are responsible for the pathological calcium release, regarding the tissue origin of the arrh

231 h bursts of action potentials, we found that calcium responses have the capacity to encode action pot

232 eral PAR-2 polarization, suggesting that the calcium responses originated from nonciliated cells.

233 accompanied by actin-Rho dependent growth of calcium rich axonal spheroids that eventually rupture, r

234 d femoral plaque volume; and coronary artery calcium score (CACS) at baseline and 2.8 years later.

235 in, we review the use of the coronary artery calcium score as a decision aid in individuals with type

236 CT calcium score was 1373.3+/-1392.9 Agatston units.

237 ompared with those without uptake (change in calcium score, 97 [39-166] versus 35 [7-93] AU; P<0.0001

238 f cardiovascular risk score, coronary artery calcium score, or coronary artery area stenosis.

239 ry artery, thoracic aorta, and cardiac valve calcium scores and pulse wave velocity were not signific

240 Breast arterial calcification and calcium scores were determined for each patient, and the

241 for calcium homeostasis, TRPV5 and TRPV6 are calcium-selective channels belonging to the transient re

242 Luminal calcium levels are determined by calcium-sensing proteins that trigger calcium dynamics i

243 The calcium-sensing receptor (CaSR) regulates serum calcium

244 ships (metabotropic glutamate receptor 5 and calcium-sensing receptor).

245 of Ca(2+) Only AtSCS-A has the features of a calcium sensor.

246 Cortical astrocyte calcium signaling also altered the acute stimulatory and

247 rall activity, accelerates the refinement of calcium signaling and excitatory inputs without affectin

248 i2 as a potential intermediary between early calcium signaling and subsequent tissue regeneration.

249 one hand, specific Ship1 inhibition enhanced calcium signaling and thereby abrogated an anergic respo

250 ting granule localization and/or priming and calcium signaling in concert.

251 Alterations in calcium signaling in pancreatic acinar cells can result

252 We report that (1) calcium signaling increases with the application of ultr

253 podocytes become sensitized to AngII-induced calcium signaling upon injury might explain results from

254 dy indicate a role for endoplasmic reticulum calcium signaling via calreticulin in the differentiatio

255 les in ATP production, metabolic regulation, calcium signaling, generation of reactive oxygen species

256 tion) triggered increased microglial process calcium signaling, often concomitant with process extens

257 ells from patients with CF without impacting calcium signaling.

258 tored activation of the Galpha(q/11)-coupled calcium-signaling pathway, beta-arrestin recruitment, an

259 Recently, characterizing calcium signalling in neurons related to interactions wi

260 Calcium signalling through NMDA-type glutamate receptors

261 t various stages, including somatic spiking, calcium signals at somata and axons, and striatal dopami

262 the responsiveness of CaMKII holoenzymes to calcium signals can be tuned by varying the relative lev

263 However, these calcium signals were delayed relative to channel activat

264 suggest that precise control of ionic flux (calcium, sodium, and potassium) contributes to in utero

265 ase in response to caffeine and the troponin-calcium stabilizer tirasemtiv, similar to responses meas

266 ed to a phase transformation to an anhydrous calcium sulfate, anhydrite, which was formed via repreci

267 dy BMD compared to participants on vitamin D/calcium supplementation and exercise alone.

268 Overall, the meta-analysis indicates that calcium supplementation does not provide clinically impo

269 Calcium supplements have increasingly been used at pre-

270 e 1 strong recommendation for baseline serum calcium testing, 13 conditional recommendations, and 1 b

271 VC1 and sRAGE in the absence or presence of calcium that acted as a competitor.

272 ng a mathematical model, that dissolution of calcium that has aggregated within the mitochondria of v

273 lcium angle was 292.5 +/- 76.5 degrees , and calcium thickness was 0.96 +/- 0.25 mm at the site of ma

274 esponses require the influx of extracellular calcium through ion channels.

275 mor microenvironment (TME) by sustaining the calcium transients and neurotransmitter-dependent commun

276 Local synaptic calcium transients decreased, leaving a GluR2 lacking AM

277 l somata and processes exhibited spontaneous calcium transients in a chronic window preparation.

278 m photon count required for the detection of calcium transients in GCaMP6s-expressing neurons for 920

279 ng of spontaneous and neural activity-evoked calcium transients in mural cells.

280 astrocytes respond to neurotransmitters with calcium transients stimulating the release of gliotransm

281 orescence intensity recordings >1.40 for the calcium transients.

282 ed, let alone the molecular mechanism of the calcium transport activity.

283 s the hypothesis that impaired mitochondrial calcium transport contributes to the pathogenesis of Bar

284 es involved in cellular transport, including calcium transporters and cytoskeletal regulators, that a

285 oxidation as a consequence of mitochondrial calcium uniporter complex (MCUC) inhibitory subunit MCUb

286 minimal functional unit of the mitochondrial calcium uniporter complex in metazoans, a highly selecti

287 The mitochondrial calcium uniporter is a Ca(2+)-gated ion channel complex

288 endent anion channel 1 and the mitochondrial calcium uniporter, respectively.

289 Moreover, mitochondrial calcium uptake at mitochondria-lysosome contact sites wa

290 s axon regrowth through axonal mitochondrial calcium uptake.

291 rial compared progression of coronary artery calcium volume score and other measurements of cardiovas

292 end point was change in log coronary artery calcium volume score from baseline to week 52.

293 pared with placebo attenuated progression of calcium volume score in the aortic valve (14% [95% CI, 5

294 The mean change in coronary artery calcium volume score was 11% (95% CI, 7-15) for the comb

295 e, calcification grade in raphe, and leaflet calcium volume were assessed with CT analysis in a maske

296 nteraction between 25(OH)D3 and magnesium or calcium was assessed by investigating 1) joint compared

297 Calcium wave induces the polarized movement of the surro

298 Instead, phosphorus and calcium were found to permeate through the destabilized

299 mation is pH-sensitive in apo state (lacking calcium), whereas in a calcium-containing solution it is

300 me quercetin derivatives was also favored by calcium, while other flavonols and flavan-3-ols were aff