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1 (NSP4) induces dramatic changes in cellular calcium homeostasis.
2 f AD, including altered lipid metabolism and calcium homeostasis.
3 actin-mediated, and disrupted intracellular calcium homeostasis.
4 ular system protein, is a major regulator of calcium homeostasis.
5 e force-frequency curve, suggesting improved calcium homeostasis.
6 are important in the regulation of cellular calcium homeostasis.
7 l function and survival, i.e., intracellular calcium homeostasis.
8 ell proliferation, cell differentiation, and calcium homeostasis.
9 ered markers of mitochondrial biogenesis and calcium homeostasis.
10 resiliency factor through its modulation of calcium homeostasis.
11 le membrane fragility, but also dysregulated calcium homeostasis.
12 eticulum Ca(2+) ATPase (SERCA) that disrupts calcium homeostasis.
13 and has been suggested to have functions in calcium homeostasis.
14 iating calcium spike activity and regulating calcium homeostasis.
15 cers of energy and play an important role in calcium homeostasis.
16 lism plays in the development of diseases of calcium homeostasis.
17 ation through increased load on dysregulated calcium homeostasis.
18 ochondria cooperate with the SER to maintain calcium homeostasis.
19 , impairs cell cycle progression and affects calcium homeostasis.
20 r barrier function, resulting in the loss of calcium homeostasis.
21 he endoplasmic reticulum and plays a role in calcium homeostasis.
22 eoclasts are essential for bone dynamics and calcium homeostasis.
23 trophy (DMD) include, among others, abnormal calcium homeostasis.
24 a mechanism involving the modulation of the calcium homeostasis.
25 not required for viability, reproduction, or calcium homeostasis.
26 min, a drug known to perturb ER ceramide and calcium homeostasis.
27 t through the affected channels and disrupts calcium homeostasis.
28 gin and clotrimazole (CLT), which disrupt ER calcium homeostasis.
29 id hormone (PTH), the principal regulator of calcium homeostasis.
30 ics of dark adaptation through modulation of calcium homeostasis.
31 al cells is tightly controlled during normal calcium homeostasis.
32 ranes that, among other functions, modulates calcium homeostasis.
33 te important processes such as apoptosis and calcium homeostasis.
34 lastic cells to regulate bone remodeling and calcium homeostasis.
35 cardiac muscle by maintaining cardiomyocyte calcium homeostasis.
36 ractile dysfunction through dysregulation of calcium homeostasis.
37 response to acute hypoxia and regulation of calcium homeostasis.
38 tion pathway and regulation of intracellular calcium homeostasis.
39 l, we arrive at a simple dynamical model for calcium homeostasis.
40 ients has been reported to result in altered calcium homeostasis.
41 remodeling and as an essential regulator of calcium homeostasis.
42 regulators in cardiac energy metabolism and calcium homeostasis.
43 ultures, SMA astrocytes exhibited defects in calcium homeostasis.
44 urther insights into the function of WFS1 in calcium homeostasis.
45 The kidney has a major role in extracellular calcium homeostasis.
46 hich allow for longitudinal monitoring of ER calcium homeostasis.
47 ation influx and disruption of intracellular calcium homeostasis.
48 MTC1 and TMTC2 as ER proteins involved in ER calcium homeostasis.
49 identify a new role for AP2 in extracellular calcium homeostasis.
50 als within a cell including dysregulation of calcium homeostasis.
51 optimization of the mechanisms that regulate calcium homeostasis.
52 o PPT1-deficiency increases ROS and disrupts calcium homeostasis activating caspase-9 and (ii) caspas
54 viously reported disruption of mitochondrial calcium homeostasis after chronic doxorubicin administra
56 PS is also involved in the regulation of calcium homeostasis, although the precise site of its ac
58 a link between myocardial isoform switching, calcium homeostasis and altered metabolism in the develo
59 response to mefloquine-induced disruption of calcium homeostasis and appropriate control agents were
60 ic hematopoiesis through maintenance of bone calcium homeostasis and are consistent with the concept
61 clude tissues involved in the maintenance of calcium homeostasis and bone development and remodeling.
63 yroid hormone (PTH) is the major mediator of calcium homeostasis and bone remodeling and is now known
65 es MTM1 mutations do not dramatically affect calcium homeostasis and calcium release mediated through
66 he major organelle involved in intracellular calcium homeostasis and calcium signaling, including cal
68 ion channels/pumps that alter intracellular calcium homeostasis and cause renin-independent aldoster
69 yzed the sequential steps leading to altered calcium homeostasis and cell death in response to activa
72 l or cell-matrix interaction, Rho signaling, calcium homeostasis and copper-binding/sensitive activit
73 -term OVL did not increase the alteration in calcium homeostasis and did not deplete muscle cell prog
74 wth with activation involving the effects on calcium homeostasis and downstream effects involving the
76 M as redox sensors that function to modulate calcium homeostasis and energy metabolism in response to
77 ng the mechanisms involved in the control of calcium homeostasis and have provided evidence for a rol
79 lso support a role for ICS1 (SA) in iron and calcium homeostasis and identify components of SA cross
81 whose actions include those associated with calcium homeostasis and immune responses as well as cell
83 ption of high-protein diets does not disrupt calcium homeostasis and is not detrimental to skeletal i
84 combined lead to disruption of intracellular calcium homeostasis and isoproterenol-induced arrhythmia
85 ctor, which is shown to play a major role in calcium homeostasis and keratinocyte differentiation.
88 These data signify the essential role of calcium homeostasis and NCX1h in establishing rhythmic c
89 findings link mutations in TRPV4 to altered calcium homeostasis and peripheral neuropathies, implyin
91 oid hormone-related protein (PTHrP) in fetal calcium homeostasis and placental calcium transport was
92 cts of the anti-Abeta antibody aducanumab on calcium homeostasis and plaque clearance in aged Tg2576
93 of oxygen radicals as well as alteration in calcium homeostasis and possibly alteration in contracti
97 her module encloses many genes important for calcium homeostasis and signaling and contains SCA genes
98 hat sigma-1 receptor activation can regulate calcium homeostasis and signaling in RGCs, likely by dir
99 The overrepresentation of genes involved in calcium homeostasis and signaling may indicate an import
101 BP-D28k plays a critical role in maintaining calcium homeostasis and skeletal mineralization and sugg
102 teraction patterns with proteins involved in calcium homeostasis and sphingolipid metabolism could in
104 These findings establish a role for ERO1 in calcium homeostasis and suggest that modifying the lumen
105 ctively, our findings show that PS regulates calcium homeostasis and synaptic function via RyR and su
106 lications for the long-term monitoring of ER calcium homeostasis and the development of therapeutic a
108 onstrate that modulation of dynamic cellular calcium homeostasis and TXNIP suppression present viable
109 ding neurofilament filled swellings, loss of calcium homeostasis, and accumulation of reactive oxygen
111 se mitochondrial membrane potential controls calcium homeostasis, and AMP-activated protein kinase (A
115 neurotransmitter signaling, perturbations in calcium homeostasis, and damage-associated molecular pat
116 These channels couple lipid metabolism, calcium homeostasis, and electrophysiological properties
117 urite retraction, loss of synapses, aberrant calcium homeostasis, and imbalanced neurotransmitter rel
121 servation of erythrocyte membrane integrity, calcium homeostasis, and osmotic resistance through an a
124 ve been implicated in synaptic transmission, calcium homeostasis, and structural function and thus ma
125 transduction, regulation of gene expression, calcium homeostasis, and the maintenance of a unique ext
126 ed in several cellular processes, apoptosis, calcium homeostasis, and transcriptional regulation.
127 egulation of de novo sphingolipid synthesis, calcium homeostasis, and unfolded protein response.
128 ents), this study suggests that disorders of calcium homeostasis are associated with fatal and nonfat
131 channels TRPV5 and TRPV6 play vital roles in calcium homeostasis as Ca(2+) uptake channels in epithel
132 rant beta-adrenergic signaling and depressed calcium homeostasis, associated with an imbalance of pro
136 rm black carbon [BC] and PM2.5 levels, serum calcium homeostasis biomarkers (parathyroid hormone, cal
137 tes, mutations in the presenilins also alter calcium homeostasis, but the mechanism linking presenili
138 oupled receptor family C, regulates systemic calcium homeostasis by activating G(q)- and G(i)-linked
139 s (CaR) contribute to regulation of systemic calcium homeostasis by activation of G(q)- and G(i)-link
142 is used to examine the regulation of ROS and calcium homeostasis by local, subcellular X-ROS signalin
145 Here we show that modulation of cellular calcium homeostasis can mitigate cytokine- and ER stress
148 The epidermal adrenergic signal controls calcium homeostasis, cell growth, differentiation, motil
149 Thus, although alterations in intracellular calcium homeostasis contribute to glucocorticoid-induced
150 through modulation of SERCA and maintaining calcium homeostasis could be a therapeutic aim for bette
151 line in mechanisms controlling intracellular calcium homeostasis could contribute to altered neuronal
153 r endothelial cells, TRPV4 channels regulate calcium homeostasis, cytoskeletal signalling and the org
154 ypercalcemia type 3 (FHH3), an extracellular calcium homeostasis disorder affecting the parathyroids,
155 oid plaques in an acute setting and restores calcium homeostasis disrupted in a mouse model of AD upo
156 ty, injuring sarcolemmal membranes, altering calcium homeostasis due to effects on the sarcoplasmic r
157 d the hypothesis that alterations in cardiac calcium homeostasis due to sepsis underlie the observed
158 nflux at afferent ribbon synapses influences calcium homeostasis during long-lasting cholinergic inhi
160 ing low-dose caffeine to mimic the defective calcium homeostasis encountered under these conditions.
161 on, modulation of endoplasmic reticulum (ER) calcium homeostasis, ER stress signaling, autophagy, rea
164 usly expressed membrane protein essential in calcium homeostasis for many cells including those in ma
165 eal a regulatory role of the PLN pentamer in calcium homeostasis, going beyond the previously hypothe
168 ogenesis, cell proliferation, apoptosis, and calcium homeostasis have been attributed to its N termin
170 s a critical role in cellular energetics and calcium homeostasis; however, how MAM is affected under
172 n up by neurons causing: (i) deregulation of calcium homeostasis, (ii) endoplasmic reticulum-calcium
173 ite degeneration, loss of synapses, aberrant calcium homeostasis, imbalanced neurotransmitter release
174 in vivo, we quantitatively imaged astrocytic calcium homeostasis in a mouse model of Alzheimer's dise
176 te the effect of sigma-1 receptor ligands on calcium homeostasis in a retinal ganglion cell line (RGC
177 n of caspase-12 activation and its effect on calcium homeostasis in an ER stress-induced model of apo
179 turbance in endoplasmic reticulum-associated calcium homeostasis in cultured embryonic motor neurons
181 n D3 (1,25(OH)2D3) plays an integral role in calcium homeostasis in higher organisms through its acti
182 n contractility despite normal intracellular calcium homeostasis in intact cardiomyocytes and resulte
183 t manner, demonstrating the critical role of calcium homeostasis in maintaining embryonic cardiac fun
184 levels of ion channels involved in cellular calcium homeostasis in mouse cortical microglial cells i
186 nserved role of dematin in the regulation of calcium homeostasis in other cell types will be discusse
187 glutamate receptor signalling and disrupted calcium homeostasis in PNs form a common, early pathophy
188 bellar ataxia type 2 (SCA2) mouse model that calcium homeostasis in PNs is disturbed across a broad r
190 ous system, where it regulates intracellular calcium homeostasis in response to excitatory signaling.
195 elation between IP(3)R elevation and altered calcium homeostasis in terms of either kinetics or dose
197 iquitin-proteasome system and alterations of calcium homeostasis in the neuronal loss observed during
198 se may alter glutamate neurotransmission and calcium homeostasis in the retina, which may have implic
199 The hypertension-induced alterations of calcium homeostasis in the soleus muscle of SHRs occurre
200 a simple and sensitive method to monitor ER calcium homeostasis in vitro or in vivo by analyzing cul
201 onstrate that senile plaques impair neuritic calcium homeostasis in vivo and result in the structural
202 harmacological approach to restore cytosolic calcium homeostasis in vivo, we administered the clinica
205 Cellular stresses such as disruption of calcium homeostasis, inhibition of protein glycosylation
206 ellular stress signals such as disruption of calcium homeostasis, inhibition of protein glycosylation
207 t 9-fold from the target organs required for calcium homeostasis (intestine, bone, kidney, and parath
209 al changes, supports the view that disturbed calcium homeostasis is an early feature of Parkinson's d
210 strongly suggests that imbalance in cellular calcium homeostasis is an important factor leading to CD
212 To address whether the role of CaBP-D28k in calcium homeostasis is compensated by CaBP-D9k, we gener
217 grity, and active adaptation at the level of calcium homeostasis is not mechanistic in protection.
218 y support the hypothesis that maintenance of calcium homeostasis is one function of complex gangliosi
221 ave shown that ion homeostasis, particularly calcium homeostasis, is critical to limiting tissue dama
222 osphatase (SERCA)2a, a critical regulator of calcium homeostasis, is known to be decreased in heart f
223 lcitonin (CT), a peptide hormone involved in calcium homeostasis, is transiently expressed in the rec
224 uggest that mutant LRRK2 causes a deficit in calcium homeostasis, leading to enhanced mitophagy and d
225 PC1 disease pathogenesis that causes altered calcium homeostasis, leading to the secondary storage of
227 enes involved in cell adhesion and motility, calcium homeostasis, lipid transport and metabolism, and
228 ght to occur include a loss of intracellular calcium homeostasis, loss of energy supply to the cell,
230 Together, the results indicate that altered calcium homeostasis may be a key early event in basal to
231 and suggest that disruption of intracellular calcium homeostasis may be an early pathogenic event lea
232 Altered glutamatergic neurotransmission and calcium homeostasis may contribute to retinal neural cel
233 ta suggest that BI-1, through its actions on calcium homeostasis, may confer affective resiliency in
234 licated in many neuronal processes including calcium homeostasis, membrane excitability, synaptic tra
235 been used to study metabolism, mitochondrial calcium homeostasis, mitochondrial membrane potential, a
236 the MPT differentially affect mitochondrial calcium homeostasis: mitoK(ATP) channels suppress calciu
243 n implicated as one of the causes of altered calcium homeostasis observed during human heart failure.
246 show that blocking this channel perturbs the calcium homeostasis of the cells and inhibits the prolif
248 se observations suggest an important role of calcium homeostasis on the Apaf-1-dependent apoptotic pa
249 dentified have functions related to neuronal calcium homeostasis or central nervous system developmen
250 nd this effect was not due to alterations in calcium homeostasis or myosin light chain phosphorylatio
251 D3 [1,25(OH)2D3] to perform its function in calcium homeostasis, or it is activated by lithocholic a
255 rticoid-induced alterations in intracellular calcium homeostasis promote apoptosis, but the mechanism
256 etoxification enzymes, antioxidant proteins, calcium homeostasis proteins, growth factors, neuron-spe
257 ive oxygen species production and signaling, calcium homeostasis, regulated cell death, and heme bios
258 ; consistently, tissue-specific induction of calcium homeostasis-related genes and suppression of gro
259 tabolic derangements (particularly involving calcium homeostasis), renal failure, and possibly, morta
260 phenotypes, such as alkaline pH sensitivity, calcium homeostasis, respiratory defects, and cell wall
261 oA dehydrogenase, and uncoupling protein 3), calcium homeostasis (sarcoplasmic reticulum Ca(2+)-ATPas
262 naptic cistern may play an essential role in calcium homeostasis, serving as sink or source, dependin
264 and rcy1), all were found to have defective calcium homeostasis, supporting a correlation with amiod
265 tions at the level of glial gene expression, calcium homeostasis, swelling, and volume regulation.
266 oid hormone (PTH), an important regulator of calcium homeostasis, targets most of its complex actions
268 min D is a secosteroid with known effects on calcium homeostasis that has recently been shown to have
269 ole for alpha 3 gap junctions in maintaining calcium homeostasis that in turn is required to control
270 oncentrations induce a stochastic failure of calcium homeostasis that precedes both mitochondrial dep
271 to the generation of ATP and maintenance of calcium homeostasis, the effective delivery of mitochond
272 nes are known to play a contributory role in calcium homeostasis, the entire caste of key components
273 itially thought to play a restricted role in calcium homeostasis, the pleiotropic actions of vitamin
274 aused a phenotype-dependent dysregulation of calcium homeostasis; the resting intracellular calcium o
276 hyroid hormone (PTH) regulates extracellular calcium homeostasis through the type 1 PTH receptor (PTH
278 well as core biological processes mediating calcium homeostasis, tissue integrity, cornification, an
279 fficking of ion channel subunits involved in calcium homeostasis to and from the plasma membrane.
281 er se, is the key effector of Drp1, altering calcium homeostasis to modulate neuronal morphology and
282 data link defects in neuronal intracellular calcium homeostasis to the vulnerability of central auto
283 ecies, electron transport chain function and calcium homeostasis trigger altered mitochondrial dynami
284 to explore the ability of BI-1 to influence calcium homeostasis under basal conditions and also foll
285 These results suggest that disruption of calcium homeostasis underlies isoflurane-induced caspase
286 by which PS regulates synaptic function and calcium homeostasis using acute hippocampal slices from
287 have shown that mefloquine disrupts neuronal calcium homeostasis via liberation of the endoplasmic re
288 ion due to its ability to stabilize cellular calcium homeostasis via N-methyl-D-aspartate-receptor an
289 upts mitochondrial and endoplasmic reticulum calcium homeostasis via ryanodine receptor (RyR) activat
290 etabolite, NAADP(+), regulates intracellular calcium homeostasis via the 2-pore channel, ryanodine re
292 gland VDR content is an important factor in calcium homeostasis, vitamin D metabolism, and the treat
293 ne permeability and consequent disruption of calcium homeostasis were implicated in cellular degenera
295 heimer's disease (AD), disturb intracellular calcium homeostasis, which in turn activates the calcium
296 dergo increased oxidative stress and altered calcium homeostasis, which may contribute to myofiber lo
297 utophagic/lysosomal system and intracellular calcium homeostasis, which underlie vulnerability to neu
299 hat PTHrP is an important regulator of fetal calcium homeostasis with its predominant effect being on
300 suggesting a dysregulation of intracellular calcium homeostasis within the muscle or an alteration o
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