ライフサイエンスコーパス: calcium-binding protein

1 lated by SOS2 (a protein kinase) and SOS3 (a calcium-binding protein).

2 ner, and is regulated by cytosolic VILIP1, a calcium binding protein.

3 s of drugs is known to bind to calmodulin, a calcium binding protein.

4 r target of 2F11 to be Annexin A4 (Anxa4), a calcium binding protein.

5 is structurally stabilized by calmodulin, a calcium-binding protein.

6 e strongly immunoreactive for parvalbumin, a calcium-binding protein.

7 Thus, BAD-1 is a high capacity calcium-binding protein.

8 act as true calcium sensors rather than just calcium binding proteins.

9 are perceived by sensor molecules, including calcium binding proteins.

10 cell adhesion molecules, neuropeptides, and calcium binding proteins.

11 binding of target peptides to other EF-hand calcium-binding proteins.

12 s1 is a member of the S100 family of EF-hand calcium-binding proteins.

13 ne + aspartate (SD) domain that is shared by calcium-binding proteins.

14 and transmitted by sensor molecules such as calcium-binding proteins.

15 ined with ruthenium red dye, an indicator of calcium-binding proteins.

16 ing loop of the EF-hand domain found in many calcium-binding proteins.

17 and 6 members of the S100 protein family of calcium-binding proteins.

18 the calmodulin (CaM) superfamily of EF-hand calcium-binding proteins.

19 s signals as inferred by the accumulation of calcium-binding proteins.

20 mposed of protein disulfide isomerase (PDI), calcium binding protein 1 (CABP1/P5), 72 kDa endoplasmic

21 The nCaBPs calcium-binding protein 1 (CaBP1) and visinin-like prote

22 Calcium-binding protein 1 (CaBP1) is a neuron-specific m

23 In neurons, binding of calmodulin (CaM) or calcium-binding protein 1 (CaBP1) to the CaV1 (L-type) v

24 Calcium-binding protein 1 (CaBP1), a neuron-specific mem

25 Ca(2+) sensor proteins, calmodulin (CaM) and calcium-binding protein 1 (CaBP1), via multiple, partial

26 vels of an age-associated gene, Sarcoplasmic calcium-binding protein 1 (SCP-1).

27 CaBP1 (calcium-binding protein 1) is a 19.4-kDa protein of the

28 n, calbindin, calretinin, N-terminal EF-hand calcium-binding protein 1, cholecystokinin, reelin, or a

29 tion of Ca(V)2.1 channels by the CaS protein calcium-binding protein-1 (CaBP1) by analysis of chimera

30 rofiling reveals an increase of the neuronal calcium-binding protein 2 (NECAB2) in diseased neurons.

31 SPARC-Related Modular Calcium Binding Protein-2 (Smoc-2) is a broadly-expresse

32 ne such protein was SMOC-2 (secreted modular calcium-binding protein-2), classified as belonging to t

33 f the gene encoding SMOC-2 (secreted modular calcium-binding protein-2), which has been shown to syne

34 Recently, the calcium-binding protein 39 (Cab39) has emerged as a bind

35 Calcium-binding protein 7 (CaBP7) is a member of the cal

36 Calcium-binding protein-7 (CaBP7) is a phosphatidylinosi

37 ells and fibers to several markers including calcium-binding proteins, a synthetic enzyme for nitric

38 binding protein-1, forkhead box J1, and S100 calcium-binding protein A1.

39 Using proteomics, we found the S100 calcium-binding protein A11 (S100/A11) to be significant

40 otein (CRP), serum amyloid A (SAA), and S100 calcium-binding protein A12 (S100A12).

41 upregulation of the metastatic mediator S100 Calcium-binding protein A4 (S100A4) (1.78-fold, P<0.05).

42 es of key remodeling molecules, such as S100 calcium-binding protein A4 (S100A4) and miR-181b, after

43 ion using principal component analysis, S100 calcium-binding protein A4 (S100A4) was aligned to a pri

44 ignature with the proinflammation genes S100 calcium binding protein A8 (S100A8) and A9 (S100A9) up-r

45 etalloproteinase 9, chitinase 3-like-1, S100 calcium binding protein A8 (S100A8), S100A9, cathepsin B

46 ve cancer phenotype including increased S100 calcium binding protein A8, IL-6, IL-8, and tissue inhib

47 c oxide synthase, inducible (Nos2), and S100 calcium-binding protein A8 (S100a8).

48 se levels trigger neutrophil release of S100 calcium-binding protein A8/A9 (S100A8/A9), which binds t

49 se to hyperglycemia, neutrophil-derived S100 calcium-binding proteins A8/A9 (S100A8/A9) interact with

50 S100 calcium-binding protein A9 (S100A9) has previously been

51 l proline-rich protein 2C (SPRR2C), and S100 calcium-binding protein A9 (S100A9), which are down-regu

52 ecific transcripts mannose receptor and S100 calcium-binding protein A9, which significantly discrimi

53 terminals were themselves immunoreactive for calcium-binding proteins, again more commonly for ParV.

54 ished novel interactions with histidine-rich calcium-binding protein and TGF beta induced apoptosis p

55 and modulates the interactions between this calcium-binding protein and the T1 domain of the Kv4.3 c

56 thalamic neurons that do not contain typical calcium-binding proteins and do not project to other par

57 ith existing classification methods based on calcium-binding proteins and firing behavior.

58 Thus, with respect to the expression of calcium-binding proteins and neuropeptides, GINs are sur

59 onin C belongs to the EF-hand superfamily of calcium-binding proteins and plays an essential role in

60 S100P is a member of the S100 family of calcium-binding proteins and there have been several rec

61 In addition, genes coding for calcium-binding proteins and those implicated in tissue

62 nown localization such as TcFCaBP (flagellar calcium binding protein) and TcVP1 (vacuolar proton pyro

63 ease complex, consisting of aFGF, S100A13 (a calcium binding protein), and a 40 kDa (p40) form of syn

64 get genes, including S100A8, which encodes a calcium-binding protein, and DEK, a proto-oncogene.

65 ine kinase, myosin light chain, sarcoplasmic calcium-binding protein, and hemocyanin are the most rel

66 eraldehyde-3-phosphate dehydrogenase (GPDH), calcium-binding protein, and phosphoglycerate mutase wer

67 ansduction molecules, transcription factors, calcium-binding proteins, and carbohydrate-modifying enz

68 antibodies against G-protein alpha subunits, calcium-binding proteins, and general neuronal markers,

69 ing triple immunofluorescence (for biocytin, calcium-binding proteins, and neuropeptides) in conjunct

70 that includes the AMPA receptor, integrins, calcium-binding proteins, and, surprisingly, the myelin

71 This process is initiated by the calcium-binding protein-apoptosis-linked gene (ALG)-2.

72 These data support the notion that calcium binding proteins are differentially distributed

73 s and types of collagens, proteoglycans, and calcium-binding proteins are altered.

74 various small proline-rich proteins and S100 calcium-binding proteins, are significantly increased, w

75 n we have previously shown to express robust calcium binding proteins as well as display far less apo

76 sly shown to express only moderate levels of calcium binding proteins as well as display robust apopt

77 els of the astroglial injury biomarker S-100 calcium-binding protein B were also increased in players

78 marker concentrations of total tau and S-100 calcium-binding protein B were measured immediately afte

79 Total tau, S-100 calcium-binding protein B, and neuron-specific enolase c

80 tofore unrecognized up-regulation of a small calcium-binding protein, both in vitro and in vivo, whos

81 of the ITN-neostriatal (Str) projections and calcium binding protein (CaBP) immunostaining patterns o

82 Specifically, there is a calcium binding protein (CaBP)-poor region in the latera

83 We find that CaM-like calcium-binding protein (CaBP) molecules are clearly exp

84 Neurons expressing the calcium binding proteins (CaBPs) parvalbumin (PV) and ca

85 Calcium-binding proteins (CaBPs) play a buffering role f

86 Calcium-binding proteins (CaBPs) such as parvalbumin are

87 Despite the great variety of calcium-binding proteins (CaBPs), many of them contain t

88 ECL2 neurons that express mutant PS1 and the calcium binding protein calbindin-D28k in ECL2 are also

89 or GABA and glycine receptors, gephyrin; the calcium binding proteins calbindin and calretinin; the N

90 or GABA and glycine receptors, gephyrin; the calcium binding proteins calbindin and calretinin; the N

91 ession of activated caspase-3 as well as the calcium binding proteins calbindin, calretinin, and parv

92 tween the sexes, using the expression of the calcium-binding protein calbindin (CB) during embryonic

93 Expression of the intracellular calcium-binding protein calbindin-D(9K), previously show

94 elated strongly with decreased levels of the calcium-binding protein calbindin-D28k (CB) and the calc

95 The calcium-binding protein calbindin-D28k is critical for h

96 n loop is composed of cells positive for the calcium-binding protein calbindin.

97 eurofilament triplet protein (NNFP), and the calcium-binding proteins calbindin (CB), calretinin (CR)

98 amined expression of Ca(V)1 subtypes and the calcium-binding proteins calbindin, calmodulin and calre

99 eurons in which it was co-expressed with the calcium-binding proteins calbindin, calretinin, and parv

100 ctal cells were found to be negative for the calcium-binding proteins calbindin, parvalbumin, or calr

101 size of interneurons immunoreactive for the calcium-binding proteins calbindin-D(28K) (CB), parvalbu

102 the full-length human ERalpha (NCL-ER-6F11), calcium-binding proteins calbindin-D(28k), and parvalbum

103 the neuronal distribution of three cytosolic calcium-binding proteins: calbindin-D28k (CB), calretini

104 IR neurons for their colocalization with the calcium-binding proteins; calbindin-D28k (CB), parvalbum

105 The family of calcium binding proteins called KChIPs associates with K

106 Here, we report that the calcium binding protein calmodulin (CaM) binds to the C-

107 The calcium binding protein calmodulin (CaM) serves as a mol

108 bility group (HMG) box) proteins require the calcium-binding protein calmodulin (CaM) for optimal nuc

109 ecule, force-spectroscopy experiments of the calcium-binding protein calmodulin and explain it in a s

110 via the binding of the ubiquitous eukaryotic calcium-binding protein calmodulin to the cytoplasmic ta

111 compared with the apo states of the EF-hand calcium-binding proteins calmodulin, S100B, and calbindi

112 ngle high-affinity binding site, and (iii) a calcium-binding protein (calmodulin) with four binding s

113 The ubiquitous calcium binding protein, calmodulin (CaM), plays a major

114 breast cancer cells is also modulated by the calcium-binding protein, calmodulin (CaM).

115 The calcium-binding protein calreticulin (CRT) regulates pro

116 tive excitatory SDH neurons that express the calcium binding protein calretinin (CR).

117 The calcium binding protein calretinin is known to be expres

118 he vertical eye movement system contains the calcium-binding protein calretinin (CR).

119 We have found that expression of the calcium-binding proteins calretinin (CR) and calbindin (

120 The calcium-binding proteins calretinin (CR) and calbindin-D

121 We therefore used antibodies against the calcium-binding proteins calretinin (CR), parvalbumin (P

122 nefits of additionally expressing the mobile calcium binding protein Cb.

123 Calbindin is a calcium-binding protein (CBP) present in a subpopulation

124 three lysine residues is stimulated by P300/calcium-binding protein (CBP)-associated factor (PCAF) a

125 at 6 and 14 kDa matched the PMN chemotactic calcium-binding proteins (CBPs), S100A8 and S100A9, resp

126 Vps13p must be in complex with the small calcium-binding protein Cdc31p to be active.

127 verse genetics to test the role of the small calcium-binding protein, centrin2, in ciliogenesis.

128 Centrin is an EF-hand calcium-binding protein closely related to the prototypi

129 that up to 1% of all identified multidomain calcium-binding proteins contain a similarly highly char

130 d a complex of signaling proteins, including calcium-binding proteins, cytoskeletal proteins, and a n

131 lower renal calcium binding protein D9k and calcium binding protein D28k than normal mice, and bone

132 n was higher and associated with lower renal calcium binding protein D9k and calcium binding protein

133 um absorption as well as vitamin D-regulated calcium binding protein D9k and TRPV6 gene expression in

134 cific Ca(V)1 subtype or distribution of each calcium-binding protein did not associate with those reg

135 Because of the many different calcium-binding proteins distributed throughout cells, s

136 fin cells, but the role of a closely related calcium-binding protein, Doc2b, remains enigmatic.

137 The calcium-binding protein downstream regulatory element an

138 Staining for calbindin, a calcium binding protein enriched in Purkinje cells, show

139 was confirmed with staining for calbindin, a calcium binding protein enriched in Purkinje cells.

140 S100B is a calcium-binding protein expressed in, and secreted by, a

141 n of Kv3 channels and interrelationship with calcium-binding protein expression has not been investig

142 derived, but differ in morphology, location, calcium-binding protein expression, synaptic connectivit

143 roteins that is a part of the larger EF-hand calcium binding protein family.

144 Up-regulation of S100P, a member of the S100 calcium-binding protein family, is an early molecular ev

145 ted photoproteins are members of the EF-hand calcium-binding protein family.

146 The flagellar calcium-binding protein (FCaBP) of the flagellated proto

147 The flagellar calcium-binding protein (FCaBP) of the protozoan Trypano

148 The flagellar calcium-binding protein (FCaBP) of Trypanosoma cruzi is

149 For example, chromogranin B (CGB), a calcium binding protein found in secretory granules and

150 An antibody to recoverin, a calcium-binding protein found in photoreceptors and othe

151 Calreticulin is a pleiotropic calcium-binding protein found in the endoplasmic reticul

152 ded cells with an antibody for calretinin, a calcium-binding protein found specifically in Cajal-Retz

153 S100B is a calcium-binding protein found within astroglial cells.

154 is quite similar to that of the sarcoplasmic calcium-binding protein from Amphioxus although the sequ

155 Calcium overlay assay showed that FSCB is a calcium-binding protein from sperm.

156 EhCaBP1, one of the calcium-binding proteins from Entamoeba histolytica, is

157 nalyzing the patterns of immunoreactivity to calcium-binding proteins, GAD, serotonin, nNOS and the g

158 verexpression of S100A7 (psoriasin), a small calcium-binding protein, has been associated with the de

159 S100P, an EF-hand calcium-binding protein, has been reported to be associa

160 lular calcium concentrations, yet only a few calcium-binding proteins have been identified in plants.

161 In addition, a number of calcium-binding proteins have been isolated in several p

162 Also, osteocalcin, a calcium-binding protein highly expressed in bone, dose-d

163 The histidine-rich calcium-binding protein (HRCBP) is expressed in the junc

164 Calmodulin is the primary calcium binding protein in living cells.

165 nalyze the immunohistochemical expression of calcium-binding proteins in the dorsal thalamus of Fmr1

166 gorized based on their expression of various calcium-binding proteins, including parvalbumin, calbind

167 h mobility group box-1 protein (HMGB1), S100 calcium binding proteins] inducers of inflammation.

168 Centrins are calcium binding proteins involved in cell division in eu

169 Calmodulin (CaM) is a 16.8-kDa calcium-binding protein involved in calcium-signal trans

170 The fungal protein CBP (calcium binding protein) is a known virulence factor wit

171 matricellular protein SMOC (Secreted Modular Calcium binding protein) is conserved phylogenetically f

172 (Ocm), a member of the parvalbumin family of calcium binding proteins, is expressed predominantly by

173 sin (S100A7), a member of the S100 family of calcium-binding proteins, is richly expressed in keratin

174 An antibody against recoverin, the calcium-binding protein, labels photoreceptors, cone bip

175 , cochlear-driven activity appears to affect calcium binding protein levels in both neuropil and neur

176 with immunogold-silver to identify different calcium-binding proteins localized within separate popul

177 S100B is a calcium-binding protein, localized to astroglial cells,

178 This calcium-binding protein localizes to the junctional SR (

179 rdiac calsequestrin (CASQ2), a high-capacity calcium-binding protein located in the sarcoplasmic reti

180 d CaBP-D9k are cytosolic vitamin D-dependent calcium-binding proteins long thought to play an importa

181 Two S100 family calcium-binding proteins, macrophage inhibitory-related

182 of GABAergic neurons identified by distinct calcium-binding proteins may exert unique roles in the p

183 ar components include the EF-hand-containing calcium-binding proteins mitochondrial calcium uptake 1

184 he Tc1 include increased levels of the S100B calcium-binding protein, mTOR proteins RAPTOR and P70S6,

185 The calcium-binding proteins myeloid-related protein (MRP)-8

186 t conducted a systematic comparison of three calcium-binding proteins, namely, parvalbumin, calretini

187 ial modulation of these channels by neuronal calcium-binding proteins (nCaBPs) may contribute to syna

188 One product that may play a role is the calcium binding protein, neurocalcin.

189 We have discovered that the calcium-binding protein nuclebindin-1 (NUCB1) is a novel

190 The calcium binding proteins of the EF-hand super-family are

191 The calcium-binding proteins of the human S100A7/A15 (hS100A

192 stinguished on the basis of their content of calcium-binding proteins or peptides.

193 lated MMTV integration site 5A (WNT5A), S100 calcium-binding protein P (S100P) and cysteine-rich prot

194 he MS/DB, including neurons that express the calcium binding protein parvalbumin (marker of fast spik

195 hybridization measures of the mRNAs for the calcium binding protein parvalbumin (PV) and the GABA sy

196 ctivity in inhibitory neurons expressing the calcium binding protein parvalbumin (PV) in the mouse pr

197 ss of inhibitory interneurons expressing the calcium binding protein parvalbumin plays a central role

198 utter-firing interneurons also expressed the calcium-binding protein parvalbumin (PV(+)).

199 Positive immunoreactivity to the calcium-binding protein parvalbumin (PV) and nitric oxid

200 Interneurons containing the calcium-binding protein parvalbumin (PV) constitute abou

201 iking inhibitory interneurons expressing the calcium-binding protein parvalbumin (PV).

202 by two populations of neurons containing the calcium-binding protein parvalbumin (PV): local inhibito

203 ortical GABAergic interneurons expresses the calcium-binding protein parvalbumin and plays a critical

204 fast-spiking phenotype and expression of the calcium-binding protein parvalbumin have been suggested

205 set of GABAergic interneurons expressing the calcium-binding protein parvalbumin.

206 nits with neurochemical markers, such as the calcium-binding proteins parvalbumin (PV) and calbindin

207 In rodents, the calcium-binding proteins parvalbumin (PVB) and calbindin

208 here to be little if any overlap between the calcium-binding proteins parvalbumin and calretinin in i

209 urons--identified by their expression of the calcium-binding proteins parvalbumin, calbindin, and cal

210 to GABAergic interneuron subtypes expressing calcium-binding proteins parvalbumin, calbindin, or calr

211 y peptide (cholecystokinin, somatostatin) or calcium-binding protein (parvalbumin, calretinin) conten

212 ket cells or interneurons expressing various calcium-binding proteins (parvalbumin, calbindin, and ca

213 The EF-hand calcium binding protein, parvalbumin, is a major fish al

214 of GABA-containing neurons that express the calcium-binding protein, parvalbumin (PV).

215 ically projecting neurons, which contain the calcium-binding protein, parvalbumin (PV).

216 ulation of projection neurons containing the calcium-binding protein, parvalbumin (PV).

217 ssurance acted through the regulation of the calcium-binding protein PAT-10.

218 ine kinase, the adaptor protein Fyb, and the calcium-binding protein Pdcd-6/Alg-2.

219 that CUL3 and its adaptor KLHL12 require two calcium-binding proteins, PEF1 and ALG2, for recognition

220 Secretagogin (SCGN), a hexa EF-hand calcium binding protein, plays key roles in insulin secr

221 S100A8 and S100A9 are calcium-binding proteins predominantly expressed by neut

222 , chaperones and/or chaperone-like proteins, calcium-binding proteins, proteases, signal transduction

223 -spiking interneuron clusters expressing the calcium-binding protein Pvalb were identified, one co-ex

224 We used antibodies against the calcium-binding protein recoverin and the carbohydrate e

225 In the habenula, these calcium-binding proteins revealed right-left asymmetry o

226 95% of the axonemal tektins, and >95% of the calcium-binding proteins, Rib74 and Rib85.5, whose human

227 interneurons, which do not contain any known calcium-binding protein(s), kappafixed amounted to only

228 We further show that 1q21.3-encoded S100 calcium-binding protein (S100A) family members, mainly S

229 d for expression of phospholipase D1 and the calcium-binding protein S100A3.

230 High levels of the S100 calcium binding protein S100A4 also called fibroblast sp

231 The interaction between the calcium-binding protein S100A4 and the C-terminal fragme

232 Nuclear expression of the calcium-binding protein S100A4 is a biomarker of increas

233 The calcium-binding protein S100A4 is expressed at elevated

234 We previously showed that the calcium-binding protein S100A4 is overexpressed during t

235 correlated with the expression of the small calcium-binding protein S100A4.

236 Transgenic mice overexpressing the calcium binding protein, S100A4/Mts1, occasionally devel

237 Increased levels of the homodimeric calcium-binding protein, S100A4, have been shown to caus

238 Heightened expression of the S100 calcium-binding protein, S100A4/Mts1, is observed in pul

239 ne signaling, notably the heterodimeric S100 calcium-binding proteins S100a8 and S100a9.

240 emarkably, UG-KO mouse lungs overexpress two calcium-binding proteins, S100A8 and S100A9, whereas B16

241 The EF-hand calcium-binding protein S100B also binds one zinc ion pe

242 ression of Cav1, which then acts through the calcium-binding protein S100P to promote metastasis.

243 The calcium-binding protein S100P was prominent among PEGA g

244 In Arabidopsis thaliana, the calcium binding protein Salt Overly Sensitive3 (SOS3) in

245 In the present study the calcium-binding protein secretagogin was localized in a

246 that the selective co-expression of another calcium-binding protein, secretagogin (Scgn), separates

247 demonstrate that antibodies for the EF-hand calcium-binding protein, secretagogin, strongly label th

248 that Calnuc and NUCB2, two highly homologous calcium-binding proteins, share a common motif with GIV

249 Interneuron markers using calcium-binding proteins showed that LS GABAergic neuron

250 elected Drosophila genes has revealed that a calcium-binding protein, stromal interaction molecule (S

251 Calcium-binding proteins such as parvalbumin and calbind

252 S100 calcium-binding proteins such as S100B are elevated in p

253 TSF includes many low-affinity high-capacity calcium binding proteins, such as serum albumin and case

254 ncoding small proline-rich proteins and S100 calcium-binding proteins, suggest that keratinization pl

255 We recently identified a family of calcium-binding proteins, termed KChIPs (Kv channel inte

256 Neuronal calcium sensor-1 (NCS-1) is a small calcium binding protein that plays a key role in the int

257 Tescalcin, an EF-hand calcium binding protein that regulates the Na(+)/H(+) ex

258 Centrins are calcium binding proteins that belong to the EF-hand supe

259 We recently identified KChIPs as a family of calcium binding proteins that coassociate and colocalize

260 calmodulin, NCS-1 is a member of a family of calcium binding proteins that contain EF-hand motifs, wh

261 he S100 proteins make up a family of dimeric calcium binding proteins that function in response to ch

262 the distance between these channels and the calcium binding proteins that serve as the molecular tar

263 otassium channel interacting protein 3) is a calcium-binding protein that binds at the N terminus of

264 DREAM (calsenilin/KChIP3) is an EF-hand calcium-binding protein that binds to specific DNA seque

265 terferon (IFN)- and growth factor-inducible, calcium-binding protein that either inserts into the pla

266 CaBP4 is a calmodulin-like neuronal calcium-binding protein that is crucial for the developm

267 lammatory factor-1 (AIF-1) is a cytoplasmic, calcium-binding protein that is expressed in VSMCs by al

268 S100A4 is a calcium-binding protein that is known to form homodimers

269 BYR is a highly polymorphic, sperm flagellar calcium-binding protein that is tyrosine as well as seri

270 identified as a binding partner of CABYR, a calcium-binding protein that is tyrosine-phosphorylated

271 Calmodulin (CaM) is a highly flexible calcium-binding protein that mediates signal transductio

272 matrix protein 1 (DMP1) is a non-collagenous calcium-binding protein that plays a critical role in bi

273 ne, cardiac troponin C, codes for a neuronal calcium-binding protein that regulates actin binding and

274 DREAM (calsenilin/KChIP3) is an EF-hand calcium-binding protein that represses transcription of

275 m and integrin binding protein 1 (CIB1) is a calcium-binding protein that was initially identified as

276 r to derive from matrix vesicles enriched in calcium-binding proteins that are released by cells with

277 Calcineurin B-like (CBL) proteins are calcium-binding proteins that are thought to function as

278 S100A4 is a member of the S100 family of calcium-binding proteins that is directly involved in tu

279 etastasin) is a member of the S100 family of calcium-binding proteins that is directly involved in tu

280 In sections labeled for calcium binding proteins, the two walls of the sPCS were

281 It involves two major calcium-binding proteins, the voltage-gated calcium chan

282 ly or by exogenous dopamine, by expressing a calcium-binding protein to buffer calcium levels in sens

283 or-1 (NCS-1), a high-affinity, low-capacity, calcium-binding protein, to purified InsP3R type 1 (InsP

284 -to-noise version of cameleon, a fluorescent calcium-binding protein, to quantify the activity of the

285 alcium-dependent sequestration of PID by the calcium-binding protein TOUCH3 (TCH3).

286 Calmodulin is a calcium-binding protein ubiquitous in eukaryotic cells,

287 Here we show that S100A11, a calcium-binding protein upregulated in a variety of meta

288 ently cloned member of the EF-hand family of calcium binding proteins, was localized in the mouse, ra

289 All three calcium-binding proteins were expressed in nucleus media

290 All three calcium-binding proteins were expressed in the auditory

291 n the amount of both Ca(V)1 subtypes and the calcium-binding proteins were found throughout the brain

292 The HRC gene encodes the histidine-rich calcium-binding protein, which is found in the lumen of

293 -like domain beta (DOC2B) gene encodes for a calcium-binding protein, which is involved in neurotrans

294 nflammatory factor (AIF)-1 is a cytoplasmic, calcium-binding protein whose expression in transplanted

295 1 (NUCB1) is a widely expressed multidomain calcium-binding protein whose precise physiological and

296 calcium indicators are fusions of endogenous calcium-binding proteins whose functionality in vivo may

297 Calbindin-D28k is a calcium binding protein with six EF hand domains.

298 S100B is a calcium-binding protein with both extracellular and intr

299 It is an EF-hand calcium-binding protein with homology to calmodulin but

300 Centrins are a family of small, calcium-binding proteins with diverse cellular functions