ライフサイエンスコーパス: calcium-binding protein

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

36 an increase in synthetic marker S100A4 (S100 calcium binding protein A4) compared with contractile VS

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

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

39 We have previously demonstrated that S100 calcium-binding protein A4 (S100a4) is a driver of tendo

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

41 Here, we found that S100 calcium-binding protein A4 (S100A4), a major metastasis-

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

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

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

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

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

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

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

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

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

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

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

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

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 cognized on the basis of their expression of calcium-binding proteins and neuropeptides, including pa

60 f inhibitory interneurons expressing various calcium-binding proteins and neuropeptides.

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

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

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

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

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

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

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

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

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

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

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

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

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

74 eurodegeneration, especially when protective calcium binding proteins are lost from the cytosol.

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

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

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

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

79 ein, ubiquitin c-terminal hydrolase-L1, S100 calcium binding protein B, alpha-II-spectrin breakdown p

80 CSF levels of S100 calcium-binding protein B and glial fibrillary acidic pr

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

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

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

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

85 al Fibrillary Acidic Protein (GFAP) and S100 Calcium-Binding Protein beta (S100beta); and the inflamm

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

105 ergic, and a quarter of these co-express the calcium-binding protein, calbindin.

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

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

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

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

110 Binding of a regulatory calcium-binding protein calmodulin (CaM) to the proximal

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

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

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

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

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

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

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

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

119 The calcium binding protein calretinin is known to be expres

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

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

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

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

124 Mutations in the calcium-binding protein calsequestrin cause the highly l

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

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

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

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

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

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

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

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

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

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

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

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

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

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

139 The calcium-binding protein downstream regulatory element an

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

161 iffering densities of neurons expressing the calcium-binding proteins in specific nuclei are noted.

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

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

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

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

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

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

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

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

170 gene that encodes a putative histidine-rich calcium-binding protein, is the key determinant of Fhb1-

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

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

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

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

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

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

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

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

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

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

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

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

183 Increased levels of the calcium-binding protein neuronal calcium sensor 1 (NCS1)

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

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

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

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

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

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

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

191 The expression of the calcium binding protein parvalbumin (PV) has been observ

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

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

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

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

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

197 basal forebrain (BF) neurons containing the calcium-binding protein parvalbumin (PV) increased broad

198 of TRN GABAergic neurons, which express the calcium-binding protein parvalbumin (PV), and are implic

199 xpresses the vesicular GABA transporter, the calcium-binding protein parvalbumin (PV), and the Kv3.3

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

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

202 ateral hypothalamic neurons that express the calcium-binding protein parvalbumin (PVALB; LH(PV) neuro

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 lpha-Estradiol reduced the expression of the calcium-binding protein parvalbumin, decreased the integ

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

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

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

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

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

211 in the density of structures expressing the calcium-binding proteins parvalbumin, calbindin, and cal

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

228 95% of the axonemal tektins, and >95% of the calcium-binding proteins, Rib74 and Rib85.5, whose human

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

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

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

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

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

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

235 The calcium-binding protein S100A4 is expressed at elevated

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

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

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

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

240 The S100 calcium binding proteins S100A8 and S100A9, and their ex

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

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

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

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

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

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

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

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

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

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

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

252 he folding of a ribosome-bound, multi-domain calcium-binding protein stalled at different points in t

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

254 Calcium-binding proteins such as parvalbumin and calbind

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

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

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

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

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

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

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

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

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

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

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

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

267 monstration that overexpression of S100A4, a calcium-binding protein that is frequently overexpressed

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

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

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

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

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

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

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

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

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

277 Doc2a and Doc2b are high-affinity calcium-binding proteins that interact with SNARE protei

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

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

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

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

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

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

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

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

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

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

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

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

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

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

294 1 (NUCB1) is a widely expressed multidomain calcium-binding protein whose precise physiological and

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

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

297 Calmodulin is a calcium binding protein with two lobes, N-lobe and C-lob

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