ライフサイエンスコーパス: binding capacity

1 quences have confirmed function (e.g. target binding capacity).

2 ion between RGD structure and their integrin-binding capacity.

3 rotein interaction, independent of SPDEF DNA binding capacity.

4 R) at Ser101 and Ser241 to attenuate its DNA binding capacity.

5 tains its protein stability and tetrapyrrole binding capacity.

6 ond domain, without compromising its calcium binding capacity.

7 orbed to a porous membrane with high protein binding capacity.

8 recipitate pri-miRs, suggesting possible RNA-binding capacity.

9 ut hydroxyprolines displayed a very weak IgE-binding capacity.

10 s is consistent with a change in the maximum binding capacity.

11 tophosphorylation abolished its carbohydrate-binding capacity.

12 en screened for clones with restored antigen binding capacity.

13 an acetylation mimic, reduces NDPK-A FBXO24 binding capacity.

14 nsactivation ability and upregulation of DNA binding capacity.

15 monary fibrosis (IPF) exhibit enhanced FXIIa binding capacity.

16 nd transcriptional activity, through its RNA-binding capacity.

17 asomes are asymmetric in their polyubiquitin binding capacity.

18 with WT, presumably due to enhanced membrane-binding capacity.

19 proteins showed significantly decreased IgE binding capacity.

20 of HCAs may significantly contribute to the binding capacity.

21 S100B homodimers do not exhibit such Mn(II)-binding capacity.

22 fic anti-HLA antibodies and their complement-binding capacity.

23 basic motif, causes the loss of p17 heparin-binding capacity.

24 , also could be highly promiscuous in its GF-binding capacity.

25 to integrins, thereby enhancing their ligand binding capacity.

26 ion associated with loss of activity and DNA binding capacity.

27 lected since it provided the highest protein binding capacity.

28 essitates knowledge of the precise metal-ion binding capacity.

29 lysis, cysteine activation, and metal (zinc) binding capacity.

30 king density is used to achieve high protein binding capacity.

31 t in SpoVAD essentially abolish its DPA(2,6)-binding capacity.

32 ues is diminished in the absence of FcgammaR binding capacity.

33 assessed strain-specific differences in GAG binding capacity.

34 LISA and protein arrays to confirm their IgM-binding capacity.

35 inetics, replication stability, and receptor-binding capacity.

36 somerase activity and decrease the multidrug binding capacity.

37 ing relatively inexpensive quantification of binding capacity.

38 l ties, we could maintain ThreeFoil's glycan-binding capacity.

39 ut antibody leakage or reduction in antibody binding capacity.

40 which results in maintenance of their ligand-binding capacities.

41 l the isolates and MR and VOR had high metal binding capacities.

42 /DP heteromers without altering their ligand-binding capacities.

43 Cationic MBs (+15.8 mV; DNA binding capacity, 0.03 pg per MB) partially protected bo

44 gen parvalbumin demonstrated the highest IgE-binding capacity (10%-49%), followed by triosephosphate

45 a dissociation constant of 3 nM and maximum binding capacity 83 fmol/10(6) SKOV3 cells.

46 nt K(c) = 10(19.8) at 25 degrees C) and high binding capacity (9.5 mg Hg disk(-1)) toward Hg(2+).

47 cell wall hydrolytic activity and ampicillin binding capacity, a characteristic of most bacterial CWM

48 cence intensity, DSA IgG3 positivity and C1q binding capacity adequately reclassified patients at low

49 anges in serum ferritin level and total iron-binding capacity, adverse effects.

50 ious micro-organisms, we assessed whether HS-binding capacity affects MHC class II-restricted present

51 polymorphism, amylopectin content and water-binding capacity all along heating, cooling and storage

52 that the parasite decreases its endothelial binding capacity, allowing increased splenic clearance a

53 matin similarly in mitosis and how different binding capacities among them relate to function.

54 pproach utilizing crystal structures, Ca(2+) binding capacities, analytical ultracentrifugation, and

55 Water retention and oil binding capacities and pasting properties significantly

56 Detergent-binding capacities and phospholipid contents of the mode

57 rking temperature during the synthesis, high binding capacity and affinity.

58 tructural homolog and suggest that its lipid-binding capacity and association with COQ7 are key featu

59 Moreover, other Sirtuins share some DSB-binding capacity and DDR activation.

60 -alphaPEG, hybrid-type cells) to improve the binding capacity and detection limit for free PEG and PE

61 ity through measurements of iron solubility, binding capacity and dialyzability.

62 lsifying activity, emulsion stability, water binding capacity and dispersibility, whereas, foaming ca

63 types of peel flour showed interesting water binding capacity and fat absorption capacity.

64 of CRT2 is responsible for its high calcium-binding capacity and function in regulating the endogeno

65 amily can diversify while maintaining ligand-binding capacity and identifies features that should be

66 amino acids 43 and 67 showed promiscuous HLA-binding capacity and induced memory CD4(+) T-cell respon

67 stronger T cell-stimulatory and reduced IgE-binding capacity and induced murine Bet v 1-specific ant

68 ermembrane space domain of Mic60 has a lipid-binding capacity and induces membrane curvature even in

69 The calcium buffering power, binding capacity and non-linear binding properties of th

70 er and lactic acid retention capacities, oil binding capacity and Rapid Visco Analyzer indices).

71 of MAP4 at T927ES928E partially abolished E7-binding capacity and rescued mitotic progression in host

72 d (palmitic acid analog) to Uox with the HSA binding capacity and retained enzyme activity.

73 th esterified starches increased their water binding capacity and solubility in water.

74 ysis) on the functional properties, in vitro binding capacity and structural properties of succinylat

75 allenge model of inflammation, Treg selectin binding capacity and the molecular basis of Treg rolling

76 nctional ingredients is related to the water binding capacity and the presence of dietary fiber.

77 ters (serum iron, serum ferritin, total iron-binding capacity and transferrin saturation), serum hepc

78 fic adsorption typically accompanies loss of binding capacity and vice versa for many surface coating

79 ility (pH 7.4-9), emulsificant capacity, oil binding capacity and water adsorption capacity.

80 roperty study demonstrates that toxicity, NA binding capacity, and biodistribution could be balanced

81 Diabetic albumin showed impaired NEFA binding capacity, and both structural and functional alt

82 vitro cholesterol and 25-hydroxycholesterol-binding capacity, and cholesterol extraction from liposo

83 tein family, originally defined by their RNA binding capacity, and forms a complex with SLIRP that ha

84 d that RAP has an intrinsic and specific RNA binding capacity, and the RAP binding site was mapped to

85 The SMZ-MIPs had SMZ binding capacity approximately more than eight times hig

86 vation states possessing differential myosin binding capacities are also visible.

87 volume ratios and subsequently large protein binding capacities are of interest for advanced immunoso

88 Fermentation increased water- and oil-binding capacity as well as protein solubility at pH 4.0

89 ed large ranges of affinity, specificity and binding capacity as well as substantial lot-to-lot varia

90 kingly, their application in quantitative Ab-binding capacity assays combined with high-dimensional p

91 phic approaches and radiolabeled competitive binding-capacity assays, we report here how two nonstero

92 There was no effect on water binding capacity assessed by centrifuge, however, low-fi

93 that USFS exhibited the highest cholesterol binding capacity at both pH 2.0 (1.86 mg/g) and pH 7.0 (

94 cessive variants were enriched in nucleotide binding capacity, ATPase activity, and the dynein heavy

95 for in vitro biofilm formation, fibronectin-binding capacity, autolysis, and protease and nuclease a

96 e present study were differences in 11C-PBB3 binding capacity between groups, and the association of

97 of 1 mM ACh with Kd, 4.23 nM, and saturable binding capacity (Bmax), 6.38 pmol/mg protein.

98 , electrostatic interactions affect membrane-binding capacity, but do not appear to affect the curvat

99 d to Ara h 2 significantly decreased the IgE binding capacity by 37% and 50%, respectively.

100 These results suggest that FcgammaR binding capacity by anti-HA antibodies was dependent on

101 burden in TBI brains, we calculated 11C-PBB3 binding capacity (cm3), which is a summed voxel value of

102 of chemical and physical stability and high binding capacity combined with the intrinsic advantages

103 significantly higher swelling power and fat binding capacity compared to other fractions (F1, F2 and

104 S-CoV-2 has a 10- to 20-fold higher receptor-binding capacity compared with previous pandemic coronav

105 ndependent in vivo; the presence of FcgammaR-binding capacity compromises their anti-tumor activity.

106 use of processed walnuts with decreased IgE binding capacity could be a potential strategy for walnu

107 noclonal antibody (mAb) effectively, but the binding capacity decays over repeated purification cycle

108 Mean total iron-binding capacity decreased from 501 to 389 mug/dL (ferro

109 he cross-linked surface retained the antigen binding capacity demonstrating its robustness in being r

110 ely with O(4)-alkyldT-harboring DNA, and the binding capacity depends mainly on the HMG box-A domain

111 binding domains (RBDs), whose integrated RNA-binding capacity determines whether LLPS occurs upon RNA

112 ncated CDC37 (DeltaC-CDC37) that lacks HSP90 binding capacity did not affect kinase client expression

113 A mutant reporter with reduced PI(4,5)P(2) binding capacity did not show these accumulations.

114 s that lack either alpha-actinin or Ena/VASP-binding capacity display compromised response to mechani

115 Loss of MGP or its BMP4-binding capacity disrupted the retinal vasculature, resu

116 A carried J chain and displayed selective SC binding capacity either in a mixture with monomeric IgA

117 Thus, PCM size and binding capacity emerge from the regulated polymerizatio

118 This study shows that removal of receptor binding capacity enhances potency of the subunit HCR vac

119 umic colloids lost up to 50% of their copper-binding capacity, expressed as a molar ratio to organic

120 on of laminarin to ovalbumin reduced its IgE binding capacity fivefold and increased its immunogenici

121 The columns exhibited excellent binding capacities for microaffinity enrichment: Con A w

122 main-engineered bNAb variants with selective binding capacity for activating FcgammaRs displayed augm

123 L blasts, whereas endothelial cells with low binding capacity for AT1413 remained unaffected.

124 ation between LARGE-glycan extension and its binding capacity for extracellular matrix ligands.

125 that controls muscle growth by altering the binding capacity for myostatin.

126 tios were optimised in order to maximise the binding capacity for phosphate.

127 or histocompatibility complex (MHC) class II-binding capacity for rapid production as synthetic poly-

128 higher surface densities, yielding a higher binding capacity for the analyte.

129 This can be attributed to a loss of binding capacity for the microRNAs (miRNAs) Let-7e and L

130 uired to be stored at 4 degrees C) with high binding capacity for the separation and purification und

131 ed MMSNs were highly effective and had large binding capacity for U sequestration from high salt wate

132 g motif of Mamu-A2*05:01, and elucidated the binding capacity for virus-derived peptides.

133 Vaccines that lack receptor binding capacity have the added property of limited off-

134 llergenic activity in terms of patients' IgE-binding capacity, human basophil activation, and positiv

135 (T) /A at least 30% below intravascular B(T) binding capacity (i.e., B(T) /A = 1.0).

136 a mechanism that is independent of its dsRNA binding capacity.IMPORTANCE We use mammalian reovirus as

137 d that patients with TBI had higher 11C-PBB3 binding capacities in the neocortical grey and white mat

138 d to adsorb via a Langmuir model and to have binding capacities in the order Zn(++)>Co(++)>Ni(++).

139 k showing low midbrain serotonin transporter binding capacity in depressed suicides and may partially

140 a CADD score of 29.6, and increases protein binding capacity in silico.

141 11C-PBB3 binding capacity in the white matter segment correlated

142 cephalopathy syndrome showed higher 11C-PBB3 binding capacity in the white matter segment than those

143 ion was found between psychosis and 11C-PBB3 binding capacity in the white matter.

144 that LRPPRC displays a broad and strong RNA binding capacity in vitro in contrast to SLIRP that asso

145 Addition of DSA IgG3 positivity or C1q binding capacity increased discrimination performance of

146 an Rbd2 mutant with diminished PtdIns(4,5)P2-binding capacity indicates that this interaction is nece

147 HHP treatment decreased the IgE and IgG-binding capacities, indicating a significant decrease in

148 ion of Fox-1 by WNK3 does not change its RNA binding capacity; instead, WNK3 increases the cytoplasmi

149 The results show that absolute binding capacity is a better predictor of immunogenicity

150 In conclusion, increased 11C-PBB3 binding capacity is associated with late-onset neuropsyc

151 In contrast, its DNA-binding capacity is enhanced on IgM stimulation in respo

152 ility involves its N-glycosylation, its pili-binding capacity is insufficient, and it cannot be confe

153 iation constant of ~30 muM, and its arginine-binding capacity is required for arginine to activate mT

154 rA mispairs is fully inhibited, although its binding capacity is retained.

155 eron-stimulated gene (ISG) with possible RNA-binding capacity, is an important restriction factor for

156 rum ferritin level >15 ng/mL, and total iron-binding capacity <425 mug/dL at the 12-week visit), chan

157 L1 exhibits high affinity for ADP and ATP, a binding capacity not reported in any D7.

158 in by two purification circuits altering the binding capacities of albumin by biochemical (changing o

159 ly affect the protein solubility and the IgE-binding capacities of both the soluble and insoluble haz

160 This assay was used to compare the binding capacities of different auxin response factor (A

161 Amino acid substitutions may disrupt binding capacities of dystrophin and have a major impact

162 Bile acid (BA)-binding capacities of in vitro digested samples and nutr

163 p120 (surface HIV-1 glycoprotein of 120 kDa) binding capacities of isolated Lg-CRD.

164 accompanied by substantial decreases in ATP-binding capacities of many kinases.

165 erms, we obtained dissociation constants and binding capacities of the membranes.

166 To further examine peptide-binding capacities of these two allelic variants, we use

167 The BA-binding capacities of WFB and FBSC were 1.94 and 37.50mu

168 ndicated an imprinting factor, IF, of ~10, a binding capacity of 0.5-2 mg/g, and the ability to rebin

169 a dissociation constant of 2 nM and maximum binding capacity of 18 fmol/10(6) cells, and (18)F-FES h

170 Additionally, the overall binding capacity of 293T/SL-alphaPEG cells for PEGylated

171 tudy was developed in order to determine the binding capacity of 4-EG by PANI materials in 12% ethano

172 This DGT method had a binding capacity of 4.24 mug per binding gel disk (3.14

173 Substitution of E45 reduces the binding capacity of 6H4, confirming that it is critical

174 F binding sites and increased expression and binding capacity of activity-regulated TFs.

175 g to the high selectivity and cost-effective binding capacity of affinity resins for capture of the F

176 ctive metabolites in platelets when the NEFA binding capacity of albumin is blunted by glycoxidation.

177 levant levels of fatty acids modulate the Zn-binding capacity of albumin, with far-reaching implicati

178 In summary, these data show that glycogen-binding capacity of AMPKbeta is regulated by Thr-148 aut

179 Determining the binding capacity of AMPs to the bacterial cell envelope

180 brium dissociation constant (KD) and maximum binding capacity of analyte (Bmax) values for the intera

181 Equilibrium constant (KD) and maximum binding capacity of analyte (Bmax) values for the intera

182 We investigated whether the complement-binding capacity of anti-HLA antibodies plays a role in

183 The IgE-binding capacity of Ara h 2 was then recapitulated with

184 blocks and then used to saturate the biotin binding capacity of avidin coated wells.

185 analogous results, suggesting that the dsRNA binding capacity of B2 somehow played a role in coat pro

186 In this study, metal binding capacity of barley protein hydrolysates and thei

187 The water and fat binding capacity of beta-chitosan presently studied was

188 a h 6, Ara h 6 immune complexes, and the IgE binding capacity of breast milk samples were measured us

189 aggressively than MgCl2 and NaCl due to the binding capacity of Ca(2+) ions with hydroxyl and carbon

190 , respectively, higher and lower than the Hb-binding capacity of CSF haptoglobin.

191 oxOL binding to CSQ2 reduced both the Ca(2+) binding capacity of CSQ2 (by 48%-58%) and its aggregatio

192 The ICAM-1-binding capacity of DC4 was mapped to the C-terminal thi

193 vity with and cross-inhibition of the ICAM-1 binding capacity of domain cassette 4 PfEMP1s.

194 Assessment of the complement-binding capacity of donor-specific anti-HLA antibodies a

195 We conclude that assessment of the C3d-binding capacity of DSA at the time of AMR diagnosis all

196 tavidin is used to quantify the streptavidin binding capacity of each mesh type through confocal micr

197 the inter-RRM interaction or the loss of RNA binding capacity of either RRM impairs splicing repressi

198 We show that this requires DNA binding capacity of EVI1, suggesting that downstream tar

199 described that Ala258Ser leads to increased binding capacity of ficolin-2 to N-acetylglucosamine.

200 cytometry examination revealed the specific binding capacity of fluorescein isothiocyanate-RamAb to

201 In vitro bile acid-binding capacity of FVJ was about 4.30times higher than

202 This PSD-95 binding capacity of GPR30 is specific and determined by

203 nuclear translocation, dimerization, or DNA binding capacity of GR.

204 However, the overall Pu binding capacity of HA (particulate + colloidal-Pu) decr

205 ans as an important determinant of the FXIIa binding capacity of HLF.

206 The binding capacity of HMF to casein was about 10% but did

207 ns could be limited by the concentration and binding capacity of humic ligands, and provide a summary

208 The binding capacity of hybrid-type cells for PEG-like molec

209 SA surface expression, leading to higher C4S-binding capacity of infected erythrocytes.

210 acid increased the affinity and the maximum binding capacity of LPMO for cellulose.

211 tofusins (Mfns) 1 and 2-and enhances the GTP-binding capacity of Mfn2, suggesting that IHG-1 acts as

212 d by autopsy, we directly compared the Abeta-binding capacity of multiple receptor candidates while a

213 Binding capacity of N8-GP on human monocyte-derived dend

214 IgE-binding capacity of oleosins derived from in-shell roast

215 s UBAN domain at S473, thereby expanding the binding capacity of OPTN to diverse Ub chains.

216 The phosphatidylinositol 4,5-bisphosphate-binding capacity of PBP10 was not in its own sufficient

217 polar amino acids to alanine diminished the binding capacity of PCV2 to heparin.IMPORTANCE It has be

218 0min, produces a significant decrease of IgE-binding capacity of peanut allergens.

219 study was to investigate the changes in IgE binding capacity of peanut proteins produced by thermal-

220 Importantly, the double-stranded DNA-binding capacity of protein p6 is essential for its relo

221 ds, which we named regacin, disrupts the DNA binding capacity of RegA by interacting with amino acid

222 nduced activation of mTORC1 requires the SAM binding capacity of SAMTOR.

223 The leucine-binding capacity of Sestrin2 is required for leucine to

224 ting titer to determine the infectious prion binding capacity of SLS and Mte.

225 Our data reveal significant prion-binding capacity of soil and the utility of BASICS to es

226 oil has complicated attempts to quantify the binding capacity of soil for prion infectivity.

227 Thus, the antigen binding capacity of the attached Abs was enhanced by up

228 The binding capacity of the bioadsorbent is partially loaded

229 HLA restriction of the specific TCLs and the binding capacity of the epitope-containing peptides to c

230 The ubiquitin-binding capacity of the FAAP20 UBZ is required for recru

231 stics were associated with a decrease in the binding capacity of the HS for Fe and Al but not Cu whil

232 time did not affect the carbon specific iron-binding capacity of the humic substances which was [L]/[

233 ino acid sequences double the carbon dioxide binding capacity of the previously reported fiber formed

234 The maximum binding capacity of the protein G-coupled membrane was 4

235 The antibody binding capacity of the protein G-coupled membrane was e

236 ation in the SEMA3C promoter reduces the DNA binding capacity of the region.

237 OH was synthetically deleted, and the sterol binding capacity of the resulting derivative, C2'deOAmB,

238 The microtubule-binding capacity of the SAH domain is important for mito

239 arted by this particular region inhibits the binding capacity of the tri-domain protein for GPIbalpha

240 gulated molecule, SULF2, normalizes the VLDL-binding capacity of their hepatocytes and abolishes post

241 tivation of TTP by MK2, whereas retained RNA-binding capacity of TTP-AA to 3'UTRs caused profound cha

242 Our study thus reveals that the RNA-binding capacity of uL18 ribosomal proteins has been rep

243 In uninfected cells, the impaired RNA-binding capacity of Y315A was evident by a shift of A3G

244 xhibited distinct activity patterns, various binding capacities on cellulosic substrates, and differe

245 or allergen, Der p 13 may, through its lipid-binding capacity, play a role in the initiation of the H

246 metals in non bioavailable forms, the metal-binding capacity provided by OC and iron and manganese o

247 Maximum IgG binding capacities, Qm of 6.7, 3.8, and 4.1mgm(-2) were

248 In general, this reduction increased antigen-binding capacity, resulting in, for example, enhanced tu

249 Equilibrium constant (KD), maximum binding capacity (Rmax) and Gb values for interaction of

250 h include incomplete template removal, small binding capacity, slow mass transfer, and irregular mate

251 functional properties (water-holding and oil-binding capacities, solubility, emulsifying and foaming

252 ulting in soluble Shh clusters with their HS binding capacities strongly reduced.

253 e-relevant non-canonical Wnt ligands lack HS binding capacity, suggesting that Sulfs indirectly repre

254 Hg(2+) ion from all other metal ions, and a binding capacity that is >/=18 times that of thio-crown

255 transferrin saturation (SAT) and total iron binding capacity (TIBC) in 2347 AAs participating in the

256 vailable serum iron, ferritin and total iron binding capacity (TIBC) values were ultimately included

257 association study of serum iron, total iron binding capacity (TIBC), transferrin saturation, and fer

258 l dynamics of AADC, potentially lowering its binding capacity to a cofactor.

259 protein isolates (CPIs) revealed the highest binding capacity to all aldehydes followed by wheat glut

260 A high-throughput screen to analyse TINCR binding capacity to approximately 9,400 human recombinan

261 dent, comprehensive functional assays of DNA-binding capacity to explore the evolution of DNA-binding

262 r MoS2 nanosheets also exhibit a much higher binding capacity to pesticides and a much larger specifi

263 evels in vivo selectively reduces Alba3 mRNA-binding capacity to specific target transcripts and can

264 VIM1-binding capacity to target genes was significantly reduc

265 nse against both CIDR Ags, with an increased binding capacity to the cognate endothelial protein C re

266 etalg aggregation, which in turn affects its binding capacity to the FA.

267 rface-exposed epitope conferring optimal IgE-binding capacity to the folded allergen.

268 ing either WT or mutant CaM that lack Ca(2+)-binding capacity to the pore-forming alpha-subunit of Ca

269 ENaC-alpha, displayed significantly reduced binding capacity to TIP peptide and to TNF.

270 its function in cancer, even while retaining binding capacity to WBP2.

271 e index and increased serum iron, total iron binding capacity, transferrin saturation, and serum albu

272 e 45 min process and is capable of achieving binding capacities up to 1 000 000 times greater than si

273 shown to have reduced immunoglobulin E (IgE)-binding capacity upon calcium depletion.

274 To determine whether GAG binding capacity varies among CHIKV strains, a represent

275 at the NA of the zoonotic H7N9 viruses has a binding capacity via both the secondary binding site and

276 functional properties and in vitro bile acid-binding capacities was performed.

277 Pigment-binding capacity was completely lost in each of the OHPs

278 In case of IgE antibodies, the lowest binding capacity was detected in the 24 h hydrolysates o

279 High cobalamin-binding capacity was found in trout stomach (210 pmol/g)

280 rmocomp/glass substrates in terms of protein binding capacity was observed for at least two months.

281 A higher antibody binding capacity was observed on the GalCer-diluted flui

282 on (DOC) concentration above ca. 250 muM the binding capacity was only 50% of the theoretical value o

283 The MIP with the highest binding capacity was selected.

284 olic Ca binding affinity, whereas maximal Ca binding capacity was unchanged.

285 found, on the basis of measurements of water binding capacity, water solubility and intrinsic viscosi

286 Based on its nucleic acid binding capacity, we propose a dual location and functio

287 Because of their pigment-binding capacity, we suggest that OHPs function in the d

288 th differing (defined) heparin- and integrin-binding capacities were applied directly to resistance a

289 of anti-HLA antibodies and their complement binding capacity were associated with increased severity

290 ies such as the swelling power and bile acid binding capacity were increased by acetylation.

291 c strength, and hydrophobicity of liquids on binding capacity, were examined using a well-mixed conta

292 PPW showed interesting water-holding and fat-binding capacities which were 4.097 +/- 0.537 g/g and 4.

293 These effects rely on Phf19 histone-binding capacity, which is critical for the recruitment

294 , such boron-selective resins have a limited binding capacity with a maximum free base content of 0.7

295 Our results suggest that the loss of copper-binding capacity with increasing residence time is cause

296 ps, and the association of regional 11C-PBB3 binding capacity with neuropsychiatric symptoms.

297 rial, we show that there is plasticity in ER-binding capacity, with distinct combinations of cis-regu

298 hat lipid membranes have substantial calcium-binding capacity, with several types of binding sites pr

299 ic acid monomers, which guarantees a uniform binding capacity within the pH range of intestinal fluid

300 o a therapeutic protein resulting in the HSA binding capacity without compromising therapeutic activi