ライフサイエンスコーパス: basic protein

1 3p22 MOBP (myelin-associated oligodendrocyte basic protein).

2 lase), astrocytes (S100b), and axons (myelin basic protein).

3 ot occur due to a genetic deletion of myelin basic protein.

4 kinetics between protein-, DNA-, or RNA- and basic protein.

5 lation in a robust in vitro substrate myelin basic protein.

6 TcR, which recognizes the autoantigen myelin basic protein.

7 nd Western blotting indicated reduced myelin basic protein.

8 ts' sera contained an IgG specific to myelin basic protein.

9 ne for MS, encoding full-length human myelin basic protein.

10 togenic determinant of the guinea pig myelin basic protein.

11 VEGF165 is a basic protein.

12 sphorylated the artificial substrate, myelin basic protein.

13 immunodominant N-terminal epitope of myelin basic protein.

14 rmn), and by immunohistochemistry for myelin basic protein.

15 rmined the location of methylation on myelin basic protein.

16 oth immunodeficient and deficient for myelin basic protein.

17 y neuron-specific enolase and finally myelin basic protein.

18 iption factor Oct-6 and expression of myelin basic protein.

19 rosis and recognizes the self-antigen myelin basic protein.

20 Hpa2, but not Hpa3, acetylated certain small basic proteins.

21 petitive sequences, respectively, and encode basic proteins.

22 these secondary granules (by mass) are major basic protein 1 (MBP-1) and eosinophil peroxidase (EPX).

23 inhibition of the polymerase acidic protein-basic protein 1 (PA-PB1) interaction is a promising stra

24 interaction of the polymerase acidic protein-basic protein 1 (PA-PB1) subunits of influenza virus (Fl

25 otein 1 [M1], nucleoprotein [NP], polymerase basic protein 1 [PB1]).

26 ependent upon eosinophil peroxidase or major basic protein 1 and did not correlate with activity of t

27 ondria membrane potential via its polymerase basic protein 1-frame 2 (PB1-F2) accessory protein.

28 n transcription factor 1 and round spermatid basic protein 1.

29 Finally, treatment of myelin basic protein(1-11) T cell receptor transgenic mice with

30 e 2), eosinophil peroxidase (EPO), and major basic protein-1 (MBP1) intradermally into guinea pig and

31 Major basic protein-1 activation of CBMC primed with fibroblas

32 Major basic protein-1-induced CBMC activation is mediated part

33 granule protein double knock-out mice (major basic protein-1/eosinophil peroxidase dual gene deletion

34 maging and sections immunostained for myelin basic protein, 15/28 being mixed white and grey matter a

35 pressing TL3A6, an MS patient-derived myelin basic protein 83-99-specific TCR.

36 ) that also recognizes a peptide from myelin basic protein, a candidate MS autoantigen.

37 We show that myelin basic protein, a protein essential for CNS myelin wrappi

38 that GPR17 activation also diminishes myelin basic protein abundance by lessening stimulation of the

39 immunodominant N-terminal epitope of myelin basic protein, Ac1-9.

40 apparent Km values of PKC betaII for myelin basic protein; activation was independent of phospholipi

41 Myelin basic protein and 2', 3'-cyclic nucleotide 3'-phosphodie

42 cs) demonstrated that peptides from platelet basic protein and C1 inhibitor achieved both 100% sensit

43 nally, the eosinophil granule proteins major basic protein and eosinophil peroxidase were more freque

44 a was determined by immunostaining for major basic protein and flow cytometry for cell-surface recept

45 bunit NR-2A), and myelin-derived Ags (myelin basic protein and myelin oligodendrocyte glycoprotein) i

46 Myelin basic protein and neurofilament immunolabelling demonstr

47 mice exhibited enhanced expression of myelin basic protein and promoter of proteolipid protein.

48 esponse, and a small response against myelin basic protein and proteolipid protein epitopes.

49 n basic protein (r = 0.58, P < 0.01), myelin basic protein and T(2) (r = -0.59, P < 0.01), and neuron

50 rtem sections show concurrent loss of myelin basic protein and TAL from sites of demyelination.

51 toplasmic granules with immunoreactive major basic protein and they express surface Siglec F and tran

52 ) and EDTA regressive staining indicate that basic proteins and DNA are major constituents of the inn

53 The electrostatic interaction between the basic proteins and the negatively charged C1 chip surfac

54 rker O1 and the mature OL marker MBP (myelin basic protein), and also prevents the long-term reductio

55 evels of myelin regulatory factor and myelin basic protein, and decreased numbers of myelinated axons

56 s including ubiquitin, beta-thymosin, myelin basic protein, and hemoglobin were spatially mapped and

57 al myelin proteins, such as periaxin, myelin basic protein, and myelin protein zero, was decreased, g

58 inal domain of fibrillarin (GST-GAR), myelin basic protein, and recombinant human histones H2A, H2B,

59 e-like protein-2 (CRMP2/DRP2/DPYSL2), myelin basic protein, and syntaxin-binding protein-1 (STXBP1/Mu

60 e number of axons, immunostaining for myelin basic protein, and TUNEL assays were performed.

61 growth factor (TGF)-beta secretion by myelin basic protein- and MOG-peptide-specific T cells, as well

62 ple Sclerosis (MS) autoantibody, Anti-Myelin Basic Protein (Anti-MBP) was developed by immobilization

63 reatment biased the class of elicited myelin basic protein antibodies from IgG2a to IgG1 and IgG2b, s

64 ing that a triad of enzyme, acidic lipid and basic protein are necessary for interfacial activity.

65 Epx (eosinophil peroxidase) and Prg2 (major basic protein) as well as lower interleukin 1beta (IL-1b

66 Serum myelin basic protein at 24 and 72 hours correctly classified su

67 Efficient separations of unlabeled basic proteins at low pH and FITC-labeled proteins at hi

68 ed theoretically, apparently all recombinant basic proteins (at least pI-1 > or = 6.94) may be purifi

69 solution and in the lipid-free state, myelin basic protein belongs to that class of proteins.

70 itro studies to advance our understanding of basic protein biochemistry, the emergence of new extrins

71 cessfully detected phosphorylation of myelin basic protein by PKC-alpha kinase.

72 ped a novel method for measuring bindings to basic proteins by SPR, wherein the naturally positive ch

73 Histones are the basic protein components of nucleosomes.

74 HIV-1 nucleocapsid (NC) protein is a small, basic protein containing two retroviral zinc fingers.

75 mology with stathmins and encode small, very basic proteins containing several KKD/E repeats.

76 atoracidic AA ratios were >1 suggesting high basic protein contents.

77 action of bromine on fluorescein and stains basic proteins due to its acidic nature.

78 induced in Lewis rats by injection of myelin basic protein emulsified in complete Freund's adjuvant (

79 They are all small basic proteins, encoded by genes present at the end of t

80 face Siglec F and transcripts encoding major basic protein, eosinophil peroxidase, and GATA-1, -2, an

81 host defense peptides, neuropeptides, major basic protein, eosinophil peroxidase, and many US Food a

82 P in processing of the immunodominant myelin basic protein epitope.

83 Aggarwal et al. present evidence that myelin basic protein, essential for myelination by oligodendroc

84 totic pathway specifically in mature, myelin basic protein expressing oligodendrocytes (MBP-iCP9).

85 Myelin basic protein expression and CC1(+) oligodendroglia decr

86 ition, nsf mutants exhibit defects in Myelin basic protein expression and in localization of sodium c

87 1H-indole-3-propionic acid) decreases myelin basic protein expression levels mainly by triggering the

88 s, showed bilateral reduction in MBP (myelin basic protein) expression with 24 h exposure to 80% oxyg

89 Here we present two basic protein extraction protocols that have successfull

90 t encode a small RNA (FsrA) and three small, basic proteins (FbpA, FbpB, and FbpC).

91 functions, in collaboration with three small basic proteins (FbpABC), to repress many "low-priority"

92 latin-induced changes in coherency of myelin basic protein fibers in the cingular cortex and loss of

93 4 +/- 2.1 mm(3) and augmented loss of myelin basic protein from 13.4 +/- 6.0 to 70.6 +/- 5.3%.

94 can be applied for purifying any recombinant basic protein from Escherichia coli.

95 and our previous reports, a model for myelin basic protein gene control is proposed.

96 Golli proteins, products of the myelin basic protein gene, can modulate voltage-gated Ca(2+) up

97 Golli proteins, products of the myelin basic protein gene, function as a new type of modulator

98 alternatively spliced product of the myelin basic protein gene, plays a critical role in regulating

99 ultimeric peptides such as guinea pig myelin basic protein GPBP(72-84) MAP (a dendrimeric octamer com

100 ncephalitogenic peptide of guinea pig myelin basic protein (GPMBP; i.e., neuroantigen or NAg).

101 lar myelin compaction and the role of myelin basic protein has been investigated, the forces that med

102 mammals of the WRB protein (tryptophan-rich basic protein), homologous to yeast Get1, in combination

103 encephalitogenic 73-87 determinant of myelin basic protein (i.e., the neuroantigen, or NAg) could pre

104 essed eosinophil numbers by using anti-major basic protein immunostaining, goblet cell hyperplasia by

105 Histones form an octameric complex of basic proteins important in regulating DNA organization

106 ination, and histological analysis of myelin basic protein in human postmortem specimens confirmed a

107 with immunocytochemical staining for myelin basic protein in single-labelled neurons.

108 Degraded myelin basic protein in the gray matter medial to the CCFM of b

109 P-selectin, platelet factor 4, and platelet basic protein in the population-based Bruneck study (n=6

110 hosphorylation and phosphorylation of myelin basic protein in vitro.

111 11S A3, and 11S acidic subunits and the 11S basic proteins in the soymilk supernatant fraction (SSF)

112 as been introduced to provide easy access to basic protein information.

113 These results were corroborated by myelin basic protein intensity and staining pattern in these ar

114 h as eosinophil-derived neurotoxin and major basic protein, into the extracellular milieu and onto th

115 of proteolytic autoantibodies against myelin basic protein is now considered as a characteristic feat

116 Pou3f1, Egr2, myelin protein zero and myelin basic protein, is reduced.

117 this paper, we show that TAL, but not myelin basic protein, is specifically cleaved by human GrB.

118 conjunction with one or more of three small, basic proteins, known as FbpA, FbpB, and FbpC.

119 ed of myelinated fibers, with reduced myelin basic protein levels (MBP) compared to levels in the C57

120 orescence for 4-hydroxy-2-nonenal and myelin basic protein localized free-radical-induced oxidative d

121 We use the highly basic protein lysozyme at nearly neutral and lower pH as

122 The protein mixtures contained four basic proteins (lysozyme, cytochrome c, alpha-chymotryps

123 from the acetylated N-terminal end of myelin basic protein: mass-to-charge (m/z) 795.81 (+2) molecula

124 m S100b, neuron-specific enolase, and myelin basic protein may aid in outcome classification of child

125 reported a strong interaction between myelin basic protein (MBP) and Abeta peptides that resulted in

126 nificant role in the fragmentation of myelin basic protein (MBP) and demyelination.

127 silencing of EGO results in decreased major basic protein (MBP) and eosinophil derived neurotoxin (E

128 ent in the eosinophil granule products major basic protein (MBP) and eosinophil peroxidase (EPO), it

129 Mice that have been immunized with myelin basic protein (MBP) and infected exhibit the features of

130 tion of a label-less immunosensor for myelin basic protein (MBP) and its interrogation using an ac im

131 demonstrated widespread reduction of myelin basic protein (MBP) and myelin in the sensorimotor corte

132 associates with the mRNA encoding the myelin basic protein (MBP) and rescues MBP expression from the

133 or the simultaneous quantification of Myelin Basic Protein (MBP) and Tau proteins in cerebrospinal fl

134 nd optimized based on the autoantigen myelin basic protein (MBP) and the MBP-derived peptide MBP85-99

135 MS2-3C8) bound to a self-peptide from myelin basic protein (MBP) and the multiple sclerosis-associate

136 s were found to contain citrullinated myelin basic protein (MBP) and were surrounded by astrocytes im

137 Transcripts of myelin basic protein (mbp) are expressed in normal and regenera

138 and mass spectrometry, we identified myelin basic protein (MBP) as a prominent brain parenchymal fac

139 l-time fluorogenic kinase assay using myelin basic protein (MBP) as a substrate is reported.

140 actin-based cytocortex, and requires myelin basic protein (MBP) as its major structural component.

141 p-nitrophenyl phosphate (pNPP) or 32P-myelin basic protein (MBP) as substrates, with matching Km and

142 Here we show that myelin basic protein (MBP) binds to L1 in a Lewis(x)-dependent

143 stigation, we find that the release of major basic protein (MBP) by eosinophils is a prominent featur

144 eta4 demonstrated an amplification of myelin basic protein (MBP) expression and differentiation of OP

145 znf16l mutant larvae have reduced myelin basic protein (mbp) expression and reduced CNS myelin.

146 e performed an image-based screen for myelin basic protein (MBP) expression using primary rat optic-n

147 The myelin basic protein (MBP) gene encodes two families of protein

148 ter birth) promotes activation of the myelin basic protein (Mbp) gene with an accelerated loss of MBP

149 A novel highly sensitive impedimetric Myelin Basic Protein (MBP) immunosensor for the determination o

150 yelin at various surface coverages of myelin basic protein (MBP) indicate that maximum adhesion and m

151 Myelin basic protein (MBP) is a major component of central nerv

152 We previously reported that myelin basic protein (MBP) is a potent inhibitor of Abeta fibri

153 Myelin basic protein (MBP) is the major structural protein comp

154 We screened for myelin basic protein (mbp) mRNA by in situ hybridization and id

155 ss fail to localize normal amounts of myelin basic protein (mbp) mRNA in cellular processes, and fail

156 afficking factor that associates with myelin basic protein (MBP) mRNA.

157 pid composition and concentrations of myelin basic protein (MBP) on the structure of model lipid bila

158 cell receptor (TCR) specific for the Myelin Basic Protein (MBP) peptide Ac1-9, making the animals su

159 yelin membranes, mostly occupied by a myelin basic protein (MBP) phase.

160 Myelin basic protein (MBP) plays an important structural and fu

161 Interestingly, after myelin basic protein (MBP) priming, the expression of Foxp3 dec

162 transgenic pMBP-eGFP-NTR tadpoles the myelin basic protein (MBP) regulatory sequences, specific to ma

163 In this study, euthymic myelin basic protein (MBP) TCR transgenic mice are protected fr

164 duction in the net positive charge of myelin basic protein (MBP) via deimination of arginine to citru

165 Our previous studies determined that myelin basic protein (MBP) was capable of inhibiting fibril for

166 We show that MHC class I-restricted myelin basic protein (MBP) was presented by oligodendrocytes an

167 e specific for the Ac1-11 fragment of myelin basic protein (MBP) with Ac1-11 elicits T cells with dom

168 of OPs into oligodendrocytes forming myelin basic protein (MBP)(+) and proteolipid protein-positive

169 stricted T cells specific for classic myelin basic protein (MBP), a component of the myelin sheath, i

170 Among soluble mediators, eosinophil major basic protein (MBP), a hallmark of allergy, is particula

171 further reveal that the expression of myelin basic protein (MBP), a myelin-specific protein that is s

172 translation of a key sheath protein, myelin basic protein (MBP), by reversing the inhibitory effect

173 bnormalities in the charge pattern of myelin basic protein (MBP), changes linked to adaptive immunolo

174 In multiple sclerosis (MS), myelin basic protein (MBP), critical for the maintenance of mye

175 A critical component of myelin is myelin basic protein (MBP), expression of which requires antero

176 ial fibrillary acidic protein (GFAP), myelin basic protein (MBP), interferon gamma (IFNgamma), lipid

177 myelin multilayered membrane sheath, myelin basic protein (MBP), is hydrolyzed by the 26S proteasome

178 ial fibrillary acidic protein (GFAP), myelin basic protein (MBP), or F4/80 as determined by Western b

179 de, the immunodominant determinant of myelin basic protein (MBP), produced a single episode of EAE fo

180 of neurofilament light chain (NF-L), myelin basic protein (MBP), S100B, and heart-type fatty acid bi

181 n the central nervous system (CNS) of myelin basic protein (MBP)-induced EAE mice, especially in cell

182 antibodies and subsequently mature to myelin basic protein (MBP)-positive cells prior to formation of

183 oligodendrocytes and weakly in mature myelin basic protein (MBP)-positive oligodendrocytes.

184 Interestingly, we found that myelin basic protein (MBP)-primed T cells from female and castr

185 Earlier we have demonstrated that myelin basic protein (MBP)-primed T cells induce the expression

186 spontaneous EAE, we demonstrated that myelin basic protein (MBP)-specific CD4(+) T cells up-regulate

187 Here we found that CD8(+) myelin basic protein (MBP)-specific T cell tolerance was broken

188 Myelin basic protein (MBP)-specific T cells are thought to play

189 redirect therapeutic T cells against myelin basic protein (MBP)-specific T lymphocytes implicated in

190 ptide induces peripheral tolerance in myelin basic protein (MBP)-specific TCR transgenic mice.

191 KO mice, accompanied by a decrease in myelin basic protein (MBP).

192 such as myelin protein zero (MPZ) and myelin basic protein (MBP).

193 ell tolerance to myelin proteins like myelin basic protein (MBP).

194 specific for myelin proteins such as myelin basic protein (MBP).

195 xic proteins, including the eosinophil major basic protein (MBP-1).

196 rentially expressed in schizophrenia (myelin basic protein [MBP], myelin-oligodendrocyte glycoprotein

197 n the lipid and the adhesive protein (myelin basic protein, MBP) composition.

198 Human eosinophil granule major basic protein (MBP1) is an exceedingly basic (isoelectri

199 The basic protein model used was a minimalist Go model using

200 We identified a novel basic protein motif consisting of a cluster of three dib

201 These basic protein motifs exhibit weak but physiologically re

202 itionally, IL-13, IL-10 and eosinophil major basic protein mRNA levels were greater in patients with

203 required for the localization of mbp (myelin basic protein) mRNA to processes of myelinating oligoden

204 expression of myelin-specific genes (myelin basic protein, myelin oligodendrocyte glycoprotein, 2',3

205 myelin-associated proteins including myelin basic protein, myelin proteolipid protein, and 2'3'-cycl

206 that the inferred HIM-5 product is a highly basic protein of 252 amino acids with no clear orthologs

207 IHF and HU are small basic proteins of eubacteria that bind as homodimers to

208 er(+)), and terminal-differentiation (myelin basic protein(+)) of OPs was significantly increased in

209 m neuron-specific enolase, S100b, and myelin basic protein on days 1-4 and 7 after cardiac arrest.

210 ects were identified for soy protein or milk basic protein on lumbar spine BMD.

211 ins chondroitin sulfate proteoglycan, myelin basic protein, or Nogo-A (reticulon 4).

212 N-gamma- or IL-17-skewed responses to myelin basic protein over the course of a year.

213 eir degranulation/activation products (major basic protein [p < 0.001, r = 0.7353] and eosinophil-der

214 ge product of chemotactically inert platelet basic protein (PBP), not previously identified in the in

215 T-cell receptor that is specific for myelin basic protein peptide Ac1-9 (ASQKRPSQR).

216 ansgenic mouse model specific for the myelin basic protein peptide Ac1-9.

217 decreases in the mean (SD) number of myelin basic protein peptide-specific cells secreting IL-6 and

218 Mean (SD) number of myelin basic protein peptide-specific cells secreting interfero

219 that recognizes two I-A(u)-restricted myelin basic protein peptides and one of its peptide/major hist

220 nly when specifically stimulated with myelin basic protein, peripheral blood mononuclear cell culture

221 Many basic proteins (pI>7) and putative disease biomarkers ar

222 SCA, a small ( approximately 9.4 kDa), basic protein plus low esterified pectin from this extra

223 y can be terminally differentiated to myelin basic protein-positive (MBP(+)) oligodendrocytes.

224 ment of optic nerve whereas decreased myelin basic protein-positive axon counts were seen in all segm

225 lin Associated Glycoprotein-positive, Myelin Basic Protein-positive oligodendrocytes, rather than Gli

226 Pro-platelet basic protein (PPBP) is a potent neutrophil chemoattract

227 related protein 9 (C1QTNF9) and pro-platelet basic protein (PPBP).

228 Small basic proteins present in most Archaea share a common an

229 Similarly, treatment of myelin basic protein-primed SJL/J lymph node cells with SB-3317

230 s from collagen-primed DBA/1 mice and myelin basic protein-primed SJL/J mice with Ag in the presence

231 t NaB switched the differentiation of myelin basic protein-primed T cells from Th1 to Th2 mode, enric

232 scriptional activator Puralpha to the myelin basic protein promoter.

233 lineage progression and inhibits MBP (myelin basic protein) promoter activity and Sox10 function.

234 tively assayed for reactivity against myelin basic protein, proteolipid protein, and myelin oligodend

235 myelin protein expression, including myelin basic protein, proteolipid protein, myelin oligodendrocy

236 he well-characterized myelin antigens myelin basic protein, proteolipid protein, or myelin oligodendr

237 yelitis of SJL mice induced by MP4, a myelin basic protein-proteolipid protein (PLP) fusion protein.

238 ween phosphorylated neurofilament and myelin basic protein (r = 0.58, P < 0.01), myelin basic protein

239 s had marked inhibition on autologous myelin basic protein-reactive T cells and displayed two distinc

240 munization with irradiated autologous myelin basic protein-reactive T cells.

241 sity, intensity of immunostaining for myelin basic protein (reflecting myelin content) and phosphoryl

242 Major basic protein released from eosinophils to airway parasy

243 ical staining for the granule protein, major basic protein, revealed that eosinophils accumulated exc

244 ) that mediate dendritic targeting of myelin basic protein RNA by the A2 pathway in oligodendrocytes.

245 e outcome and survival, whereas serum myelin basic protein's best accuracy occurred at 48 hours.

246 kering with different variations of the same basic protein scaffold.

247 al vulnerability in mice deficient in myelin basic protein (shiverer), also expressing yellow fluores

248 nophils (bmEos) express immunoreactive major basic protein, Siglec F, IL-5R alpha-chain, and transcri

249 h 9 was much lower than reactivity to other basic proteins, some of which bound IgE well in the RAST

250 gulatory T cells, with an increase in myelin basic protein-specific T cell proliferation and secretio

251 in the CNS as well as suppression of myelin basic protein-specific Th1 autoreactive T cells.

252 mutant (Gal-9(-/-)) mice as well as a myelin basic protein-specific Tim-3(+) encephalitogenic T-cell

253 ncreasing oligodendrocyte density and myelin basic protein staining in CNS lesions.

254 , and their brains were processed for myelin basic protein staining.

255 ficantly reduced FA (P < .05) and antimyelin basic protein staining.

256 reduction in transphosphorylation of myelin basic protein substrate.

257 assembled from two mutant forms of the same basic protein subunit.

258 ins could involve interactions with acylated basic proteins such as GAP-43.

259 irectly interacts with, and is activated by, basic proteins such as histone H1 and Tau with nm affini

260 mRNA molecules, namely those encoding small basic proteins such as MBP, to prevent aberrant effects

261 Many basic proteins, such as histones, transcription factors,

262 cted individuals from one family lack myelin basic protein, suggesting that this disease in affected

263 peared to mediate the effect: an anti-myelin basic protein T-cell line treated with cefuroxime or pen

264 ental autoimmune encephalomyelitis in myelin basic protein TCR transgenic mice, and showed that the h

265 ly reduced the number of peribronchial major basic protein(+)/TGF-beta(+) cells, suggesting that redu

266 rotein G0/G1 switch gene 2 (G0S2) is a small basic protein that functions as an endogenous inhibitor

267 containing the N-terminal epitope of myelin basic protein that is associated with experimental autoi

268 CC1 is a 6-kDa, monomeric, basic protein that is expressed at a high level in T. te

269 ns shaker (les) rat has a mutation in myelin basic protein that results in severe CNS dysmyelination

270 Protein V is a highly basic protein that strongly binds to DNA in a nonspecifi

271 mitochondrial, filamentous structure rich in basic proteins that links the kDNA discs during their se

272 n addition to identifying aptamers to highly basic proteins, these results suggest that aptamers prov

273 e major protein in the myelin sheath, myelin basic protein, through Fyn kinase-dependent signaling.

274 antigens, such as phosphatidylserine, myelin basic protein, thyroglobulin, histone, insulin, cytochro

275 lling stimulates local translation of myelin basic protein to initiate myelination.

276 s stimulates CREB phosphorylation and myelin basic protein transcription and increases survival.

277 ethod was established to measure bindings to basic proteins under physiological conditions.

278 The change in charge of the myelin basic protein upon phosphorylation by the protein kinase

279 ellow mottle virus codes for a 16-kDa highly basic protein using novel modalities for coding, transla

280 ases demonstrated a substrate preference for basic protein variants, which indicates a possible recog

281 autoimmunity, oral tolerization with myelin basic protein was abrogated as well in Grail(-/-) mice.

282 utcome, whereas greater reactivity to myelin basic protein was correlated with stroke severity on adm

283 Myelin basic protein was identified as a major citrullinated pr

284 Expression of myelin basic protein was increased, and activity of MMP-9 was r

285 Myelin basic protein was significantly reduced in all regions a

286 ning for protein gene product 9.5 and myelin basic protein was used to evaluate morphological feature

287 PR, wherein the naturally positive charge of basic protein was utilized to immobilize ligand.

288 y cultures of mature OLs that express myelin basic protein, we found that 3-morpholinosydnonimine, a

289 nohistochemistry analyses of CCL26 and major basic protein were done on bronchial biopsy specimens.

290 ficiency and diminished expression of myelin basic protein were noted in GBDK brains.

291 l levels of IL-6, IL-5, and eosinophil major basic protein were observed in CRSwNP patients.

292 drocytes and their ability to produce myelin basic protein were significantly decreased.

293 Prefractionated basic proteins were compared with total tissue lysates f

294 eptides and three times the number of unique basic proteins when compared with total lysates.

295 Myelin basic protein, when added to the CYT monolayer, increase

296 riptional control of the promoter for myelin basic protein, which is oligodendrocyte-specific.

297 umour suppressor gene encodes a small highly basic protein whose known functions are largely determin

298 e mutated the TRC40 receptor tryptophan-rich basic protein (Wrb) in hair cells of zebrafish and mice

299 HD5), which is also known as tryptophan-rich basic protein (WRB), a gene located on chromosome 21 in

300 s induced in rats using a fragment of myelin basic protein, yielding acute clinical disease that refl