ライフサイエンスコーパス: microtubule-associated protein

1 s; plus end regulators) and structural MAPs (microtubule-associated proteins).

2 ereas tau is a brain-specific, axon-enriched microtubule-associated protein.

3 The TON1a gene encodes a microtubule-associated protein.

4 rganization of microtubules are regulated by microtubule-associated proteins.

5 evealed that SYK phosphorylates tubulins and microtubule-associated proteins.

6 vitro conditions via direct interaction with microtubule-associated proteins.

7 the catalytic subunit of Katanin, and other microtubule-associated proteins.

8 or the binding of RASSF family proteins with microtubule-associated proteins.

9 f microtubular function and interaction with microtubule-associated proteins.

10 r network of contractile ring components and microtubule-associated proteins.

11 out how the effects of MTAs are modulated by microtubule-associated proteins.

12 bulin dimers and the binding of drugs and/or microtubule-associated proteins.

13 d with mutations in microtubule subunits and microtubule-associated proteins.

14 etween isotypes, specifies interactions with microtubule-associated proteins.

15 resence of autophagy and endosomal proteins, microtubule-associated protein 1 light chain (MAP1LC3B)

16 of childhood, we developed and piloted a GFP-microtubule-associated protein 1 light chain 3 (GFP-LC3)

17 ed in increased punctate distribution of GFP-microtubule-associated protein 1 light chain 3 (LC3) and

18 tophagosomes, and enhanced the occurrence of microtubule-associated protein 1 light chain 3 (LC3) at

19 tg4c and Atg7 (involved in the lipidation of microtubule-associated protein 1 light chain 3 (LC3) B-I

20 hagy proteins involved in the conjugation of microtubule-associated protein 1 light chain 3 (LC3) to

21 CGD patients display minimal recruitment of microtubule-associated protein 1 light chain 3 (LC3) to

22 utophagy receptors [sequestosome 1 (SQSTM1), microtubule-associated protein 1 light chain 3 (LC3), ga

23 f autophagy, sequestosome 1 (SQSTM1/p62) and microtubule-associated protein 1 light chain 3 (LC3), we

24 Microtubule-associated protein 1 light chain 3 (LC3)-II

25 Among them, the microtubule-associated protein 1 light chain 3 (LC3)-II

26 iciency as evidenced by reduced formation of microtubule-associated protein 1 light chain 3 (LC3)-II,

27 oid leukemia (PICALM) as binding proteins of microtubule-associated protein 1 light chain 3 (LC3).

28 al p62/sequestosome 1 (SQSTM1) and processed microtubule-associated protein 1 light chain 3 (LC3-II).

29 ar defense programs, specifically xenophagy, microtubule-associated protein 1 light chain 3 alpha (LC

30 was required for decorin-evoked Beclin 1 and microtubule-associated protein 1 light chain 3 alpha exp

31 Peg3, induced transcription of Beclin 1 and microtubule-associated protein 1 light chain 3 alpha gen

32 The autophagosome marker LC3 (microtubule-associated protein 1 light chain 3 alpha) wa

33 in containing 3 and autophagosome-associated microtubule-associated protein 1 light chain 3 associate

34 essed a key step in autophagy, lipidation of microtubule-associated protein 1 light chain 3 beta (LC3

35 Instead, staining with acridine orange and microtubule-associated protein 1 light chain 3 revealed

36 th several autophagy markers, including LC3 (microtubule-associated protein 1 light chain 3) (3,4) .

37 ulation of the autophagosome marker LC3 (rat microtubule-associated protein 1 light chain 3), autopha

38 e presence of autophagy markers such as LC3 (microtubule-associated protein 1 light chain 3), Beclin-

39 as the autophagy-related protein-7 (ATG-7), microtubule-associated protein 1 light chain 3, ATG-12,

40 dant anion channels (VDACs) interacting with microtubule-associated protein 1 light chain 3, could or

41 ositive phagophores is crucial for producing microtubule-associated protein 1 light chain 3-II (LC3-I

42 uitin-like protein autophagy-related (Atg)8 (microtubule-associated protein 1 light chain 3/LC3 in ma

43 s encoding the essential autophagy component microtubule-associated protein 1 light chain 3B (LC3B) a

44 addition, colocalization of autophagy marker microtubule-associated protein 1 light chain 3B (LC3B) w

45 reased lysosomal protease activities) higher microtubule-associated protein 1 light chain 3B-II/I rat

46 mation and markers of autophagy BECLIN-1 and microtubule-associated protein 1 light chain 3beta (LC3-

47 sed transcription of the autophagy component microtubule-associated protein 1 light chain 3beta (Lc3b

48 S typhimurium colocalized with microtubule-associated protein 1 light chain 3beta (Map1

49 recruitment of the autophagy component LC3 (microtubule-associated proteins 1 light chain 3) to TLR-

50 es from 22 patients with HCV infection using microtubule-associated protein-1 light chain 3 immunoblo

51 dependent decrease in autophagosome markers, microtubule-associated protein-1 light chain beta II (LC

52 The MNV RC was marked by the microtubule-associated-protein-1-light-chain-3 (LC3) con

53 Microtubule-associated protein 1A (MAP1A) is one of the

54 response DNA-binding protein 43, ubiquitin, microtubule-associated protein 1A/1B light chains 3, and

55 luation, and western blotting light chain 3 (microtubule-associated protein 1A/1B-LC3) expression wer

56 ic and autophagic pathways, a process called microtubule-associated protein 1A/1B-light chain 3 (LC3)

57 luorescent staining for the autophagy marker microtubule-associated protein 1A/1B-light chain 3 (LC3)

58 r the autophagic structure LC3-I and LC3-II (microtubule-associated protein 1A/1B-light chain 3) frac

59 d colocalization between MUC4 and LAMP1/LC3 (microtubule-associated protein 1A/1B-light chain 3) in P

60 l form of non-canonical autophagy where LC3 (microtubule-associated protein 1A/1B-light chain 3) is c

61 E1B 19-kDa protein-interacting protein 3 and microtubule-associated proteins 1A/1B light chain 3B gra

62 Microtubule-associated protein 1B (MAP1B) is expressed p

63 ase-1 (DAPK1) was rerouted to the cell base, microtubule-associated protein 1B (MAP1B) was dephosphor

64 orrelating with increased phosphorylation of microtubule-associated protein 1B and reduced microtubul

65 The presence of Futsch-positive (microtubule-associated protein 1B) supernumerary microtu

66 The microtubule associated protein 2 (Map2) helps stabilize

67 -SPION-rIgPxcIgY carries chick polyclonal to microtubule-associated protein 2 (MAP2) as Ran-SPION-rIg

68 Using microtubule-associated protein 2 (MAP2) immunohistochemi

69 Microtubule-associated protein 2 (MAP2) is a neuronal pr

70 y diminished neuronal damage, as assessed by microtubule-associated protein 2 (MAP2), class III beta-

71 feration (+16%), decreased neurogenesis into microtubule-associated protein 2 (MAP2)-positive neurons

72 uroendocrine tumor markers synaptophysin and microtubule-associated protein 2 (MAP2).

73 ciated with activity/anxiety behaviours, and microtubule-associated protein 2 (Map2, rs13475902) was

74 eflectivity and by immunohistochemistry with microtubule-associated protein 2 antibody.

75 When immunoreactivity for microtubule-associated protein 2 was assessed in the cor

76 f class III neuron-specific beta-tubulin and microtubule-associated protein 2 were significantly incr

77 splayed multipotency by differentiating into microtubule-associated protein 2, beta-III tubulin, and

78 This was evidenced by loss of microtubule-associated protein 2, synaptophysin, and neu

79 thod for the determination of the density of microtubule-associated protein 2-immunolabeled neurons i

80 EC24C is disrupted, remained confined to the microtubule-associated protein 2-positive somatodendriti

81 protein kinase Cgamma and phosphorylation of microtubule-associated protein 2.

82 ajority of M1 and M2 ipRGCs expressed Isl-1, microtubule associated protein-2 (MAP2), gamma-synuclein

83 nd immunoreactivity to neuronal derived Ags (microtubule-associated protein-2 and N-methyl d-aspartat

84 cidic protein immunoreactivity and increased microtubule-associated protein-2 immunoreactivity in the

85 synaptotoxicity (decreased synaptophysin and microtubule-associated protein-2 staining) and reactive

86 tin-positive neuroblasts (-28%), and mature, microtubule-associated protein-2-positive neurons (-36%)

87 Microtubule-associated protein 2c (MAP2c) is involved in

88 However, we also identified microtubule-associated protein 4 microtubule-binding pro

89 regulator of microtubule stability via MAP4 (microtubule-associated protein 4).

90 untingtin, cytoplasmic linker protein 3, and microtubule-associated protein 6.

91 We investigated the role of the Arabidopsis microtubule associated proteins 65-1 and 65-2 (MAP65-1 a

92 lmodulin (CaM), as a co-factor to target the microtubule-associated protein 65 (MAP65), an important

93 crotubule-associated protein ensconsin (Ens)/microtubule-associated protein 7 (MAP7) and kinesin heav

94 rray analysis, we have identified a role for microtubule-associated protein 7 (MAP7) during collatera

95 branch development, we identified a role for microtubule-associated protein 7 (MAP7) in dorsal root g

96 Microtubule-associated protein 7 (MAP7) plays an importa

97 s tightly regulated in cells via a number of microtubule associated proteins and enzymes.

98 ies but completely loses the ability to bind microtubule-associated proteins and complex with microtu

99 for understanding the mechanism of action of microtubule-associated proteins and microtubule-directed

100 to use heterologous systems for the study of microtubule-associated proteins and motor proteins, whic

101 gh the organization of the filament network, microtubule-associated proteins, and tubulin posttransla

102 Microtubules and microtubule-associated proteins are fundamental for mult

103 Mutations in genes encoding tubulins and microtubule-associated proteins are known to cause neuro

104 robe atomic resolution dynamic profiles of a microtubule-associated protein assembled on polymeric mi

105 Structures of microtubule-associated proteins assembled on polymeric m

106 mic resolution analysis of dynamics in other microtubule-associated protein assemblies, including but

107 processing bodies (PBs), where it acts as a microtubule-associated protein capable of linking mRNP c

108 Mutations in the gene MAPT encoding tau, a microtubules-associated protein, cause a subtype of fami

109 0-NH12 exhibits impaired localization of the microtubule-associated protein complex Alp7/transforming

110 In the closed mitosis of fission yeast, a microtubule-associated protein complex, Alp7-Alp14 (tran

111 nces for catastrophe regulation in cells, as microtubule-associated proteins could promote catastroph

112 he leading process through activation of the microtubule-associated protein doublecortin (DCX).

113 hes in birds, with specific reference to the microtubule-associated protein, doublecortin (DCX), that

114 Proteins of the echinoderm microtubule-associated protein (EMAP)-like (EML) family

115 Here we identify the microtubule-associated protein ensconsin (Ens)/microtubu

116 es ensconsin (MAP7, E-MAP-115), a ubiquitous microtubule-associated protein, for its primary function

117 including synaptojanin-1 (pThr1131) and the microtubule-associated protein futsch (pSer4106) in the

118 Two microtubule-associated proteins, homologs of Clip170 and

119 quent mitotic spindle and to phosphorylate a microtubule-associated protein important for mitotic spi

120 is driven by GTP hydrolysis and regulated by microtubule-associated proteins, including the plus-end

121 the expression of doublecortin-like (DCL), a microtubule-associated protein involved in embryonic neu

122 Doublecortin (DCX) is an important microtubule-associated protein involved in the migration

123 An important microtubule-associated protein is the protein Tau, becau

124 Tau, the microtubule-associated protein, is a hallmark of several

125 Doublecortin (DCX), a microtubule-associated protein, is essential for neurona

126 Tau, a microtubule-associated protein, is implicated in the pat

127 ate receptor 5 (mGluR5) is phosphorylated by microtubule-associated protein kinase (MAPK), which we s

128 indicated microtubule polymerization and the microtubule-associated proteins Kinesin-1 and dynein all

129 rgeting of HIV Ags to autophagosomes using a microtubule-associated protein L chain 3 (LC3) fusion pr

130 utophagosomes by promoting the lipidation of microtubule-associated protein LC3 (light chain 3).

131 The turnover of microtubule associated protein light chain 3b in Acsl1(T

132 e-associated membrane protein 2 (LAMP2), and microtubule-associated protein light chain (LC) 3 and LC

133 tophagy, as determined by immunoblotting for microtubule-associated protein light chain 3 (LC3) and p

134 analysis, in drug combination-treated cells, microtubule-associated protein light chain 3 (LC3) assoc

135 METHODOLOGY: Microtubule-associated protein light chain 3 (LC3) has e

136 Since the autophagosomal membrane component microtubule-associated protein light chain 3 (LC3) is de

137 omal cathepsin B, cathepsin D, Beclin-1, and microtubule-associated protein light chain 3 (LC3) sugge

138 tophagosome formation and the recruitment of microtubule-associated protein light chain 3 (LC3).

139 ic engulfment through their association with microtubule-associated protein light chain 3 (LC3).

140 eptozotocin as assessed by protein levels of microtubule-associated protein light chain 3 form 2 (LC3

141 62/sequestosome 1, and the lipidated form of microtubule-associated protein light chain 3 isoform B.

142 use hippocampal HT22 cells, characterized by microtubule-associated protein light chain 3 membrane tr

143 thout affecting the increased levels of LC3 (microtubule-associated protein light chain 3) conversion

144 s, p62(SQSTM1) degradation and conversion of Microtubule-associated Protein Light Chain 3-I (LC3-I) t

145 nucleophagy characterized by accumulation of microtubule-associated protein light chain 3/lysosomal-a

146 pression of green fluorescent protein-tagged microtubule-associated protein light chain-3 to induce i

147 rotubule-associated protein light-chain-3-II/microtubule-associated protein light-chain-3-I ratio.

148 ion of p62 and a concomitant decrease in the microtubule-associated protein light-chain-3-II/microtub

149 ple is a fusion between the genes echinoderm microtubule-associated protein like 4 (EML4) and anaplas

150 on proteins nucleophosmin-ALK and echinoderm microtubule-associated protein like 4-ALK, which are abe

151 Because plus end-localized microtubule-associated proteins like p150(Glued) may als

152 stranded breaks (DSB) within the echinoderm microtubule-associated protein-like 4 (EML4) gene and AL

153 In the treatment of echinoderm microtubule-associated protein-like 4 (EML4)-anaplastic

154 Of the 67 primary NSCLCs, 17 were echinoderm microtubule-associated protein-like 4-ALK translocated (

155 The echinoderm microtubule-associated protein-like 4-anaplastic lymphom

156 er, we provide the first evidence of a novel microtubule-associated protein-like function of LC8 that

157 The microtubule-associated protein lissencephaly 1 (Lis1) is

158 Protein levels of subunits of the microtubule associated proteins (MAP) 1A and 1B, light c

159 To report the identification of microtubule-associated protein (MAP) 1B as the antigen o

160 trated previously that GEC1, a member of the microtubule-associated protein (MAP) family, bound to th

161 in activity depends upon the behavior of the microtubule-associated protein (MAP) SPIRAL2 (SPR2).

162 onal microtubule (MT) bundles crosslinked by microtubule-associated protein (MAP) tau are responsible

163 The molecular mechanism by which the microtubule-associated protein (MAP) tau regulates the f

164 pecifically increased, and the expression of microtubule-associated protein (MAP)-1A was significantl

165 and repressed translational activator GCN1, microtubule-associated protein (MAP)1B, thioredoxin redu

166 er, although both isoforms were expressed in microtubule-associated protein (MAP)2-positive dendrites

167 g overlapping portions of the light chain of microtubule-associated protein Map1b (Mtap1b) were recov

168 n this work, we uncovered a new role for the microtubule-associated protein MAP1B in modulating acces

169 In this study, we found that a microtubule-associated protein, MAP1B light chain (MAP1B

170 The predominant brain microtubule-associated proteins MAP2 and tau play a crit

171 the dissociation of Polo from the PBD-bound microtubule-associated protein Map205, which acts as an

172 o antibodies, one antibody against dendritic microtubule-associated proteins (MAP2a,b) and the second

173 microtubule-binding domain of the mammalian microtubule-associated protein MAP4 and with green fluor

174 tify a previously uncharacterised isoform of microtubule-associated protein MAP4, oMAP4, as a microtu

175 effector, HopE1, targets calmodulin and the microtubule-associated protein MAP65-1 to subvert plant

176 abundance and reduced phosphorylation of the microtubule-associated protein MAP65-1, thus providing a

177 for the expression of several major neuronal microtubule associated proteins (MAPs), which are import

178 Studying the in vitro responses of RNPs to microtubule-associated proteins (MAPs) and microtubule e

179 ol the architecture of microtubule networks, microtubule-associated proteins (MAPs) and motor protein

180 The structural microtubule-associated proteins (MAPs) are critical for

181 Within these dynamic motifs, microtubule-associated proteins (MAPs) are frequently un

182 lular motility, but the factors that control microtubule-associated proteins (MAPs) are poorly unders

183 spindle assembly regulators, we isolated 855 microtubule-associated proteins (MAPs) from Drosophila m

184 bulin and may directly affect the binding of microtubule-associated proteins (MAPs) or motors.

185 rowth and shrinkage are tightly regulated by microtubule-associated proteins (MAPs) that bind to micr

186 e tracks, microtubules are bound by numerous microtubule-associated proteins (MAPs) that have the cap

187 ouble RNAi screen to identify genes encoding Microtubule-Associated Proteins (MAPs) that interact wit

188 Structural microtubule-associated proteins (MAPs), like MAP1, not o

189 ciently around the many obstacles, including microtubule-associated proteins (MAPs), that are found o

190 rs are linked to aberrant phosphorylation of microtubule-associated proteins (MAPs).

191 tial for cell functions and involves various microtubule-associated proteins (MAPs).

192 our efforts to obtain atomic information on microtubule-associated protein/microtubule interactions

193 s the first atomic-resolution structure of a microtubule-associated protein on polymeric microtubules

194 cting in the autophagy/apoptosis (MAP1LC3C - microtubule-associated protein) or signal transduction (

195 We now report that the microtubule-associated protein p600 (also known as UBR4)

196 NuSAP, a microtubule-associated protein, plays a critical role in

197 Doublecortin is a microtubule-associated protein produced during neurogene

198 The tumor suppressor and microtubule-associated protein Ras association domain fa

199 Microtubule-associated proteins regulate microtubule (MT

200 titution assays that PRC1 and kinesin-4, two microtubule-associated proteins required for midzone ass

201 y of pure tubulin as well as the assembly of microtubule-associated protein rich tubulin.

202 Our data reveal how inhibitory microtubule-associated proteins selectively regulate mot

203 g the phosphorylation status of the cellular microtubule-associated protein stathmin by its known ass

204 further highlight the essential role of the microtubule-associated protein stathmin in MCPyV ST-medi

205 The microtubule-associated protein Stu2 (XMAP215) has the re

206 ule ends, distinct from the effects of other microtubule-associated proteins such as kinesin-1 and EB

207 which polyglutamylation can target selected microtubule-associated proteins, such as CSAP, to microt

208 The microtubule-associated protein targeting protein for Xen

209 elerated accumulation of hyperphosphorylated microtubule associated protein tau in AD + P.

210 Aggregation of the microtubule associated protein Tau is associated with se

211 The microtubule associated protein tau promotes neuronal sur

212 ar inclusions of abnormal fibrillar forms of microtubule associated protein tau, accumulate in Alzhei

213 Recently the microtubule associated protein tau, MAPT, which is assoc

214 associated with the aggregation of modified microtubule associated protein tau.

215 sphorylatable peptide derived from the human microtubule associated protein tau.

216 Microtubule-associated protein tau (MAPT) H1H1 genotype

217 ly in one of three genes: progranulin (GRN), microtubule-associated protein tau (MAPT), or chromosome

218 a) and intraneuronal hyperphosphorylation of microtubule-associated protein tau (MAPT)--remain to be

219 caused by mutations in the gene encoding the microtubule-associated protein TAU (MAPT).

220 The microtubule-associated protein tau (MAPT, tau) forms neu

221 The microtubule-associated protein tau accumulates in neurod

222 The microtubule-associated protein tau accumulates into toxi

223 ccount for familial frontotemporal dementia: microtubule-associated protein tau and progranulin.

224 ormal phosphorylation and aggregation of the microtubule-associated protein Tau are hallmarks of vari

225 Herein, we investigated the microtubule-associated protein tau as a new link between

226 hetic lethal interaction between CDA and the microtubule-associated protein Tau deficiencies, and rep

227 l interaction between cytidine deaminase and microtubule-associated protein Tau deficiencies.

228 's disease and frontotemporal dementias, the microtubule-associated protein Tau forms intracellular p

229 dically and on the basis of mutations in the microtubule-associated protein tau gene and healthy olde

230 k factors and the disease-predisposing H1/H1 microtubule-associated protein tau haplotype.

231 The microtubule-associated protein tau has a critical role i

232 The microtubule-associated protein tau has been implicated i

233 Reducing levels of the microtubule-associated protein tau has shown promise as

234 Abnormal phosphorylation of the microtubule-associated protein tau in neurodegenerative

235 sing Drosophila, we demonstrate roles of the microtubule-associated protein Tau in regulating synapse

236 heimer's disease is the self-assembly of the microtubule-associated protein tau into fibers termed "p

237 Subcellular mislocalization of the microtubule-associated protein Tau is a hallmark of Alzh

238 The axonal-enriched microtubule-associated protein tau is a key mediator of

239 Microtubule-associated protein tau is an axonal phosphop

240 The neuronal microtubule-associated protein Tau is expressed in diffe

241 In Alzheimer disease (AD), the microtubule-associated protein tau is highly phosphoryla

242 The microtubule-associated protein tau is implicated in vari

243 The microtubule-associated protein tau is involved in a numb

244 Although the disease-relevant microtubule-associated protein tau is known to severely

245 The microtubule-associated protein Tau is mainly expressed i

246 The microtubule-associated protein tau is predominantly loca

247 The hyperphosphorylated microtubule-associated protein tau is present in several

248 Recent evidence suggests that microtubule-associated protein tau may mediate amyloid-b

249 Microtubule-associated protein tau mutations cause a gro

250 lized (predominantly temporal lobe) atrophy (microtubule-associated protein tau mutations); strongly

251 ficantly less temporal lobe involvement than microtubule-associated protein tau mutations.

252 The microtubule-associated protein Tau plays a central role

253 The microtubule-associated protein Tau plays a critical role

254 Accumulation of the microtubule-associated protein tau prevented the clearan

255 ng the kinase Nuak1 from phosphorylating the microtubule-associated protein tau reduces the level of

256 ver, it remains to be determined whether the microtubule-associated protein tau regulates the differe

257 A pathway from the natively unfolded microtubule-associated protein Tau to a highly structure

258 Investigations on the microtubule-associated protein tau yielded innovative ta

259 utations in the gene encoding for tau (MAPT, microtubule-associated protein tau) cause frontotemporal

260 accumulation of aberrantly aggregated MAPT (microtubule-associated protein Tau) defines a spectrum o

261 The MAPT (microtubule-associated protein tau) locus is one of the

262 opin-releasing hormone receptor 1) and MAPT (microtubule-associated protein Tau)) and on chromosome 1

263 In addition, calpain cleaved the microtubule-associated protein Tau, a major component of

264 les, composed of insoluble aggregates of the microtubule-associated protein Tau, are a pathological h

265 splicing generates multiple isoforms of the microtubule-associated protein Tau, but little is known

266 , including TDP-43, alpha-synuclein, and the microtubule-associated protein tau, can be driven out of

267 An important regulator of this system, the microtubule-associated protein Tau, has been shown to pa

268 In the microtubule-associated protein tau, hyperphosphorylation

269 alsy, are characterized by aggregates of the microtubule-associated protein tau, which are linked to

270 ieved to result from loss-of-function of the microtubule-associated protein tau, which becomes hyper-

271 beta) peptides and pathological forms of the microtubule-associated protein tau.

272 rized by the pathological aggregation of the microtubule-associated protein tau.

273 ntotemporal lobar degeneration involving the microtubule-associated protein tau.

274 sociated with the cytoplasmic aggregation of microtubule-associated protein tau.

275 d aggregates of amyloid beta protein and the microtubule-associated protein tau.

276 lary tangles composed of hyperphosphorylated microtubule-associated protein, tau.

277 stimulate hyperphosphorylation of the axonal microtubule-associated protein, tau.

278 Tpx2 is a microtubule-associated protein that activates the cell-c

279 that CESA interactive protein 1 (CSI1) is a microtubule-associated protein that bridges CESA complex

280 Tau is a microtubule-associated protein that functions in regulat

281 rtially rescued by overexpression of LIS1, a microtubule-associated protein that has previously been

282 Tau is a microtubule-associated protein that is genetically linke

283 Tau is a microtubule-associated protein that is highly soluble an

284 Human MID1 (midline-1) is a microtubule-associated protein that is postulated to tar

285 TPX2 is a microtubule-associated protein that is required for mito

286 archetypal member of this family, TRM1, is a microtubule-associated protein that localizes to cortica

287 toskeleton-associated protein 2, CKAP2, is a microtubule-associated protein that localizes to spindle

288 Tau is a microtubule-associated protein that stabilizes microtubu

289 CLASPs are microtubule-associated proteins that have a conserved ro

290 The XMAP215 family is comprised of conserved microtubule-associated proteins that use an array of tub

291 sion yeast Ndc80 directly binds the Dis1/TOG microtubule-associated protein, thereby coupling spindle

292 The microtubule-associated protein, TPX2, regulates the acti

293 Prior work demonstrated that a microtubule-associated protein, TPX2, targets kinesin-5

294 ed on the mitotic spindle via binding to the microtubule-associated protein, TPX2.

295 ny studies advanced our understanding of how microtubule-associated proteins tune microtubule dynamic

296 The microtubule associated protein type-2 (MAP-2) modulates

297 Tau is a microtubule-associated protein well known for its stabil

298 tially redundant EB1-binding sites provide a microtubule-associated protein with the means to modulat

299 (DCLK), closely related family members, are microtubule-associated proteins with overlapping functio

300 We also verified that the microtubule-associated protein XTP or the depolymerizati