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

1 further found that WDR90 is an evolutionary microtubule associated protein.

2 The TON1a gene encodes a microtubule-associated protein.

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

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

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

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

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

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

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

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

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

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

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

14 Elevated LC3 (microtubule associated protein 1 light chain 3)-I/-II co

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 phagy machinery components and modulation of microtubule-associated protein 1 light chain 3 (LC3).

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

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

31 Microtubule-associated protein 1 light chain 3 alpha (LC

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

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

34 Methamphetamine and HIV proteins increased microtubule-associated protein 1 light chain 3 beta-II (

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

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

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

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

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

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

43 phagosome-associated protein MAP1LC3B (LC3B; microtubule-associated protein 1 light chain 3beta) to p

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

45 alian Atg8) homologs, including the MAP1LC3 (microtubule-associated protein-1 light chain 3) family a

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

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

48 oteins, we identified C7orf43 (also known as microtubule-associated protein 11 (MAP11)) as being requ

49 ed analysis across ASD and ADHD, identifying microtubule-associated protein 1A (MAP1A) as a new exome

50 (NR2B), postsynaptic density-95 (PSD-95) and microtubule-associated protein 1A (MAP1A) in PV(+) neuro

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

52 interact with both the autophagosome protein microtubule-associated protein 1A/1B light chain 3 (LC3)

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

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

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

56 y in renal tubules, as assessed by measuring microtubule-associated protein 1A/1B-light chain 3 (LC3)

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

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

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

60 Moreover, the autophagy marker microtubule-associated proteins 1A-1B light chain 3B was

61 agy-related gene (Atg)5, Atg7, beclin-1, and microtubule-associated proteins 1A/1B light chain 3 (LC3

62 G 5-12 [autophagy related 5-12] and LC3B-II [microtubule-associated proteins 1A/1B light chain 3B-II]

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

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

65 e formation or autophagic process, including microtubule-associated protein 1B-light chain 3, autopha

66 d hepatocarcinogenesis through activation of microtubule associated protein 1S (MAP1S)-mediated autop

67 The microtubule associated protein 2 (Map2) helps stabilize

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

69 uction and mitochondrial damage, and reduced microtubule-associated protein 2 (MAP2) dendrites in hum

70 Using microtubule-associated protein 2 (MAP2) immunohistochemi

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

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

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

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

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

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 in reaction (RT-PCR), and levels of KLK8 and microtubule-associated protein 2, c isoform (MAP2c) prot

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

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

81 he neuronal-markers; neuronal nuclei (NeuN), microtubule-associated protein-2 (MAP-2) and betaIII-tub

82 We also previously demonstrated that microtubule-associated-protein-2 immunoreactivity (MAP2-

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

84 Microtubule-associated protein 4 (MAP4) interacts with a

85 ed by phosphorylation status of stathmin and microtubule-associated protein 4 (MAP4), the latter of w

86 cell by direct binding to the C terminus of Microtubule-Associated Protein 4 (MAP4).

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

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

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

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

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

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

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

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

95 , accumulation of hyperphosphorylated tau, a microtubule-associated protein and a hallmark of Alzheim

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

97 e adaptor KLHL15 in proteostasis of neuronal microtubule-associated proteins and identify a regulator

98 Apart from microtubule-associated proteins and motors, two factors

99 ed by biochemical signaling, cargo adaptors, microtubule-associated proteins, and mechanical forces.

100 enriched for genes encoding microtubules and microtubule-associated proteins, and this enrichment hig

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

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

103 cs approach to identify a family of neuronal microtubule-associated proteins as KLHL15 substrates, wh

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 Using the kinetochore and microtubule-associated protein, Astrin, as a molecular p

108 encoding the mitotic kinase AtAurora 1, the microtubule-associated proteins AtEDE1 and AtMAP65-4, an

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

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

111 A new in vitro study finds that the microtubule-associated protein CLASP repairs lattice dam

112 Previous work showed that the microtubule-associated protein CLASP sustains root apica

113 We validate the microtubule-associated proteins Clasp2, Elys, tubulin ty

114 0-NH12 exhibits impaired localization of the microtubule-associated protein complex Alp7/transforming

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

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

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

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

119 MTUS1 gene, whose major product, ATIP3, is a microtubule-associated protein down-regulated in aggress

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

121 LRPPRC interacts with one of microtubule-associated protein family MAP1S that promote

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

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

124 ains microtubule stability/dynamics with the microtubule-associated protein futsch/MAP1B, which is al

125 Two microtubule-associated proteins, homologs of Clip170 and

126 of cell elongation include microtubules and microtubule-associated proteins; however, upstream regul

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

128 Tau is an abundant microtubule-associated protein in neurons.

129 Tau is a multifunctional microtubule-associated protein in the neuron.

130 , and differences in activities or levels of microtubule-associated proteins in the egg cytoplasm bet

131 cells also revealed two rice (Oryza sativa) microtubule-associated proteins in the phragmoplast and

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

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

134 Tau is a microtubule-associated protein involved in the regulatio

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

136 gical aggregation and accumulation of tau, a microtubule-associated protein, is a common feature amon

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

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

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

140 MAD2 is a microtubules-associated protein known to be greatly over

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

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

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

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

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

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

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

148 al integrity and increased expression of the microtubule-associated protein light chain 3 (LC3), the

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

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

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

152 62/sequestosome 1, and the lipidated form of microtubule-associated protein light chain 3 isoform B.

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

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

155 p53-ablation reduced microtubule-associated protein light chain 3-mediated mi

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

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

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

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

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

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

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

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

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

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

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

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

168 Microtubule-associated protein (MAP) 2 has been perceive

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

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

171 In Alzheimer's disease (AD), tau, a microtubule-associated protein (MAP), becomes hyperphosp

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

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

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

175 As previously demonstrated, the microtubule associated protein MAP1B binds the cytoplasm

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

177 dant response elements (AREs) localized to a microtubule-associated protein (Map1b) gene enhancer and

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

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

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

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

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

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

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

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

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

187 Microtubule-associated proteins (MAPs) are a functionall

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

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

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

191 destabilize microtubules by phosphorylating microtubule-associated proteins (MAPs) of the MAP2/Tau f

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

193 Microtubule-associated proteins (MAPs) regulate microtub

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

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

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

197 of purified motor proteins and non-enzymatic microtubule-associated proteins (MAPs) to demonstrate th

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

199 predict that the combinatory effects of four microtubule-associated proteins (MAPs), namely EB1, XMAP

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

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

202 ubules, which are thought to be regulated by microtubule-associated proteins (MAPs).

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

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

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

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

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

208 Accumulation of hyperphosphorylated tau, a microtubule-associated protein, plays an important role

209 Doublecortin is a microtubule-associated protein produced during neurogene

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

211 Microtubule-associated proteins regulate microtubule (MT

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

213 Tau, a member of the MAP2/tau family of microtubule-associated proteins, stabilizes and organize

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

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

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

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

218 The microtubule associated protein tau is another neuronal p

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

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

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

222 ing frame 72 (C9orf72), progranulin (GRN) or microtubule-associated protein tau (MAPT) and their firs

223 missense mutations in the tau-encoding gene microtubule-associated protein tau (MAPT) can cause fron

224 Mutations in the microtubule-associated protein tau (MAPT) underlie multi

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

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

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

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

229 diated phosphorylation of target residues in microtubule-associated protein tau (MAPTAU) contributes

230 consisting primarily of hyperphosphorylated microtubule-associated protein tau (p-tau) and extracell

231 The microtubule-associated protein tau accumulates in neurod

232 The microtubule-associated protein tau accumulates into toxi

233 Aggregates of Abeta peptide and the microtubule-associated protein tau are key molecular hal

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

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

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

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

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

239 The microtubule-associated protein tau has a central role in

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

241 The microtubule-associated protein tau has been implicated i

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

243 d-beta (Abeta) protein precedes and requires microtubule-associated protein tau in a sort of trigger-

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

245 Assembly of microtubule-associated protein tau into filamentous incl

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

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

248 Microtubule-associated protein tau is an axonal phosphop

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

250 The microtubule-associated protein tau is implicated in vari

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

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

253 The microtubule-associated protein tau is predominantly loca

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

255 Microtubule-associated protein tau mutations cause a gro

256 The microtubule-associated protein Tau plays a central role

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

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

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

260 The microtubule-associated protein tau undergoes aberrant mo

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

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

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

264 linked to neurodegenerative diseases is tau (microtubule-associated protein tau), which can cause fro

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 Microtubule-associated protein tau, which is considered

272 ons between the human sHSP HspB1 (Hsp27) and microtubule-associated protein tau, which is implicated

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

274 rocess is mediated by the phosphorylation of microtubule-associated protein tau.

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

276 mulation of hyperphosphorylated forms of the microtubule-associated protein tau.

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

278 Tau is a microtubule-associated protein that becomes dysregulated

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

280 Tau is an intrinsically disordered, microtubule-associated protein that has a role in regula

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 Tau is an intrinsically disordered microtubule-associated protein that is implicated in sev

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

286 Tau, a microtubule-associated protein that modifies the dynamic

287 Tau is a microtubule-associated protein that plays a major role i

288 opoietic PBX-interacting protein (HPIP) is a microtubule-associated protein that plays a pivotal role

289 EML4 is a microtubule-associated protein that promotes microtubule

290 Sperm flagellar 1 (also called CLAMP) is a microtubule-associated protein that regulates microtubul

291 Tau is a microtubule-associated protein that stabilizes microtubu

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

293 As the microtubule-associated protein TPX2 appeared, efficient

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

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

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

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

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

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

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