ライフサイエンスコーパス: microtubule-associated

1 CAP-Gly domain of dynactin, a microtubule-associated activator of dynein motor, partic

2 The latter also binds to microtubule-associated Bim1p, thereby connecting both ty

3 how that small CESA compartments (SmaCCs) or microtubule-associated cellulose synthase compartments (

4 k, and small CESA-containing compartments or microtubule-associated cellulose synthase compartments,

5 We have identified KIAA0556 as a novel microtubule-associated ciliary base protein mutated in J

6 xpression of cellular proteins implicated in microtubule-associated cytoskeletal organization and dyn

7 The microtubule-associated formin, mDIA2, localized to actin

8 ng protein, and much work has focused on its microtubule-associated functions.

9 We also found that the expression levels of microtubule-associated genes, such as MAP70-5 and CLASP,

10 Here we show that the activation of the microtubule-associated guanine nucleotide exchange facto

11 Here, we report that the microtubule-associated histone deacetylase 6 (HDAC6) dif

12 into autophagosomes labeled by Beclin 1 and microtubule-associated light chain 3.

13 Here we discover that microtubule-associated lipid droplets (LDs) in COS1 cell

14 Some of these are found to be microtubule associated, making actin polymerization from

15 nal early endosome motility, indicating that microtubule-associated membrane trafficking enhances dif

16 nal coregulation with its host gene, MICAL3 (microtubule-associated monooxygenase, calponin, and LIM

17 omic-resolution structural analysis of other microtubule-associated motors.

18 ealed that TRPC3 functionally interacts with microtubule-associated NADPH oxidase (Nox) 2, and inhibi

19 that learning causes biphasic changes in the microtubule-associated network in the hippocampus.

20 Our results demonstrate that the microtubule-associated perturbations of mdx muscle are d

21 The microtubule-associated phosphoprotein tau regulates micr

22 associated, making actin polymerization from microtubule-associated platforms possible.

23 The microtubule associated protein 2 (Map2) helps stabilize

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

80 Using microtubule-associated protein 2 (MAP2) immunohistochemi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

103 0-NH12 exhibits impaired localization of the microtubule-associated protein complex Alp7/transforming

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

122 62/sequestosome 1, and the lipidated form of microtubule-associated protein light chain 3 isoform B.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

139 Doublecortin is a microtubule-associated protein produced during neurogene

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

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

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

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

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

145 The microtubule-associated protein targeting protein for Xen

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

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

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

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

150 The microtubule-associated protein tau accumulates in neurod

151 The microtubule-associated protein tau accumulates into toxi

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

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

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

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

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

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

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

159 The microtubule-associated protein tau has been implicated i

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

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

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

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

164 Microtubule-associated protein tau is an axonal phosphop

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

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

167 The microtubule-associated protein tau is implicated in vari

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

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

170 The microtubule-associated protein Tau is mainly expressed i

171 The microtubule-associated protein tau is predominantly loca

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

173 Microtubule-associated protein tau mutations cause a gro

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

175 The microtubule-associated protein Tau plays a central role

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

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

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

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

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

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

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

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

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

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

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

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

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

189 In the microtubule-associated protein tau, hyperphosphorylation

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

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

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

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

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

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

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

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

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

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

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

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

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

203 Tau is a microtubule-associated protein that stabilizes microtubu

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

229 The TON1a gene encodes a microtubule-associated protein.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

257 Microtubules and microtubule-associated proteins are fundamental for mult

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

259 Structures of microtubule-associated proteins assembled on polymeric m

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

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

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

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

264 Microtubule-associated proteins regulate microtubule (MT

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

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

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

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

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

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

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

272 Two microtubule-associated proteins, homologs of Clip170 and

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

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

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

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

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

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

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

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

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

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

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

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

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

286 Proteomic analysis revealed that microtubule-associated Rho guanine nucleotide exchange f

287 reen for proteins interacting with HvMAGAP1 (Microtubule Associated ROP-GTPase Activating Protein 1).

288 p encodes the single Drosophila homologue of microtubule-associated Ser/Thr (MAST) kinases.

289 high, doses promoted AICD transactivation of microtubule associated serine/threonine kinase family me

290 also phosphorylated in vitro and in vivo by microtubule-associated serine/threonine kinase 3 (MAST3

291 In mitosis, the Greatwall kinase (called microtubule-associated serine/threonine kinase like [Mas

292 d a genetic screen and identified MAST205 (a microtubule-associated serine/threonine kinase with a mo

293 Of these, Microtubule-Associated Stress Protein 1 (MASP1), an unch

294 The self-assembly of the microtubule associated tau protein into fibrillar cell i

295 intraneuronal tangles of hyperphosphorylated microtubule-associated tau protein (tau, gene MAPT) are

296 One of the most well-known IDPs is the microtubule-associated tau protein, which regulates micr

297 ng in embryonic hair cells, probably through microtubule-associated Tiam1, a guanine nucleotide excha

298 ically dividing human cells that kinetochore-microtubules associated to old centrosomes are more stab

299 The disordered microtubule associated Tubulin Polymerization Promoting

300 alpha4 forms a complex with PP2A and MID1, a microtubule-associated ubiquitin E3 ligase that facilita