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

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

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

5 membrane-associated Ankyrin (UNC-44) and the microtubule-associated CRMP (UNC-33).

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

7 ream from and is negatively regulated by the microtubule-associated deacetylase HDAC6, which function

8 alpha-tubulin acetylation by inhibiting the microtubule-associated deacetylase histone deacetylase 6

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

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

11 ferroptotic 15LO1 and the autophagic protein microtubule-associated light chain-3 (LC3).

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

13 alytic half of LRRK2, and an atomic model of microtubule-associated LRRK2 built using a reported cryo

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 Surprisingly, we find that the classically microtubule-associated Pavarotti binds directly to actin

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

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

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

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

25 The microtubule associated protein 2 (Map2) helps stabilize

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

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

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

29 The microtubule associated protein tau is another neuronal p

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

84 Using microtubule-associated protein 2 (MAP2) immunohistochemi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

126 62/sequestosome 1, and the lipidated form of microtubule-associated protein light chain 3 isoform B.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

154 The microtubule-associated protein tau accumulates into toxi

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

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

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

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

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

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

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

162 The microtubule-associated protein tau has been implicated i

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

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

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

166 Assembly of microtubule-associated protein tau into filamentous incl

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

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

169 Microtubule-associated protein tau is an axonal phosphop

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

171 The microtubule-associated protein tau is implicated in vari

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

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

174 Microtubule-associated protein tau mutations cause a gro

175 The microtubule-associated protein Tau plays a central role

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

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

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

179 The microtubule-associated protein tau undergoes aberrant mo

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

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

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

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

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

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

186 In the microtubule-associated protein tau, hyperphosphorylation

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

188 Microtubule-associated protein tau, which is considered

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

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

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

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

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

194 Tau is a microtubule-associated protein that becomes dysregulated

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

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

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

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

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

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

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

205 EML4 is a microtubule-associated protein that promotes microtubule

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

207 Tau is a microtubule-associated protein that stabilizes microtubu

208 As the microtubule-associated protein TPX2 appeared, efficient

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

229 The TON1a gene encodes a microtubule-associated protein.

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

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

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

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

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

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

238 Microtubule-associated proteins (MAPs) are a functionall

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

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

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

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

243 Microtubule-associated proteins (MAPs) regulate microtub

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

260 Structures of microtubule-associated proteins assembled on polymeric m

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

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

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

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

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

266 Microtubule-associated proteins regulate microtubule (MT

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

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

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

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

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

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

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

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

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

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

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

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

282 onal avenues for further characterization of microtubule-associated regulatory molecules as putative

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

284 tion, we found that GEF-H1/GEF-H1/AHRGEF2, a microtubule-associated Rho-GEF, was necessary for the in

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

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

287 Microtubule-associated Ser/Thr kinase 2 (MAST2) inhibits

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

289 Microtubule-associated serine/threonine kinase 1 (MAST1)

290 Specifically, the dysregulation of microtubule-associated serine/threonine kinase 2 and pro

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

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

293 Microtubule-associated serine/threonine-protein kinase-l

294 These findings suggest that microtubule-associated signaling proteins such as EB3 co

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

296 fied GTPases, membrane channel proteins, and microtubule associated targets that promote an osteoindu

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

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

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

300 The disordered microtubule associated Tubulin Polymerization Promoting