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1 ormation through developmental regulation of cytoplasmic dynein.
2  forces on astral microtubules (MTs) through cytoplasmic dynein.
3  driven exclusively by the microtubule motor cytoplasmic dynein.
4  transport motors: kinesin-1, kinesin-3, and cytoplasmic dynein.
5 for the minus-end-directed microtubule motor cytoplasmic dynein.
6 first specific small-molecule antagonists of cytoplasmic dynein.
7  of the cellular functions and regulation of cytoplasmic dynein.
8 f two ~300-kilodalton motor domains of yeast cytoplasmic dynein.
9 1 in the regulation of the microtubule motor cytoplasmic dynein.
10  interact directly with one another and with cytoplasmic dynein.
11 e force-dependent stepping behavior of yeast cytoplasmic dynein.
12 back to the cytoplasm (retrograde) driven by cytoplasmic dynein.
13 d by myosin V, heterotrimeric kinesin-2, and cytoplasmic dynein.
14 directly modulates the enzymatic activity of cytoplasmic dynein.
15 orged between Lis1 and the microtubule motor cytoplasmic dynein.
16 gene, which is involved in the regulation of cytoplasmic dynein.
17                                              Cytoplasmic dynein 1 (dynein) is a minus end-directed mi
18               All animal cells use the motor cytoplasmic dynein 1 (dynein) to transport diverse cargo
19                                          The cytoplasmic dynein 1 cargo binding domain is formed by f
20 ediate Chain 2), encoding a component of the cytoplasmic dynein 1 complex.
21 f the microtubule-based motors kinesin 1 and cytoplasmic dynein 1 in vitro.
22                Recent experiment showed that cytoplasmic dynein 1, a molecular motor responsible for
23                                              Cytoplasmic dynein-1 (dynein) is the motor responsible f
24                                          The cytoplasmic dynein-1 (dynein) motor plays a central role
25                                              Cytoplasmic dynein-1 (dynein-1) plays roles in mitosis a
26 cently identified an interaction between the cytoplasmic dynein-1 activating adaptor Hook3 and the ki
27      We decorated microtubules with MTBDs of cytoplasmic dynein-1 and axonemal dynein DNAH7 and deter
28 t a previously unrecognized link between the cytoplasmic dynein-1 and IFT dynein-2 motors.
29 novel model by which stationary complexes of cytoplasmic dynein-1 are responsible for the shuttling o
30                                              Cytoplasmic dynein-1 binds dynactin and cargo adaptor pr
31                                              Cytoplasmic dynein-1 is a molecular motor that drives ne
32 work is essential for neuronal function, and cytoplasmic dynein-1 is an established molecular motor t
33                              In human cells, cytoplasmic dynein-1 is essential for long-distance tran
34           DYNC1H1 encodes the heavy chain of cytoplasmic dynein-1, a 1.4-MDa motor complex that traff
35 gical and genetic manipulation, we show that cytoplasmic dynein-1, which localizes to the junction be
36 essential cofactor for the microtubule motor cytoplasmic dynein-1.
37         The microtubule motors kinesin-2 and cytoplasmic dynein 1b drive IFT particles (protein compl
38 re, we report that the retrograde IFT motor, cytoplasmic dynein 1b, is required in the cytoplasm for
39 nt away from the flagellar tip is powered by cytoplasmic dynein 1b/2.
40 his identifies potential novel components of cytoplasmic dynein 2 and furthermore provides fresh insi
41 nts IFT88, the kinesin-II subunit KIF3A, and cytoplasmic dynein 2 appeared compromised.
42 , a mammalian homologue of the Chlamydomonas cytoplasmic dynein 2 intermediate chain that also locali
43 both requiring the ciliary retrograde motor, cytoplasmic dynein 2, for ciliary exit.
44  Wdr34 gene encodes an intermediate chain of cytoplasmic dynein 2, the motor for retrograde intraflag
45                                              Cytoplasmic dynein-2 (dynein-2) performs intraflagellar
46  the light intermediate chain (D2LIC) of the cytoplasmic dynein-2 complex are essential for retrograd
47                            Zebrafish lacking cytoplasmic dynein-2 function exhibited small eyes, kidn
48                                      Loss of cytoplasmic dynein-2 function resulted in a significant
49 the first time, that the dync2-i1 subunit of cytoplasmic dynein-2 is necessary for retrograde IFT.
50 y mutations in a new disease-producing gene, cytoplasmic dynein-2 light intermediate chain 1, DYNC2LI
51 e present the crystal structure of the human cytoplasmic dynein-2 motor bound to the ATP-hydrolysis t
52 nally, the ERG results indicate that loss of cytoplasmic dynein-2 reduces the photoreceptor light res
53 nd intermediate chain (dync2-i1) subunits of cytoplasmic dynein-2 were injected into zebrafish embryo
54 oreceptors lacking the retrograde IFT motor, cytoplasmic dynein-2.
55 complex required for the in vivo function of cytoplasmic dynein, a microtubule (MT)-based motor.
56 1 and an interacting protein, NDEL1, bind to cytoplasmic dynein, a microtubule motor protein.
57 nhibitor nocodazole and by the inhibition of cytoplasmic dynein, a microtubule-associated motor prote
58                                              Cytoplasmic dynein, a microtubule-based motor protein, t
59 , Nudel/NudE, and dynactin are regulators of cytoplasmic dynein, a minus end-directed, microtubule (M
60                                              Cytoplasmic dynein, a minus-end-directed microtubule mot
61  is central to the functional versatility of cytoplasmic dynein, a motor involved in intracellular tr
62 uggesting that dop is involved in regulating cytoplasmic dynein activity through direct or indirect m
63                         Here we identify the cytoplasmic dynein adaptor Spindly as an additional comp
64                                 In addition, cytoplasmic dynein also depended on EBA to track on most
65 antibody-Fab tag to mark the position of the cytoplasmic dynein amino-terminal tail domain, as it eme
66                             Contacts between cytoplasmic dynein and astral microtubules (MTs) at the
67 r migration (INM) that is driven apically by cytoplasmic dynein and basally by the kinesin KIF1A, whi
68                                              Cytoplasmic dynein and dynactin interact to drive microt
69                                              Cytoplasmic dynein and dynactin participate in retrograd
70    Although LIS1 binds the microtubule motor cytoplasmic dynein and has been linked to dynein functio
71                        The microtubule motor cytoplasmic dynein and its activator dynactin drive vesi
72 the trafficking of TYR and Pmel17 depends on cytoplasmic dynein and its interaction with the spectrin
73                        The microtubule motor cytoplasmic dynein and its partner complex dynactin driv
74                                              Cytoplasmic dynein and kinesin are both microtubule-base
75 t, bidirectional capsid motility mediated by cytoplasmic dynein and kinesin during entry, whereas egr
76                                              Cytoplasmic dynein and kinesin-1 are microtubule-based m
77 endosomes are transported bidirectionally by cytoplasmic dynein and kinesin-3, but how the movements
78 udEL are related proteins that interact with cytoplasmic dynein and LIS1.
79 1 in developing hair cells causes defects in cytoplasmic dynein and microtubule organization, resulti
80 precursor migration and the effects of LIS1, cytoplasmic dynein and myosin II inhibition.
81                     In Aspergillus nidulans, cytoplasmic dynein and NUDF/LIS1 are found at the spindl
82                               Dynactin links cytoplasmic dynein and other motors to cargo and is invo
83 in is a multiprotein complex that works with cytoplasmic dynein and other motors to support a wide ra
84 that kinesin-5 works in part by antagonizing cytoplasmic dynein and that these motor-driven forces fu
85 telomere attachment sites must be coupled to cytoplasmic dynein and the microtubule system to ensure
86 ation activities associated with NuMA (i.e., cytoplasmic dynein) and HSET are not necessary for pole
87 d moved by microtubule motors (kinesin-1 and cytoplasmic dynein), and that binding of motors and move
88 sported by microtubule motors, kinesin-2 and cytoplasmic dynein, and an actin motor, myosin-V.
89 ransport machinery: specifically, kinesin-1, cytoplasmic dynein, and the dynein regulators Lis1 and d
90                                Kinesin-1 and cytoplasmic dynein are microtubule (MT) motors that tran
91                                  Kinesin and cytoplasmic dynein are microtubule-based motor proteins
92                        Our studies implicate cytoplasmic dynein as a more thermally tunable motor and
93                    We identify Kinesin-1 and cytoplasmic dynein as major PrP(C) vesicle motor complex
94  are integral parts of the microtubule motor cytoplasmic dynein, as they directly associate with dyne
95 ts, but not control transcripts, recruit the cytoplasmic Dynein-associated co-factors Bicaudal D (Bic
96                       A single major form of cytoplasmic dynein associates with membranous organelles
97              We find that PKA phosphorylates cytoplasmic dynein at a novel site in light intermediate
98 itotic checkpoint protein and the anchor for cytoplasmic dynein at mitotic kinetochores, though it is
99 ons to model the molecular motor function of cytoplasmic dynein at the single-molecule level.
100    Dynamitin is a commonly used inhibitor of cytoplasmic dynein-based motility in living cells.
101 rotubules are polarity sorted in the axon by cytoplasmic dynein but that additional factors are also
102                    The velocity of mammalian cytoplasmic dynein, but not of mammalian kinesin-1, exhi
103  cellular functions of the microtubule motor cytoplasmic dynein, but the mechanism by which dynactin
104  in vivo evidence that distinct mutations in cytoplasmic dynein can either result in a pure sensory n
105 l trap, we were now able to demonstrate that cytoplasmic dynein can generate a discrete power stroke
106 tubule movements so that polarity sorting by cytoplasmic dynein can occur in a manner unimpeded by ot
107 ncoding the heavy chain subunit (DYNC1H1) of cytoplasmic dynein cause spinal muscular atrophy with lo
108                The microtubule motor protein cytoplasmic dynein clusters into a ring at the synapse,
109 at mutations in the minus-end-directed motor cytoplasmic dynein, completely block the increased DCVs
110 microtubule transport, the recombinant human cytoplasmic dynein complex is an active, microtubule min
111 n performed either with the native mammalian cytoplasmic dynein complex purified from tissue or, more
112             Here, we reconstitute a complete cytoplasmic dynein complex using recombinant human subun
113 ssed by disrupting the retrograde motor, the cytoplasmic dynein complex.
114 ays demonstrate that Bub3 interacts with the cytoplasmic dynein complex.
115 his nomenclature recognizes the two distinct cytoplasmic dynein complexes and has the flexibility to
116                      We find that Drosophila cytoplasmic dynein components are direct PKA phosphoryla
117 essing of tagged and truncated Dictyostelium cytoplasmic dynein constructs, we show that the heart of
118 TrkB) signaling endosomes are transported by cytoplasmic dynein containing the neuron-specific IC-1B
119                           The heavy chain of cytoplasmic dynein contains four nucleotide-binding doma
120 minus-end directed microtubule motor protein cytoplasmic dynein contributes to many aspects of cell d
121 al channels and annular cylinders, even when cytoplasmic dynein-dependent pulling mechanisms were inh
122                 Specifically, MPP+ increased cytoplasmic dynein-dependent retrograde FAT and reduced
123 crotubule-associated proteins (MAPs) but not cytoplasmic dynein-depleted MAPs.
124 n of kinesin-1 (KLC1) and the heavy chain of cytoplasmic dynein (DHC1) on vesicles.
125 o measure stall forces of both kinesin-1 and cytoplasmic dynein-driven lipid droplets in Drosophila e
126 for why Lis1 is a required cofactor for most cytoplasmic dynein-driven processes in cells.
127 r et al. and Hashimoto-Tane et al. show that cytoplasmic dynein drives microcluster centralization al
128                                              Cytoplasmic dynein drives the majority of minus end-dire
129 ei migrate basally during G1, apically using cytoplasmic dynein during G2, and undergo mitosis at the
130                                              Cytoplasmic dynein, dynactin, and pericentrin are all re
131                           Single kinesin and cytoplasmic dynein-dynactin molecules fused with green-f
132  mutation in p150(Glued), a component of the cytoplasmic dynein/dynactin microtubule motor complex, r
133                                 In contrast, cytoplasmic dynein efficiently navigates both axons and
134 , hexon, directly recruits the motor protein cytoplasmic dynein following virion entry.
135 ond switch, depending on magnesium, converts cytoplasmic dynein from a nonprocessive to a processive
136                              Single-molecule cytoplasmic dynein function is well understood, but ther
137      Bipolar spindle fusion was blocked when cytoplasmic dynein function was perturbed, suggesting a
138                                              Cytoplasmic dynein functions at several sites during mit
139                                              Cytoplasmic dynein functions in the checkpoint, apparent
140 ducts of the 6 kinesin gene family and the 1 cytoplasmic dynein gene.
141                                              Cytoplasmic dynein has been implicated in diverse mitoti
142           A few small-molecule inhibitors of cytoplasmic dynein have been identified.
143                            A mutation in the cytoplasmic dynein heavy chain (DHC) gene was discovered
144 ioning in different systems, associates with cytoplasmic dynein heavy chain (DYNC1H1) in a Galphai-re
145  comprises different subunits assembled on a cytoplasmic dynein heavy chain 1 (DYNC1H1) dimer.
146 ant, c.917A>G, in DYNC1H1, which encodes the cytoplasmic dynein heavy chain 1 (here, novel refers to
147 to identify a nine base-pair deletion in the cytoplasmic dynein heavy chain 1 gene (Dync1h1) in this
148   The library was examined for inhibition of cytoplasmic dynein heavy chain and cell growth.
149                         Partial depletion of cytoplasmic dynein heavy chain by RNA interference block
150 le-stimulated ATPase activity of recombinant cytoplasmic dynein heavy chain motor domain.
151  of CLIPA, green fluorescent protein-labeled cytoplasmic dynein heavy chain, p150(Glued) dynactin, an
152 ganelle movement by conventional kinesin and cytoplasmic dynein in a cell.
153 n hexon recruits the molecular motor protein cytoplasmic dynein in a pH-dependent manner, a function
154                     FAK also associated with cytoplasmic dynein in a Ser-732 phosphorylation-dependen
155                       Functional analysis of cytoplasmic dynein in Caenorhabditis elegans has reveale
156 at both Hook1 and Hook3 effectively activate cytoplasmic dynein, inducing longer run lengths and high
157 d a genomic region that contained DYNC2H1, a cytoplasmic dynein involved in retrograde transport in t
158                                              Cytoplasmic dynein is a 1.2-MDa multisubunit motor prote
159                                              Cytoplasmic dynein is a complex containing heavy chains
160                                              Cytoplasmic dynein is a dimeric AAA(+) motor protein tha
161                                              Cytoplasmic dynein is a dimeric motor that transports in
162                                              Cytoplasmic dynein is a eukaryotic motor protein complex
163                                              Cytoplasmic dynein is a homodimeric AAA+ motor that tran
164                                              Cytoplasmic dynein is a homodimeric microtubule (MT) mot
165                                              Cytoplasmic dynein is a large minus end-directed motor c
166                                              Cytoplasmic dynein is a large multisubunit complex invol
167                                              Cytoplasmic dynein is a large multisubunit motor protein
168                                              Cytoplasmic dynein is a large, microtubule-dependent mol
169                                              Cytoplasmic dynein is a microtubule motor involved in ca
170                                              Cytoplasmic dynein is a microtubule-based molecular moto
171                                              Cytoplasmic dynein is a microtubule-based motor protein
172                                              Cytoplasmic dynein is a microtubule-based motor required
173                                              Cytoplasmic dynein is a minus end-directed microtubule m
174                                              Cytoplasmic dynein is a minus-end-directed microtubule m
175                                              Cytoplasmic dynein is a molecular motor responsible for
176                                              Cytoplasmic dynein is a molecular motor that transports
177                                              Cytoplasmic dynein is a motor protein that walks along m
178                                              Cytoplasmic dynein is a multisubunit microtubule motor c
179                                              Cytoplasmic dynein is activated by forming a complex wit
180 in vivo and in vitro, we found evidence that cytoplasmic dynein is active during minus- and plus-end
181                                              Cytoplasmic dynein is an AAA(+) motor that drives the tr
182                                              Cytoplasmic dynein is an abundant kinetochore protein wh
183  Here, we report that the stalk shaft of rat cytoplasmic dynein is an antiparallel alpha-helical coil
184                                              Cytoplasmic dynein is an approximately 1.4 MDa multi-pro
185                                              Cytoplasmic dynein is an enormous minus end-directed mic
186                  The functional diversity of cytoplasmic dynein is in part attributed to multiple int
187                                              Cytoplasmic dynein is involved in a multitude of essenti
188                                              Cytoplasmic dynein is involved in a wide range of cellul
189                        In higher eukaryotes, cytoplasmic dynein is involved in silencing the SAC by r
190  endosomes from the axon to the cell body by cytoplasmic dynein is necessary for axonal and neuronal
191                                              Cytoplasmic dynein is particularly important for neurons
192                                      Whereas cytoplasmic dynein is primarily known as a minus-end-dir
193                   Furthermore, we found that cytoplasmic dynein is required for the spindle pole accu
194                                              Cytoplasmic dynein is responsible for a wide range of ce
195                                              Cytoplasmic dynein is responsible for many aspects of ce
196                          The molecular motor cytoplasmic dynein is responsible for most minus-end-dir
197     The minus end-directed microtubule motor cytoplasmic dynein is responsible for the intracellular
198                                              Cytoplasmic dynein is responsible for transport of sever
199                                              Cytoplasmic dynein is the main retrograde motor in all e
200                                              Cytoplasmic dynein is the major microtubule minus end-di
201                                              Cytoplasmic dynein is the major microtubule minus-end-di
202                                              Cytoplasmic dynein is the major minus end-directed micro
203                                              Cytoplasmic dynein is the major motor protein responsibl
204                                              Cytoplasmic dynein is the molecular motor responsible fo
205                                              Cytoplasmic dynein is the most complex cytoskeletal moto
206         We have previously demonstrated that cytoplasmic dynein is the motor involved in the perinucl
207                                              Cytoplasmic dynein is the motor protein responsible for
208                                              Cytoplasmic dynein is the multisubunit motor protein for
209                                              Cytoplasmic dynein is the multisubunit protein complex r
210                                              Cytoplasmic dynein is the predominant minus-end-directed
211                                              Cytoplasmic dynein is the primary minus-end-directed mic
212                                              Cytoplasmic dynein is the primary molecular motor respon
213                                              Cytoplasmic dynein is the primary motor for microtubule
214                                              Cytoplasmic dynein is well characterized as an organelle
215 al cortex involves Nesprin-2, which recruits cytoplasmic dynein, kinesin, and actin to the nuclear en
216                        Previously, the 8-kDa cytoplasmic dynein light chain (LC8) was demonstrated to
217 nal kinesin, reductions in the levels of the cytoplasmic dynein light chain Tctex type 3 subunit were
218  studies, we show that in rodents Tctex-1, a cytoplasmic dynein light chain, is selectively enriched
219                                          The cytoplasmic dynein light intermediate chains (LICs) 1 an
220                        Dominant mutations in cytoplasmic dynein (Loa or Cra) have been reported to pr
221  MTOC, in which the minus end-directed motor cytoplasmic dynein, localized at the synapse through an
222  is a highly conserved protein necessary for cytoplasmic dynein-mediated nuclear migration in Aspergi
223 say was used to evaluate the hypothesis that cytoplasmic dynein mediates AAV interaction with microtu
224                                              Cytoplasmic dynein mediates retrograde transport in axon
225                                              Cytoplasmic dynein mediates spindle orientation from the
226                                              Cytoplasmic dynein mediates spindle positioning in buddi
227   Recently, an x-ray structure of the murine cytoplasmic dynein microtubule binding domain (MTBD) in
228  a mutation in dhc-1, the heavy chain of the cytoplasmic dynein minus-end directed microtubule motor,
229 along microtubules is powered by kinesin and cytoplasmic dynein molecular motors.
230                                              Cytoplasmic dynein motility along microtubules is critic
231 ight chain LC8 is an integral subunit of the cytoplasmic dynein motor complex that binds directly to
232      Tctex-1, a light-chain component of the cytoplasmic dynein motor complex, can function independe
233                        We show that a single cytoplasmic dynein motor frequently transitions into an
234                                          The cytoplasmic dynein motor generates pulling forces to cen
235 ion of a specific role for these proteins in cytoplasmic dynein motor regulation has remained elusive
236 lization to elucidate relative kinesin-1 and cytoplasmic dynein motor subunit composition of individu
237         Dynactin is an essential part of the cytoplasmic dynein motor that enhances motor processivit
238 , dynactin, is an essential component of the cytoplasmic dynein motor.
239          Our data also suggest kinesin-1 and cytoplasmic dynein motors assemble in stable mixtures on
240 re under the influence of forces mediated by cytoplasmic dynein motors associated with the cell corte
241  MTs to test the hypothesis that immobilized cytoplasmic dynein motors transport short MTs with their
242                                              Cytoplasmic dynein moves processively along microtubules
243                                     Metazoan cytoplasmic dynein moves processively along microtubules
244                     Our results suggest that cytoplasmic dynein moves processively through the coordi
245  microtubules in the cell periphery, whereas cytoplasmic dynein moves to the minus ends in the cell c
246 We report the crystal structure of the mouse cytoplasmic dynein MTBD and a portion of the coiled coil
247 single molecule motility properties of yeast cytoplasmic dynein mutants bearing mutations that preven
248  (chromokinesin and Eg5) and minus-directed (cytoplasmic dynein oligomers) motors walking on microtub
249 litates the localization of Mcp5 and that of cytoplasmic dynein on the membrane.
250 y distribution of melanosomes transported by cytoplasmic dynein or kinesin-2 under conditions of aggr
251 terfering RNA (siRNA)-mediated inhibition of cytoplasmic dynein or the kinesin 1 heavy chain KIF5B de
252                                              Cytoplasmic dynein participates in multiple aspects of n
253                              Proteins in the cytoplasmic dynein pathway accumulate at the microtubule
254                                              Cytoplasmic dynein performs multiple cellular tasks but
255  phenotype than the control, indicating that cytoplasmic dynein plays a role in chromosome segregatio
256                                              Cytoplasmic dynein plays critical roles within the devel
257                                              Cytoplasmic dynein plays important roles in membrane tra
258           During mitosis, the motor molecule cytoplasmic dynein plays key direct and indirect roles i
259                                              Cytoplasmic dynein powers intracellular movement of carg
260                     In axons of PNS neurons, cytoplasmic dynein provides force for retrograde movemen
261 e compelling evidence that the motor protein cytoplasmic dynein provides the necessary force for micr
262                        The AAA+ ATPase motor cytoplasmic dynein regulates ciliary trafficking, mitoti
263 erkinetic nuclear migration, consistent with cytoplasmic dynein regulation.
264 ave coevolved with an autoinhibitory mode of cytoplasmic dynein regulation.
265                          We propose that the cytoplasmic dynein regulators are a critical component o
266   It is specifically blocked by RNAi for the cytoplasmic dynein regulators LIS1 and NudE/L (Nde1/Ndel
267                                          The cytoplasmic dynein regulatory factor Lis1, which induces
268                                Kinesin-1 and cytoplasmic dynein require each other for bidirectional
269  motor axons are kinesin-1 (anterograde) and cytoplasmic dynein (retrograde), and interestingly that
270                                Regulation of cytoplasmic dynein's motor activity is essential for div
271 cture we are able to draw new conclusions on cytoplasmic dynein's stepping mechanism.
272           In contrast, the velocity of yeast cytoplasmic dynein showed a break from Arrhenius behavio
273                        RNAi directed against cytoplasmic dynein specifically inhibited nuclear moveme
274           We propose names for the mammalian cytoplasmic dynein subunit genes and proteins that refle
275 ctions in levels of conventional kinesin and cytoplasmic dynein subunits were recapitulated in a rat
276                       It has been shown that cytoplasmic dynein, targeted to cortical actin, removes
277 is a highly conserved light-chain subunit of cytoplasmic dynein that interacts with a wide variety of
278                                              Cytoplasmic dynein, the 1.2 MDa motor driving minus-end-
279 an interaction between the microtubule motor cytoplasmic dynein, the adenomatous polyposis coli tumor
280  contain a large number of kinesins but lack cytoplasmic dynein, the foremost processive retrograde t
281                                              Cytoplasmic dynein, the major motor driving retrograde a
282 orted to regulate the mechanical behavior of cytoplasmic dynein, the primary minus-end-directed micro
283                               The ability of cytoplasmic dynein to recognize such diverse forms of ca
284  binding to Trk initiates the recruitment of cytoplasmic dynein to signaling endosomes through ERK1/2
285 es attachment of the microtubule-based motor cytoplasmic dynein to the cortex, where it exerts a pull
286  nuclear INT complex promotes recruitment of cytoplasmic dynein to the NE, possibly via a mechanism i
287 pAR63, nearly eliminates the localization of cytoplasmic dynein to the spindle poles, but it has no a
288       To do this, we fused the MTBD of mouse cytoplasmic dynein, together with 12-36 residues of its
289                                              Cytoplasmic dynein transports cargoes for a variety of c
290                          The multi-component cytoplasmic dynein transports cellular cargoes with the
291                                              Cytoplasmic dynein transports membranous cargoes along m
292                                              Cytoplasmic dynein transports various cellular cargoes i
293     The minus end-directed microtubule motor cytoplasmic dynein transports various cellular cargoes,
294 s proplatelet elongation and is dependent on cytoplasmic dynein under static and physiological shear
295                        The microtubule motor cytoplasmic dynein was a critical part of this coalescin
296 sitioning, are mediated by the motor protein cytoplasmic dynein, which produces force on the microtub
297  critical regulator of the microtubule motor cytoplasmic dynein, which transports numerous cargoes th
298     We also predict that acute inhibition of cytoplasmic dynein will disrupt the polarity sorting of
299 oups of motor proteins, such as kinesins and cytoplasmic dynein, work together to ensure the supply a
300 to the soma is driven by the molecular motor cytoplasmic dynein, yet it remains unclear how dynein is

 
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