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1 f C. neoformans stress response pathways and cell morphogenesis.
2 ation, meristemoid differentiation and guard cell morphogenesis.
3 3 pathway links actin filament nucleation to cell morphogenesis.
4 dynamically reorganizes the cytoplasm during cell morphogenesis.
5  regulation of plant signal transduction and cell morphogenesis.
6 n important role in F-actin organization and cell morphogenesis.
7 en I and laminin-1 in regulating endothelial cell morphogenesis.
8  cortical array, which is critical for plant cell morphogenesis.
9  polymers in the biomechanical regulation of cell morphogenesis.
10 the MAPK-dependent stimulation of epithelial cell morphogenesis.
11                     The cytoskeleton governs cell morphogenesis.
12 ot ERK, prevented polycystin-1-mediated IMCD cell morphogenesis.
13 and each contributes to different aspects of cell morphogenesis.
14 al mechanical properties of the wall support cell morphogenesis.
15 es we observe are consistent with defects in cell morphogenesis.
16  its mammalian homolog CRB1 in photoreceptor cell morphogenesis.
17 he signals and mechanisms that control plant cell morphogenesis.
18 /APN functions in the control of endothelial cell morphogenesis.
19 ossibility that ES might regulate epithelial cell morphogenesis.
20  that targets the cytoskeleton and regulates cell morphogenesis.
21 al role of the MreB-controlled elongasome in cell morphogenesis.
22 ant strain defective in chitin synthesis and cell morphogenesis.
23 we questioned whether it induces endothelial cell morphogenesis.
24 a role for multiple integrins in endothelial cell morphogenesis.
25 ntial for cell migration, cell division, and cell morphogenesis.
26 ate levels of PECAM-1 stimulate, endothelial cell morphogenesis.
27 s active in the root until the initiation of cell morphogenesis.
28  and Cdc42Hs suggest a role for the Golgi in cell morphogenesis.
29 eptor in order to support mammary epithelial cell morphogenesis.
30  by immuno-deficiencies and defects in blood cell morphogenesis.
31 since these PBPs are known to participate in cell morphogenesis.
32 ange of functions, including cytokinesis and cell morphogenesis.
33  morphology at the EPCS and for normal plant cell morphogenesis.
34 l relation between NPF self-organization and cell morphogenesis.
35 p that solicits BR signaling and coordinates cell morphogenesis.
36 en cell shape and actin regulators instructs cell morphogenesis.
37 FAZ), a cytoskeletal structure important for cell morphogenesis.
38 onal consequences on filament properties and cell morphogenesis.
39 omoting cell wall metabolism and influencing cell morphogenesis.
40 tructure required for flagellum adhesion and cell morphogenesis.
41  V0 and V1 domains are required for terminal cell morphogenesis.
42 e the polarization process during epithelial cell morphogenesis.
43 o understanding the biomechanical control of cell morphogenesis.
44 dures as one of the central enigmas in plant cell morphogenesis.
45 ole of the p12 protein in modulation of host cell morphogenesis.
46 aromyces cerevisiae as a protein involved in cell morphogenesis.
47 that autolysins control different aspects of cell morphogenesis.
48 Tbx16-Fgf2 pathway that regulates epithelial cell morphogenesis.
49 ulate cortex structure, which in turn drives cell morphogenesis.
50  unexpected role of Vangl2 during supporting cell morphogenesis.
51 erve as a valuable model in studies of plant cell morphogenesis.
52 egulation of the microtubule cytoskeleton in cell morphogenesis.
53 echanism by which endocytosis contributes to cell morphogenesis.
54 acks for CHSs delivery and both cooperate in cell morphogenesis.
55 the role of asymmetric lipid distribution in cell morphogenesis.
56 ions in root tissue patterning and root hair cell morphogenesis.
57       The cytoskeleton is a key regulator of cell morphogenesis.
58 polarity mechanisms, and MTs responsible for cell morphogenesis.
59 ial actin homologue MreB plays a key role in cell morphogenesis.
60 g proteins often control multiple aspects of cell morphogenesis.
61 st polarization but also leads to defects in cell morphogenesis.
62 been implicated in septin organization [14], cell morphogenesis [15], and mitotic exit [16, 17], spec
63  traE genes could be involved in S. kunkelii cell morphogenesis, adhesion and DNA recombination.
64 airway epithelium, including those involving cell morphogenesis, adhesion, and motility.
65 ily tyrosine kinases have been implicated in cell morphogenesis, adhesion, motility, and oncogenesis.
66 that are essential regulators of endothelial cell morphogenesis and angiogenesis.
67 le-associated protein tau may be involved in cell morphogenesis and axonal maintenance.
68 l seed coats and document its importance for cell morphogenesis and barrier function of the seed coat
69 onstitutively active Erk5 blocks endothelial cell morphogenesis and causes HIF1-alpha destabilization
70 threonine kinase involved in regulating both cell morphogenesis and cell cycle control.
71 nce in the host and has a great influence on cell morphogenesis and cell division.
72 s and that its absence has severe effects on cell morphogenesis and cell division.
73         We conclude that Kel1p has a role in cell morphogenesis and cell fusion and may antagonize th
74 egulation of gene expression, cell adhesion, cell morphogenesis and cell migration.
75  proteins directly and indirectly related to cell morphogenesis and cell wall components such as mann
76 hat fgd-1 plays a critical role in excretory cell morphogenesis and cellular organization.
77 onomous mechanisms that regulate coordinated cell morphogenesis and cytodifferentiation of the retina
78 to provide the first detailed description of cell morphogenesis and cytokinesis in the early-branchin
79 omes use a microtubule-focused mechanism for cell morphogenesis and cytokinesis.
80 genesis; or (2) alterations of somatic gonad cell morphogenesis and differentiation in larval life.
81  White (d/d) mutants have defects in pigment cell morphogenesis and differentiation, whereas albino (
82  maturation late in development by promoting cell morphogenesis and differentiation.
83  dual regulator for Ras and Rho signaling in cell morphogenesis and differentiation.
84 f a physiologic role for Git2a in regulating cell morphogenesis and directed cell migration via myosi
85 re involved in the same aspects of epidermal cell morphogenesis and division.
86 TPs) in three-dimensional mammary epithelial cell morphogenesis and ERBB2 signaling.
87 omyosin contractility is required for bottle cell morphogenesis and further suggest a novel and unpre
88 ver, simultaneous melatonin supply supported cell morphogenesis and growth, reduced ROS and superoxid
89 e in directing early processes in intestinal cell morphogenesis and in the maintenance of the differe
90  KRAS signaling leads to altered endothelial cell morphogenesis and increased cell size, ectopic spro
91 brane components involved in tracheal fusion cell morphogenesis and lumenal development.
92                         Proper regulation of cell morphogenesis and migration by adhesion and growth-
93 espective contribution of these functions to cell morphogenesis and migration in 3D matrices is uncle
94      Here we demonstrate that Abi2 modulates cell morphogenesis and migration in vivo.
95 es have been implicated in the regulation of cell morphogenesis and migration, but the molecular mech
96 ing for effective membrane protrusion during cell morphogenesis and migration.
97 he generation of branched actin networks for cell morphogenesis and migration.
98 aling cascades, they have important roles in cell morphogenesis and mitogenesis.
99 he ability of actin filaments to function in cell morphogenesis and motility is coupled to their capa
100 ant non-redundant roles in the regulation of cell morphogenesis and motility.
101 cs at the cell cortex play a crucial role in cell morphogenesis and neuronal development.
102 ts designed to uncover general principles of cell morphogenesis and of cell shape function.
103 polarity is a fundamental feature underlying cell morphogenesis and organismal development.
104 s a potential coordination mechanism between cell morphogenesis and polarity during budding yeast mat
105           The conserved NDR kinase regulates cell morphogenesis and polarized cell growth in differen
106 Ndr/Warts family are important regulators of cell morphogenesis and proliferation.
107 al cells is important for cell integrity and cell morphogenesis and protects against harmful environm
108 e actin cytoskeleton is a major regulator of cell morphogenesis and responses to biotic and abiotic s
109 CP function with the hormone response during cell morphogenesis and shows that developmental and envi
110 ned considerable insight into the process of cell morphogenesis and the establishment of positional i
111 ain impaired the ability of Cla4 to regulate cell morphogenesis and the mitotic exit network (localiz
112  to probe molecular mechanisms underlying 3D cell morphogenesis and to test the intriguing possibilit
113 , as FoxO-regulated mediators of endothelial cell morphogenesis and vascular homeostasis.
114 ng epithelial polarity and, in photoreceptor cells, morphogenesis and stability.
115 flagellum that is involved in cell motility, cell morphogenesis, and cell division.
116  is critical for intercellular connectivity, cell morphogenesis, and cognitive functions.
117 s two paralogues: FAMA, a regulator of guard cell morphogenesis, and SPEECHLESS (SPCH).
118 ar distribution of molecules and organelles, cell morphogenesis, as well as segregation of the geneti
119 ornea in vivo and in the ex vivo endothelial cell morphogenesis assay is also MAPK- and PI3K-dependen
120 re, the WAVE complex has additional roles in cell morphogenesis beyond Arp2/3 complex activation.
121    These cells are a prime example of single-cell morphogenesis, branching significantly over time to
122 r dynamic remodeling of the cytoskeleton and cell morphogenesis, but the mechanisms driving actin dis
123 ults suggest that Cdc42Hs may play a role in cell morphogenesis by acting on targets in the Golgi tha
124 ules and F-actin both play critical roles in cell morphogenesis by guiding the deposition of wall mat
125  highly ordered parallel arrays that mediate cell morphogenesis by orienting cellulose deposition.
126 ide exchange factors control many aspects of cell morphogenesis by turning on Rho-GTPases.
127 lements to perform many functions, including cell morphogenesis, cell division, DNA partitioning, and
128 ing mating differentiation to mediate proper cell morphogenesis, cell fusion, and other steps of the
129 e-activating protein (RhoGAP) that regulates cell morphogenesis, cell migration, and ERK signaling by
130 ignaling, extracellular matrix interactions, cell morphogenesis, cell motility and migration.
131 range of important cell processes, including cell morphogenesis, chromosome segregation and cell pola
132 follows MreB and retains its crucial role in cell morphogenesis, demonstrating conservation of functi
133  altered functional gene networks related to cell morphogenesis, dendritic development, and cytoskele
134 utant cells develop into aberrant pharyngeal cells (Morphogenesis/Differentiation stage).
135 he expression of many genes that orchestrate cell morphogenesis during differentiation.
136 development is required for correct palisade cell morphogenesis during leaf development.
137                                Understanding cell morphogenesis during metazoan development requires
138         We report a role for puc in follicle cell morphogenesis during oogenesis.
139 le (otd), a homeobox gene, is required for R-cell morphogenesis during pupation.
140  are similarly involved in the regulation of cell morphogenesis during the yeast-to-hypha transition
141 nisms evolved is essential for understanding cell morphogenesis evolution.
142 eveals differences in expression dynamics of cell morphogenesis factors, including ZEB2, a known epit
143 review of this current knowledge of pavement cell morphogenesis, generated from a wealth of experimen
144 The alpha(v)beta(3) integrin participates in cell morphogenesis, growth factor signaling, and cell su
145 for cell curvature can cause a disruption of cell morphogenesis, highlighting the delicate harmony am
146  cr4 functions cell autonomously to regulate cell morphogenesis, implying that CR4 signal transductio
147 ulogenesis, VEGF can induce renal epithelial cell morphogenesis in a Nrp-1-dependent fashion.
148 of growth sites are tightly regulated during cell morphogenesis in all organisms.
149 otic cellular processes, including epidermal cell morphogenesis in Arabidopsis thaliana.
150 pathway of ROP2-mediated regulation of plant cell morphogenesis in Arabidopsis.
151 ought to function in spatially co-ordinating cell morphogenesis in conjunction with MreC, a protein t
152 s in live cells is critical to understanding cell morphogenesis in development and disease.
153 ts both chloroplast development and palisade cell morphogenesis in leaves.
154  advances in the quantitative imaging of all-cell morphogenesis in living organisms.
155                                              Cell morphogenesis in most bacteria is governed by spati
156 PDZ domain (MPDZ) protein during apical hair cell morphogenesis in mouse.
157  a novel role for Fgf signaling during glial cell morphogenesis in promoting axonal regeneration afte
158  compared the signaling pathways for mIMCD-3 cell morphogenesis in response to EGF and HGF.
159 lecular networks through which TbPLK directs cell morphogenesis in T. brucei.
160  cytoskeleton-dependent mechanisms governing cell morphogenesis in the maize leaf epidermis.
161 nfirmed the role of PhMYB1 in the control of cell morphogenesis in the petal epidermis.
162 the attached flagellum plays a major role in cell morphogenesis in this organism.
163 nding implicates the concept of cytotaxis in cell morphogenesis in trypanosomes.
164 n actin cytoskeleton that governs lens fiber cell morphogenesis in vivo.
165 p both participate in bud site selection and cell morphogenesis in yeast, and spa2delta cdc10-10 cell
166 ture involved in many key processes in plant cell morphogenesis including nuclear and cell division,
167 d protein kinase kinase inhibition abrogated cell morphogenesis induced by OSM, indicating an importa
168 naling pathways are required for endothelial cell morphogenesis into capillary-like networks.
169                                  Endothelial cell morphogenesis is a carbohydrate-dependent process,
170                                              Cell morphogenesis is a complex process that relies on a
171  of expansion is necessary to understand how cell morphogenesis is controlled in plants.
172                                              Cell morphogenesis is crucial for the physiology of anim
173 es their levels and connects their action to cell morphogenesis is less clear.
174              We show that slow-twitch muscle cell morphogenesis is marked by behaviors typical of cel
175 In mouse lenses lacking Tmod1, initial fiber cell morphogenesis is normal, but fiber cell hexagonal s
176                            However, follicle cell morphogenesis is unaffected by point mutations that
177  from Saccharomyces cerevisiae indicate that cell morphogenesis may involve cell cycle regulation by
178 at are upregulated during mammary epithelial cell morphogenesis may reveal novel regulators of tumori
179 Actin demonstrated that giActin functions in cell morphogenesis, membrane trafficking, and cytokinesi
180 d contractility, and accompanied problems in cell morphogenesis, migration, invasion, and mechanosens
181 res exquisite spatiotemporal coordination of cell morphogenesis, migration, proliferation, and differ
182  peri/intracellular, and subcellular ENS for cell morphogenesis, molecular imaging, cancer therapy, a
183 ctin-rich membrane protrusions essential for cell morphogenesis, motility, and cancer invasion.
184 or tyrosine kinases has an important role in cell morphogenesis, motility, and proliferation.
185      Contractile actin cortex is involved in cell morphogenesis, movement, and cytokinesis, but its o
186 diate downstream effects specific for either cell morphogenesis or pathogenesis.
187 l GTPase with roles in migration, epithelial cell morphogenesis, osteoclastogenesis, and oncogenic tr
188  and Hym1p function to regulate two distinct cell morphogenesis pathways: an ACE2-independent pathway
189 fy a critical role for SIPA1L3 in epithelial cell morphogenesis, polarity, adhesion and cytoskeletal
190 ber assembly and consequent abnormalities in cell morphogenesis, polarity, and migration.
191                                   Models for cell morphogenesis postulate that the effects of turgor
192 d by multiple and specific interactions with cell morphogenesis proteins that are linked to a dynamic
193 s of peptidoglycan synthases, hydrolases and cell morphogenesis proteins, but the details of these in
194             The molecular basis of bacterial cell morphogenesis remains largely an open question.
195                                    Bacterial cell morphogenesis requires coordination among multiple
196 type and act1/act1 mutants indicates that PH cell morphogenesis requires the maintenance of a highly
197                                 During plant cell morphogenesis, signal transduction and cytoskeletal
198                                As such, many cell morphogenesis studies have focused on the mechanism
199 f these GTPases is crucial for some forms of cell morphogenesis, the nature of such coordination duri
200 of which Cdc42Hs is a member, is involved in cell morphogenesis through a GTPase cascade which regula
201 putative Arabidopsis Arp2/3 complex controls cell morphogenesis through its roles in cell polarity es
202 portant for induction of gene expression and cell morphogenesis throughout embryonic development.
203  orchestrates essential genetic programs for cell morphogenesis, tissue organization, and development
204 ional culture of MCF10A cells, which undergo cell morphogenesis to form polarized spheroids with holl
205 es many essential biological processes, from cell morphogenesis to motility.
206  that turgor pressure evolved early and that cell morphogenesis underwent a major transition during e
207 n Candida albicans, GlcNAc stimulates hyphal cell morphogenesis, virulence genes, and the genes neede
208 ugh a panel of yeast mutants with defects in cell morphogenesis, we report here that the polarity est
209 s receptor in in vitro assays of endothelial cell morphogenesis where defined steps can be examined.
210            Flt-1 is required for endothelial cell morphogenesis whereas KDR is involved primarily in
211 cular motors drive deformations required for cell morphogenesis, while actin-filament disassembly dyn
212  distinctive aspects of PCP-mediated granule cell morphogenesis with CELSR1 regulating the direction
213 Shk1, forming part of a pathway coordinating cell morphogenesis with progression through the cell cyc
214     The molecular mechanisms that coordinate cell morphogenesis with the cell cycle remain largely un
215 ctivation correlated with periodic rounds of cell morphogenesis, with each peak preceding the formati

 
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