ライフサイエンスコーパス: cell morphogenesis

1 al role of the MreB-controlled elongasome in cell morphogenesis.

2 regulation of plant signal transduction and cell morphogenesis.

3 n important role in F-actin organization and cell morphogenesis.

4 en I and laminin-1 in regulating endothelial cell morphogenesis.

5 cortical array, which is critical for plant cell morphogenesis.

6 the MAPK-dependent stimulation of epithelial cell morphogenesis.

7 The cytoskeleton governs cell morphogenesis.

8 ot ERK, prevented polycystin-1-mediated IMCD cell morphogenesis.

9 and each contributes to different aspects of cell morphogenesis.

10 es we observe are consistent with defects in cell morphogenesis.

11 its mammalian homolog CRB1 in photoreceptor cell morphogenesis.

12 tructure required for flagellum adhesion and cell morphogenesis.

13 he signals and mechanisms that control plant cell morphogenesis.

14 /APN functions in the control of endothelial cell morphogenesis.

15 ossibility that ES might regulate epithelial cell morphogenesis.

16 that targets the cytoskeleton and regulates cell morphogenesis.

17 ant strain defective in chitin synthesis and cell morphogenesis.

18 we questioned whether it induces endothelial cell morphogenesis.

19 a role for multiple integrins in endothelial cell morphogenesis.

20 V0 and V1 domains are required for terminal cell morphogenesis.

21 ntial for cell migration, cell division, and cell morphogenesis.

22 ate levels of PECAM-1 stimulate, endothelial cell morphogenesis.

23 s active in the root until the initiation of cell morphogenesis.

24 and Cdc42Hs suggest a role for the Golgi in cell morphogenesis.

25 eptor in order to support mammary epithelial cell morphogenesis.

26 by immuno-deficiencies and defects in blood cell morphogenesis.

27 since these PBPs are known to participate in cell morphogenesis.

28 e the polarization process during epithelial cell morphogenesis.

29 o understanding the biomechanical control of cell morphogenesis.

30 dures as one of the central enigmas in plant cell morphogenesis.

31 ole of the p12 protein in modulation of host cell morphogenesis.

32 aromyces cerevisiae as a protein involved in cell morphogenesis.

33 that autolysins control different aspects of cell morphogenesis.

34 Tbx16-Fgf2 pathway that regulates epithelial cell morphogenesis.

35 ulate cortex structure, which in turn drives cell morphogenesis.

36 unexpected role of Vangl2 during supporting cell morphogenesis.

37 erve as a valuable model in studies of plant cell morphogenesis.

38 egulation of the microtubule cytoskeleton in cell morphogenesis.

39 echanism by which endocytosis contributes to cell morphogenesis.

40 acks for CHSs delivery and both cooperate in cell morphogenesis.

41 the role of asymmetric lipid distribution in cell morphogenesis.

42 ions in root tissue patterning and root hair cell morphogenesis.

43 The cytoskeleton is a key regulator of cell morphogenesis.

44 polarity mechanisms, and MTs responsible for cell morphogenesis.

45 ial actin homologue MreB plays a key role in cell morphogenesis.

46 g proteins often control multiple aspects of cell morphogenesis.

47 st polarization but also leads to defects in cell morphogenesis.

48 omoting cell wall metabolism and influencing cell morphogenesis.

49 ation, meristemoid differentiation and guard cell morphogenesis.

50 3 pathway links actin filament nucleation to cell morphogenesis.

51 dynamically reorganizes the cytoplasm during cell morphogenesis.

52 traE genes could be involved in S. kunkelii cell morphogenesis, adhesion and DNA recombination.

53 airway epithelium, including those involving cell morphogenesis, adhesion, and motility.

54 ily tyrosine kinases have been implicated in cell morphogenesis, adhesion, motility, and oncogenesis.

55 that are essential regulators of endothelial cell morphogenesis and angiogenesis.

56 le-associated protein tau may be involved in cell morphogenesis and axonal maintenance.

57 l seed coats and document its importance for cell morphogenesis and barrier function of the seed coat

58 onstitutively active Erk5 blocks endothelial cell morphogenesis and causes HIF1-alpha destabilization

59 threonine kinase involved in regulating both cell morphogenesis and cell cycle control.

60 s and that its absence has severe effects on cell morphogenesis and cell division.

61 We conclude that Kel1p has a role in cell morphogenesis and cell fusion and may antagonize th

62 egulation of gene expression, cell adhesion, cell morphogenesis and cell migration.

63 hat fgd-1 plays a critical role in excretory cell morphogenesis and cellular organization.

64 onomous mechanisms that regulate coordinated cell morphogenesis and cytodifferentiation of the retina

65 to provide the first detailed description of cell morphogenesis and cytokinesis in the early-branchin

66 omes use a microtubule-focused mechanism for cell morphogenesis and cytokinesis.

67 genesis; or (2) alterations of somatic gonad cell morphogenesis and differentiation in larval life.

68 White (d/d) mutants have defects in pigment cell morphogenesis and differentiation, whereas albino (

69 dual regulator for Ras and Rho signaling in cell morphogenesis and differentiation.

70 maturation late in development by promoting cell morphogenesis and differentiation.

71 f a physiologic role for Git2a in regulating cell morphogenesis and directed cell migration via myosi

72 re involved in the same aspects of epidermal cell morphogenesis and division.

73 TPs) in three-dimensional mammary epithelial cell morphogenesis and ERBB2 signaling.

74 omyosin contractility is required for bottle cell morphogenesis and further suggest a novel and unpre

75 ver, simultaneous melatonin supply supported cell morphogenesis and growth, reduced ROS and superoxid

76 e in directing early processes in intestinal cell morphogenesis and in the maintenance of the differe

77 brane components involved in tracheal fusion cell morphogenesis and lumenal development.

78 Proper regulation of cell morphogenesis and migration by adhesion and growth-

79 espective contribution of these functions to cell morphogenesis and migration in 3D matrices is uncle

80 Here we demonstrate that Abi2 modulates cell morphogenesis and migration in vivo.

81 es have been implicated in the regulation of cell morphogenesis and migration, but the molecular mech

82 ing for effective membrane protrusion during cell morphogenesis and migration.

83 he generation of branched actin networks for cell morphogenesis and migration.

84 aling cascades, they have important roles in cell morphogenesis and mitogenesis.

85 he ability of actin filaments to function in cell morphogenesis and motility is coupled to their capa

86 ant non-redundant roles in the regulation of cell morphogenesis and motility.

87 cs at the cell cortex play a crucial role in cell morphogenesis and neuronal development.

88 ts designed to uncover general principles of cell morphogenesis and of cell shape function.

89 The conserved NDR kinase regulates cell morphogenesis and polarized cell growth in differen

90 Ndr/Warts family are important regulators of cell morphogenesis and proliferation.

91 al cells is important for cell integrity and cell morphogenesis and protects against harmful environm

92 e actin cytoskeleton is a major regulator of cell morphogenesis and responses to biotic and abiotic s

93 CP function with the hormone response during cell morphogenesis and shows that developmental and envi

94 ned considerable insight into the process of cell morphogenesis and the establishment of positional i

95 ain impaired the ability of Cla4 to regulate cell morphogenesis and the mitotic exit network (localiz

96 , as FoxO-regulated mediators of endothelial cell morphogenesis and vascular homeostasis.

97 ng epithelial polarity and, in photoreceptor cells, morphogenesis and stability.

98 is critical for intercellular connectivity, cell morphogenesis, and cognitive functions.

99 s two paralogues: FAMA, a regulator of guard cell morphogenesis, and SPEECHLESS (SPCH).

100 ornea in vivo and in the ex vivo endothelial cell morphogenesis assay is also MAPK- and PI3K-dependen

101 r dynamic remodeling of the cytoskeleton and cell morphogenesis, but the mechanisms driving actin dis

102 ults suggest that Cdc42Hs may play a role in cell morphogenesis by acting on targets in the Golgi tha

103 ules and F-actin both play critical roles in cell morphogenesis by guiding the deposition of wall mat

104 highly ordered parallel arrays that mediate cell morphogenesis by orienting cellulose deposition.

105 ide exchange factors control many aspects of cell morphogenesis by turning on Rho-GTPases.

106 lements to perform many functions, including cell morphogenesis, cell division, DNA partitioning, and

107 ing mating differentiation to mediate proper cell morphogenesis, cell fusion, and other steps of the

108 e-activating protein (RhoGAP) that regulates cell morphogenesis, cell migration, and ERK signaling by

109 ignaling, extracellular matrix interactions, cell morphogenesis, cell motility and migration.

110 range of important cell processes, including cell morphogenesis, chromosome segregation and cell pola

111 follows MreB and retains its crucial role in cell morphogenesis, demonstrating conservation of functi

112 utant cells develop into aberrant pharyngeal cells (Morphogenesis/Differentiation stage).

113 he expression of many genes that orchestrate cell morphogenesis during differentiation.

114 development is required for correct palisade cell morphogenesis during leaf development.

115 Understanding cell morphogenesis during metazoan development requires

116 We report a role for puc in follicle cell morphogenesis during oogenesis.

117 le (otd), a homeobox gene, is required for R-cell morphogenesis during pupation.

118 are similarly involved in the regulation of cell morphogenesis during the yeast-to-hypha transition

119 The alpha(v)beta(3) integrin participates in cell morphogenesis, growth factor signaling, and cell su

120 for cell curvature can cause a disruption of cell morphogenesis, highlighting the delicate harmony am

121 cr4 functions cell autonomously to regulate cell morphogenesis, implying that CR4 signal transductio

122 ulogenesis, VEGF can induce renal epithelial cell morphogenesis in a Nrp-1-dependent fashion.

123 of growth sites are tightly regulated during cell morphogenesis in all organisms.

124 otic cellular processes, including epidermal cell morphogenesis in Arabidopsis thaliana.

125 ought to function in spatially co-ordinating cell morphogenesis in conjunction with MreC, a protein t

126 s in live cells is critical to understanding cell morphogenesis in development and disease.

127 ts both chloroplast development and palisade cell morphogenesis in leaves.

128 advances in the quantitative imaging of all-cell morphogenesis in living organisms.

129 Cell morphogenesis in most bacteria is governed by spati

130 a novel role for Fgf signaling during glial cell morphogenesis in promoting axonal regeneration afte

131 compared the signaling pathways for mIMCD-3 cell morphogenesis in response to EGF and HGF.

132 lecular networks through which TbPLK directs cell morphogenesis in T. brucei.

133 cytoskeleton-dependent mechanisms governing cell morphogenesis in the maize leaf epidermis.

134 nfirmed the role of PhMYB1 in the control of cell morphogenesis in the petal epidermis.

135 the attached flagellum plays a major role in cell morphogenesis in this organism.

136 nding implicates the concept of cytotaxis in cell morphogenesis in trypanosomes.

137 n actin cytoskeleton that governs lens fiber cell morphogenesis in vivo.

138 p both participate in bud site selection and cell morphogenesis in yeast, and spa2delta cdc10-10 cell

139 ture involved in many key processes in plant cell morphogenesis including nuclear and cell division,

140 d protein kinase kinase inhibition abrogated cell morphogenesis induced by OSM, indicating an importa

141 naling pathways are required for endothelial cell morphogenesis into capillary-like networks.

142 Endothelial cell morphogenesis is a carbohydrate-dependent process,

143 Cell morphogenesis is a complex process that relies on a

144 of expansion is necessary to understand how cell morphogenesis is controlled in plants.

145 es their levels and connects their action to cell morphogenesis is less clear.

146 We show that slow-twitch muscle cell morphogenesis is marked by behaviors typical of cel

147 In mouse lenses lacking Tmod1, initial fiber cell morphogenesis is normal, but fiber cell hexagonal s

148 However, follicle cell morphogenesis is unaffected by point mutations that

149 from Saccharomyces cerevisiae indicate that cell morphogenesis may involve cell cycle regulation by

150 at are upregulated during mammary epithelial cell morphogenesis may reveal novel regulators of tumori

151 Actin demonstrated that giActin functions in cell morphogenesis, membrane trafficking, and cytokinesi

152 or tyrosine kinases has an important role in cell morphogenesis, motility, and proliferation.

153 Contractile actin cortex is involved in cell morphogenesis, movement, and cytokinesis, but its o

154 diate downstream effects specific for either cell morphogenesis or pathogenesis.

155 l GTPase with roles in migration, epithelial cell morphogenesis, osteoclastogenesis, and oncogenic tr

156 and Hym1p function to regulate two distinct cell morphogenesis pathways: an ACE2-independent pathway

157 fy a critical role for SIPA1L3 in epithelial cell morphogenesis, polarity, adhesion and cytoskeletal

158 ber assembly and consequent abnormalities in cell morphogenesis, polarity, and migration.

159 Models for cell morphogenesis postulate that the effects of turgor

160 s of peptidoglycan synthases, hydrolases and cell morphogenesis proteins, but the details of these in

161 The molecular basis of bacterial cell morphogenesis remains largely an open question.

162 Bacterial cell morphogenesis requires coordination among multiple

163 type and act1/act1 mutants indicates that PH cell morphogenesis requires the maintenance of a highly

164 During plant cell morphogenesis, signal transduction and cytoskeletal

165 f these GTPases is crucial for some forms of cell morphogenesis, the nature of such coordination duri

166 of which Cdc42Hs is a member, is involved in cell morphogenesis through a GTPase cascade which regula

167 putative Arabidopsis Arp2/3 complex controls cell morphogenesis through its roles in cell polarity es

168 portant for induction of gene expression and cell morphogenesis throughout embryonic development.

169 ional culture of MCF10A cells, which undergo cell morphogenesis to form polarized spheroids with holl

170 n Candida albicans, GlcNAc stimulates hyphal cell morphogenesis, virulence genes, and the genes neede

171 ugh a panel of yeast mutants with defects in cell morphogenesis, we report here that the polarity est

172 s receptor in in vitro assays of endothelial cell morphogenesis where defined steps can be examined.

173 Flt-1 is required for endothelial cell morphogenesis whereas KDR is involved primarily in

174 distinctive aspects of PCP-mediated granule cell morphogenesis with CELSR1 regulating the direction

175 Shk1, forming part of a pathway coordinating cell morphogenesis with progression through the cell cyc

176 The molecular mechanisms that coordinate cell morphogenesis with the cell cycle remain largely un

177 ctivation correlated with periodic rounds of cell morphogenesis, with each peak preceding the formati