ライフサイエンスコーパス: morphogenesis

1 hat captures the key features of the organ's morphogenesis.

2 be precisely coordinated for proper cardiac morphogenesis.

3 ization, protein phosphorylation, and tissue morphogenesis.

4 afish was associated with abnormal epidermal morphogenesis.

5 their maxillary molar tooth germs completed morphogenesis.

6 remodeling required for mammalian epithelial morphogenesis.

7 icated in regulation of adherence and hyphal morphogenesis.

8 els of plant cell wall structure, growth and morphogenesis.

9 both in vitro and in vivo and induces hyphal morphogenesis.

10 ion and motility during epithelial branching morphogenesis.

11 control of ezrin localization and epithelial morphogenesis.

12 mpartment before the initiation of branching morphogenesis.

13 nalling instructs axon guidance and neuronal morphogenesis.

14 ctomyosin contractile machinery drive embryo morphogenesis.

15 acting downstream of Pax9 to regulate palate morphogenesis.

16 , and force transmission critical for tissue morphogenesis.

17 adenylyl cyclase to form cAMP induces hyphal morphogenesis.

18 This stability affects neuronal morphogenesis.

19 vel studies of notochord gene regulation and morphogenesis.

20 est ideas of patterning, differentiation and morphogenesis.

21 rtunities for future research into branching morphogenesis.

22 controlling neuron migration, polarity, and morphogenesis.

23 m that is known to drive adult megakaryocyte morphogenesis.

24 e that has broad implications for epithelial morphogenesis.

25 upling in the dysregulation of heart and jaw morphogenesis.

26 ntegrin alpha5beta1 in regulating epithelial morphogenesis.

27 pillars are also necessary for proper somite morphogenesis.

28 e of vertebrates, as a paradigm of embryonic morphogenesis.

29 ent signaling pathways that regulate neurite morphogenesis.

30 gnaling pathway that specifies cell fate and morphogenesis.

31 ds to dramatic disruptions of patterning and morphogenesis.

32 a set of common enhancers during epithelial morphogenesis.

33 el GRN for the major gene batteries in heart morphogenesis.

34 actile material for driving cell- and tissue morphogenesis.

35 issues plays a central role in guiding organ morphogenesis.

36 signals to control CPC expansion and cardiac morphogenesis.

37 from the bud stage and throughout branching morphogenesis.

38 of apoptotic modulation during urinary tract morphogenesis.

39 ynamic forces and mechanotransduction during morphogenesis.

40 ive gut lengthening and digestive epithelial morphogenesis.

41 dent HIR histone chaperone complex in fungal morphogenesis.

42 xtensive gene regulation to mediate cellular morphogenesis.

43 rinsic behaviours confers robustness to limb morphogenesis.

44 rinsic regulator of palatal shelf growth and morphogenesis.

45 heir functions and are essential for cardiac morphogenesis.

46 ting in a continuous lumen and normal tubule morphogenesis.

47 d AIR9 during phragmoplast guidance and root morphogenesis.

48 ion of Sertoli cells that orchestrate testis morphogenesis.

49 (CE) type cell rearrangements during tissue morphogenesis.

50 auxin transport and distribution during root morphogenesis.

51 resolution systematic analyses of C. elegans morphogenesis.

52 nscription factors govern lens and optic cup morphogenesis.

53 ved in wound healing, cancer metastasis, and morphogenesis.

54 at connect gene regulation and 3D epithelial morphogenesis.

55 ular mechanisms that underpin patterning and morphogenesis.

56 for TAG and/or its metabolites in spore wall morphogenesis.

57 ide the cell movements that initiate cardiac morphogenesis.

58 sential non-classical role in vertebrate gut morphogenesis.

59 tion and AJ protein levels during epithelial morphogenesis.

60 of epithelium formation leads to defects in morphogenesis.

61 mitotic spindle orientation and 3D glandular morphogenesis.

62 and to control active tissue dynamics during morphogenesis.

63 at are regulated by Shh signaling during lip morphogenesis.

64 n for Fgf20 in mammary budding and branching morphogenesis.

65 elium and mesenchyme are required for normal morphogenesis.

66 or the developmental control of Crb-mediated morphogenesis.

67 of the Twist-family bHLH dimer pool in limb morphogenesis.

68 the transcriptional circuitry that controls morphogenesis.

69 provide a deeper understanding of growth and morphogenesis.

70 ves; which confirmed their roles in frustule morphogenesis.

71 ellent model of developmental patterning and morphogenesis.

72 r Daam1 (Dishevelled associated activator of morphogenesis 1), and functionally suppresses Dvl --> Da

73 During varphiX174 morphogenesis, 240 copies of the external scaffolding pr

74 During morphogenesis, adherens junctions (AJs) remodel to allow

75 a non-essential role for Hand1 in mouse limb morphogenesis, altering Hand1 phosphoregulation, and con

76 Vis-a-vis virion morphogenesis, an improper protein-protein interaction w

77 between cellular redox sensing and community morphogenesis analogous to the functions performed by PA

78 strong link between the regulation of axonal morphogenesis and a new ALS-associated gene variant medi

79 excitatory synapses where it regulates spine morphogenesis and AMPA receptor confinement.

80 many biological functions, including tissue morphogenesis and architecture, extracellular matrix-med

81 ical processes, including biofilm formation, morphogenesis and cancer invasion.

82 on to control essential functions, including morphogenesis and cell wall biosynthesis, as well as the

83 gly related to embryonic development, tissue morphogenesis and cellular differentiation, including HO

84 sexual dimorphism, bud induction, branching morphogenesis and cellular differentiation.

85 rtant adaptations with respect to growth and morphogenesis and defense against biotic and abiotic str

86 ore molecule in substrate modulus-controlled morphogenesis and define a mechanism whereby neuronal ce

87 lts reveal tissue-level coordination between morphogenesis and differentiation during HT formation an

88 r multiple signalling pathways in epithelial morphogenesis and differentiation of fundic cell types,

89 al transcription factors that specify tissue morphogenesis and differentiation.

90 nces actin dynamics and is essential for OPC morphogenesis and differentiation.

91 eas MEF2C, despite its major role in cardiac morphogenesis and direct reprogramming, was dispensable

92 s responsible for Twist1-induced mesenchymal morphogenesis and expression of certain EMT markers.

93 in E12.5 mouse dermal fibroblasts delayed HF morphogenesis and growth and prevented new HF formation

94 gm for cross-tissue coordination of vascular morphogenesis and growth.

95 arious biological processes including tissue morphogenesis and homeostasis, as well as pathogenesis o

96 h and differentiation is essential to tissue morphogenesis and homeostasis.

97 s within their niche is essential for tissue morphogenesis and homeostasis.

98 or cell subpopulations driving mammary gland morphogenesis and homoeostasis are poorly understood.

99 wing transplantation into mice, HCOs undergo morphogenesis and maturation to form tissue that exhibit

100 ts into microtubule regulation during axonal morphogenesis and may shed light on MAP7 function in neu

101 g pathway known to regulate cellular growth, morphogenesis and metabolism.

102 etic analysis shows that BOP2 promotes photo-morphogenesis and modulates thermomorphogenesis by suppr

103 n of MAP7 and demonstrate its role in branch morphogenesis and neural circuit function.

104 soderm migration is necessary for the proper morphogenesis and organ formation during embryonic devel

105 e gross defects in chorioallantoic branching morphogenesis and placental vascular patterning.

106 nal activation and regulates dendritic spine morphogenesis and plasticity.

107 molecular cues controlling astrocyte branch morphogenesis and positioning during neural circuit asse

108 with lung buds failing to undergo branching morphogenesis and progressive atrophy of the proximal lu

109 ro-niches, tissues gain precise control over morphogenesis and regeneration: some progenitors specify

110 Target of Rapamycin (TOR) pathway regulates morphogenesis and responses to host cells in the fungal

111 utionarily conserved mechanism of nerve cord morphogenesis and reveal a role for SAX-3/Robo in this p

112 intrinsic biochemical mechanisms underlying morphogenesis and secondary metabolism are rarely reveal

113 The pathway of HCV morphogenesis and secretion has not been fully understoo

114 light the importance of apoptosis for tissue morphogenesis and suggest that Ntn1 may play divergent c

115 Consistent with a role in fungal morphogenesis and symbiotic interface differentiation, C

116 ts that occur in the MHB at the onset of MHB morphogenesis and that calcium mediates phosphorylation

117 r, the mechanisms that regulate diencephalic morphogenesis and the involvement of RA signaling in thi

118 rmal papilla cells during hair follicle (HF) morphogenesis and the postnatal hair cycle, preceding de

119 ssing the role of the gene in lip and palate morphogenesis and thus ensuring survival to adulthood.

120 Despite their fundamental role in tissue morphogenesis and tissue homeostasis, how adhesion molec

121 ymal-like cell layers is critical for embryo morphogenesis and tissue repair, yet we know little of t

122 el of salivary cells, disorganized branching morphogenesis, and a lack of differentiated mucous acina

123 rogram involving cell lineage determination, morphogenesis, and dynamic spatiotemporal gene expressio

124 many cellular processes, such as migration, morphogenesis, and endocytosis.

125 Bile duct differentiation, morphogenesis, and function were dysregulated in newborn

126 es, stress fibers, are crucial for adhesion, morphogenesis, and mechanosensing in nonmuscle cells.

127 o dissect the cellular basis of development, morphogenesis, and polarity in the lateral line of Danio

128 es the central logic of PCP signaling during morphogenesis, and provides new insight into PCP-related

129 Ps) are required for phototransduction, disk morphogenesis, and rod structural integrity.

130 CC mesenchyme proliferation during upper lip morphogenesis, and that disruption of this sequence resu

131 ivision and is crucial for cell fate, tissue morphogenesis, and the development of an organism.

132 ling on maxillary and mandibular molar tooth morphogenesis are mainly due to the differential express

133 MII to mediate cell shape changes during MHB morphogenesis are not known.

134 hanisms they require for their role in heart morphogenesis are not well understood.

135 including terminal differentiation and axon morphogenesis, are less well understood.

136 ion and migration, which contribute to joint morphogenesis, are mechanically controlled and are signi

137 regulation of contractility is essential for morphogenesis as loss of N-cadherin disrupts cell rearra

138 Other miRNAs also participate in wing morphogenesis, as well as in programmed cell and tissue

139 mbryos and uncovered alterations in cochlear morphogenesis, auditory hair cell differentiation, and c

140 eal an important role of PI(4,5)P2 for HIV-1 morphogenesis beyond Gag recruitment to the PM and sugge

141 rces are increasingly recognized to regulate morphogenesis, but how this is accomplished in the conte

142 nts and processes contributing to organismal morphogenesis, but the mathematical and physical princip

143 EN controls three-dimensional (3D) glandular morphogenesis by coupling juxtamembrane signaling to mit

144 hat it links redox conditions to PA14 colony morphogenesis by modulating levels of bis-(3',5')-cyclic

145 Hedgehog proteins control morphogenesis by promoting GLI-dependent transcriptional

146 the dynamics of cardiac differentiation and morphogenesis by tracking individual cells in live analy

147 anism by which blood flow mediates DA and CV morphogenesis, by regulating arterial-venous specificati

148 ts point to an ancient role for brachyury in morphogenesis, cell polarity and the patterning of both

149 actin cytoskeleton is important for growth, morphogenesis, cellular trafficking, and fungal pathogen

150 Thus, HF morphogenesis, commensal microbe colonization, and local

151 ey-specific and shared programs of branching morphogenesis, comparative expression studies on the dev

152 Branching morphogenesis creates arborized epithelial networks.

153 Disheveled-associated activator of morphogenesis (DAAM) is a diaphanous-related formin prot

154 lacking (Vvl) largely ameliorates the airway morphogenesis defects of grh mutants.

155 Cell and tissue morphogenesis depends on the correct regulation of non-m

156 a pivotal function in epithelial and hepatic morphogenesis, differentiation and cell-type identity, d

157 phages are important regulators of branching morphogenesis during development and postnatally in the

158 ppaB activity is also involved in hair fiber morphogenesis during HF cycling.

159 Proper lumen morphogenesis during pancreas development is critical to

160 trategies for more robustly directing tissue morphogenesis ex vivo.

161 gulatory mechanisms to ensure that flagellar morphogenesis follows a defined path, with each componen

162 Expression of genes involved in branching morphogenesis, Gcm1, Syna and Synb, and in patterning of

163 expression of Sox17 increases expression of morphogenesis genes and promotes integration of transpla

164 ve Akt signalling increases expression of EC morphogenesis genes, including Sox17, shifts the genomic

165 ntribution of AJ remodeling to developmental morphogenesis has been intensively studied, less is know

166 ently, biomechanical inputs into neural tube morphogenesis have also been identified.

167 atially localized signals that control islet morphogenesis have not been discovered.

168 ioning of this boundary is critical for leaf morphogenesis, how the boundary is established and how i

169 evelops with the epithelium during branching morphogenesis; however, it is not known whether the vasc

170 modeling and show that central lumen network morphogenesis impacts pancreatic endocrine mass.

171 vessels, edema, defective lymphovenous valve morphogenesis, improper lymphatic drainage, defective ly

172 We analyzed dendritic morphogenesis in a functionally characterized RGC type,

173 tructure and function, we analyzed dendritic morphogenesis in a single retinal ganglion cell (RGC) ty

174 the normal invasive mammary gland branching morphogenesis in an epithelial cell extrinsic manner by

175 extensively, especially in relation to wing morphogenesis in both hemimetabolan and holometabolan sp

176 espite its conserved expression during canal morphogenesis in chicken and mouse.

177 to achieve the ambitious goal of programming morphogenesis in complex tissues and organoids.

178 ACKR2 is an important regulator of branching morphogenesis in diverse biological contexts and provide

179 signaling pathway, rescues mandibular molar morphogenesis in Inhba(-/-) embryos.

180 ibitor IIIC3a rescued mandibular molar tooth morphogenesis in Inhba(-/-) embryos.

181 Considering the importance of branching morphogenesis in multiple taxa, our findings have genera

182 as ischemic macrophages triggered tube-like morphogenesis in neighboring endothelial cells that coul

183 canonical Wnt signaling, also rescued palate morphogenesis in Pax9-deficient mice.

184 that SHANK3 has a critical role in neuronal morphogenesis in placodal neurons and that early defects

185 and a signaling component to fine-tune plant morphogenesis in response to environmental conditions.

186 platform has been applied to study vascular morphogenesis in response to hypoxia and to understand h

187 Therefore, PTPRB regulates branching morphogenesis in the mammary epithelium by modulating th

188 Here we show that astrocyte morphogenesis in the mouse cortex depends on direct cont

189 Evidence that sex influences dendritic morphogenesis in two models of neurodevelopment in a reg

190 at Btbd7 is a crucial regulator of branching morphogenesis in vivo.

191 a model for post-pubertal mammary branching morphogenesis in which position-dependent, lineage-restr

192 human are important regulators of epithelial morphogenesis including Cdh1, Ck19, Cldn3 and 4, Ddr1, a

193 e, no differentiation occurs while extensive morphogenesis, including splanchnic mesoderm sliding ove

194 nstricting surfaces.Various stages of tissue morphogenesis involve the contraction of epithelial surf

195 Jaw morphogenesis is a complex event mediated by inductive s

196 Branching morphogenesis is a fundamental program for tissue patter

197 attern cell walls during this form of tissue morphogenesis is an important research challenge.

198 When the delicate process of craniofacial morphogenesis is disrupted, the result is orofacial clef

199 Here we show that morphogenesis is driven by proliferative terminal end bu

200 standing of the mechanisms that regulate lip morphogenesis is limited.

201 sional scaffold to generate structures whose morphogenesis is markedly similar to that of natural emb

202 timing of a landmark event during embryonic morphogenesis is mediated by the concerted action of fou

203 Netrin-dependent morphogenesis is preceded by multimerization of DCC, act

204 , Sema3a- and Nrp2-mediated control of islet morphogenesis is strikingly homologous to mechanisms tha

205 How left-right patterning drives asymmetric morphogenesis is unclear.

206 ut whether they can recreate early embryonic morphogenesis is unclear.

207 The most obvious entry of physics into morphogenesis is via tissue mechanics.

208 mutants also grow slowly and have defects in morphogenesis, making it unclear whether hyphal inducers

209 enrichment of genes involved in development, morphogenesis, migration, adhesion, regulation of proces

210 tin, have an essential role in the epidermal morphogenesis necessary to form the initial dorsal and v

211 nervous system, Lpd contributes to neuronal morphogenesis, neuronal migration during development and

212 During branching morphogenesis, new branches form by "budding" or "clefti

213 ts that occur during cardiac development and morphogenesis, notably muscle creation through division

214 sculpting tissue interfaces by directing the morphogenesis of a variety of folded tissue forms from p

215 en cortical tension, material properties and morphogenesis of an entire embryo.

216 Here the authors describe the morphogenesis of astrocyte-like glia in the Drosophila o

217 The morphogenesis of branched organs remains a subject of ab

218 Branching morphogenesis of developing organs requires coordinated

219 promising cell survival, and suppressed tube morphogenesis of ECs, whereas over-expression of EMCN le

220 ammals, large wounds in mice lead to de novo morphogenesis of hair follicles.

221 Finally, the morphogenesis of herpesviral growth in three-dimensional

222 ty is critical for the lumenal epiblast-like morphogenesis of human pluripotent stem cells (hPSCs).

223 Inspired by the differential-growth-driven morphogenesis of leaves, flowers, and other tissues, the

224 pealing features of the bottom-up process in morphogenesis of living tissues.

225 The functions of blood flow in the morphogenesis of mammalian arteries and veins are not we

226 final laminar position is essential for the morphogenesis of neuronal circuits.

227 hermore, loss of release did not disrupt the morphogenesis of presynaptic terminals and dendritic spi

228 lications for the integrity, arrangement and morphogenesis of proliferative tissues.

229 y, is required for the proper patterning and morphogenesis of SMG epithelium.

230 tation clock is translated into the periodic morphogenesis of somites remains poorly understood.

231 tains the invariant cleavage pattern driving morphogenesis of the ascidian blastula.

232 P signaling plays a critical role in looping morphogenesis of the avian small intestine.

233 ve Shh signaling is responsible for abnormal morphogenesis of the cerebellum of Npc1-deficient mice a

234 s of the developing air pore complex and the morphogenesis of the complex is defective in plants with

235 e I describe how our quest to understand the morphogenesis of the fission yeast Schizosaccharomyces p

236 , results in severe hyperplasia and abnormal morphogenesis of the gland by the end of gestation.

237 ow provide essential mechanical cues for the morphogenesis of the heart.

238 results provide new insights into branching morphogenesis of the intrahepatic biliary network.

239 ion of epithelium-derived signaling controls morphogenesis of the mandible remains elusive.

240 egulation of mesenchymal genes important for morphogenesis of the mandibular arch.

241 ctions that differentially contribute to the morphogenesis of the respiratory tract.

242 protein sans, which is involved both in the morphogenesis of the stereociliary bundle, the sensory a

243 the temporal pattern of Dpp presentation for morphogenesis of the wing.

244 The morphogenesis of tissues, like the deformation of an obj

245 aviors is a crucial step in the assembly and morphogenesis of tissues.

246 factor, Pax9, is critical for patterning and morphogenesis of tooth and taste buds.

247 Cell cycle-dependent morphogenesis of unicellular organisms depends on the sp

248 ession, but the impact of cell behaviour and morphogenesis on neural specification is not understood.

249 Cell migration is essential for morphogenesis, organ formation, and homeostasis, with re

250 (DKK) activity in utero during palatal shelf morphogenesis partly rescued secondary palate developmen

251 ut tube is an essential aspect of intestinal morphogenesis, permitting proper placement of the length

252 ssembly and consequent abnormalities in cell morphogenesis, polarity, and migration.

253 tially expressed unigenes (DEGs) involved in morphogenesis, primary carbohydrate metabolism, cold sti

254 LD physiology directly to a unique membrane morphogenesis process critical for development.

255 The duct morphogenesis process was interrupted by inhibiting Notc

256 n fetal progenitors do not execute the adult morphogenesis program of enlargement, polyploidization,

257 We concluded that I2 is required for virion morphogenesis, release of the D13 scaffold, and the asso

258 Embryo morphogenesis relies on highly coordinated movements of

259 Tissue morphogenesis relies on the coordinated action of actin

260 in serial passage culture and in vivo breast morphogenesis relies on the preservation of a myoepithel

261 Instead, morphogenesis relies upon lineage-restricted heterogeneo

262 that participate in mammary gland branching morphogenesis remain contested.

263 genetic modifiers underlying lymphatic valve morphogenesis remain elusive.

264 ral plate, ectoderm, endoderm) to drive axis morphogenesis remain largely unknown.

265 ne to such instabilities can rveliably drive morphogenesis remains an outstanding question.

266 Plant morphogenesis requires differential and often asymmetric

267 Joint morphogenesis requires mechanical activity during develo

268 Branching morphogenesis requires the coordinated interplay of mult

269 Tissue morphogenesis requires the coordinated regulation of cel

270 We conclude that proper denticle morphogenesis requires transcriptional regulation by bot

271 insights into peripheral nerve microvascular morphogenesis, restrictive barrier formation, influx and

272 ntricate relationship between metabolism and morphogenesis, showing that glycolysis facilitates body

273 rforms prominent ciliogenic functions during morphogenesis, such as in the skin.

274 tralization of the phagosome promotes hyphal morphogenesis, sufficient for induction of caspase-1-med

275 ly to form a cardiac crescent, while limited morphogenesis takes place.

276 nd with unrelated mutants blocked earlier in morphogenesis that also accumulated viral membranes reta

277 chanism of extra-embryonic control of embryo morphogenesis that couples the mechanical properties of

278 ify a regulatory axis affecting blood vessel morphogenesis that highlights exquisite post-translation

279 a non-local input into the control of early morphogenesis that is mediated by neurotransmitters and

280 al modeling has changed our understanding of morphogenesis - the shaping of an organism during develo

281 h that, on timescales relevant to epithelial morphogenesis, the cytoplasm is predominantly viscous, w

282 ransmural pressure controls airway branching morphogenesis, the frequency of airway smooth muscle con

283 y control the bud-to-cap transition of tooth morphogenesis through antagonistic regulation of express

284 ed by cortical astrocytes, control astrocyte morphogenesis through interactions with neuronal neurexi

285 novel role for Osr2 in regulation of palatal morphogenesis through preventing aberrant activation of

286 lium of the Islet1 mutant rescued mandibular morphogenesis through sonic hedgehog (SHH) signaling to

287 f the Wnt signaling pathway to promote tooth morphogenesis through the bud-to-cap transition and that

288 Many embryonic organs undergo branching morphogenesis to maximize their functional epithelial su

289 Saccharomyces cerevisiae that couples spore morphogenesis to the completion of chromosome segregatio

290 During morphogenesis, vacuolated cells maintain their structura

291 similarity in developmental stages, although morphogenesis was greatly expanded in humans.

292 Unexpectedly, morphogenesis was interrupted at a stage after immature

293 Right after birth, hair follicle (HF) morphogenesis was transiently delayed, along with reduce

294 owed that the early defects observed in hair morphogenesis were caused by the absence of adipose tiss

295 Afadin and RhoA in pancreatic central lumen morphogenesis, which subsequently determines endocrine c

296 rowth factor (FGF) pathway to promote branch morphogenesis, while correct positioning is essential fo

297 ryonic tissues to orchestrate and coordinate morphogenesis with changes in developmental potential.

298 Salivary glands are formed by branching morphogenesis with epithelial progenitors forming a netw

299 ances are generated is a central question of morphogenesis, with existing paradigms focusing on asymm

300 e end effectors of cell migration, division, morphogenesis, wound healing and cancer invasion.