ライフサイエンスコーパス: organogenesis

1 ated cytokinin signaling in symbiotic nodule organogenesis.

2 o the liver vasculature and defects in liver organogenesis.

3 nately induce rhizobial infection and nodule organogenesis.

4 liferation to differentiation is crucial for organogenesis.

5 an integrated transcriptomic atlas of human organogenesis.

6 the meristematic competence of cells during organogenesis.

7 acid (RA) metabolism is critical for spleen organogenesis.

8 gnaling pathway, which is essential for skin organogenesis.

9 for infection thread progression and nodule organogenesis.

10 ent despite loss of LTbetaR-mediated medulla organogenesis.

11 es during mammalian cell differentiation and organogenesis.

12 ECM markers, contribute to morphogenesis and organogenesis.

13 controls both rhizobial infection and nodule organogenesis.

14 at ligand back-signaling contributed to skin organogenesis.

15 ial for specific aspects of auditory-related organogenesis.

16 I) endocrine-committed cells during pancreas organogenesis.

17 ing the fate of epithelial stem cells during organogenesis.

18 pecies are needed to infer the principles of organogenesis.

19 ndoderm patterning, organ specification, and organogenesis.

20 he nucleus and cytoplasm during lateral root organogenesis.

21 late later developmental events during petal organogenesis.

22 o define how this hypertrophy contributes to organogenesis.

23 ed by massive cell death and defect in liver organogenesis.

24 ad implications for understanding epithelial organogenesis.

25 rebrain and establish novel roles of Pax6 in organogenesis.

26 es such as proliferation, transcription, and organogenesis.

27 l the transcriptional programs that underpin organogenesis.

28 mone signaling pathway that is essential for organogenesis.

29 ystem to study adaptive immune regulation of organogenesis.

30 pathological processes, including regulating organogenesis.

31 ovel role for mouse Hox6 genes in pancreatic organogenesis.

32 cell expansion during murine salivary gland organogenesis.

33 lyamine biosynthesis functions in pancreatic organogenesis.

34 the mitotic spindle in stem cells underlies organogenesis.

35 tion, and apoptosis is of key importance for organogenesis.

36 matin-remodeling factors contribute to plant organogenesis.

37 x1 is instead a negative regulator of thymus organogenesis.

38 the early embryo and local remodeling during organogenesis.

39 evealed that the cross-link is essential for organogenesis.

40 shed roles in host defense and immune system organogenesis.

41 ty by modifying local growth patterns during organogenesis.

42 rization and organ architecture during fetal organogenesis.

43 the auxin stream directionality during plant organogenesis.

44 ges in AOC1 expression, has a role in kidney organogenesis.

45 NPC and the COPII functions of Sec13 during organogenesis.

46 nd participates in critical functions during organogenesis.

47 processes in early embryonic development and organogenesis.

48 alpha1beta2-LTbeta receptor-dependent thymic organogenesis.

49 obium loti, in the initial absence of nodule organogenesis.

50 eneration of mesothelia exists in vertebrate organogenesis.

51 ith ex vivo cultures for the induction of 3D organogenesis.

52 3rd pp endoderm is a prerequisite for thymus organogenesis.

53 ethylation to the normal process of prostate organogenesis.

54 s are absent or downregulated during initial organogenesis.

55 mplantation development and subsequent early organogenesis.

56 nates multiple steps in tubulogenesis during organogenesis.

57 nt, cell fate determination, and ultimately, organogenesis.

58 2 also plays crucial regulatory roles during organogenesis.

59 proliferation and survival during mammalian organogenesis.

60 pment, maintaining a pool of progenitors for organogenesis.

61 ear how lineages are regulated during kidney organogenesis.

62 ex 3D environments such as morphogenesis and organogenesis.

63 interaction required for proper fetal thymus organogenesis.

64 divisions is a fundamental part of metazoan organogenesis.

65 tiation, and multicellular patterning during organogenesis.

66 for proliferation and differentiation during organogenesis.

67 l-conserved mechanism in regulating multiple organogenesis.

68 ormal segmentation of nephrons during kidney organogenesis.

69 al differentiation, body axis formation, and organogenesis.

70 of signaling factors that regulate pituitary organogenesis.

71 operly specified during tissue formation and organogenesis.

72 . elegans vulval development, a paradigm for organogenesis.

73 rucial for postnatal tissue homoeostasis and organogenesis.

74 he establishment of vascular networks during organogenesis.

75 sible for KIT(+) progenitor expansion during organogenesis.

76 ts are critical for proper embryogenesis and organogenesis.

77 proach to study the mechanism of human liver organogenesis.

78 ty in nephron progenitor cells during kidney organogenesis.

79 required for multiple aspects of pancreatic organogenesis.

80 -1958 bp) affects minor or major aspects of organogenesis.

81 offers an attractive model for investigating organogenesis.

82 hy of periodic patterning modes operating in organogenesis.

83 ing programs and are essential for mammalian organogenesis.

84 and fate determination critically influences organogenesis.

85 ghly migratory and significant to vertebrate organogenesis.

86 emains one of the least understood phases of organogenesis.

87 subset transcripts associated with prostate organogenesis.

88 of estrogen's direct effect on mammary gland organogenesis.

89 on of appropriate lineage differentiation in organogenesis.

90 apitulate cell interactions occurring during organogenesis.

91 ester, the etiologically relevant period for organogenesis.

92 l, differentiation, and proliferation during organogenesis.

93 mice by study of embryos undergoing advanced organogenesis.

94 e, specification of pancreatic cell fate and organogenesis.

95 nds on its adequate supply to achieve proper organogenesis.

96 e lineage-restricted progenitor cells during organogenesis.

97 specify this cellular spatial domain during organogenesis.

98 oth cell types during fate specification and organogenesis.

99 ate the role of Pol II pausing in vertebrate organogenesis.

100 indings define a novel mechanism of impaired organogenesis, accelerated ubiquitin-directed proteasoma

101 to the specific role of CHRDL1 during cornea organogenesis, among others by the establishment of the

102 cesses, including early cell fate decisions, organogenesis and adult tissue homeostasis.

103 amental communication between tissues during organogenesis and are primarily regulated by growth fact

104 -YC1) was shown to play a key role in nodule organogenesis and bacterial infection during the nitroge

105 d to better evaluate effects of chemicals on organogenesis and begin classification of chemicals by t

106 implicated in noncanonical Wnt signaling in organogenesis and cancer metastasis.

107 any pathways including developmental timing, organogenesis and development in eukaryotes.

108 d to play essential tissue-specific roles in organogenesis and disease and can provide starting point

109 vide new insights into the dynamics of tooth organogenesis and growth.

110 Gremlin-1/Drm is crucial in embryo-/organogenesis and has been shown to be expressed in the

111 ace heparan sulfate (HS) proteoglycans shape organogenesis and homeostasis by capture and release of

112 ole for polyamine biosynthesis in pancreatic organogenesis and identified that it may be possible to

113 lopment is severely compromised by defective organogenesis and in particular by defective cardiogenes

114 cent work in understanding the regulation of organogenesis and in particular leaf formation, highligh

115 progenitors for mesenchymal lineages during organogenesis and indicate that signals controlling meso

116 ntral role in cross signaling between nodule organogenesis and infection processes; and Symbiosis Rec

117 for thymic tolerance segregates from medulla organogenesis and instead involves LTbetaR-mediated regu

118 ysis of Mnx1 function during murine pancreas organogenesis and into the adult uncovered novel stage-s

119 ng pathway, is indispensible for both nodule organogenesis and intracellular colonization of symbiont

120 rce for the molecular understanding of human organogenesis and its associated disorders.

121 -7 exerts essential roles in lymph node (LN) organogenesis and lymphocyte development and homeostasis

122 II regulation and is implicated in embryonic organogenesis and maintenance of embryonic stem cell plu

123 aning), with only a small effect on pancreas organogenesis and no deficiencies in their female counte

124 NFR5, and SYMRK initiate spontaneous nodule organogenesis and nodulation-related gene expression in

125 extend our understanding of gastrointestinal organogenesis and of how Wnt and BMP might coordinate ge

126 models suboptimal for studying human stomach organogenesis and pathogenesis, and there is no experime

127 of the gynoecium and female gametophyte, and organogenesis and phyllotaxy in the shoot.

128 eta Receptor (LTbetaR) resulting in lymphoid organogenesis and propagation of inflammatory signals is

129 atory mechanisms that underlie early thyroid organogenesis and provide a significant step toward cell

130 e paradigm for studying players of postnatal organogenesis and provides insights into immune surveill

131 rcing the view that the capacity for de novo organogenesis and regeneration from mature plant tissues

132 Organogenesis and regeneration require coordination of c

133 onsider their possible contribution to heart organogenesis and regeneration.

134 tem for multidisciplinary studies, including organogenesis and regenerative medicine.

135 capitulated several aspects of hepatobiliary organogenesis and resulted in concomitant formation of p

136 tems with which to study tissue development, organogenesis and stem cell behavior ex vivo.

137 ed and new roles of senescence in vertebrate organogenesis and support the view that cellular senesce

138 Foxn1 is essential for thymic organogenesis and T lymphopoiesis.

139 imordial innovation of the ECM essential for organogenesis and tissue evolution.

140 filament phosphorylation during mitosis for organogenesis and tissue homeostasis was uncertain.

141 tic, and environmental factors that regulate organogenesis and tissue homeostasis.

142 lia are sensory organelles indispensable for organogenesis and tissue pattern formation.

143 Organogenesis and tumor metastasis involve the transform

144 re critical but poorly understood inputs for organogenesis and wound healing.

145 for malformations and spontaneous abortion (organogenesis), and the second/third trimesters are the

146 ndary transition, their rapid decline during organogenesis, and absence from the mature organ.

147 the discrete action of extrinsic factors in organogenesis, and allow for the discovery of relationsh

148 tiation of progenitor cells is a key step in organogenesis, and alterations in this process can lead

149 cell proliferation, cell fate specification, organogenesis, and epithelial-mesenchymal transition.

150 ation can dramatically affect morphogenesis, organogenesis, and growth.

151 ultiple stages to regulate infection, nodule organogenesis, and nitrogen fixation in L. japonicus.

152 Notch1, plays indispensable roles in kidney organogenesis, and Notch2 haploinsufficiency is associat

153 essential for cell-type differentiation and organogenesis, and plant cells produce amounts of GlcCer

154 gnals act on tissue-level mechanics to drive organogenesis, and suggest a possible mechanism by which

155 reciated role of metabolic regulation during organogenesis, and suggests that it might contribute to

156 erning organelle biogenesis are simpler than organogenesis, and therefore organelle size scaling in t

157 However, their roles in vertebrate organogenesis are poorly understood.

158 verse differentiated cell types required for organogenesis, are not understood.

159 T helper 1 cells participate in MG postnatal organogenesis as negative regulators, locally orchestrat

160 phage differentiation is an integral part of organogenesis, as colonization of organ anlagen by pMacs

161 Teeth are a classic model system of organogenesis, as repeated and reciprocal epithelial and

162 ant biological functions, including lymphoid organogenesis, B-lymphocyte function, and cell growth an

163 tors like kinases required either for nodule organogenesis, bacterial infection or both, and transcri

164 s suggested that Tbx1 is required for thymus organogenesis because loss of Tbx1 in individuals with D

165 Neoblast lineages arise as organogenesis begins and are required for construction o

166 t Pals1 is not only essential for cerebellum organogenesis, but also for preventing premature differe

167 Hedgehog (Hh) signaling regulates organogenesis, but is silent in adult livers until injur

168 hoid tissue inducer (LTi) cells and lymphoid organogenesis, but its role in postnatal ILC3s is unknow

169 gous pluripotent cells can result in de-novo organogenesis, but the technique is complex, not widely

170 duce acinar, endocrine and duct cells during organogenesis, but their existence and location in the m

171 transcription factors are known to regulate organogenesis, but their molecular targets and function

172 quired for lymph node and Peyer's patch (PP) organogenesis, but where these specialized group 3 innat

173 the percentage of eggs successfully reaching organogenesis by 80%.

174 cale-bridging, in vivo studies of vertebrate organogenesis by cell-accurate structure-function mappin

175 Blood vessels serve as key regulators of organogenesis by providing oxygen, nutrients and molecul

176 together, our data show that normal blastema organogenesis cannot occur without timely infiltration o

177 During organogenesis, cell fate specification and patterning ar

178 0(-/-) mice die shortly after birth owing to organogenesis defects as in ciliopathies.

179 Tooth organogenesis depends on genetically programmed sequenti

180 Organogenesis depends on orchestrated interactions betwe

181 Proper organogenesis depends upon defining the precise dimensio

182 ging from pharyngeal pouch endoderm in early organogenesis, differential Foxa1/Foxa2 expression disti

183 erivatives in several tissues of gene-edited organogenesis-disabled mice.

184 Phyllotaxis arises from reiterative organogenesis driven by lateral inhibitions at the shoot

185 Organogenesis during embryonic development occurs throug

186 cell differentiation, lineage commitment and organogenesis during mammalian development.

187 ine by embryonic day (E) 13.5 and, before PP organogenesis (E14.5-15), are broadly dispersed in the p

188 r, many other programs of postembryonic root organogenesis exist in angiosperms.

189 During organogenesis, FGFs are diffusible communication signals

190 and cellular dynamics across the entirety of organogenesis, focusing on two key nephrogenic progenito

191 gen-fixing rhizobia that trigger root nodule organogenesis for bacterial accommodation.

192 Recapitulating organogenesis from purified progenitor cells that can be

193 e-resident myeloid cells that develop during organogenesis from yolk-sac erythro-myeloid progenitors

194 f the auxin-signaling pathways that regulate organogenesis, growth, and environmental response.

195 of four developmental mechanisms that guide organogenesis: growth, patterning, branching rate, and n

196 ural folds, and in early tadpoles undergoing organogenesis gtpbp2 is expressed prominently in the bra

197 hether DNA methylation of Cdh1 occurs during organogenesis has not been determined.

198 , but how metabolic changes are coupled with organogenesis has remained unclear.

199 temporal gene expression trajectories during organogenesis have been challenging because diverse cell

200 ling pathways and its roles in mammary gland organogenesis, how they contribute to normal organ speci

201 De novo shoot organogenesis (i.e., the regeneration of shoots on nonme

202 XCL12 mediate directed cell migration during organogenesis, immune responses, and metastatic disease.

203 ls, and is a longstanding model for studying organogenesis in a small, simple embryo.

204 tion inhibits embryonic white adipose tissue organogenesis in a tissue-autonomous manner.

205 In a rare example akin to organogenesis in adult mammals, large wounds in mice lea

206 in treatment only very weakly induced nodule organogenesis in amsh1 mutants, suggesting that AMSH1 fu

207 e mechanisms behind nephrogenesis and kidney organogenesis in an ex vivo organ culture/organoid setti

208 ectivity accompany and regulate lateral root organogenesis in Arabidopsis.

209 PAHs disrupts several pathways critical for organogenesis in fish.

210 ll deployment that may have implications for organogenesis in general.

211 em cell (ESC) culture allow investigation of organogenesis in human cells.

212 redundant manner with LHK1 to mediate nodule organogenesis in L. japonicus.

213 zyme are thus involved in both infection and organogenesis in Lotus japonicus.

214 eogenesis (WIHN)--is a rare example of adult organogenesis in mammals.

215 Mutations in lamins cause defective organogenesis in mouse models and human diseases that af

216 important roles in stem cell regulation and organogenesis in plants.

217 ed activation of SYMRK hyperactivates nodule organogenesis in the absence of rhizobia, but its ectodo

218 ly driven self-assembly of cells that mimics organogenesis in the developing embryo.

219 nt to promote cytokinin signaling and nodule organogenesis in the inner root cortex.

220 se factors have been shown to play a role in organogenesis in various diverse model species, revealin

221 xin stream redirection, such as lateral root organogenesis, in which a gradual PIN polarity switch de

222 nt signaling pathways play a crucial role in organogenesis, including tooth development.

223 unctionally replace Lhk1 in mediating nodule organogenesis, indicating that the ability to perform th

224 This provides powerful evidence that initial organogenesis involves a process of multilineage priming

225 Prostate organogenesis involves epithelial growth controlled by i

226 Mammalian kidney organogenesis involves reciprocal epithelial-mesenchymal

227 Organogenesis is a complex developmental process, which

228 Prostate organogenesis is a complex process that is primarily med

229 hemical and transcriptional factors to shape organogenesis is an important question in developmental

230 process throughout fetal life and found that organogenesis is composed of two distinct developmental

231 Proper execution of asymmetric organogenesis is critical to health, making furthering o

232 Vertebrate organogenesis is critically sensitive to gene dosage and

233 ticular type of metabolism during vertebrate organogenesis is currently unknown.

234 Pituitary organogenesis is dependent on signaling factors that are

235 wledge of the mechanisms that drive prostate organogenesis is far from complete.

236 surface and the cortical cells where nodule organogenesis is initiated.

237 ower frequency and are smaller at birth, but organogenesis is mostly normal.

238 ation of stem/progenitor cells during kidney organogenesis is not well defined.

239 t what directs this patterning during kidney organogenesis is not well understood.

240 n in vitro, their function during vertebrate organogenesis is poorly understood.

241 alance expansion with differentiation during organogenesis is still little understood.

242 l and hematopoietic cells are present during organogenesis is unclear.

243 ement, how acinar cells are generated during organogenesis is unclear.

244 factor-dependent progenitor expansion during organogenesis is unknown.

245 function of PDGFRalpha during adipose tissue organogenesis is unknown.

246 Human organogenesis is when severe developmental abnormalities

247 lular source for LTalpha1beta2 during thymic organogenesis, marked by expression of IL-7Ralpha, which

248 We adapted a Caenorhabditis elegans organogenesis model to enable a genome-wide mesodermal-s

249 d have important functions during intestinal organogenesis, morphogenesis, and homeostasis.

250 asing recognition as important regulators of organogenesis motivate the development of methods to eff

251 tresia-like phenotypes and hepatitis in late organogenesis mouse embryos, but the molecular and cellu

252 o ask questions we still ask today: How does organogenesis occur?

253 sis, but remained unspecialized until target organogenesis occurred postnatally.

254 Postnatal organogenesis occurs in an immune competent environment

255 Organogenesis occurs through cell division, expansion, a

256 circulation during the first trimester, when organogenesis occurs.

257 First, we used immunohistochemistry to chart organogenesis of continually replacing cichlid teeth and

258 Additionally, de novo organogenesis of inducible LAs resembling mammalian tert

259 ROPICA (DGT), have been shown to abolish the organogenesis of lateral roots; however, a mechanistic e

260 During organogenesis of the kidney, SCL/Tal1(+) progenitors gav

261 rgy-demanding processes of cell division and organogenesis of the new seedling.

262 racterize the transcriptome during the early organogenesis of the nodule and during its functioning.

263 Organogenesis of the ovary is a highly orchestrated proc

264 The Abdominal-B selector protein induces organogenesis of the posterior spiracles by coordinating

265 Organogenesis of the testis is initiated when expression

266 ositive and negative roles in patterning and organogenesis of the thymus and parathyroids.

267 y which spatial differences of Vmem regulate organogenesis of the vertebrate brain, and suggest volta

268 ritic cells, and osteoclasts, as well as for organogenesis of thymic and secondary lymphoid tissues.

269 Organogenesis often starts with the formation of charact

270 y overlap with genes associated with SIX1 in organogenesis or human tumors, and show coincident regul

271 RA2 is a CEP peptide receptor mediating both organogenesis programs.

272 A three-dimensional organogenesis protocol was optimised whereby embryoid bo

273 noids, three-dimensional cultures that model organogenesis, provide a new platform to investigate hum

274 Teeth undergo postnatal organogenesis relatively late in life and only complete

275 Organogenesis relies on the spatiotemporal balancing of

276 he functions of Dnmt1 and DNA methylation in organogenesis remain unclear.

277 organization of the vasculature during fetal organogenesis remained unclear.

278 essful root infection by rhizobia and nodule organogenesis require the activation of symbiotic genes

279 Plant organogenesis requires control over division planes and

280 ion of all aspects of lens specification and organogenesis, resulting in aphakia.

281 otes lateral root growth but prevents nodule organogenesis, rhizobial infection, and the induction of

282 Women who are treated with lithium during organogenesis should undergo fetal echocardiography and

283 let vascularization process during embryonic organogenesis significantly precedes islet innervation.

284 ring the hyperglycemia-susceptible period of organogenesis significantly reduced NTDs and cell apopto

285 During organogenesis, specific adhesions between adjoining tiss

286 transcription factor Pdx1 controls pancreas organogenesis, specification of endocrine pancreas proge

287 ns, they have been shown to be important for organogenesis, spermatogenesis, and male hormone product

288 from in vivo and three dimensional in vitro organogenesis studies, we review the novel contribution

289 We now show that, during organogenesis, the Arabidopsis endomembrane system speci

290 During the earliest phases of organogenesis, the liver acquires a separate lineage fro

291 heir contributions to hepatic and pancreatic organogenesis throughout life.

292 least in part through suppression of p21 and organogenesis via factors yet to be discovered.

293 izobial invasion of the epidermis and nodule organogenesis was unaffected but rhizobia remain restric

294 c Drosophila hindgut as an in vivo model for organogenesis, we show that the tightening of hindgut cu

295 d an indispensable role for Pdx1 in pancreas organogenesis, we used Elastase-Cre-mediated recombinati

296 treated drMM also recovered the capacity for organogenesis when recombined with the UB.

297 ermis is also a unique mechanical barrier to organogenesis, which must be overcome through chemical a

298 anscription factors, important regulators of organogenesis, with the Hippo tumor suppressor pathway t

299 , genes of signaling components important in organogenesis (Wnt, TGFbeta/ BMP, FGF, Notch, SHH, Erbb)

300 l and systemic roles in murine mammary gland organogenesis, yet specific functions remain undefined.