ライフサイエンスコーパス: morphogenic

1 ulation of spatially and temporally confined morphogenic 2-AG signals remain unexplored.

2 r with erythroid (Ery) hypoplasia and tissue morphogenic abnormalities.

3 ronal progenitor domains is dependent on the morphogenic action of the secreted protein Sonic hedgeho

4 renal injury and are known to induce marked morphogenic actions in cultured tubular epithelial cells

5 hyte have been identified and, recently, the morphogenic activity of the plant hormone auxin has been

6 ify the structural motif responsible for the morphogenic activity.

7 d in invasive progression, yet with striking morphogenic and behavioral differences.

8 These signals control both vascular morphogenic and regression events, and thus a molecular

9 wth factor, Met signaling confers mitogenic, morphogenic, and motogenic activity to various cells.

10 system that facilitates the dissection of 3D morphogenic behaviors and bidirectional signaling betwee

11 Formation of cell clusters is a common morphogenic cell behavior observed during tissue and org

12 have yielded insights into the regulation of morphogenic cell migration, such as the zebrafish latera

13 nd growth factor gene expression highlighted morphogenic cell processes within the embryoid bodies, s

14 migrating into the tissues before undergoing morphogenic change to cause tissue damage.

15 survival, motility, and invasion as well as morphogenic changes that stimulate tissue repair and reg

16 The dramatic morphogenic changes to the bacterium during germination

17 We reasoned that this process, named morphogenics, could be used to improve suboptimal hybrid

18 ble mechanistic insight into the coordinated morphogenic crosstalk between the epithelium and vascula

19 ew model for how an evolutionarily conserved morphogenic cue and its cognate receptors can pattern a

20 Morphogenic cues and biochemical interactions that are c

21 etastatic disease, little is known about the morphogenic cues and signaling pathways that govern glan

22 We also show that a morphogenic cycle driven by the PT leads to extensive re

23 nts) using morpholinos caused severe cardiac morphogenic defects including a cardiac looping failure

24 ApoER2 knock-out (KO) mice had rod bipolar morphogenic defects, altered A-II amacrine dendritic dev

25 type, single rpn5a mutants display a host of morphogenic defects, including abnormal embryogenesis, p

26 at PpPTEN is a suppressor of cell growth and morphogenic development in plants.

27 eages, despite their major developmental and morphogenic differences.

28 targeting this axis in dealing with vascular morphogenic disorders and vascular normalization of tumo

29 ed regions (UTRs) along with suppressor with morphogenic effect on genitalia 5 (SMG5) and SMG7 but no

30 These morphogenic effects of VEGF-165 require activation of bo

31 enal tubular epithelial cells and that these morphogenic effects require activation of the phosphatid

32 known to influence neoplasia and also exert morphogenic effects via the urogenital sinus mesenchyme.

33 Following organ injury, morphogenic epithelial responses can vary depending on l

34 shown to lose cell polarity during the early morphogenic event of germ tube emergence.

35 However, morphogenic events and molecular mechanisms governing an

36 ghly coordinated succession of molecular and morphogenic events during development.

37 trula, their ability to recapitulate complex morphogenic events such as gastrulation is limited, poss

38 these compartments results in molecular and morphogenic events that closely mimic those observed in

39 Because wound healing largely mimics the morphogenic events that occur during development, we pro

40 e cell polarity is an intrinsic organizer of morphogenic events, environmental cues in the germinal z

41 for a wide range of cellular and subcellular morphogenic events, from cell migration to cytokinesis a

42 rolled during these highly dynamic and rapid morphogenic events.

43 e-derived cell types resulting in control of morphogenic events.

44 Tenascin-C (TNC) is a mechano-regulated, morphogenic, extracellular matrix protein that is associ

45 The S protein serves as the morphogenic factor for both types of particles, while th

46 nt osteoinductivity of EBM demonstrates that morphogenic factors expressed by ESCs undergoing osteoge

47 is, identify REEP3/4 as specific and crucial morphogenic factors mediating ER tubulation during mitos

48 g forces physically distort the shape of the morphogenic field, causing local maxima of epithelial si

49 accumulating in a gradient fashion through a morphogenic field.

50 differences in the abilities of these three morphogenic forms of C. albicans to adhere to endotheliu

51 hus, although TTF1 appears to fulfill only a morphogenic function in the ventral telencephalon, once

52 pathway is well known for its mitogenic and morphogenic functions during development, and HH signali

53 dependent protein kinase II (CaMKII)beta has morphogenic functions in neurons not shared by the alpha

54 tment and regulation of proteins involved in morphogenic functions, especially elongation and divisio

55 vents aberrant Hh signaling posterior to the morphogenic furrow, which is essential for normal eye de

56 nd growth and differentiation factor-5 joint morphogenic gene expressions.

57 cells and associated with developmental and morphogenic gene groups.

58 nt, in turn, is established in response to a morphogenic gradient of fibroblast growth factor signall

59 rong evidence against the role of long-range morphogenic gradients or biased cell exchange in the dis

60 Morphogenic gradients originating from signaling centers

61 to direct guidance of cell migration by Wnt morphogenic gradients, cell migration can also be contro

62 g deleted on chromosome ten (PTEN) regulates morphogenic growth of benign MDCK (Madin Darby Canine Ki

63 receptor (VDR) are required for normal post-morphogenic hair cycles; however, the molecular mechanis

64 undantly and partially differentially at the morphogenic level in this process.

65 network junctions are formed by two separate morphogenic mechanisms of anastomosis and cluster thinni

66 To investigate the distinct morphogenic mechanisms shared by these organisms, we per

67 ad a unique small RNA signature comprised of morphogenic miRNAs that induce microglia cytokine releas

68 le is known about the role of these vascular morphogenic molecules in the pathogenesis of atheroscler

69 ates how spatiotemporal coordination between morphogenic movements and fate determination critically

70 ll-cell signaling, and cellular forces cause morphogenic movements during dorsal closure.

71 The morphogenic movements that characterize embryonic develo

72 r, little is known about Rac function in the morphogenic movements that drive epithelial tube formati

73 r study revealed fewer (and different) inter-morphogenic pathway crosstalk connections than expected;

74 tin, sheds light for the first time into the morphogenic pathway of cytoskeletal structures that are

75 results suggest that MreC and MreD act in a morphogenic pathway that couples the helical cytosolic M

76 Crosstalk was measured by the ability of one morphogenic pathway to cross-activate core transcription

77 uxiliary mechanism of metabolic control by a morphogenic pathway with relevant implications in develo

78 ption factors and/or target genes of another morphogenic pathway.

79 Many dsDNA viruses have morphogenic pathways utilizing an intermediate capsid, k

80 Here, we investigated pairs of morphogenic pathways, previously reported to have multip

81 e maintenance of the mucosal architecture by morphogenic pathways.

82 In lymphoma, transcriptomes and morphogenic patterns of the vasculature are distinct fro

83 the protein responsible for recruitment of a morphogenic PG remodeling complex, SpmX, is distinct fro

84 ersity plays a crucial role in driving these morphogenic phenomena, via spatial segregation.

85 Tweak stimulates a branching morphogenic phenotype, similar to that induced by pro-on

86 seedling development, leading to a distinct morphogenic plan (skotomorphogenesis) [1], characterized

87 MARY-X exhibited distinct proliferative and morphogenic potencies in vitro.

88 nt specify and arrange themselves during the morphogenic process based on cell-cell interactions.

89 Tissue fusion, the morphogenic process by which epithelial sheets are drawn

90 ch overexpression and alteration of a normal morphogenic process promote the development of cancer in

91 g the involution of mouse mammary tissues, a morphogenic process requiring cellular apoptosis.

92 nergistic and nonadditive manner during this morphogenic process.

93 al cells is dynamically regulated during the morphogenic process.

94 suitable for genetic optimization using the morphogenics process and have shown potential for large-

95 ) cytoskeleton has been proposed to regulate morphogenic processes by integrating the cell fate signa

96 last stage, providing a model to explore key morphogenic processes in early human embryos.

97 potential Ca(2)(+) mediator of many of these morphogenic processes is CaMK-II, a conserved calmodulin

98 hanced Cdc42 activation and rescued aberrant morphogenic processes of PTEN-deficient cultures.

99 How then do cells define alternative morphogenic processes that are distinct from cell elonga

100 ol of cell proliferation and apoptosis, plus morphogenic processes that sculpt vasculature, parenchym

101 othesize that PTEN controls Cdc42 -dependent morphogenic processes through a beta-Arrestin1-ARHGAP21

102 that plays important roles in developmental morphogenic processes, is abnormally elevated in the bon

103 endogenous Eph signaling in endothelial cell morphogenic processes, uncovers a novel link between Eph

104 al mechanoenzyme in a wide range of cellular morphogenic processes.

105 trolling the expression of genes involved in morphogenic processes.

106 ined an unidentified SocA substrate that had morphogenic properties.

107 Similar to bone morphogenic protein (BMP) 2, application of the recombin

108 ates endothelial cells (ECs) to produce bone morphogenic protein (BMP) 4, which in turn activates inf

109 K14-Noggin transgenic mouse to modulate bone morphogenic protein (BMP) activity and test the extent o

110 ignaling induces down-regulation of the bone morphogenic protein (BMP) and activin membrane-bound inh

111 Bone morphogenic protein (BMP) and fibroblast growth factor (

112 hese proteins play an important role in bone morphogenic protein (BMP) and transforming growth factor

113 The bone morphogenic protein (BMP) antagonist gremlin is elevated

114 Wnt and bone morphogenic protein (BMP) gradients drive this polarity,

115 cyte lineage specificity in response to bone morphogenic protein (BMP) remain unclear.

116 ansforming growth factor (TGF)-beta and bone morphogenic protein (BMP) signaling after specification

117 apid bouton budding requires retrograde bone morphogenic protein (BMP) signaling and local alteration

118 and murine hematopoietic cells induced bone morphogenic protein (BMP) signaling and resulted in a ma

119 We show that bone morphogenic protein (BMP) signaling and the transcriptio

120 reduction of synaptic growth-promoting bone morphogenic protein (BMP) signaling at the neuromuscular

121 st whether adult neuronal expression of bone morphogenic protein (BMP) signaling components also play

122 rrespondingly, the distribution of both bone morphogenic protein (BMP) signaling domains and BMP2 imm

123 in injection in neonatal mice increased bone morphogenic protein (BMP) signaling in the ventral hypot

124 In the present study, we show that bone morphogenic protein (Bmp) signaling is a critical regula

125 Canonical bone morphogenic protein (BMP) signaling is mediated via the

126 gulatory hormone, hepcidin, through the bone morphogenic protein (BMP) signaling pathway by acting as

127 through the inhibition of both Wnt and bone morphogenic protein (BMP) signaling pathways.

128 Although bone morphogenic protein (BMP) signaling promotes chondrogene

129 Bone morphogenic protein (BMP) signaling was the apparent cau

130 nsic sensitivity and local elevation in bone morphogenic protein (BMP) signaling.

131 n transforming growth factor (TGF)-beta/bone morphogenic protein (BMP) signaling.

132 Bone morphogenic protein (BMP) signalling contributes towards

133 rosophila homologue spichthyin inhibits bone morphogenic protein (BMP) signalling, although the relev

134 blocking TGF-beta signalling, promoting bone morphogenic protein (BMP) signalling.

135 expression of embryonic globin and key bone morphogenic protein (BMP) target genes, including the he

136 of cerberus RNA, which encodes a Nodal, bone morphogenic protein (BMP), and Wnt inhibitor.

137 that a signaling cascade involving the Bone Morphogenic Protein (BMP), WNT, and NODAL pathways is ne

138 n is controlled jointly by at least the bone morphogenic protein (BMP), WNT, fibroblast growth factor

139 Osteocalcin and bone morphogenic protein (BMP)-2 expression was evaluated imm

140 Although GlaMGP binds and inactivates bone morphogenic protein (BMP)-2, a proposed mediator of vasc

141 The bone morphogenic protein (BMP)/small mothers against decapent

142 Screening data revealed bone morphogenic protein (BMP)4 as a factor that inhibited ce

143 Bone morphogenic protein 1 (BMP1) is an enzyme responsible fo

144 Bone morphogenic protein 1 (Bmp1)/Tolloid-like metalloprotein

145 /C1s, Uegf sea urchin fibropellins, and bone morphogenic protein 1 (CUB) domains, but was severely de

146 complement component Clr/Cls, Uegf, and bone morphogenic protein 1).

147 r markers atrial natriuretic factor and bone morphogenic protein 10 indicated that proliferating card

148 the suppressive effects of TGF-beta and bone morphogenic protein 2 (BMP-2) on epithelial gene express

149 repression is established by utilizing bone morphogenic protein 2 (BMP-2)-induced chondrogenic diffe

150 e Food and Drug Administration-approved bone morphogenic protein 2 (BMP-2).

151 -osteogenic factors [Fgf-2, Fgf-18, and bone morphogenic protein 2 (Bmp-2)] still were present in Fgf

152 osteogenic activity of ihOCM surpasses bone morphogenic protein 2 (BMP2) driving healing of calvaria

153 We explored the role of bone morphogenic protein 2 (BMP2) in defocus-induced ocular g

154 We previously found that bone morphogenic protein 2 (BMP2) induces export of HDAC7 fro

155 tein 1 (SMAD1) and SMAD4 in response to bone morphogenic protein 2 (BMP2) signaling.

156 Importantly, bone morphogenic protein 2 (BMP2) was able to intensify the d

157 erived factor-1 (SDF-1), is involved in bone morphogenic protein 2 (BMP2)-induced osteogenic differen

158 n of mesenchymal C2C12 cells induced by bone morphogenic protein 2 (BMP2).

159 or activator of nuclear factor kappa B, bone morphogenic protein 2, and muscle segment homeobox 2, th

160 or optimal expression in ECs, including bone morphogenic protein 2, cbp/p300-interacting transactivat

161 fferentiated in vitro by treatment with bone morphogenic protein 2, the OBs from TIEG(+/+) calvaria d

162 tor receptor beta polypeptide (PDGFRb), bone morphogenic protein 4 (BMP-4), and stem cell factor (SCF

163 elial nitric oxide synthase (eNOS), and bone morphogenic protein 4 (BMP-4).

164 Human ES cells (hESC) exposed to bone morphogenic protein 4 (BMP4) in the absence of FGF2 have

165 ocyte, corresponding to upregulation of bone morphogenic protein 4 mRNA and CTGF mRNA (inhibitors of

166 Dual-SMAD inhibition followed by bone morphogenic protein 4 stimulation induced self-organizat

167 ating aggregates by cytokines including bone morphogenic protein 4.

168 lants of Hepcidin transcription include bone morphogenic protein 6 (BMP6) and interleukin-6 (IL-6) by

169 haplotypes composed of several SNPs in bone morphogenic protein 6, annexin A2, and klotho were assoc

170 thelial cells to undergo EndMT, whereas bone morphogenic protein 7 (BMP-7) preserved the endothelial

171 In the absence of the growth factor bone morphogenic protein 7 (BMP7), kidney development arrests

172 the genes common to both data sets was bone morphogenic protein 7 (BMP7), whose expression is also s

173 tituent of the antifibrotic activity of bone morphogenic protein 7 (BMP7).

174 cleotide polymorphisms (SNPs) were near bone morphogenic protein 7 [BMP7: rs75161997, P = 5.34 x 10(-

175 sms, such as fetuin-A, osteopontin, and bone morphogenic protein 7, among others, will be necessary t

176 HOXC6 directly regulates expression of bone morphogenic protein 7, fibroblast growth factor receptor

177 In the case of bone morphogenic protein 9 (BMP9), however, the pro-domains d

178 rming growth factor-beta [TGF-beta] and bone morphogenic protein [BMP]) in the dentine that are belie

179 CHRDL1 encodes ventroptin, a bone morphogenic protein antagonist with a proposed role in s

180 ructure of the homeodomain of the Drosophila morphogenic protein Bicoid (Bcd) complexed with a TAATCC

181 In response to bone morphogenic protein BMP2, Hoxa10 is rapidly induced and

182 of inhibiting activin signaling but not bone morphogenic protein or platelet-derived growth factor si

183 leads to an up-regulation of endogenous bone morphogenic protein pathway activation, as indicated by

184 transforming growth factor-beta/activin/bone morphogenic protein pathways, we demonstrate a specializ

185 -acylated in mouse NSCs and showed that bone morphogenic protein receptor 1a (BMPR1a), a core mediato

186 Bone morphogenic protein receptor 2 (BMPR2) gene mutations ar

187 This gene encodes the type I bone morphogenic protein receptor ALK2, with the residues aff

188 t is driven by direct inhibition of the bone morphogenic protein receptor kinase activin A receptor,

189 including mutations in the gene coding bone morphogenic protein receptor type 2 (BMPR2) and related

190 ed to changes in cell cycle control and bone morphogenic protein receptor type 2 (BMPR2) signaling, a

191 synaptic growth signaling by activated bone morphogenic protein receptors, and live imaging in neuro

192 we demonstrate that the cytosolic leaflet ER morphogenic protein reticulon (RTN) protects ER membrane

193 roinsulin aggregation, while the ER membrane morphogenic protein reticulon-3 (RTN3) disposes of aggre

194 sistent with a role for activin but not bone morphogenic protein signaling in cardiac dysfunction.

195 encoding inhibitors of WNT and activin/bone morphogenic protein signaling were overrepresented in th

196 d for regulation of synaptic growth via bone morphogenic protein signaling.

197 t differentiation, Ciz, interferes with bone morphogenic protein signaling.

198 Sonic hedgehog (Shh) is a morphogenic protein that operates through the Gli transc

199 Pretreatment with a bone morphogenic protein type I receptor inhibitor showed tha

200 Germ-line mutations in bone morphogenic protein type II receptor (Bmpr2) confer susc

201 t mutations in p3 likely had changes in p12 (morphogenic protein), a region that was not polymorphic

202 oaches to fusion, as well as the use of bone morphogenic protein, disk arthroplasty, and interspinous

203 nt findings regarding the roles of Wnt, bone morphogenic protein, PtdIns(3,4,5) kinase, and Notch pat

204 arding signaling pathways, such as Wnt, bone morphogenic protein, PtdIns(3,4,5) kinase, and Notch, in

205 Here we discover a morphogenic protein, RodZ, which is widely conserved acr

206 where DCVs contain neuropeptides and a bone morphogenic protein, show that activity-dependent replen

207 ortance of pathways such as Wnt, Notch, bone morphogenic protein, Sonic hedgehog and fibroblast growt

208 of leukemia inhibitory factor (LIF) and bone-morphogenic protein-2 (BMP-2)-induced mouse ES cell (mES

209 IL-3 inhibited basal and bone morphogenic protein-2 (BMP-2)-stimulated osteoblast form

210 tion inducers, including ascorbic acid, bone morphogenic protein-2, or fibroblast growth factor 2.

211 Nf1 ablation also prevents bone morphogenic protein-2-induced osteoprogenitor differenti

212 including many expressed in response to bone morphogenic protein-4.

213 studies demonstrate a pivotal role for bone morphogenic protein-6 (BMP6) and matriptase-2, a protein

214 Both hemojuvelin (HJV) and bone morphogenic protein-6 (BMP6) are essential for hepcidin

215 , we tested the therapeutic efficacy of bone morphogenic protein-7 (BMP-7) and inhibitors of advanced

216 and is associated with a loss of renal bone morphogenic protein-7 (BMP-7) expression.

217 Bone morphogenic protein-7 (BMP-7) is a key protein involved

218 1 because a combination of IGFBP-3 with bone morphogenic protein-7 (BMP-7), another member of the TGF

219 Furthermore, we demonstrate that bone morphogenic protein-7 (BMP7), a member of the TGFbeta su

220 e phosphorylation of Smad1 and Smad2 by bone morphogenic protein-7 and transforming growth factor-bet

221 ion of TGF-beta1 with recombinant human bone morphogenic protein-7 prevents this process and prevents

222 testinal epithelial cells in vitro, and bone morphogenic protein-7, an antagonist of TGF-beta1, inhib

223 o showed hyperactivation of alternative bone morphogenic protein-activated Smad1/5/8 signaling and in

224 formation of the caudal vein plexus, a bone morphogenic protein-responsive process, an effect rescue

225 rotein involved in protein translation, is a morphogenic protein.

226 esis by targeting endothelial cell (EC) bone morphogenic protein/SMAD1 signaling in vitro and in vivo

227 s demonstrate that miR-26a inhibits the bone morphogenic protein/SMAD1 signaling pathway in ECs by bi

228 ngs establish miR-26a as a regulator of bone morphogenic protein/SMAD1-mediated EC angiogenic respons

229 Multiple signaling molecules, including bone morphogenic proteins (BMP) and fibroblast growth factors

230 se include the Notch, Wnt/beta-catenin, bone morphogenic proteins (Bmp) and Sonic Hedgehog (Shh) path

231 We report that DeltaNp63alpha activates bone morphogenic proteins (BMP) signaling by inducing the exp

232 e cerebellar region of the neural tube, bone morphogenic proteins (BMP6/7 and GDF7) that induce early

233 ive conditions induce the expression of bone morphogenic proteins (BMPs 2 and 4) in cultured endothel

234 Bone morphogenic proteins (BMPs) and blood flow regulate vasc

235 linositol-linked protein and binds both bone morphogenic proteins (BMPs) and neogenin.

236 Gremlin 1 (GREM1) inhibits bone morphogenic proteins (BMPs) and plays a role in kidney d

237 or beta (TGF-beta) superfamily, such as bone morphogenic proteins (BMPs) and TGF-beta, are key regula

238 (AV) cusps have increased expression of bone morphogenic proteins (BMPs) and transforming growth fact

239 Bone morphogenic proteins (BMPs) are involved in axon pathfin

240 Bone morphogenic proteins (BMPs) directly augment bone regene

241 We found that activity of bone morphogenic proteins (BMPs) is required for neural crest

242 Although bone morphogenic proteins (BMPs) maintain pluripotency of und

243 Bone morphogenic proteins (BMPs) play pleotrophic roles in ne

244 of the transforming growth factor-beta, bone morphogenic proteins (BMPs), and activin signaling.

245 sses endogenous growth factors, such as bone morphogenic proteins (BMPs), which facilitate maintenanc

246 Bone morphogenic proteins 2 and 4 (BMP2 and BMP4) inhibit pro

247 nd associated hepcidin up-regulation by bone morphogenic proteins 2 and 4 (BMP2/BMP4).

248 g that they represent a widespread family of morphogenic proteins controlling cell wall biogenesis by

249 Concentration gradients of morphogenic proteins pattern the embryonic axes of Droso

250 This review will focus on bone morphogenic proteins, Hedgehog, Notch, ephrins, neuropil

251 hanges depend on SPP-mediated cleavage of ER morphogenic proteins, including the SNARE protein syntax

252 odulates the ER shape through degradation of morphogenic proteins.

253 mented with LIF; even in the absence of bone morphogenic proteins.

254 The shape and oligomerization of the "morphogenic" proteins could explain the formation of the

255 We propose that these "morphogenic" proteins partition into and stabilize highl

256 of polo-like kinase (TbPLK) as an essential morphogenic regulator.

257 temporal dynamics of stem cell signaling and morphogenic remodeling to direct the differentiation of

258 MAPK activity in successful cell fusion and morphogenic reorganization.

259 ocks VEGF-165 binding to Nrp-1) prevents the morphogenic response and the phosphorylation of VEGFR-2

260 PA14 colony biofilms show a profound morphogenic response to phenazines resulting from electr

261 ated to be critical in coordinating vascular morphogenic responses by controlling hematopoietic cytok

262 M (OSM) induces potent growth-inhibitory and morphogenic responses in several different tumor cell ty

263 cascades alter gene expression and initiate morphogenic responses.

264 ork that regulates a diversity of downstream morphogenic responses.

265 tion) signal and GATA-6 is required to sense morphogenic (retinoic acid) signal.

266 fully mature RGP has distinct protective and morphogenic roles for S. mutans, and these structures ar

267 ous experimental and theoretical analyses of morphogenic scaling that have focused on compensatory ch

268 We propose this complex delivers morphogenic secretory traffic along polarized actin fila

269 We infer that TGFbeta is an essential morphogenic signal for the neural crest cell lineage in

270 ce is given here that light acts mainly as a morphogenic signal in the triggering of bud outgrowth an

271 previously proposed, but functions as an ER morphogenic signal.

272 discuss the emerging role of Wnt proteins in morphogenic signaling and ciliary biology during health

273 t the mechanisms that coordinate and control morphogenic signaling during effective liver regeneratio

274 Channeling morphogenic signaling gradients intrinsic to intestinal

275 Morphogenic signaling in HSCs is necessary to reprogram

276 Morphogenic signaling pathways that are active during fe

277 ic stellate cells (HSCs) and reactivation of morphogenic signaling pathways that modulate epithelial-

278 The distribution and activities of morphogenic signaling proteins such as Hedgehog (Hh) and

279 hen localized to the cytoplasmic surface and morphogenic signaling when localized to the extracellula

280 Our study thus links spine morphogenic signaling with age-dependent, delayed, disea

281 ral nervous system and generates dorsalising morphogenic signals along the length of the neuraxis.

282 Morphogenic signals are crucial in defining neuronal ide

283 The integration of morphogenic signals by cells is not well understood.

284 of meninges, we have identified a cascade of morphogenic signals initiated by the meninges that regul

285 al epithelial cells to the dedifferentiating morphogenic signals of hepatocyte growth factor (HGF) wa

286 ing during gastrulation, and is regulated by morphogenic signals such as the FGF/MAPK and activin pat

287 cient mesenchymal progenitors cause aberrant morphogenic signals, and identify an expression signatur

288 r within the organism, presumably via mobile morphogenic signals.

289 function as a receptor for growth factors or morphogenic signals.

290 ant formed near-normal levels of the various morphogenic stages of infectious virus particles and sup

291 er cells in mitosis, but their role in other morphogenic states is poorly understood.

292 a general framework to study and predict the morphogenic states of contractile fibrous tissues under

293 quired for virus replication.IMPORTANCE In a morphogenic step that is exceedingly rare for nonenvelop

294 ncluding autoinducers, virulence factors and morphogenic substances.

295 lar mechanisms that underlie the C. albicans morphogenic switch.

296 In growth conditions that elicit morphogenic switching, vph1Delta was defective in formin

297 These findings not only identify a morphogenic target for Ca(2+) during heart development,

298 platform process that combines hybridoma and morphogenics technologies for the generation of fully hu

299 infection appears to be associated with the morphogenic transformation of C. albicans yeasts into in

300 Thus, the morphogenic transition can be targeted as an efficient t