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 We introduce a concept that Wnt3A morphogenic action relies on crosstalk with both Shh and

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

6 tropic factor with mitogenic, motogenic, and morphogenic activities on a number of different cell typ

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

8 ify the structural motif responsible for the morphogenic activity.

9 n development, but not CaMKIIalpha, has this morphogenic activity.

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

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

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

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

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

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

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

17 The dramatic morphogenic changes to the bacterium during germination

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

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 that these ECM filaments have a reproducible morphogenic destiny that is characterized by directed tr

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

28 ardiac function is directly linked to normal morphogenic development of heart and vasculature.

29 eages, despite their major developmental and morphogenic differences.

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

31 ses, and it appeared to represent a specific morphogenic effect because neither axonal growth nor cel

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

33 We have previously reported that these morphogenic effects are dependent on MAPK activation at

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

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

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

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

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

39 However, morphogenic events and molecular mechanisms governing an

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

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

42 expressed in the epithelium throughout these morphogenic events, and mice lacking either factor exhib

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

44 rolled during these highly dynamic and rapid morphogenic events.

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

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

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

48 ch is in turn dependent on the Wnt family of morphogenic factors for autophosphorylation or transacti

49 indicating that these eicosanoids are major morphogenic factors in the serum.

50 er angiogenic CXC chemokines as well as bone morphogenic factors.

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

52 accumulating in a gradient fashion through a morphogenic field.

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

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

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

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

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

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

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

60 cells and associated with developmental and morphogenic gene groups.

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

62 Morphogenic gradients originating from signaling centers

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

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

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

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

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

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 The morphogenic pathway of these cells strongly resembles th

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

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

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

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

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

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

82 e maintenance of the mucosal architecture by morphogenic pathways.

83 Combined with the robust visible morphogenic phenotype of the phyB mutant in Rc, these da

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

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

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

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

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

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

90 nergistic and nonadditive manner during this morphogenic process.

91 al cells is dynamically regulated during the morphogenic process.

92 integrin alpha6 signaling during a cellular morphogenic process; 2) the decreased surface expression

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

94 of gonad formation, indicating that separate morphogenic processes are at work during gonadogenesis.

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

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

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

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

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

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

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

102 trolling the expression of genes involved in morphogenic processes.

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

104 atrix and integrin signaling, suggest that a morphogenic program integrates cell-cell and cell-extrac

105 grown in Matrigel, are restored to a normal morphogenic program when transfected with CEACAM1-4S, th

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 ion are likely to involve a gradient of bone morphogenic protein (BMP) in conjunction with FGF and Wn

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

131 nsic sensitivity and local elevation in 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 expression of embryonic globin and key bone morphogenic protein (BMP) target genes, including the he

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

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

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

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

139 Bone morphogenic protein (BMP)-7 is a 35-kDa homodimeric prot

140 Recombinant human bone morphogenic protein (BMP)-7, a morphogen that is essenti

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

158 superfamily, activin A, TGF-beta1, and bone morphogenic protein 4 (BMP-4) have various effects on he

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

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

161 on, and functional studies, we identify bone morphogenic protein 4 (BMP4) as a mechanosensitive and p

162 f pluripotent C3H10T1/2 stem cells with bone morphogenic protein 4 (BMP4) during proliferation follow

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

164 osure induces endothelial expression of bone morphogenic protein 4 (BMP4), which in turn may activate

165 em cells to the growth factors FGF2 and bone morphogenic protein 4 (BMP4), which normally promote and

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

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

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

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

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

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

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

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

174 Quite unexpectedly, bone morphogenic protein 7 prevents EMT and protects lupus mi

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 Bone morphogenic protein receptor 2 (BMPR2) gene mutations ar

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

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

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

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

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

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

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

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

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

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

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

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

198 cted with noggin, an antagonist of BMP (Bone Morphogenic Protein), we found that BMP expression is re

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

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

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

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

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

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

205 revealed that procollagen C-proteinases bone morphogenic protein-1 and mammalians Tolloid and procoll

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

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

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

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

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

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

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

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

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

215 1 because a combination of IGFBP-3 with bone morphogenic protein-7 (BMP-7), another member of the TGF

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

235 of local peptide signals, primarily the bone morphogenic proteins (BMPs) and the Wingless-related gen

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

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

238 Bone morphogenic proteins (BMPs) directly augment bone regene

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

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

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

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

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

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

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

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

247 s in the PLAB gene, encoding one of the bone morphogenic proteins in the transforming growth factor-b

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

249 gnals from adjacent endoderm, including bone morphogenic proteins, and is antagonized by a second sec

250 lated by neuregulin, notch ligands, and bone morphogenic proteins, as these factors are expressed in

251 two homologous secreted antagonists of bone morphogenic proteins, have been shown to regulate early

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

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

254 osylation and is not interfered with by bone morphogenic proteins.

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

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

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

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

259 MAPK activity in successful cell fusion and morphogenic reorganization.

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

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

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

263 K-ras is sufficient to elicit mitogenic and morphogenic responses in pancreatic ductal cells and hen

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

265 cascades alter gene expression and initiate morphogenic responses.

266 ork that regulates a diversity of downstream morphogenic responses.

267 on of light signals to control circadian and morphogenic responses.

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

269 ll fusion, whereas Ste20 fulfills a distinct morphogenic role and is required to maintain polarity in

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

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

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

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

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

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

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

277 Morphogenic signaling in HSCs is necessary to reprogram

278 Morphogenic signaling pathways that are active during fe

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

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

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

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

283 skeleton converges or coordinates with other morphogenic signalling systems to control feather bud de

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

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

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

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

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

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

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

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

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

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

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