ライフサイエンスコーパス: morphogenetic

1 First, polyP shows morphogenetic activity, i.e., induces cell differentiati

2 dels that tonic signalling leads to superior morphogenetic activity, with syndecan-binding growth fac

3 ar structures, which are governed by similar morphogenetic and gene regulatory processes as animal de

4 Morphogenetic and transcriptome profiling analyses revea

5 neural and yolk sac ciliogenesis, leading to morphogenetic anomalies resulting from impaired hedgehog

6 However, the cellular control of morphogenetic apoptosis is poorly understood, notably th

7 der wall, represents an exquisite example of morphogenetic apoptosis, requiring the receptor protein

8 rge suite of effector genes that control the morphogenetic behaviors and biomineral-forming activitie

9 innovations collectively contribute to novel morphogenetic behaviors and unprecedented increases in t

10 tion with specific cellular interactions and morphogenetic behaviors is necessary for stripe developm

11 online through the newly developed Morphonet morphogenetic browser.

12 ize, premature flowering and increased shoot morphogenetic capacity in culture.

13 oot apical meristem cell size increases, and morphogenetic capacity of cultured hypocotyls is reduced

14 he cAMP pulses that coordinate Dictyostelium morphogenetic cell movement and is highly expressed at t

15 nscriptional thresholds required for driving morphogenetic cell-fate decisions.

16 Testes and ovaries undergo sex-specific morphogenetic changes and adopt strikingly different mor

17 and adult stage, allowed us to describe the morphogenetic changes shaping the adult SEZ.

18 ss comprising multiple lineage decisions and morphogenetic changes that are inaccessible to deep anal

19 ngus Magnaporthe oryzae involves a series of morphogenetic changes, essential for its ability to caus

20 lengths, which stabilize to produce lasting morphogenetic changes.

21 e axes could potentially underlie the entire morphogenetic chromosomal program.

22 d LDTs function independently of the primary morphogenetic complexes to support growth, provide prote

23 applications and hold promise as adhesive or morphogenetic control units that can be genetically enco

24 lly specify fates within developing tissues, morphogenetic cues must be correctly positioned and inte

25 ric JH isomers to induce gene expression and morphogenetic effects in the developing insects.

26 entral body wall in amniotes is an important morphogenetic event and is essential for life.

27 CM) (Tnc, Postn, Spon2, Thbs2) as a key lung morphogenetic event associating with eosinophils.

28 that collectively extend in a multicellular morphogenetic event that occurs during C. elegans embryo

29 This is a complex morphogenetic event where expulsion of the apoptotic cel

30 fficient to recapitulate all aspects of this morphogenetic event, including anisotropic apical constr

31 et of ventral cells and is required for this morphogenetic event.

32 rheostat-like responses of an ERK-dependent morphogenetic event.

33 Here, we review three morphogenetic events common to most animals: apical cons

34 Gene regulatory networks and tissue morphogenetic events drive the emergence of shape and fu

35 Out-of-plane tissue deformations are key morphogenetic events during plant and animal development

36 ell-lineage allocation and recapitulated key morphogenetic events during preimplantation and early po

37 ity (PCP) signaling pathway orients numerous morphogenetic events in both invertebrates and vertebrat

38 is of mitochondrial dynamics and function in morphogenetic events in early metazoan embryogenesis has

39 It controls early morphogenetic events in embryos, maintains stem cell nic

40 One of the first morphogenetic events in the vertebrate brain is the form

41 organ anlages, which then recapitulate early morphogenetic events including the invagination and bran

42 al morphology and activity in supporting the morphogenetic events that drive cellularization in Droso

43 ay is shared by two embryologically distinct morphogenetic events that previously were considered ind

44 be that then undergoes multiple simultaneous morphogenetic events to obtain its mature shape.

45 een identified as critically contributing to morphogenetic events, but the interplay between the vari

46 associated with ABMs as tools for examining morphogenetic events.

47 of reproducible shapes, through stereotyped morphogenetic events.

48 sue behaviors during early vertebrate embryo morphogenetic events.

49 e biochemically controlled to robustly drive morphogenetic events.

50 etween these tissues is key to understanding morphogenetic evolution.

51 ver, the mechanisms by which these different morphogenetic factors are coordinated and how they may b

52 ll be useful for decoupling other downstream morphogenetic factors from hyphal growth.

53 at they capture the early footprint of known morphogenetic features, reveal new ones, and quantitativ

54 The lateral boundaries of the morphogenetic field are determined by phloem-adjacent pe

55 spread through a tissue to establish such a morphogenetic field remain elusive.

56 Furthermore, FC recruitment establishes a morphogenetic field where laterally peripheral cells hav

57 Morphogenetic flows in developmental biology are charact

58 a pupal dorsal thorax epithelium responds to morphogenetic forces, we found that the number of apical

59 ssential to brace the cells against external morphogenetic forces.

60 nd have distinct but incompletely understood morphogenetic functions during cell elongation and divis

61 sentative for insects, that Fog has multiple morphogenetic functions.

62 uses preferential cell death anterior to the morphogenetic furrow in the eye disc and within wing pou

63 he CG membrane, which is slightly behind the morphogenetic furrow that marks the front of PR differen

64 G1 arrest and neuronal specification at the morphogenetic furrow.

65 However, the nature of the AR-regulated morphogenetic genes and the mechanisms whereby AR contro

66 (AR) is thought to control the expression of morphogenetic genes in inductive UGS mesenchyme, which p

67 ity conforms to the ICM, following a linear, morphogenetic gradient along the molar row.

68 Previous study showed that a "morphogenetic gradient" of molar proportions was explain

69 Tissue internalisation is a key morphogenetic mechanism by which embryonic tissues gener

70 ere, we describe an evolutionarily conserved morphogenetic mechanism for epidermal ensheathment of so

71 tic spindles is believed to be a fundamental morphogenetic mechanism in multicellular organisms [3-6]

72 that epithelial bending can be achieved by a morphogenetic mechanism of coordinated cell rearrangemen

73 Convergent extension (CE) is a fundamental morphogenetic mechanism that underlies numerous processe

74 Moreover, these morphogenetic mechanisms provide new perspectives regard

75 by transcriptional regulation as well as by morphogenetic mechanisms that shape organ primordia, alt

76 ll described, little is understood about the morphogenetic mechanisms.

77 nce 1997 relevant to TBM and other candidate morphogenetic mechanisms.

78 ven local tissue fluidization as a conserved morphogenetic module for closure of epithelial gaps.

79 r accurate mapping of sub- to multi-cellular morphogenetic motifs using a time series data mining fra

80 ithelial cell properties required for proper morphogenetic movement and pattern formation.

81 Here, we describe a morphogenetic movement in which the intertwined socket a

82 that knockdown of mondoa impaired the early morphogenetic movement of epiboly in zebrafish embryos a

83 n many tissues, allowing cells to coordinate morphogenetic movements and function.

84 Mechanisms governing such morphogenetic movements have been studied only within a

85 ducing gut endoderm-like gene expression and morphogenetic movements in all cells within this region.

86 different signaling thresholds and that the morphogenetic movements of gastrulation are robust to a

87 activating key endoderm GRN factors and the morphogenetic movements of gastrulation.

88 n IF network accompanies collective cellular morphogenetic movements that occur during early embryoni

89 cell behaviors that mediate the tissue-level morphogenetic movements that shape the neural tube (NT),

90 yostelia always initiates at the site of the morphogenetic organizer.

91 patial organization of forces determines the morphogenetic output.

92 tor 2), and WLS (Wntless), genes involved in morphogenetic pathways known to mediate tracheoesophagea

93 of mechanics and chemistry combine to drive morphogenetic pattern formation.

94 represses the Hedgehog pathway and promotes morphogenetic patterning.

95 h increasing tissue size, and it responds to morphogenetic perturbations that impact organ growth.

96 nparalleled flexibility for studying various morphogenetic phenomena at multiple levels and have the

97 These findings unveil the surprising morphogenetic potential of mESCs to execute key aspects

98 polymers at the periclinal wall regulate the morphogenetic process in epidermal pavement cells and me

99 Drosophila dorsal closure (DC), a morphogenetic process in which an extraembryonic tissue

100 enchymal transition (EMT) represents a basic morphogenetic process of high cell plasticity underlying

101 The morphogenetic process of mammalian cardiac development i

102 ergent extension is a particularly important morphogenetic process to which George Oster gave signifi

103 y at the onset of animals or it evolved from morphogenetic processes already present in their unicell

104 ys controls the complexity and order of lens morphogenetic processes and lens transparency.

105 rn regulatory networks that direct essential morphogenetic processes and organogenesis in vertebrate

106 suggest that the mechanisms underlying these morphogenetic processes are conserved.

107 al constraints: at any stage of ontogenesis, morphogenetic processes are constrained to operate withi

108 Collectively, our results indicate that lung morphogenetic processes associated with heightened Type

109 For each part of the cell, morphogenetic processes create internal structures such

110 y has ramifications for our understanding of morphogenetic processes in plant leaves and animal epith

111 trated a startling array of regenerative and morphogenetic processes in this single-celled organism,

112 We know that the patterning and morphogenetic processes involved in development are deep

113 e-tissue interactions needed for the complex morphogenetic processes of native organogenesis.

114 Intra-organ communication guides morphogenetic processes that are essential for an organ

115 s evolve is understanding the origins of the morphogenetic processes that form these features.

116 Ca(2+) sensors, they may participate in the morphogenetic processes that shape RGC dendrite and axon

117 Pulsed actomyosin contractions drive morphogenetic processes, but how cyclic frequencies and

118 prehensive mechanistic insights into complex morphogenetic processes, the meeting provided an ideal p

119 th and internal organization reflect complex morphogenetic processes.

120 ement of the mechanochemical organization of morphogenetic processes.

121 pment to orchestrate critical patterning and morphogenetic processes.

122 ebrate mutants are related to other types of morphogenetic processes.

123 k-STRIPAK complex in the control of multiple morphogenetic processes.

124 lar mechanisms may orient other lateralizing morphogenetic processes.

125 Together, this work identifies a unique morphogenetic program during OFT valve formation and pla

126 These results reveal a morphogenetic program of patterned apical constriction g

127 despread strategy to ensure the integrity of morphogenetic programs.

128 n synovial MSCs transduced with Bmp7 display morphogenetic properties by patterning a joint-like orga

129 system essential for generating the hallmark morphogenetic properties of pancreatic islets.

130 s and vascular calcification, including bone morphogenetic protein (BMP) and transforming growth fact

131 The bone morphogenetic protein (Bmp) family of secreted molecules

132 The Bone Morphogenetic Protein (BMP) family reiteratively signals

133 pment, with a classic example being the bone morphogenetic protein (BMP) gradient's conserved role in

134 Here we show that bone morphogenetic protein (BMP) growth factor signaling and

135 The bone morphogenetic protein (BMP) pathway is essential for the

136 e transforming growth factor (TGF)-beta/bone morphogenetic protein (BMP) pathway, which is one of the

137 Beta-catenin/Tcf and the TGF-beta bone morphogenetic protein (BMP) provide critical molecular s

138 surrogate surface marker P2RY1, and the bone morphogenetic protein (BMP) receptor 1A (BMPR1A)/activin

139 that OA-MSC expressed the same level of Bone Morphogenetic Protein (BMP) Receptor-1A as OAC but only

140 orming growth factor beta (TGFbeta) and bone morphogenetic protein (BMP) signal transduction in postn

141 eogenic hair follicles, which triggered bone morphogenetic protein (BMP) signaling and then activatio

142 nd genetic epistasis studies identified bone morphogenetic protein (BMP) signaling as a mediator of t

143 To assess whether bone morphogenetic protein (BMP) signaling contributes to the

144 were carried out to assess the role of bone morphogenetic protein (BMP) signaling in psoriatic skin

145 ryptic "secondary cells." Inhibition of bone morphogenetic protein (BMP) signaling in secondary cells

146 Bone morphogenetic protein (BMP) signaling is critical in ren

147 Bone morphogenetic protein (BMP) signaling is known to contri

148 tion of an activity-dependent autocrine Bone Morphogenetic Protein (BMP) signaling pathway at the Dro

149 Ras signaling and may also activate the bone morphogenetic protein (BMP) signaling pathway in colorec

150 Hepcidin expression is induced via the bone morphogenetic protein (BMP) signaling pathway that prefe

151 In the anterior, it activates the bone morphogenetic protein (BMP) signaling pathway through ex

152 that RNAi silencing of a member of the Bone Morphogenetic Protein (BMP) signaling pathway, Decapenta

153 se mutants target the components of the Bone Morphogenetic Protein (BMP) signaling pathway, revealing

154 Bone morphogenetic protein (BMP) signaling pathways control m

155 ough modulation of Hedgehog, Notch, and bone morphogenetic protein (BMP) signaling pathways.

156 Bone morphogenetic protein (BMP) signaling performs multiple

157 ansforming growth factor beta (TGFbeta)/bone morphogenetic protein (BMP) signaling system.

158 ment-binding protein (SREBP) signaling, bone morphogenetic protein (BMP) signaling, and glycosylphosp

159 1/5 transcription factors, activated by bone morphogenetic protein (BMP) signaling, are major regulat

160 ltiple invasion pathways including EMT, bone morphogenetic protein (BMP) signaling, chemokine signali

161 t and Notch signaling while suppressing bone morphogenetic protein (BMP) signaling.

162 R-spondin signaling with inhibition of bone morphogenetic protein (BMP) signaling.

163 eta and activin signals while enhancing bone morphogenetic protein (BMP) signaling.

164 TSP-14, function redundantly to promote bone morphogenetic protein (BMP) signaling.

165 tion, and their dysregulating effect on bone morphogenetic protein (BMP) signaling.

166 ansforming growth factor-beta (TGFbeta)/bone morphogenetic protein (BMP) signalling and illustrate ho

167 ess-related integration site (WNT), and bone morphogenetic protein (BMP) signalling interactions capa

168 om a murine myeloma model, we find that bone morphogenetic protein (BMP) signalling is upregulated in

169 pled fibroblast growth factor (FGF) and bone morphogenetic protein (BMP) signalling together with mes

170 ss enhanced by mating and controlled by bone morphogenetic protein (BMP) signalling.

171 ion and signaling are up-regulated, and bone morphogenetic protein (BMP) signals are impaired.

172 In the Drosophila ovarian germline, Bone Morphogenetic Protein (BMP) signals released by niche ce

173 ess-integrated site (Wnt)/beta-catenin, bone morphogenetic protein (Bmp), and fibroblast growth facto

174 commonly increase signaling of the Wnt, bone morphogenetic protein (BMP), or Ras/ERK pathways, conver

175 ells (recell-dTBs); 3) dTBs seeded with bone morphogenetic protein (BMP)-2 (dTB-BMPs); and 4) freshly

176 inducible nitric oxide synthase (iNOS), bone morphogenetic protein (BMP)-2, matrix metalloproteinase

177 at iSMCs from HGPS donors overexpressed bone morphogenetic protein (BMP)-4, which plays a key role in

178 The bone morphogenetic protein (BMP)-Smad signaling pathway plays

179 tor and function as coreceptors for the bone morphogenetic protein (BMP)/growth differentiation facto

180 hepcidin, which is regulated by hepatic bone morphogenetic protein (BMP)/SMAD signalling.

181 pathway and activation of the parallel bone morphogenetic protein (BMP)/Smad1/5 axis (recently ident

182 t mutations in the type II receptor for bone morphogenetic protein (BMPRII) underlie the majority of

183 hat the extracellular metalloproteinase bone morphogenetic protein 1 (BMP-1) is involved in endotroph

184 ocessing by the C-propeptide proteinase bone morphogenetic protein 1 (BMP-1).

185 Mutations in bone morphogenetic protein 1 (BMP1) in humans or deletion of

186 ed the secreted zinc metalloproteinase, bone morphogenetic protein 1 (BMP1), as responsible for the c

187 1s, urchin embryonic growth factor, and bone morphogenetic protein 1 domain indicate that Mt2I286F ca

188 e with thrombospondin motifs) and BMP1 (bone morphogenetic protein 1)/Tolloid-like families, respecti

189 Bone morphogenetic protein 10 (BMP10), one member of the BMP

190 l delivery of essential growth factors, bone morphogenetic protein 2 (BMP-2) and vascular endothelial

191 mining role of these residues, BG bound bone morphogenetic protein 2 (BMP-2) weakly or not at all, an

192 In calcified arteries, bone morphogenetic protein 2 (BMP-2)levels were increased at

193 Otic-specific knockout of bone morphogenetic protein 2 (Bmp2) results in absence of all

194 viously identified a nuclear variant of bone morphogenetic protein 2 (BMP2), named nBMP2, that is tra

195 Recombinant human bone morphogenetic protein 2 (rhBMP-2) is an osteoinductor fr

196 ith the growth factor recombinant human bone morphogenetic protein 2 (rhBMP-2), producing a scaffold

197 osteoblast mineralization by regulating bone morphogenetic protein 2 and p53.

198 A bone morphogenetic protein 2 gradient, presented across a gel

199 nanostructures amplified signalling of bone morphogenetic protein 2 significantly more than the natu

200 Bone morphogenetic protein 2-inducible kinase (BMP2K) has bee

201 histochemical, and immunohistochemical (bone morphogenetic protein 2/4 [BMP2/4], osteocalcin [OCN], a

202 Furthermore, bone morphogenetic protein 4 (BMP-4), which also induces AKT

203 tein 1 (GLG1) expression and downstream bone morphogenetic protein 4 (BMP4) signaling and also reduce

204 -gastrulation-like fate patterning upon bone morphogenetic protein 4 (BMP4) treatment of geometricall

205 We show that bone morphogenetic protein 4 (BMP4), an important differentia

206 We and others showed that Bone Morphogenetic Protein 4 (BMP4), and other BMPs are upreg

207 TGF-beta signaling mediated by pSMAD2, bone morphogenetic protein 4 (BMP4), EGF, or PDGF was unaffec

208 R-18a decreased the expression of BMP4 (bone morphogenetic protein 4) and HIF-1alpha (hypoxia-inducib

209 ecomes CDNF-dependent after exposure to bone morphogenetic protein 4.

210 ecent work has suggested that increased bone morphogenetic protein 6 (BMP6) expression could alter ce

211 Bone morphogenetic protein 6 (BMP6) signaling in hepatocytes

212 Its expression is regulated by the bone morphogenetic protein 6 (BMP6)/SMAD1/5/8 pathway and by

213 We further identify bone morphogenetic protein 7 as one of them.

214 o increased renal expression of klotho, bone morphogenetic protein 7, and Smad7.

215 othelial cell signalling in response to bone morphogenetic protein 9 (BMP9) and BMP10 is of significa

216 Bone morphogenetic protein 9 (BMP9) is a circulating factor p

217 Circulating bone morphogenetic protein 9 (BMP9), a vascular quiescence an

218 BMP9 (bone morphogenetic protein 9) is a circulating endothelial qu

219 itation-sequencing experiments on BMP9 (bone morphogenetic protein 9)-stimulated endothelial cells (E

220 We found an interaction between WNT, bone morphogenetic protein and hedgehog signalling with SFRP1

221 nhibitors, activin traps, hepcidin, and bone morphogenetic protein antagonists in treating cancer-ass

222 nels regulate release of the Drosophila bone morphogenetic protein Dpp in the developing fly wing and

223 show that the bone morphogenetic protein gradient is decoded through freque

224 alcium deposition and the expression of bone morphogenetic protein isoform (BMPs).

225 Treatment with bone morphogenetic protein or SHH pathway inhibitors decrease

226 ocaine due to severe down-modulation of bone morphogenetic protein receptor (BMPR) axis: the anti-pro

227 oallelic mutations in the gene encoding bone morphogenetic protein receptor 2 ( Bmpr2) are the main g

228 n SMC and EC contact cocultures, BMPR2 (bone morphogenetic protein receptor 2) is required by both ce

229 CLIC4 reduced BMPRII (bone morphogenetic protein receptor II) expression and signal

230 of SMAD1 by activin A receptor type 1L, bone morphogenetic protein receptor type 1A, and bone morphog

231 hogenetic protein receptor type 1A, and bone morphogenetic protein receptor type 1B and phosphorylati

232 BMPR2 (bone morphogenetic protein receptor type 2) mutations account

233 MCs from PAH patients with mutations in bone morphogenetic protein receptor type II.

234 o track the expression of a manipulated bone morphogenetic protein receptor within the Brainbow conte

235 cumulation of synaptic growth-promoting bone morphogenetic protein receptors in the cell body and cor

236 We found cell-autonomous activation of bone morphogenetic protein signaling in proprioceptor sensory

237 ur demonstration that the activation of bone morphogenetic protein signaling in proprioceptors allevi

238 ulatory hormone that is induced via the bone morphogenetic protein signaling pathway.

239 ranscriptional programs associated with bone morphogenetic protein signaling, alveolar specification,

240 /Erk1/2 signaling and downregulation of bone morphogenetic protein signaling, with negative and posit

241 axis depends on a morphogen gradient of Bone Morphogenetic Protein signaling.

242 ther by erythroferrone or by inhibiting bone morphogenetic protein signaling.

243 damage and impaired signaling of BMPR2 (bone morphogenetic protein type 2 receptor) via two downstrea

244 Heterozygous germ-line mutations in the bone morphogenetic protein type-II receptor (BMPR-II) gene un

245 ENG (endoglin) is a coreceptor for BMP (bone morphogenetic protein) 9/10 and is strongly expressed in

246 BMP9 and BMP10 (bone morphogenetic protein) are known to regulate endothelial

247 entaplegic, a homolog of the vertebrate bone morphogenetic protein) from the wing imaginal disc.

248 BMP (bone morphogenetic protein) signaling activity is precisely c

249 yclin-dependent kinase 1 decreases BMP (bone morphogenetic protein) signaling activity specifically d

250 GDF2 encodes the circulating BMP (bone morphogenetic protein) type 9, which is a ligand for the

251 Here we show that bone morphogenetic protein-1 (BMP1)/Tolloid (TLD)-like protei

252 r and C1s, sea urchin protein Uegf, and bone morphogenetic protein-1) domains (distal domains).

253 r and C1s, sea urchin protein Uegf, and bone morphogenetic protein-1) domains.

254 wth differentiation factor-9 (GDF9) and bone morphogenetic protein-15 (BMP15) are co-expressed exclus

255 y, sustained in vivo delivery of active bone morphogenetic protein-2 (BMP-2) protein to responsive ta

256 The bone marrow cryogel (BMC) releases bone morphogenetic protein-2 to recruit stromal cells and pre

257 RUNX)-2, integrin binding sialoprotein, bone morphogenetic protein-2, osteocalcin, and cementum prote

258 Here, we show that bone morphogenetic protein-4 (BMP4) blocks metastasis in anim

259 1 and Six2 regulate both endothelin and bone morphogenetic protein-4 signaling pathways to pattern th

260 Bone morphogenetic protein-9 (BMP-9) is a circulating cytokin

261 hemojuvelin and other components of the bone morphogenetic protein-signaling pathway.

262 and that they activate cardioprotective bone-morphogenetic-protein signalling in cardiomyocytes.

263 CSCs to chemotherapy and the ability of bone morphogenetic proteins (BMP) to promote colonic stem cel

264 An activating bone morphogenetic proteins (BMP) type I receptor ACVR1 (ACVR

265 Bone morphogenetic proteins (BMPs) are important mediators of

266 Bone morphogenetic proteins (BMPs) are members of the TGF-bet

267 Bone morphogenetic proteins (BMPs) are multifunctional cytoki

268 Bone morphogenetic proteins (BMPs) are secreted ligands of th

269 Bone morphogenetic proteins (BMPs) are secreted proteins that

270 K19/14 sites in the promoter regions of bone morphogenetic proteins (BMPs) genes, which were associat

271 a with an osteo-inductive agent such as bone morphogenetic proteins (BMPs) has been considered as an

272 ng involves binding to and sequestering bone morphogenetic proteins (BMPs) in the extracellular matri

273 cludes TGFbeta, activins, inhibins, and bone morphogenetic proteins (BMPs).

274 Bone morphogenetic proteins 9 and 10 (BMP9/BMP10) are circula

275 pentaplegic (dpp), the homolog of human bone morphogenetic proteins BMP2 and BMP4, is a muscle-secret

276 Bone morphogenetic proteins BMP2 and BMP6 play key roles in s

277 The BMPs (bone morphogenetic proteins) are essential morphogens in angi

278 genes such as Sox9, Col2a1, and Acan by bone morphogenetic proteins.

279 lsatile RhoA activity is thought to underlie morphogenetic ratchets, but how RhoA governs transient c

280 bor intensive and do not naturally integrate morphogenetic readouts.

281 ip formation by interacting with an impaired morphogenetic regulation that adjusts Mnp shape, or thro

282 deficiency is modified by a Pax9-dependent 'morphogenetic regulation', which modulates Mnp shape, re

283 m6A functions to enhance translation of key morphogenetic regulators, while also destabilizing senti

284 and signal transduction pathways to control morphogenetic responses in different settings.

285 These findings reveal a morphogenetic role for IRs and demonstrate the central r

286 f extant and fossil rodent teeth to identify morphogenetic rules that influence molar morphology.

287 Sonic hedgehog (SHH) is an essential morphogenetic signal that dictates cell fate decisions i

288 nd enhanced translation, particularly of key morphogenetic signaling pathways.

289 How morphogenetic signals are prepared for intercellular dis

290 only cells that can respond to hair follicle morphogenetic signals in vivo.

291 rmis and its appendages, can respond to skin morphogenetic signals.

292 use of proteins engineered with adhesive and morphogenetic solid-binding peptides is a promising rout

293 omplex subunit Hir1 decreases sensitivity to morphogenetic stimuli.

294 road differences in vertebral structures and morphogenetic strategies occur across vertebrate groups,

295 ures, bacterial lifestyles, and/or bacterial morphogenetic strategies.

296 tivating the molecular mechanisms that drive morphogenetic transformation of neurons during developme

297 ong-awaited explanation for how Ubx controls morphogenetic transformation.

298 Because retroviruses of different morphogenetic types assemble their immature particles in

299 targeting differs among distinct retroviral morphogenetic types.

300 formation starts from the midline; then the morphogenetic wave propagates bilaterally, leaving a reg