ライフサイエンスコーパス: limpet

1 es to calculate the thermal reaction norm of limpet adductor muscle fatigue.

2 o characterize the abundance and identity of limpets along the south-eastern Pacific coast from 18 de

3 ch as the more obvious outgroup, the keyhole limpet, an observation common to other DNA sequence anal

4 The present study clearly indicated that limpet, an underutilized shellfish source can benefit th

5 rt a notable example of CGP in the Antarctic limpet, an unusually tractable system where multiple con

6 species of the genus Haliotis plus a keyhole limpet and a more distantly related gastropod, the Chile

7 Complementary, ancient and modern shells of limpets and mussels were isotopically analysed to explor

8 The highest concentrations detected were in limpets and sea urchins, followed by sea stars, ascidian

9 rms of 4 closely related intertidal Nacellid limpets, Antarctic (Nacella concinna), New Zealand (Cell

10 ation, ranging from tiny pigment-cup eyes in limpets, compound eyes in ark clams and pinhole eyes in

11 unctatus), trematode parasites for a keyhole limpet (Fissurella latimarginata), and pinnotherid pea c

12 ibrillar and sarcoplasmic protein bands from limpet flesh.

13 ritional and techno-functional properties of limpets, found attached to rocks on the shores of Cornwa

14 conomically important Cape turban shells and limpets from MSA layers along the south and west coasts

15 Focusing on keyhole limpets, genera Fissurella and Diodora from Cape Verde I

16 More importantly, our study showed that limpet had good gelling properties with a high elastic m

17 150 mug GM-CSF) or control (100 mug keyhole limpet haemocyanin) via monthly intradermal injection un

18 RvIII-specific peptide conjugated to keyhole limpet haemocyanin.

19 nt antigen, 2,4-dinitrophenyl hapten-keyhole limpet hemocyanin (DNP(23)-KLH).

20 njugated to immunocyanin monomers of keyhole limpet hemocyanin (IC(KLH)) to create the MCV ICKLH-SOO9

21 d to the immunogenic carrier protein keyhole limpet hemocyanin (Id-KLH).

22 TCR Id protein conjugated to keyhole limpet hemocyanin (KLH) (TCR Id:KLH) and injected with a

23 n conjugated to the carrier protein, keyhole limpet hemocyanin (KLH) - to be capable of inducing broa

24 Fc stimulated the production of anti-keyhole limpet hemocyanin (KLH) Ab, increasing anti-KLH IgG, IgG

25 ed by five subcutaneous boosts of Id/keyhole limpet hemocyanin (KLH) administered with adjuvant.

26 lin (Ig) idiotype (Id) conjugated to keyhole limpet hemocyanin (KLH) and administered with granulocyt

27 derivative was covalently linked to keyhole limpet hemocyanin (KLH) and monophosphoryl lipid A (MPLA

28 were pulsed with 2 foreign proteins, keyhole limpet hemocyanin (KLH) and tetanus toxoid (TT), as well

29 unization with two conjugates, Tn(c)-keyhole limpet hemocyanin (KLH) and Tn(c)-palmitic acid (PAM) wi

30 -idiotypic mAb MK2-23, conjugated to keyhole limpet hemocyanin (KLH) as a carrier and given with Baci

31 nfluenza matrix peptide (Flu-MP) and keyhole limpet hemocyanin (KLH) as control antigens.

32 Subjects were fed keyhole limpet hemocyanin (KLH) before subcutaneous immunization

33 ogenicity, we bound thiolated MEP to keyhole limpet hemocyanin (KLH) by using succinimidyl-4-(N-malei

34 bodies generated to the glycoprotein keyhole limpet hemocyanin (KLH) can cross-link with reactive car

35 njugation of the glycopeptide to the keyhole limpet hemocyanin (KLH) carrier protein completed the pr

36 and conjugated to maleimide-modified keyhole limpet hemocyanin (KLH) carrier protein through backbone

37 t regions plus GM-CSF, or linkage to keyhole limpet hemocyanin (KLH) carrier protein were increasingl

38 To solve this problem, the keyhole limpet hemocyanin (KLH) conjugates of a series of GM3 de

39 Delta71-82 alphaS, human betaS, and keyhole limpet hemocyanin (KLH) control proteins induced no symp

40 Volunteers were immunized with keyhole limpet hemocyanin (KLH) first orally and then parenteral

41 lysates and the immunogenic protein keyhole limpet hemocyanin (KLH) for 24 h and then combined.

42 cally synthesized, and conjugated to keyhole limpet hemocyanin (KLH) for examining its immunogenicity

43 ition (6OXY(Gly)(4)OH) conjugated to keyhole limpet hemocyanin (KLH) has shown early proof-of-efficac

44 ntitumor immunity induced by s.c. Id-keyhole limpet hemocyanin (KLH) immunization.

45 ,4,6-trinitrophenol (TNP)-conjugated keyhole limpet hemocyanin (KLH) in a specific pathogen-free envi

46 ation with the cocaine immunogen GNC-keyhole limpet hemocyanin (KLH) in preventing cocaine self-admin

47 th influenza matrix peptide (MP) and keyhole limpet hemocyanin (KLH) in two healthy subjects.

48 Mice immunized with the Ag keyhole limpet hemocyanin (KLH) mixed with HKL generated a KLH-s

49 neration cocaine immunoconjugate GND-keyhole limpet hemocyanin (KLH) or with the anti-cocaine mAb GNC

50 comprising Id chemically coupled to keyhole limpet hemocyanin (KLH) plus granulocyte macrophage colo

51 onjugated to the immunogenic protein keyhole limpet hemocyanin (KLH) protects mice from tumor challen

52 e PI3P hapten to maleimide-activated keyhole limpet hemocyanin (KLH) provided a PI3P immunogen, which

53 hallenge of the transgenic mice with keyhole limpet hemocyanin (KLH) resulted in a decrease in anti-K

54 l models of inflammation including a keyhole limpet hemocyanin (KLH) study and a collagen-induced art

55 compounds demonstrated efficacy in a Keyhole Limpet Hemocyanin (KLH) study in rats, where the blockad

56 her conjugated to ovalbumin (OVA) or keyhole limpet hemocyanin (KLH) to enhance immunogenicity.

57 ufactured and covalently linked with keyhole limpet hemocyanin (KLH) to generate Id/KLH.

58 immunogenic foreign carrier protein keyhole limpet hemocyanin (KLH) using glutaraldehyde has shown p

59 by adding antimyeloma idiotype (Id)-keyhole limpet hemocyanin (KLH) vaccine to vaccine-specific cost

60 Keyhole limpet hemocyanin (KLH) was beneficial in earlier studie

61 ptides and to peptides conjugated to keyhole limpet hemocyanin (KLH) were characterized by their abil

62 t linker methods, to protein carrier keyhole limpet hemocyanin (KLH) were studied in mice.

63 eptide mimetics of GXM conjugated to keyhole limpet hemocyanin (KLH) with glutaraldehyde developed Ab

64 endent (TNP-LPS) or T-dependent (TNP-keyhole limpet hemocyanin (KLH)) Ag.

65 Following challenge with TNP-keyhole limpet hemocyanin (KLH), Ab production in these mice was

66 y) is conjugated to ovalbumin (OVA), keyhole limpet hemocyanin (KLH), and a bis-maleimide; KLH conjug

67 Rats were immunized with keyhole limpet hemocyanin (KLH), and blood samples were taken.

68 ainst an exogenous, nonself antigen, keyhole limpet hemocyanin (KLH), by releasing IL-4 in the microe

69 ddition of a foreign helper protein, keyhole limpet hemocyanin (KLH), can augment the efficacy of tum

70 vaged with a single dose of 20 mg of keyhole limpet hemocyanin (KLH), followed by s.c. immunization w

71 H antigen conjugated to the protein keyhole limpet hemocyanin (KLH), has been in clinical evaluation

72 d 4-6 weeks later by DCs pulsed with keyhole limpet hemocyanin (KLH), HLA-A*0201-positive restricted

73 primary response to PC conjugated to keyhole limpet hemocyanin (KLH), T15 Id(+) Abs constitute >90% o

74 typic mAb immunization protocol (mAb-keyhole limpet hemocyanin (KLH)-Calmette-Guerin bacillus (BCG),

75 However, keyhole limpet hemocyanin (KLH)-priming of IFN-gko mice readily

76 ere cocultured with HDK-1 T cells (a keyhole limpet hemocyanin (KLH)-specific CD4+ Th1 clone) in the

77 nonprotective clone (N-MoPn), and a keyhole limpet hemocyanin (KLH)-specific cell line (KLH-1).

78 nized with ovalbumin peptide or with keyhole limpet hemocyanin (KLH).

79 onjugate, 2,4,6-trinitrophenyl (TNP)-keyhole limpet hemocyanin (KLH).

80 24 to 48 h before immunization with keyhole limpet hemocyanin (KLH).

81 h ovalbumin and a secondary antigen, keyhole limpet hemocyanin (KLH).

82 oduction following immunization with keyhole limpet hemocyanin (KLH).

83 or vehicle before immunization with keyhole limpet hemocyanin (KLH).

84 recombinant HPV16/18 E7 antigens and keyhole limpet hemocyanin (KLH; an immunological tracer molecule

85 droxy-3-nitrophenyl(5) conjugated to keyhole limpet hemocyanin (NP(5)- KLH) or infected with HSV-1, a

86 se to 4-hydroxy-3-nitrophenyl acetyl-keyhole limpet hemocyanin (NP-KLH) and NP-OVA develops within ec

87 3-nitrophenyl acetyl (NP)-conjugated keyhole limpet hemocyanin (NP-KLH) or ovalbumin(323-337) peptide

88 ce primed with 2,4, 6-trinitrophenyl-keyhole limpet hemocyanin (TNP-KLH).

89 Intratumoral VVHY, VVGMCSF, and keyhole limpet hemocyanin (to produce CD4 help) generated spleni

90 to disease-inducing (TNP-conjugated keyhole limpet hemocyanin [TNP-KLH]) and disease-inhibiting (ant

91 Inhibition of anti-keyhole limpet hemocyanin Ab response was dose-dependent in FR10

92 d with nitrophenol hapten-conjugated keyhole limpet hemocyanin adsorbed to Imject aluminum hydroxide-

93 mounted a substantial Ab response to keyhole limpet hemocyanin after completion of anti-CD40L Ab trea

94 Moreover, mDCs(ICOS) pulsed with the keyhole limpet hemocyanin Ag during the maturation phase were be

95 loantigen and secondary responses to keyhole limpet hemocyanin Ag.

96 s vaccination with GM2 conjugated to keyhole limpet hemocyanin and administered with QS-21 (GMK) for

97 ginata hemocyanin in comparison with keyhole limpet hemocyanin and C. concholepas hemocyanin, which w

98 dy responses against protein antigen keyhole limpet hemocyanin and carbohydrate antigen sTn, respecti

99 CD4+ T cell sensitization to keyhole limpet hemocyanin and CD8+ T cell sensitization to MART-

100 -hydroxykynurenine (3OHKYN)-modified keyhole limpet hemocyanin and characterized it using 3OHKYN-modi

101 e responses to two soluble proteins, keyhole limpet hemocyanin and chicken egg albumin.

102 sting of tumor Ig protein coupled to keyhole limpet hemocyanin and emulsified in an immunologic adjuv

103 Th2 immune deviation induced with keyhole limpet hemocyanin and IFA did not affect corneal allogra

104 ith cytokine-matured DCs loaded with keyhole limpet hemocyanin and MHC-I alone or MHC-I/II-restricted

105 two different immunogenic carriers, keyhole limpet hemocyanin and N-alpha-palmitoyl-S-[2,3-bis(palmi

106 ral responses to the T-dependent Ags keyhole limpet hemocyanin and OVA, as well as reduced Ag-specifi

107 its production of antibodies against keyhole limpet hemocyanin and Pneumovax in mice, indicating that

108 In response to trinitrophenol (TNP)-keyhole limpet hemocyanin and tetanus/diphtheria vaccine, CD40Lt

109 mocyanin or trinitrophenylated (TNP) keyhole limpet hemocyanin and the type 2 T-independent Ags TNP-F

110 rom the hybridoma, was conjugated to keyhole limpet hemocyanin and used to immunize Balb/c mice by ad

111 f VlsE was conjugated to the carrier keyhole limpet hemocyanin and used to immunize mice.

112 assay and immunoblots using anti-AGE-keyhole limpet hemocyanin antibody, aminoguanidine inhibited glu

113 nses of L-selectin-deficient mice to keyhole limpet hemocyanin are indistinguishable from wild-type c

114 e induced after immunization with PC-keyhole limpet hemocyanin but at significantly lower levels than

115 eactive CTL, and development of anti-keyhole limpet hemocyanin CD4+ T cells, rejection of allogeneic

116 ccine, MH6, was then contrasted with keyhole limpet hemocyanin conjugate vaccine in a subsequent expe

117 immunized with the native 38C13 IgM-keyhole limpet hemocyanin conjugate vaccine.

118 (MH2[R], MH6, and MH7) or a control keyhole limpet hemocyanin conjugate vaccine.

119 ice vaccinated with the CD20 peptide keyhole limpet hemocyanin conjugates had a 25% decrease in CD19(

120 ogenicity of three synthetic globo H-keyhole limpet hemocyanin conjugates plus the immunologic adjuva

121 ice immunized with PA1 conjugated to keyhole limpet hemocyanin developed high anti-peptide (1/13,000)

122 ) propeptide [SLS(10-30)] coupled to keyhole limpet hemocyanin evoked antibodies in rabbits that comp

123 naive mice with 3H1 conjugated with keyhole limpet hemocyanin Freund's adjuvant induced humoral and

124 ctions using the standard therapy of keyhole limpet hemocyanin Id + GM-CSF.

125 -trinitrophenyl hapten conjugated to keyhole limpet hemocyanin immunization and nephritis induction.

126 -Trinitrophenyl hapten conjugated to keyhole limpet hemocyanin immunization resulted in higher affini

127 , antigen-specific IgG1 responses to keyhole limpet hemocyanin immunization, regulated CD4(+) T-cell

128 numbers of Th1 cells in response to keyhole limpet hemocyanin immunization.

129 nd in 4-hydroxy-3-nitrophenyl acetyl-keyhole limpet hemocyanin immunized animals; recall responses we

130 a T helper 2 response (ovalbumin or keyhole limpet hemocyanin in alum) and is only seen with T cell-

131 After immunization with OVA or keyhole limpet hemocyanin in CFA, NK cell-deficient (NK-T+) mice

132 , or 100,000-mug doses of intranasal keyhole limpet hemocyanin in conjunction with adjuvant intranasa

133 Efficacy experiments in a keyhole limpet hemocyanin model in rats demonstrated that admini

134 Antibodies were raised by using keyhole limpet hemocyanin modified in vitro by 4-hydroxynonenal

135 ent with a secondary Th2 response to keyhole limpet hemocyanin or A. fumagatus extract, or by intrana

136 loading immature DCs with the neoAgs keyhole limpet hemocyanin or human immunodeficiency virus-1 p24

137 ent, secondary Th2 lung responses to keyhole limpet hemocyanin or primary responses to Nippostrongylu

138 nt (TD) Ags fluorescein-labeled (FL) keyhole limpet hemocyanin or trinitrophenylated (TNP) keyhole li

139 normal and B cell-deficient mice to keyhole limpet hemocyanin over 6 mo and observed diminished IL-2

140 d Th2 responses by immunization with keyhole limpet hemocyanin plus IFA.

141 ve prepared a conjugate vaccine (GD2-keyhole limpet hemocyanin plus immunological adjuvant QS-21) tha

142 the original tumor, including (1) Id-keyhole limpet hemocyanin protein, (2) Id single-chain variable

143 s with an F(2)Pab peptide coupled to keyhole limpet hemocyanin recognized a p53(1-39) peptide phospho

144 ermore, CLEC12A-mediated delivery of keyhole limpet hemocyanin resulted in enhanced proliferation and

145 with peptide 184- 198 conjugated to keyhole limpet hemocyanin showed significant pulmonary eosinophi

146 of ghrelin as compared with Ghr2 or keyhole limpet hemocyanin vaccinated controls.

147 ed-type hypersensitivity response to keyhole limpet hemocyanin was diminished.

148 city of coupling the glycopeptide to keyhole limpet hemocyanin was examined; although both IgM and Ig

149 Abs following immunization with DNP-keyhole limpet hemocyanin was significantly decreased for all Ig

150 networks, the primary Ab response to keyhole limpet hemocyanin was unaltered over a 20-day period.

151 s to 2,4,6-trinitrophenyl-conjugated keyhole limpet hemocyanin were measured by ELISA, and presence o

152 n of high-affinity antibodies to TNP-keyhole limpet hemocyanin were severely impaired, even after ado

153 /kg iscalimab, antibody responses to keyhole limpet hemocyanin were transiently suppressed.

154 o CR3 counterligands (fibrinogen and keyhole limpet hemocyanin) by 50%, but did not affect adhesion t

155 iophage phiX 174 and nuclear protein-keyhole limpet hemocyanin) characterized by a reduction in numbe

156 ferative response to recall antigen (keyhole limpet hemocyanin) were normal.

157 moral immunity to model Ags (OVA and keyhole limpet hemocyanin), affecting all major T-dependent Ig c

158 imarginata, and Megathura crenulata (keyhole limpet hemocyanin), on cultures of peritoneal macrophage

159 Ag (keyhole limpet hemocyanin)-specific Th1/Th2 responses of fetal-d

160 by day 3 after immunization with Ars-keyhole limpet hemocyanin, (KLH) and at day 6, large clusters of

161 has been synthesized, conjugated to keyhole limpet hemocyanin, and administered with the immunologic

162 d with caffeine covalently linked to keyhole limpet hemocyanin, and recombinant antibody techniques w

163 eptides were synthesized, coupled to keyhole limpet hemocyanin, and used to produce rabbit antisera.

164 del Ag 4-hydroxy-3-nitrophenylacetyl-keyhole limpet hemocyanin, but GrB-deficient mice produced norma

165 ted from plasma of mice immunized to keyhole limpet hemocyanin, but not from naive or OVA-immunized m

166 when immunized with nitrophenylated-keyhole limpet hemocyanin, Dbc1(-/-) mice produce significantly

167 When immunized with trinitrophenyl-keyhole limpet hemocyanin, dbh-/- mice produced less Th1 cytokin

168 Immunization with DNP-keyhole limpet hemocyanin, heat-killed Brucella abortus, or infe

169 response to the T cell-dependent Ag, keyhole limpet hemocyanin, in the PDE7A(-/-) mice was found to b

170 Imaging of DNA, keyhole limpet hemocyanin, mouse monoclonal IgG, and glucose oxi

171 sponse to Pneumovax, IgG response to keyhole limpet hemocyanin, or cytokine response to LPS).

172 ent Ag, phosphocholine conjugated to keyhole limpet hemocyanin, ppc1-5 NAA B cells mounted a quick Ig

173 DCs with the foreign helper protein, keyhole limpet hemocyanin, prior to intratumoral delivery and co

174 g vaccination with the TCR linked to keyhole limpet hemocyanin, specific anti-TCR humoral responses w

175 ter immunization with trinitrophenyl-keyhole limpet hemocyanin, specific ASC could be isolated from a

176 y response to the T-dependent Ag DNP-keyhole limpet hemocyanin, the Tg mice exhibited severely impair

177 ergic sensitization to a neoantigen, keyhole limpet hemocyanin, using a unique model of human nasal a

178 oantigens, bacteriophage phiX174 and keyhole limpet hemocyanin, was also evaluated.

179 recombinant filarial protein Ags and keyhole limpet hemocyanin, we sensitized T cells from uninfected

180 xylase (GAD), but not the control Ag keyhole limpet hemocyanin, were eliminated in NODJg mu(null) mic

181 lly administered soluble protein Ag, keyhole limpet hemocyanin, were enhanced when mice were treated

182 -I, with or without conjugation with keyhole limpet hemocyanin, were fused with P3/NS1/1-Ag4-1 myelom

183 Ig fusion protein, however, enhances keyhole limpet hemocyanin- specific T-cell proliferation and 2,4

184 Mac-1 were defective in adherence to keyhole limpet hemocyanin-coated glass, iC3b-mediated phagocytos

185 ce were immunized with a cocktail of keyhole limpet hemocyanin-conjugated peptides corresponding to t

186 distinct from those generated by the keyhole limpet hemocyanin-epitope conjugates.

187 liferation and cytokine secretion by keyhole limpet hemocyanin-experienced CD4(+) T cells.

188 cific Th2 cells, lymphoid cells from keyhole limpet hemocyanin-immune mice bearing healthy corneal al

189 various preclinical models, such as keyhole limpet hemocyanin-induced Ab responses, alloantigen-indu

190 a pigs immunized intranasally with a keyhole limpet hemocyanin-linked peptide, corresponding to the p

191 ized mice, were able to suppress the keyhole limpet hemocyanin-specific delayed-type hypersensitivity

192 avalin A-stimulated spleen cells nor keyhole limpet hemocyanin-specific proliferation of spleen cells

193 h LPS or upon 6-h coculture with the keyhole limpet hemocyanin-specific Th1 clone HDK-1 in the presen

194 h of incubation with HDK-1 T cells (keyhole limpet hemocyanin-specific TH1 clone) or with 5S8 T cell

195 t were reconstituted with a clone of keyhole limpet hemocyanin-specific Th2 cells and trinitrophenyl-

196 The sera raised against keyhole limpet hemocyanin-SV1 hapten, showed binding values of 5

197 d been immunized with trinitrophenyl-keyhole limpet hemocyanin.

198 - to 81-fold) after conjugation with keyhole limpet hemocyanin.

199 thymus-dependent Ag, phosphocholine-keyhole limpet hemocyanin.

200 g immunization of male SJL mice with keyhole limpet hemocyanin.

201 was increased by conjugating them to keyhole limpet hemocyanin.

202 using FITC-labeled tetanus, OVA, and keyhole limpet hemocyanin.

203 cluding host-restricted responses to keyhole limpet hemocyanin.

204 sponse against 2,4,6 trinitro-phenyl-keyhole limpet hemocyanin.

205 pe-matched control Ig, conjugated to keyhole limpet hemocyanin.

206 e, or to oligosaccharides present on keyhole limpet hemocyanin.

207 of sLe(a) with the benchmark carrier keyhole limpet hemocyanin.

208 scending dose groups challenged with keyhole limpet hemocyanin.

209 otoxin A, as well as to the model Ag keyhole limpet hemocyanin.

210 ith the T cell-dependent (TD) Ag DNP-keyhole limpet hemocyanin.

211 similar after immunization with DNP-keyhole limpet hemocyanin.

212 to the T cell-dependent antigen TNP-keyhole limpet hemocyanin.

213 zed with UO(2)(2+)-DCP conjugated to keyhole limpet hemocyanin.

214 es were coupled with carrier protein keyhole limpet hemocyanin.

215 ymphoma immunoglobulin conjugated to keyhole limpet hemocyanin.

216 alian cell and chemically coupled to keyhole limpet hemocyanin.

217 H2 as a hapten, conjugated to BSA or keyhole limpet hemocyanin.

218 uppression of IgE in response to DNP-keyhole limpet hemocyanin/alum and Nippostrongylus brasiliensis

219 ing MoDC with conjugates of primary (keyhole limpet hemocyanin; KLH) and recall (Bet v 1) Ags (H4B4*K

220 d GH to a carrier protein, including keyhole limpet hemocyanion, diphtheria toxoid cross-reactive mat

221 phase III clinical trial vaccine, GH-keyhole limpet hemocyanion/QS21, the GH-DT/C34 vaccine elicited

222 GNE-KLH (keyhole limpet hemocyannin) was found to elicit persistent high-

223 significantly larger than turban shells and limpets in succeeding Later Stone Age (LSA) layers that

224 ely studied bioluminescent systems (those of limpet Latia, earthworms Diplocardia and Fridericia and

225 striking increases in the recruitment of owl limpets (Lottia gigantea) and volcano barnacles (Tetracl

226 the unmineralized teeth of the giant keyhole limpet (Megathura crenulata) are shown to attain a stiff

227 thin the translucent shell of the blue-rayed limpet Patella pellucida.

228 We exposed individuals of the limpet Patella vulgata Linnaeus, 1758, to realistic expe

229 he extinction of three consumer species (the limpet Patella, the periwinkle Littorina and the topshel

230 ha-FeO(OH)) present in teeth from the Common Limpet (Patella vulgata).

231 Limpet, Patella vulgata is an underutilized gastropod mo

232 sp.), stalked barnacles, limpets, peltospiroid gastropods, anemones, and a predat

233 The limpet protein can therefore be used in a food system to

234 Our study highlighted that the addition of limpet protein improved the rheological properties and g

235 The bright colour of the limpet's stripes originates from light interference in a

236 ecific locations within the continuum of the limpet's translucent protective shell ensures the vivid

237 ing or facilitating the establishment of the limpet Scurria viridula along the south-eastern Pacific

238 nts of ostrich eggshell, coral skeleton, and limpet shell.

239 2D elemental (Mg/Ca) maps of whole limpet shells (Patella caerulea) from across the Mediter

240 e artificial intelligence techniques to four limpet species that display well-defined phylogeographic

241 aving molluscs, the chiton Chaetopleura, the limpet Tectura, and the snail Lymnaea, the MAPK pathway

242 al stage of the radula, the organ from which limpet teeth originate, identifies sequential changes in

243 d modeling, we show that the leading part of limpet teeth successfully achieves this combination of p

244 elopmental processes ex vivo, where isolated limpet tissue and cells in culture generate new biomimet

245 molecular processes behind the generation of limpet tooth and establish a platform for development of

246 Here we report on the replication of limpet tooth developmental processes ex vivo, where isol

247 A biomimetic based on limpet tooth, with corresponding high-performance mechan