ライフサイエンスコーパス: neural cell adhesion molecule

1 ker A2B5 and negative for the polysialylated neural cell adhesion molecule).

2 s, it is also a component of normal tissues (neural cell adhesion molecule).

3 cell marker PSA-NCAM (polysialylated form of neural cell adhesion molecule).

4 howed the presence of polysialic acid on the neural cell adhesion molecule.

5 nin, protein gene-regulated product 9.5, and neural cell adhesion molecule.

6 -cell-specific antibodies such as desmin and neural cell adhesion molecule.

7 ession and an increase in polysialic acid on neural cell adhesion molecule.

8 n are required for nodal-related 3 to induce neural cell adhesion molecule.

9 lls treated with BMP-7, an inducer of L1 and neural cell adhesion molecule.

10 to coexpress the polysialylated form of the neural cell adhesion molecule.

11 to those of patients with mutations in L1, a neural cell adhesion molecule.

12 yuridine and fail to express cytokeratins or neural cell adhesion molecule.

13 iclin II (FasII), the Drosophila ortholog of neural cell adhesion molecule.

14 inhibiting cell adhesion mediated by the L1 neural cell adhesion molecule.

15 sitively in reduced polysialic acid (PSA) on neural cell adhesion molecules.

16 thought to be involved in the regulation of neural cell adhesion molecules.

17 ignificant amino acid sequence similarity to neural cell adhesion molecules.

18 glycosyl-phosphatidylinositol (GPI)-anchored neural cell adhesion molecules.

19 olecule (OBCAM) comprise the IgLON family of neural cell adhesion molecules.

20 ) superfamily that represents a new class of neural cell adhesion molecules.

21 c domains of all members of the L1 family of neural cell adhesion molecules.

22 was dependent on Schwann cell expression of neural cell adhesion molecule 1 (NCAM1) and ultimately p

23 We also found that miR-200c and neural cell adhesion molecule 1 (NCAM1) expression were

24 -kit, and CD34 or the neuroepithelial marker neural cell adhesion molecule 1.

25 Changes in expression of the neural cell adhesion molecule 2 (NCAM2) have been propos

26 ast cell factor, melanocyte-specific gene 2, neural cell adhesion molecule 2, potassium inwardly-rect

27 Increases in the amounts of certain neural cell adhesion molecules a day after training migh

28 ression was up-regulated in cells expressing neural cell adhesion molecule, a marker of muscle regene

29 reduced immunoreactivity for poly-sialylated neural cell adhesion molecule, a molecule that is involv

30 Mutations in the L1 neural cell adhesion molecule, a transmembrane glycoprot

31 with keratinocyte growth factor receptor and neural cell adhesion molecule and in part via interactio

32 polysialylated N-glycans expressed mainly on neural cell-adhesion molecules and known to be present i

33 luorescence-activated cell sorting with anti-neural cell adhesion molecule antibodies, and of 144 sin

34 Members of the L1 family of homophilic neural cell adhesion molecules are thought to play an im

35 gin is often coexpressed with polysialylated-neural cell adhesion molecule, beta-III-tubulin, and cal

36 Neural cell adhesion molecules (CAMs) are important play

37 Neural cell adhesion molecules (CAMs) of the immunoglobu

38 Neural cell adhesion molecules (CAMs) of the immunoglobu

39 We have previously shown that the neural cell adhesion molecule CD56 [neural cell adhesion

40 xpression of the B-cell antigen CD19 and the neural cell adhesion molecule CD56, a natural killer cel

41 nity nerve growth factor receptor (p75NGFR), neural cell adhesion molecule (CD56/N-CAM), and growth-a

42 n a recently identified BACE1 substrate, the neural cell adhesion molecule close homolog of L1 (CHL1)

43 Members of the L1 family of neural cell adhesion molecules consist of multiple extra

44 5-fold increase in phosphacan binding to the neural cell adhesion molecule contactin.

45 onstrate that the expression of MET, but not neural cell adhesion molecule, correlates significantly

46 L1 is a neural cell adhesion molecule critical for neural develo

47 lements were evaluated by localizing nestin, neural cell adhesion molecule, distalless-2 transcriptio

48 distinguished by the expression of embryonic neural cell adhesion molecule (E-NCAM) and A2B5.

49 ing our previous observations with embryonic neural cell adhesion molecule (eN-CAM).

50 Immunoreactivity to the polysialylated neural cell adhesion molecule, expressed by the majority

51 ufficient to activate neurogenin, Xebf2, and neural cell adhesion molecule expression in animal expla

52 The punc gene, encoding a member of the neural cell adhesion molecule family expressed in the de

53 CD56 is a member of the neural cell adhesion molecule family expressed on cells

54 ppressor gene on chromosome 18q21, encodes a neural cell adhesion molecule family protein that is mos

55 The DUTT1 gene is a member of the neural cell adhesion molecule family, although its wides

56 dylinositol-YFP or the basolateral PM marker neural cell adhesion molecule-GFP.

57 that polysialic acid (PSA), presented by the neural cell adhesion molecule, has a role in the maturat

58 also show that this influence depends on the neural cell adhesion molecule homolog FasciclinII.

59 Fas II is a neural cell adhesion molecule homolog that is involved i

60 molecule Fasciclin 2, the Drosophila N-CAM (neural cell adhesion molecule) homologue.

61 B4, is primarily expressed by polysialylated neural cell adhesion molecule immature neuroblasts but i

62 Undifferentiated E-NCAM+ (embryonic neural cell adhesion molecule) immunoreactive NRPs are m

63 Neural cell adhesion molecule immunoreactivity was prese

64 in and chordin, which leads to expression of neural cell adhesion molecule in animal caps.

65 l spinal cord and of the function of Ig-like neural cell adhesion molecules in the dorsal horn.

66 The homology of RPTP-kappa's ectodomain to neural cell adhesion molecules indicates potential roles

67 this study, we show that the polysialylated neural cell adhesion molecule is expressed both on the m

68 severe congenital hydrocephalus secondary to neural cell adhesion molecule L1 (L1CAM) gene mutations

69 Mutations in the gene for neural cell adhesion molecule L1 (L1CAM) result in a deb

70 ns potentially relevant to skin homeostasis: neural cell adhesion molecule L1 and dipeptidyl peptidas

71 Two proteins, the neural cell adhesion molecule L1 and dipeptidyl peptidas

72 The neural cell adhesion molecule L1 engages the spectrin-ac

73 The neural cell adhesion molecule L1 has been implicated in

74 The neural cell adhesion molecule L1 has been shown to funct

75 Neural cell adhesion molecule L1 is a cell surface glyco

76 We investigated how the neural cell adhesion molecule L1 mediates neurite outgro

77 The neural cell adhesion molecule L1 mediates the axon outgr

78 ator, glucose-6-phosphate dehydrogenase, the neural cell adhesion molecule L1, phenylalanine hydroxyl

79 The neural cell adhesion molecule L1, which is present on ax

80 onents, alpha v beta 3 can interact with the neural cell adhesion molecule L1-CAM; a member of the im

81 m disorders (FASD) in part by disrupting the neural cell adhesion molecule L1.

82 It has long been known that the neural cell adhesion molecules L1 and NCAM-180 promote n

83 ructures, the microglomeruli did not contain neural cell adhesion molecule-labeled processes.

84 regulatory factors, interleukin 8 receptor, neural cell adhesion molecule-like adhesin, and a D-type

85 ne kinase family and is characterized by its neural cell adhesion molecule-like extracellular domain.

86 ell line, Lec2, which stably expresses human neural cell adhesion molecule (N-CAM) (Lec2-NCAM), was f

87 n carboxyl terminal hydrolase (PGP 9.5), and neural cell adhesion molecule (N-CAM) all have been desc

88 entified three murine splice-variants of the neural cell adhesion molecule (N-CAM) in the complexes,

89 We previously demonstrated that the neural cell adhesion molecule (N-CAM) inhibited the prol

90 The neural cell adhesion molecule (N-CAM) inhibits astrocyte

91 opment of the vertebrate nervous system, the neural cell adhesion molecule (N-CAM) is expressed in a

92 The neural cell adhesion molecule (N-CAM) is expressed on th

93 The neural cell adhesion molecule (N-CAM) mediates cell-cell

94 The neural cell adhesion molecule (N-CAM) mediates homophili

95 Homophilic binding of the neural cell adhesion molecule (N-CAM) mediates the calci

96 ransferases that form polysialic acid in the neural cell adhesion molecule (N-CAM), although it is no

97 are a membrane-associated adhesion molecule, neural cell adhesion molecule (N-CAM), an extracellular

98 minal hydrolase (PGP 9.5), serotonin (5-HT), neural cell adhesion molecule (N-CAM), synaptic associat

99 for the lamina-specific molecules EphA4 and neural cell adhesion molecule (N-CAM).

100 nto the forebrain along nerve fibers rich in neural cell adhesion molecule (N-CAM).

101 ng reversed, apical polarities in RPE cells, neural cell adhesion molecule (N-CAM; 140-kD isoform) an

102 ns of two cell recognition molecules (CRMs), neural-cell adhesion molecule (N-CAM) and L1 antigen hav

103 Transmembrane isoforms of the neural cell adhesion molecule, N-CAM (N-CAM-140 and N-CA

104 The neural cell adhesion molecule, N-CAM, is expressed on th

105 The mechanism by which the neural cell adhesion molecule, N-CAM, mediates homophili

106 The expression of neural cell adhesion molecule, N-CAM, was assessed immun

107 In earlier studies, the neural cell adhesion molecule, N-CAM, was found to inhib

108 y regulation in vivo of the promoter for the neural cell adhesion molecule, N-CAM, we have used homol

109 We focus on the best-studied subclasses, the neural cell adhesion molecule NCAM and the L1 family of

110 We next applied FACS for the neural cell adhesion molecule NCAM on differentiated PDi

111 cid (PSA) and its major protein carrier, the neural cell adhesion molecule NCAM, play important roles

112 Prominent family members are the neural cell adhesion molecules NCAM and L1, which were t

113 Mice that lack all three major isoforms of neural cell adhesion molecule (NCAM) (180 and 140 kDa tr

114 GF2 (200 ng, i.c.v.) or the FG loop (FGL) of neural cell adhesion molecule (NCAM) (5 microg, i.c.v.)

115 ted in Gust-BDNF mice, we used antibodies to neural cell adhesion molecule (NCAM) and ATP receptor P2

116 dage development, adhesion molecules such as neural cell adhesion molecule (NCAM) and deleted in colo

117 e adhesive properties both of membrane-bound neural cell adhesion molecule (NCAM) and of other protei

118 The distribution of E-cadherin, L1, neural cell adhesion molecule (NCAM) and the polysialate

119 The neural cell adhesion molecule (NCAM) and the receptor ty

120 us express the highly polysialylated form of neural cell adhesion molecule (NCAM) as they innervate t

121 ns are modified by polysialic acid, with the neural cell adhesion molecule (NCAM) being the most abun

122 Studied predominantly on neural cell adhesion molecule (NCAM) during development

123 The polysialylation of neural cell adhesion molecule (NCAM) evolved in vertebra

124 The function of neural cell adhesion molecule (NCAM) expression in motor

125 (ii) Hox C6 and neural cell adhesion molecule (NCAM) expression in the a

126 sed axon defasciculation, but did not affect Neural Cell Adhesion Molecule (NCAM) expression or Schwa

127 pe I cells, antigen A for type II cells, and neural cell adhesion molecule (NCAM) for type III cells]

128 he polysialic acid (PSA) modification of the neural cell adhesion molecule (NCAM) has been shown to a

129 Studies have shown neural cell adhesion molecule (NCAM) homophilic binding

130 a carbohydrate predominantly carried by the neural cell adhesion molecule (NCAM) in mammals.

131 derable evidence points to an involvement of neural cell adhesion molecule (NCAM) in myoblast fusion.

132 The role of neural cell adhesion molecule (NCAM) in the development

133 ysialic acid (PSA) is typically added to the neural cell adhesion molecule (NCAM) in the Golgi by PST

134 Neural cell adhesion molecule (NCAM) is a cell surface a

135 e TrkB, the prometastatic signaling molecule neural cell adhesion molecule (NCAM) is a downstream tar

136 The neural cell adhesion molecule (NCAM) is a membrane-assoc

137 Polysialylation of the neural cell adhesion molecule (NCAM) is catalyzed by two

138 fibroblast growth factor receptor (FGFR) by neural cell adhesion molecule (NCAM) is essential for NC

139 The neural cell adhesion molecule (NCAM) is known to partici

140 The neural cell adhesion molecule (NCAM) is the major carrie

141 The neural cell adhesion molecule (NCAM) is the major substr

142 Neural cell adhesion molecule (NCAM) is the predominant

143 Polysialic acid attached to the neural cell adhesion molecule (NCAM) is thought to play

144 Polysialylation of the neural cell adhesion molecule (NCAM) is thought to play

145 Polysialylated neural cell adhesion molecule (NCAM) is thought to play

146 n formation and function in mice lacking all neural cell adhesion molecule (NCAM) isoforms or only th

147 horibosyltransferase (Hprt) locus and at the neural cell adhesion molecule (Ncam) locus located on ch

148 Polysialic acid on the neural cell adhesion molecule (NCAM) modulates cell-cell

149 The polysialic acid (PSA) moiety of the neural cell adhesion molecule (NCAM) participates in a v

150 The Neural cell adhesion molecule (NCAM) plays an important

151 The neural cell adhesion molecule (NCAM) plays an important

152 ysialic acid is a glycan modification of the neural cell adhesion molecule (NCAM) produced by the pol

153 polybasic region (PBR) that are required for neural cell adhesion molecule (NCAM) recognition and sub

154 egulation of polysialiac acid carried by the neural cell adhesion molecule (NCAM) regulates the timin

155 Neurite outgrowth mediated by the neural cell adhesion molecule (NCAM) requires the src fa

156 xpress the highly polysialylated form of the neural cell adhesion molecule (NCAM) that has been propo

157 The lateral mobility of the neural cell adhesion molecule (NCAM) was examined using

158 Among various adhesion molecules, the neural cell adhesion molecule (NCAM) was shown to contai

159 ection for 21 days) on the expression of the neural cell adhesion molecule (NCAM) were evaluated in d

160 tributes to the adhesive interactions of the neural cell adhesion molecule (NCAM), a representative o

161 on of desmin, alphaB-crystallin, dystrophin, neural cell adhesion molecule (NCAM), and CDC2 kinase.

162 ransferases that form polysialic acid in the neural cell adhesion molecule (NCAM), and these two poly

163 iclin 2 (Fas2), the Drosophila orthologue of neural cell adhesion molecule (NCAM), as a physiological

164 eactive for vimentin, alphaB-crystallin, and neural cell adhesion molecule (NCAM), but not for desmin

165 f epithelial cell adhesion molecule (EpCAM), neural cell adhesion molecule (NCAM), cytokeratin (CK) 1

166 alpha2,8-linked sialic acid expressed on the neural cell adhesion molecule (NCAM), is thought to play

167 n-1, merosin (laminin-2), neurofilament, and neural cell adhesion molecule (NCAM), it was found that

168 and fibronectin and cell surface molecules, neural cell adhesion molecule (NCAM), L1, tenascin, chon

169 ntigens, including Islet-1/2, polysialylated neural cell adhesion molecule (NCAM), neurofilaments, an

170 As a modification of the neural cell adhesion molecule (NCAM), polySia is produce

171 Antibodies to these targets, including CD56/neural cell adhesion molecule (NCAM), promoted phagocyto

172 Found predominantly on the neural cell adhesion molecule (NCAM), PSA becomes restri

173 ic acid (PSA), a homopolymer attached to the neural cell adhesion molecule (NCAM), serves as a modula

174 nd NGF-producing fibroblast grafts expressed neural cell adhesion molecule (NCAM), suggesting that NC

175 l modification is predominantly found on the neural cell adhesion molecule (NCAM), where it is synthe

176 For these studies, we used the neural cell adhesion molecule (NCAM), which was recently

177 ating muscle precursor population, including neural cell adhesion molecule (NCAM), Xenopus kit relate

178 CNS-1 is a highly invasive neural cell adhesion molecule (NCAM)-positive rat glioma

179 regeneration; (iii) increased proportion of neural cell adhesion molecule (NCAM)-positive satellite

180 tively charged glycan mainly attached to the neural cell adhesion molecule (NCAM).

181 te neuronal function in association with the neural cell adhesion molecule (NCAM).

182 and influence the adhesive properties of the neural cell adhesion molecule (NCAM).

183 s responsible for the polysialylation of the neural cell adhesion molecule (NCAM).

184 The best studied of these proteins is the neural cell adhesion molecule (NCAM).

185 etween dynein and the 180-kDa isoform of the neural cell adhesion molecule (NCAM).

186 the fifth immunoglobulin domain (Ig5) of the neural cell adhesion molecule (NCAM).

187 the polysialyltransferases (polySTs) is the neural cell adhesion molecule (NCAM).

188 Their most abundant substrate is the neural cell adhesion molecule (NCAM).

189 cally found attached to the protein scaffold neural cell adhesion molecule (NCAM).

190 l role in brain development by modifying the neural cell adhesion molecule (NCAM).

191 to be the Aplysia homolog of the vertebrate neural cell adhesion molecule (NCAM); however, whether a

192 (ZO-1 and VE-cadherin) and PVM/M stabilizing neural cell adhesion molecule (NCAM-120).

193 he extracellular region of the transmembrane neural cell adhesion molecule (NCAM-EC) is shed as a sol

194 l-cell contacts between neurons and glia via neural cell adhesion molecules (NCAM) because NCAM signi

195 ly regulated carbohydrate found primarily on neural cell adhesion molecules (NCAM) in embryonic tissu

196 We found that surface immobilized anti-neural cell adhesion molecules (NCAM) monoclonal antibod

197 e modulation of polysialic acid (polySia) on neural cell adhesion molecules (NCAM).

198 ructure of IGSF9 closely matches that of the neural cell-adhesion molecule (NCAM) subfamily, consisti

199 igate the structure of the ectodomain of the neural-cell-adhesion molecule (NCAM).

200 monoclonal antibody that binds to the CD56 (neural cell adhesion molecule [NCAM]) antigen found on c

201 (epithelial cell adhesion molecule [EpCAM], neural cell adhesion molecule [NCAM], epithelial growth

202 a2,8-polysialic acid to the N-glycans of the neural cell adhesion molecule, NCAM, is critical for bra

203 d, anti-adhesive glycan that is added to the neural cell adhesion molecule, NCAM.

204 strate for the polysialyltransferases is the neural cell adhesion molecule, NCAM.

205 art by increased polysialic acid addition to neural cell adhesion molecule (Ncam1) in response to BMP

206 that the neural cell adhesion molecule CD56 [neural cell adhesion molecule (NCAM1)] is specifically o

207 at disrupt the extracellular interactions of neural cell adhesion molecules (NCAMs) block the formati

208 that blocks an extracellular binding site of neural cell adhesion molecules (NCAMs) did not yield tim

209 rgets of developmental MeHg exposure include neural cell adhesion molecules (NCAMs), sialoglycoconjug

210 -2 are expressed by immature polysialylated neural cell adhesion molecule neuroblasts in the SVZ.

211 or their binding to two other Ig-superfamily neural cell adhesion molecules, Ng-CAM/L1 and N-CAM.

212 thought to mediate rabies virus endocytosis (neural cell adhesion molecule, nicotinic acetylcholine r

213 uded known schizophrenia risk genes, such as neural cell adhesion molecule (NRCAM) and calcium channe

214 NrCAM is a neural cell adhesion molecule of the L1 family that has

215 acid chains found in high concentrations on neural cell adhesion molecules of the human embryo and n

216 Neural cell adhesion molecules of the immunoglobulin sup

217 nt families of guidance molecules, including neural cell adhesion molecules of the immunoglobulin sup

218 The L1 family neural cell adhesion molecules play key roles in specify

219 These results together with those related to neural cell adhesion molecule polysialylation establish

220 noreactivity was observed in polysialic acid-neural cell adhesion molecule-positive migratory progeni

221 Olig2-positive, polysialylated neural cell adhesion molecule-positive, PDGF receptor al

222 GAD with the TRC protein markers gustducin, neural cell adhesion molecule, protein gene product 9.5,

223 Doublecortin (DCX) and polysialylated neural cell adhesion molecule (PSA-NCAM) are associated

224 he up- and downregulation of polysialic acid-neural cell adhesion molecule (PSA-NCAM) expression on m

225 progenitor cells that express polysialylated neural cell adhesion molecule (PSA-NCAM) from postnatal

226 The polysialylated form of the neural cell adhesion molecule (PSA-NCAM) functions broad

227 s that express high levels of polysialylated neural cell adhesion molecule (PSA-NCAM) in adult spinal

228 development, the polysialylated form of the neural cell adhesion molecule (PSA-NCAM) is expressed by

229 The polysialylated form of neural cell adhesion molecule (PSA-NCAM) is expressed by

230 The polysialylated neural cell adhesion molecule (PSA-NCAM) plays a role in

231 Co-immunoprecipitation of PSA-carrying neural cell adhesion molecule (PSA-NCAM) with MARCKS and

232 bromodeoxyuridine (BrdU) and polysialic acid-neural cell adhesion molecule (PSA-NCAM), are also posit

233 cells expressed the polysialic acid form of neural cell adhesion molecule (PSA-NCAM), characteristic

234 at express the highly polysialylated form of neural cell adhesion molecule (PSA-NCAM).

235 express the polysialic acid-rich form of the neural cell adhesion molecule (PSA-NCAM).

236 f the neuroplasticity-related polysialylated neural cell adhesion molecule (PSA-NCAM).

237 ated protein 43 (GAP-43), and polysialylated neural cell-adhesion molecule (PSA-NCAM), was examined u

238 arrangement is a feature of the L1 family of neural cell adhesion molecules related to hemolin.

239 ndent or short-range cue in concert with the neural cell adhesion molecule SAX-7/L1CAM in the skin an

240 nvolved in damage of tissues expressing CD56/neural cell adhesion molecule, such as the central nervo

241 g a voltage-gated calcium channel (alpha1A), neural cell adhesion molecule, synapsin-II, and the neur

242 ere found to be high-affinity ligands of the neural cell adhesion molecule TAG-1/axonin-1, with disso

243 t to the dermal lamina dynamically expresses neural cell adhesion molecule, tenascin-C, and other mol

244 L1 is a neural cell adhesion molecule that has been shown to hel

245 aluated alterations in expression of MET and neural cell adhesion molecule that were proposed previou

246 belongs to a functionally conserved group of neural cell adhesion molecules that are implicated in ma

247 Neuroligins (NLs) are a family of neural cell-adhesion molecules that are involved in exci

248 Interestingly, besides the neural cell adhesion molecule, the polysialyltransferase

249 vels of EphA4, EphB1, and polysialic acid on neural cell adhesion molecule, three molecules previousl

250 ber Xenopus nodal-related 3 also induces the neural cell adhesion molecule through inhibition of bone

251 omodulators to the learning rate and linking neural cell adhesion molecules to memory maintenance.

252 0, myelin-associated glycoprotein (MAG), and neural cell adhesion molecule were used to assess the st

253 e kinetic parameters of single bonds between neural cell adhesion molecules were determined from atom

254 ily of glycosylphosphatidylinositol-anchored neural cell adhesion molecules were identified and valid

255 Other neural cell adhesion molecules were not detected in the

256 teins, including members of the L1 family of neural cell adhesion molecules, with the submembranous a