PMC:1142324 / 6780-7610 JSONTXT 4 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T2110 0-5 VBN denotes Based
T2112 6-8 IN denotes on
T2113 9-12 DT denotes the
T2115 13-17 NN denotes mRNA
T2116 18-30 NN denotes distribution
T2114 31-38 NN denotes pattern
T2117 38-40 , denotes ,
T2118 40-42 PRP denotes we
T2111 43-52 VBD denotes performed
T2119 53-76 JJ denotes immunohistopathological
T2120 77-85 NN denotes analysis
T2121 86-88 IN denotes of
T2122 89-92 DT denotes the
T2123 93-103 NN denotes cerebellum
T2124 104-107 CC denotes and
T2125 108-119 NN denotes hippocampus
T2126 120-131 RB denotes extensively
T2127 131-132 . denotes .
T2128 132-355 sentence denotes Despite the high level of expression of ADAM22 mRNAs in the cerebellar granule cells, granule cell layer was normally formed and Purkinje cell morphology (calbindin-staining) of the mutant mouse looked intact (Figs. 4A–D).
T2129 133-140 IN denotes Despite
T2131 141-144 DT denotes the
T2133 145-149 JJ denotes high
T2132 150-155 NN denotes level
T2134 156-158 IN denotes of
T2135 159-169 NN denotes expression
T2136 170-172 IN denotes of
T2137 173-179 NN denotes ADAM22
T2138 180-185 NNS denotes mRNAs
T2139 186-188 IN denotes in
T2140 189-192 DT denotes the
T2142 193-203 JJ denotes cerebellar
T2143 204-211 NN denotes granule
T2141 212-217 NNS denotes cells
T2144 217-219 , denotes ,
T2145 219-226 NN denotes granule
T2147 227-231 NN denotes cell
T2146 232-237 NN denotes layer
T2148 238-241 VBD denotes was
T2149 242-250 RB denotes normally
T2130 251-257 VBN denotes formed
T2150 258-261 CC denotes and
T2151 262-270 NNP denotes Purkinje
T2152 271-275 NN denotes cell
T2153 276-286 NN denotes morphology
T2155 287-288 -LRB- denotes (
T2157 288-297 NN denotes calbindin
T2158 297-298 HYPH denotes -
T2156 298-306 VBG denotes staining
T2159 306-307 -RRB- denotes )
T2160 308-310 IN denotes of
T2161 311-314 DT denotes the
T2163 315-321 NN denotes mutant
T2162 322-327 NN denotes mouse
T2154 328-334 VBD denotes looked
T2164 335-341 JJ denotes intact
T2165 342-343 -LRB- denotes (
T2167 343-348 NNS denotes Figs.
T2166 349-351 NN denotes 4A
T2168 351-352 SYM denotes
T2169 352-353 NN denotes D
T2170 353-354 -RRB- denotes )
T2171 354-355 . denotes .
T2172 355-416 sentence denotes Hippocampal formation was also normally formed (Figs. 4I–J).
T2173 356-367 JJ denotes Hippocampal
T2174 368-377 NN denotes formation
T2176 378-381 VBD denotes was
T2177 382-386 RB denotes also
T2178 387-395 RB denotes normally
T2175 396-402 VBN denotes formed
T2179 403-404 -LRB- denotes (
T2181 404-409 NNS denotes Figs.
T2180 410-412 NN denotes 4I
T2182 412-413 SYM denotes
T2183 413-414 NN denotes J
T2184 414-415 -RRB- denotes )
T2185 415-416 . denotes .
T2186 416-505 sentence denotes These results suggest that neuronal cell migration was not impaired in the mutant mouse.
T2187 417-422 DT denotes These
T2188 423-430 NNS denotes results
T2189 431-438 VBP denotes suggest
T2190 439-443 IN denotes that
T2192 444-452 JJ denotes neuronal
T2193 453-457 NN denotes cell
T2194 458-467 NN denotes migration
T2195 468-471 VBD denotes was
T2196 472-475 RB denotes not
T2191 476-484 VBN denotes impaired
T2197 485-487 IN denotes in
T2198 488-491 DT denotes the
T2200 492-498 NN denotes mutant
T2199 499-504 NN denotes mouse
T2201 504-505 . denotes .
T2202 505-709 sentence denotes Myelin-formation detected by MBP (myelin basic protein) staining of the mutant in the cerebellum (Fig. 4H) and spinal cord (Fig. 4L) was also indistinguishable with the wild-type littermate (Figs. 4G,K).
T2203 506-512 NN denotes Myelin
T2205 512-513 HYPH denotes -
T2204 513-522 NN denotes formation
T2207 523-531 VBN denotes detected
T2208 532-534 IN denotes by
T2209 535-538 NN denotes MBP
T2211 539-540 -LRB- denotes (
T2212 540-546 NN denotes myelin
T2214 547-552 JJ denotes basic
T2213 553-560 NN denotes protein
T2215 560-561 -RRB- denotes )
T2210 562-570 NN denotes staining
T2216 571-573 IN denotes of
T2217 574-577 DT denotes the
T2218 578-584 NN denotes mutant
T2219 585-587 IN denotes in
T2220 588-591 DT denotes the
T2221 592-602 NN denotes cerebellum
T2222 603-604 -LRB- denotes (
T2224 604-608 NN denotes Fig.
T2223 609-611 NN denotes 4H
T2225 611-612 -RRB- denotes )
T2226 613-616 CC denotes and
T2227 617-623 JJ denotes spinal
T2228 624-628 NN denotes cord
T2229 629-630 -LRB- denotes (
T2231 630-634 NN denotes Fig.
T2230 635-637 NN denotes 4L
T2232 637-638 -RRB- denotes )
T2206 639-642 VBD denotes was
T2233 643-647 RB denotes also
T2234 648-665 JJ denotes indistinguishable
T2235 666-670 IN denotes with
T2236 671-674 DT denotes the
T2238 675-679 JJ denotes wild
T2240 679-680 HYPH denotes -
T2239 680-684 NN denotes type
T2237 685-695 NN denotes littermate
T2241 696-697 -LRB- denotes (
T2243 697-702 NNS denotes Figs.
T2244 703-705 NN denotes 4G
T2245 705-706 , denotes ,
T2242 706-707 NN denotes K
T2246 707-708 -RRB- denotes )
T2247 708-709 . denotes .
T2248 709-830 sentence denotes In summary, we could not find any signs of abnormalities in the mutant mouse brain by the light microscopic examination.
T2249 710-712 IN denotes In
T2251 713-720 NN denotes summary
T2252 720-722 , denotes ,
T2253 722-724 PRP denotes we
T2254 725-730 MD denotes could
T2255 731-734 RB denotes not
T2250 735-739 VB denotes find
T2256 740-743 DT denotes any
T2257 744-749 NNS denotes signs
T2258 750-752 IN denotes of
T2259 753-766 NNS denotes abnormalities
T2260 767-769 IN denotes in
T2261 770-773 DT denotes the
T2263 774-780 NN denotes mutant
T2264 781-786 NN denotes mouse
T2262 787-792 NN denotes brain
T2265 793-795 IN denotes by
T2266 796-799 DT denotes the
T2268 800-805 NN denotes light
T2269 806-817 JJ denotes microscopic
T2267 818-829 NN denotes examination
T2270 829-830 . denotes .
R1193 T2110 T2111 prep Based,performed
R1194 T2112 T2110 prep on,Based
R1195 T2113 T2114 det the,pattern
R1196 T2114 T2112 pobj pattern,on
R1197 T2115 T2114 compound mRNA,pattern
R1198 T2116 T2114 compound distribution,pattern
R1199 T2117 T2111 punct ", ",performed
R1200 T2118 T2111 nsubj we,performed
R1201 T2119 T2120 amod immunohistopathological,analysis
R1202 T2120 T2111 dobj analysis,performed
R1203 T2121 T2120 prep of,analysis
R1204 T2122 T2123 det the,cerebellum
R1205 T2123 T2121 pobj cerebellum,of
R1206 T2124 T2123 cc and,cerebellum
R1207 T2125 T2123 conj hippocampus,cerebellum
R1208 T2126 T2111 advmod extensively,performed
R1209 T2127 T2111 punct .,performed
R1210 T2129 T2130 prep Despite,formed
R1211 T2131 T2132 det the,level
R1212 T2132 T2129 pobj level,Despite
R1213 T2133 T2132 amod high,level
R1214 T2134 T2132 prep of,level
R1215 T2135 T2134 pobj expression,of
R1216 T2136 T2135 prep of,expression
R1217 T2137 T2138 compound ADAM22,mRNAs
R1218 T2138 T2136 pobj mRNAs,of
R1219 T2139 T2132 prep in,level
R1220 T2140 T2141 det the,cells
R1221 T2141 T2139 pobj cells,in
R1222 T2142 T2141 amod cerebellar,cells
R1223 T2143 T2141 compound granule,cells
R1224 T2144 T2130 punct ", ",formed
R1225 T2145 T2146 compound granule,layer
R1226 T2146 T2130 nsubjpass layer,formed
R1227 T2147 T2146 compound cell,layer
R1228 T2148 T2130 auxpass was,formed
R1229 T2149 T2130 advmod normally,formed
R1230 T2150 T2130 cc and,formed
R1231 T2151 T2152 compound Purkinje,cell
R1232 T2152 T2153 compound cell,morphology
R1233 T2153 T2154 nsubj morphology,looked
R1234 T2154 T2130 conj looked,formed
R1235 T2155 T2156 punct (,staining
R1236 T2156 T2153 parataxis staining,morphology
R1237 T2157 T2156 npadvmod calbindin,staining
R1238 T2158 T2156 punct -,staining
R1239 T2159 T2156 punct ),staining
R1240 T2160 T2153 prep of,morphology
R1241 T2161 T2162 det the,mouse
R1242 T2162 T2160 pobj mouse,of
R1243 T2163 T2162 compound mutant,mouse
R1244 T2164 T2154 acomp intact,looked
R1245 T2165 T2166 punct (,4A
R1246 T2166 T2154 parataxis 4A,looked
R1247 T2167 T2166 compound Figs.,4A
R1248 T2168 T2169 punct –,D
R1249 T2169 T2166 prep D,4A
R1250 T2170 T2166 punct ),4A
R1251 T2171 T2130 punct .,formed
R1252 T2173 T2174 amod Hippocampal,formation
R1253 T2174 T2175 nsubjpass formation,formed
R1254 T2176 T2175 auxpass was,formed
R1255 T2177 T2175 advmod also,formed
R1256 T2178 T2175 advmod normally,formed
R1257 T2179 T2180 punct (,4I
R1258 T2180 T2175 parataxis 4I,formed
R1259 T2181 T2180 compound Figs.,4I
R1260 T2182 T2183 punct –,J
R1261 T2183 T2180 prep J,4I
R1262 T2184 T2180 punct ),4I
R1263 T2185 T2175 punct .,formed
R1264 T2187 T2188 det These,results
R1265 T2188 T2189 nsubj results,suggest
R1266 T2190 T2191 mark that,impaired
R1267 T2191 T2189 ccomp impaired,suggest
R1268 T2192 T2193 amod neuronal,cell
R1269 T2193 T2194 compound cell,migration
R1270 T2194 T2191 nsubjpass migration,impaired
R1271 T2195 T2191 auxpass was,impaired
R1272 T2196 T2191 neg not,impaired
R1273 T2197 T2191 prep in,impaired
R1274 T2198 T2199 det the,mouse
R1275 T2199 T2197 pobj mouse,in
R1276 T2200 T2199 compound mutant,mouse
R1277 T2201 T2189 punct .,suggest
R1278 T2203 T2204 compound Myelin,formation
R1279 T2204 T2206 nsubj formation,was
R1280 T2205 T2204 punct -,formation
R1281 T2207 T2204 acl detected,formation
R1282 T2208 T2207 prep by,detected
R1283 T2209 T2210 nmod MBP,staining
R1284 T2210 T2208 pobj staining,by
R1285 T2211 T2209 punct (,MBP
R1286 T2212 T2213 nmod myelin,protein
R1287 T2213 T2209 appos protein,MBP
R1288 T2214 T2213 amod basic,protein
R1289 T2215 T2210 punct ),staining
R1290 T2216 T2210 prep of,staining
R1291 T2217 T2218 det the,mutant
R1292 T2218 T2216 pobj mutant,of
R1293 T2219 T2204 prep in,formation
R1294 T2220 T2221 det the,cerebellum
R1295 T2221 T2219 pobj cerebellum,in
R1296 T2222 T2223 punct (,4H
R1297 T2223 T2221 parataxis 4H,cerebellum
R1298 T2224 T2223 compound Fig.,4H
R1299 T2225 T2223 punct ),4H
R1300 T2226 T2221 cc and,cerebellum
R1301 T2227 T2228 amod spinal,cord
R1302 T2228 T2221 conj cord,cerebellum
R1303 T2229 T2230 punct (,4L
R1304 T2230 T2228 parataxis 4L,cord
R1305 T2231 T2230 compound Fig.,4L
R1306 T2232 T2230 punct ),4L
R1307 T2233 T2206 advmod also,was
R1308 T2234 T2206 acomp indistinguishable,was
R1309 T2235 T2234 prep with,indistinguishable
R1310 T2236 T2237 det the,littermate
R1311 T2237 T2235 pobj littermate,with
R1312 T2238 T2239 amod wild,type
R1313 T2239 T2237 compound type,littermate
R1314 T2240 T2239 punct -,type
R1315 T2241 T2242 punct (,K
R1316 T2242 T2206 parataxis K,was
R1317 T2243 T2242 nmod Figs.,K
R1318 T2244 T2242 nmod 4G,K
R1319 T2245 T2242 punct ",",K
R1320 T2246 T2242 punct ),K
R1321 T2247 T2206 punct .,was
R1322 T2249 T2250 prep In,find
R1323 T2251 T2249 pobj summary,In
R1324 T2252 T2250 punct ", ",find
R1325 T2253 T2250 nsubj we,find
R1326 T2254 T2250 aux could,find
R1327 T2255 T2250 neg not,find
R1328 T2256 T2257 det any,signs
R1329 T2257 T2250 dobj signs,find
R1330 T2258 T2257 prep of,signs
R1331 T2259 T2258 pobj abnormalities,of
R1332 T2260 T2250 prep in,find
R1333 T2261 T2262 det the,brain
R1334 T2262 T2260 pobj brain,in
R1335 T2263 T2262 compound mutant,brain
R1336 T2264 T2262 compound mouse,brain
R1337 T2265 T2250 prep by,find
R1338 T2266 T2267 det the,examination
R1339 T2267 T2265 pobj examination,by
R1340 T2268 T2269 npadvmod light,microscopic
R1341 T2269 T2267 amod microscopic,examination
R1342 T2270 T2250 punct .,find