PubMed:10434303
Annnotations
c_corpus
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-10 | SO:0000781 | denotes | Transgenic |
T2 | 0-15 | 10090 | denotes | Transgenic mice |
T3 | 0-15 | D008822 | denotes | Transgenic mice |
T4 | 11-15 | PR:000005054 | denotes | mice |
T6 | 11-15 | O89094 | denotes | mice |
T8 | 50-54 | SO:0000756 | denotes | cDNA |
T9 | 50-54 | D018076 | denotes | cDNA |
T14 | 120-140 | D006816 | denotes | Huntington's disease |
T15 | 120-140 | D006816 | denotes | Huntington's disease |
T18 | 155-162 | D004194 | denotes | disease |
T19 | 155-162 | D004194 | denotes | disease |
T22 | 185-211 | D019636 | denotes | neurodegenerative disorder |
T23 | 185-211 | D019636 | denotes | neurodegenerative disorder |
T24 | 315-322 | GO:0150103 | denotes | gliosis |
T25 | 315-322 | D005911 | denotes | gliosis |
T26 | 315-322 | D005911 | denotes | gliosis |
T27 | 333-345 | D005911 | denotes | astrocytosis |
T28 | 333-345 | D005911 | denotes | astrocytosis |
T29 | 367-375 | UBERON:0002435 | denotes | striatum |
T30 | 367-375 | UBERON:0005383 | denotes | striatum |
T31 | 380-395 | UBERON:0000956 | denotes | cerebral cortex |
T34 | 437-441 | D018076 | denotes | cDNA |
T33 | 437-441 | SO:0000756 | denotes | cDNA |
T35 | 442-452 | SO:0000781 | denotes | transgenic |
T36 | 442-458 | D008822 | denotes | transgenic mouse |
T39 | 575-584 | SO:0000902 | denotes | transgene |
T40 | 601-611 | P42858 | denotes | huntingtin |
T41 | 601-611 | P42859 | denotes | huntingtin |
T42 | 601-611 | P51111 | denotes | huntingtin |
T43 | 601-611 | PR:000008840 | denotes | huntingtin |
T44 | 601-611 | P51112 | denotes | huntingtin |
T45 | 639-649 | P42858 | denotes | huntingtin |
T46 | 639-649 | P42859 | denotes | huntingtin |
T47 | 639-649 | P51111 | denotes | huntingtin |
T48 | 639-649 | PR:000008840 | denotes | huntingtin |
T49 | 639-649 | P51112 | denotes | huntingtin |
T50 | 680-686 | 37565 | denotes | tandem |
T51 | 680-686 | SO:0001513 | denotes | tandem |
T52 | 729-733 | PR:P33696 | denotes | exon |
T53 | 729-733 | SO:0000147 | denotes | exon |
T54 | 741-750 | SO:0000902 | denotes | transgene |
T55 | 779-794 | D003587 | denotes | cytomegalovirus |
T56 | 795-803 | SO:0000167 | denotes | promoter |
T57 | 822-832 | SO:0000781 | denotes | transgenic |
T58 | 822-838 | D008822 | denotes | transgenic mouse |
T61 | 870-879 | SO:0000804 | denotes | construct |
T62 | 899-909 | SO:0000781 | denotes | transgenic |
T63 | 1013-1016 | CVCL_D569 | denotes | CAG |
T64 | 1017-1023 | SO:0001068 | denotes | repeat |
T65 | 1120-1129 | SO:0000902 | denotes | transgene |
T66 | 1230-1239 | SO:0000902 | denotes | transgene |
T67 | 1243-1248 | UBERON:6110636 | denotes | brain |
T68 | 1243-1248 | UBERON:0000955 | denotes | brain |
T69 | 1257-1263 | UBERON:0002106 | denotes | spleen |
T70 | 1265-1271 | UBERON:0002113 | denotes | kidney |
T71 | 1273-1277 | UBERON:0002048 | denotes | lung |
T72 | 1279-1284 | UBERON:0002107 | denotes | liver |
T73 | 1289-1295 | UBERON:0000991 | denotes | gonads |
T74 | 1355-1364 | UBERON:0000955 | denotes | the brain |
T77 | 1366-1375 | SO:0000902 | denotes | transgene |
T78 | 1400-1415 | UBERON:0000956 | denotes | cerebral cortex |
T80 | 1417-1425 | UBERON:0002435 | denotes | striatum |
T81 | 1417-1425 | UBERON:0005383 | denotes | striatum |
T82 | 1427-1438 | UBERON:0002421 | denotes | hippocampus |
T83 | 1427-1438 | UBERON:0001954 | denotes | hippocampus |
T84 | 1427-1438 | UBERON:0002961 | denotes | hippocampus |
T85 | 1443-1453 | UBERON:0002037 | denotes | cerebellum |
T86 | 1473-1482 | SO:0000902 | denotes | transgene |
T87 | 1524-1529 | 10090 | denotes | mouse |
T88 | 1524-1529 | D051379 | denotes | mouse |
T89 | 1530-1540 | P42858 | denotes | huntingtin |
T90 | 1530-1540 | P42859 | denotes | huntingtin |
T91 | 1530-1540 | P51111 | denotes | huntingtin |
T92 | 1530-1540 | PR:000008840 | denotes | huntingtin |
T93 | 1530-1540 | P51112 | denotes | huntingtin |
T94 | 1569-1573 | PR:000005054 | denotes | mice |
T96 | 1569-1573 | O89094 | denotes | mice |
T95 | 1569-1573 | D051379 | denotes | mice |
T97 | 1569-1573 | 10095 | denotes | mice |
T98 | 1594-1597 | CVCL_D569 | denotes | CAG |
T100 | 1718-1723 | UBERON:0002100 | denotes | trunk |
T101 | 1718-1723 | UBERON:0014479 | denotes | trunk |
T99 | 1718-1723 | GO:0043198 | denotes | trunk |
T103 | 1753-1757 | PR:Q5TJ57 | denotes | fore |
T102 | 1753-1757 | CVCL_E667 | denotes | fore |
T104 | 1841-1845 | PR:000005054 | denotes | mice |
T106 | 1841-1845 | O89094 | denotes | mice |
T105 | 1841-1845 | D051379 | denotes | mice |
T107 | 1841-1845 | 10095 | denotes | mice |
T108 | 1856-1878 | D006948 | denotes | hyperkinetic movements |
T109 | 1856-1878 | D006948 | denotes | hyperkinetic movements |
T110 | 1951-1960 | GO:0007610 | denotes | behaviour |
T112 | 2122-2126 | PR:Q9V853 | denotes | lack |
T113 | 2165-2174 | GO:0051235 | denotes | retention |
T114 | 2270-2277 | D004194 | denotes | disease |
T115 | 2270-2277 | D004194 | denotes | disease |
T116 | 2311-2315 | PR:000005054 | denotes | mice |
T118 | 2311-2315 | O89094 | denotes | mice |
T117 | 2311-2315 | D051379 | denotes | mice |
T119 | 2311-2315 | 10095 | denotes | mice |
T120 | 2386-2390 | PR:000005054 | denotes | mice |
T122 | 2386-2390 | O89094 | denotes | mice |
T121 | 2386-2390 | D051379 | denotes | mice |
T123 | 2386-2390 | 10095 | denotes | mice |
T124 | 2579-2587 | UBERON:0002435 | denotes | striatum |
T125 | 2579-2587 | UBERON:0005383 | denotes | striatum |
T126 | 2589-2604 | UBERON:0000956 | denotes | cerebral cortex |
T128 | 2606-2614 | UBERON:0001897 | denotes | thalamus |
T129 | 2619-2630 | UBERON:0002421 | denotes | hippocampus |
T130 | 2619-2630 | UBERON:0001954 | denotes | hippocampus |
T131 | 2619-2630 | UBERON:0002961 | denotes | hippocampus |
T132 | 2678-2688 | GO:0008219 | denotes | cell death |
T133 | 2698-2703 | UBERON:6110636 | denotes | brain |
T134 | 2698-2703 | UBERON:0000955 | denotes | brain |
T135 | 2824-2832 | UBERON:0002435 | denotes | striatum |
T136 | 2824-2832 | UBERON:0005383 | denotes | striatum |
T137 | 2836-2840 | PR:000005054 | denotes | mice |
T139 | 2836-2840 | O89094 | denotes | mice |
T138 | 2836-2840 | D051379 | denotes | mice |
T140 | 2836-2840 | 10095 | denotes | mice |
T141 | 2890-2902 | D005911 | denotes | astrocytosis |
T142 | 2890-2902 | D005911 | denotes | astrocytosis |
T143 | 2956-2969 | C097188 | denotes | Polyglutamine |
T144 | 2956-2969 | C097188 | denotes | Polyglutamine |
T145 | 3142-3147 | UBERON:6110636 | denotes | brain |
T146 | 3142-3147 | UBERON:0000955 | denotes | brain |
T147 | 3220-3233 | C097188 | denotes | polyglutamine |
T148 | 3220-3233 | C097188 | denotes | polyglutamine |
T149 | 3349-3358 | SO:0000817 | denotes | wild-type |
T150 | 3363-3373 | SO:0000781 | denotes | transgenic |
T151 | 3363-3381 | D030801 | denotes | transgenic animals |
T152 | 3390-3393 | CVCL_D569 | denotes | CAG |
T153 | 3485-3489 | PR:000005054 | denotes | mice |
T155 | 3485-3489 | O89094 | denotes | mice |
T154 | 3485-3489 | D051379 | denotes | mice |
T156 | 3485-3489 | 10095 | denotes | mice |
T157 | 3513-3516 | CVCL_D569 | denotes | CAG |
T158 | 3517-3523 | SO:0001068 | denotes | repeat |
T159 | 3564-3567 | CVCL_D569 | denotes | CAG |
T160 | 3568-3574 | SO:0001068 | denotes | repeat |
T161 | 3641-3653 | GO:0009405 | denotes | pathogenesis |
T162 | 3752-3758 | SO:0001068 | denotes | repeat |
PMID_GLOBAL
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 47-49 | DiseaseOrPhenotypicFeature | denotes | HD | 0007739 |
T2 | 120-140 | DiseaseOrPhenotypicFeature | denotes | Huntington's disease | 0007739 |
T3 | 142-162 | DiseaseOrPhenotypicFeature | denotes | Huntington's disease | 0007739 |
T4 | 164-166 | DiseaseOrPhenotypicFeature | denotes | HD | 0007739 |
T5 | 422-424 | DiseaseOrPhenotypicFeature | denotes | HD | 0007739 |
T6 | 499-501 | DiseaseOrPhenotypicFeature | denotes | HD | 0007739 |
T7 | 948-950 | DiseaseOrPhenotypicFeature | denotes | HD | 0007739 |
T8 | 1273-1277 | DiseaseOrPhenotypicFeature | denotes | lung | 0021117 |
T9 | 3185-3187 | DiseaseOrPhenotypicFeature | denotes | HD | 0007739 |
T10 | 3293-3295 | DiseaseOrPhenotypicFeature | denotes | HD | 0007739 |
T11 | 3638-3640 | DiseaseOrPhenotypicFeature | denotes | HD | 0007739 |
PubmedHPO
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 250-274 | HP_0000708 | denotes | psychiatric disturbances |
T2 | 297-310 | HP_0002529 | denotes | neuronal loss |
T3 | 315-322 | HP_0002171 | denotes | gliosis |
T4 | 333-345 | HP_0002446 | denotes | astrocytosis |
T5 | 2495-2508 | HP_0002529 | denotes | neuronal loss |
T6 | 2539-2556 | HP_0002180 | denotes | neurodegeneration |
T7 | 2890-2902 | HP_0002446 | denotes | astrocytosis |
T8 | 2928-2945 | HP_0002180 | denotes | neurodegeneration |
T9 | 3276-3289 | HP_0002529 | denotes | neuronal loss |
UseCases_ArguminSci_Discourse
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T8 | 881-1035 | DRI_Approach | denotes | An additional six transgenic lines were obtained using full-length HD constructs that have been modified to include either 48 or 89 CAG repeat expansions. |
T1 | 0-141 | DRI_Challenge | denotes | Transgenic mice expressing mutated full-length HD cDNA: a paradigm for locomotor changes and selective neuronal loss in Huntington's disease. |
T2 | 142-396 | DRI_Challenge | denotes | Huntington's disease (HD) is a progressive neurodegenerative disorder characterized clinically by motor and psychiatric disturbances and pathologically by neuronal loss and gliosis (reactive astrocytosis) particularly in the striatum and cerebral cortex. |
T3 | 397-502 | DRI_Approach | denotes | We have recently created HD full-length cDNA transgenic mouse models that may serve as a paradigm for HD. |
T4 | 503-570 | DRI_Background | denotes | A more detailed characterization of these models is presented here. |
T5 | 571-736 | DRI_Background | denotes | The transgene encoding normal huntingtin consists of 9417 bp of the huntingtin coding sequences including 16 tandem CAGs coding for polyglutamines as part of exon 1. |
T6 | 737-804 | DRI_Approach | denotes | The transgene is driven by a heterologous cytomegalovirus promoter. |
T7 | 805-880 | DRI_Approach | denotes | Five independent transgenic mouse lines were obtained using this construct. |
T9 | 1036-1200 | DRI_Outcome | denotes | Southern blot and densitometric analyses indicated unique integration sites for the transgene in each of the lines with a copy number ranging from two to 22 copies. |
T10 | 1201-1351 | DRI_Background | denotes | Widespread expression of the transgene in brain, heart, spleen, kidney, lung, liver and gonads from each line was determined by Western blot analyses. |
T11 | 1352-1454 | DRI_Background | denotes | In the brain, transgene expression was found in cerebral cortex, striatum, hippocampus and cerebellum. |
T12 | 1455-1547 | DRI_Outcome | denotes | Expression of the transgene was as much as five times the endogenous mouse huntingtin level. |
T13 | 1548-1663 | DRI_Outcome | denotes | Phenotypically, only mice expressing 48 or 89 CAG repeats manifested progressive behavioural and motor dysfunction. |
T14 | 1664-1820 | DRI_Background | denotes | Early behavioural abnormalities were characterized by trunk curling and clasping of both fore- and hindlimbs when the animals were suspended by their tails. |
T15 | 1821-2028 | DRI_Background | denotes | Subsequently, these mice exhibited hyperkinetic movements, including heightened exploratory activities, unidirectional rotational behaviour, backflipping and excessive grooming that lasted for several weeks. |
T16 | 2029-2158 | DRI_Background | denotes | Eventually, the animals progressed to a hypokinetic phase consisting of slowed movements and lack of response to sensory stimuli. |
T17 | 2159-2245 | DRI_Background | denotes | Urine retention or incontinence was also a prominent feature of the hypokinetic phase. |
T18 | 2246-2352 | DRI_Approach | denotes | At the end stage of the disease process, HD48(B,D) and HD89(A-C) mice became akinetic just prior to death. |
T19 | 2353-2527 | DRI_Background | denotes | Neuropathological examination of mice at various stages indicated that it was only during the hypokinetic phase and thereafter when selective neuronal loss was most apparent. |
T20 | 2528-2631 | DRI_Background | denotes | Regions of neurodegeneration and loss included the striatum, cerebral cortex, thalamus and hippocampus. |
T21 | 2632-2712 | DRI_Background | denotes | TUNEL staining indicated an apoptotic mode of cell death in these brain regions. |
T22 | 2713-2880 | DRI_Outcome | denotes | Comparative neuronal counts after Nissl staining showed as much as 20% loss of small and medium neurons in the striatum in mice at the hypokinetic and akinetic stages. |
T23 | 2881-2955 | DRI_Background | denotes | Reactive astrocytosis accompanied the areas of neurodegeneration and loss. |
T24 | 2956-3188 | DRI_Background | denotes | Polyglutamine aggregates in the form of neuronal intranuclear inclusions and diffuse nuclear and perinuclear aggregations were found in a small percentage of neurons, including those in brain regions that are typically spared in HD. |
T25 | 3189-3296 | DRI_Outcome | denotes | This observation suggests that polyglutamine aggregates may not be sufficient to cause neuronal loss in HD. |
T26 | 3297-3534 | DRI_Outcome | denotes | In both behavioural and neuropathological analyses, wild-type and transgenic animals with 16 CAG repeats were indistinguishable from each other and do not exhibit the changes observed for mice carrying the 48 and 89 CAG repeat mutations. |
T27 | 3535-3769 | DRI_Challenge | denotes | Thus, animals expressing the CAG repeat expansions appear to represent clinically analogous models for HD pathogenesis, and may also provide insights into the underlying pathophysiological mechanisms of other triplet repeat disorders. |
PubMed_ArguminSci
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 142-396 | DRI_Challenge | denotes | Huntington's disease (HD) is a progressive neurodegenerative disorder characterized clinically by motor and psychiatric disturbances and pathologically by neuronal loss and gliosis (reactive astrocytosis) particularly in the striatum and cerebral cortex. |
T2 | 397-502 | DRI_Approach | denotes | We have recently created HD full-length cDNA transgenic mouse models that may serve as a paradigm for HD. |
T3 | 503-570 | DRI_Background | denotes | A more detailed characterization of these models is presented here. |
T4 | 571-736 | DRI_Background | denotes | The transgene encoding normal huntingtin consists of 9417 bp of the huntingtin coding sequences including 16 tandem CAGs coding for polyglutamines as part of exon 1. |
T5 | 737-804 | DRI_Approach | denotes | The transgene is driven by a heterologous cytomegalovirus promoter. |
T6 | 805-880 | DRI_Approach | denotes | Five independent transgenic mouse lines were obtained using this construct. |
T7 | 881-1035 | DRI_Approach | denotes | An additional six transgenic lines were obtained using full-length HD constructs that have been modified to include either 48 or 89 CAG repeat expansions. |
T8 | 1036-1200 | DRI_Outcome | denotes | Southern blot and densitometric analyses indicated unique integration sites for the transgene in each of the lines with a copy number ranging from two to 22 copies. |
T9 | 1201-1351 | DRI_Background | denotes | Widespread expression of the transgene in brain, heart, spleen, kidney, lung, liver and gonads from each line was determined by Western blot analyses. |
T10 | 1352-1454 | DRI_Background | denotes | In the brain, transgene expression was found in cerebral cortex, striatum, hippocampus and cerebellum. |
T11 | 1455-1547 | DRI_Outcome | denotes | Expression of the transgene was as much as five times the endogenous mouse huntingtin level. |
T12 | 1548-1663 | DRI_Outcome | denotes | Phenotypically, only mice expressing 48 or 89 CAG repeats manifested progressive behavioural and motor dysfunction. |
T13 | 1664-1820 | DRI_Background | denotes | Early behavioural abnormalities were characterized by trunk curling and clasping of both fore- and hindlimbs when the animals were suspended by their tails. |
T14 | 1821-2028 | DRI_Background | denotes | Subsequently, these mice exhibited hyperkinetic movements, including heightened exploratory activities, unidirectional rotational behaviour, backflipping and excessive grooming that lasted for several weeks. |
T15 | 2029-2158 | DRI_Background | denotes | Eventually, the animals progressed to a hypokinetic phase consisting of slowed movements and lack of response to sensory stimuli. |
T16 | 2159-2245 | DRI_Background | denotes | Urine retention or incontinence was also a prominent feature of the hypokinetic phase. |
T17 | 2246-2352 | DRI_Approach | denotes | At the end stage of the disease process, HD48(B,D) and HD89(A-C) mice became akinetic just prior to death. |
T18 | 2353-2527 | DRI_Background | denotes | Neuropathological examination of mice at various stages indicated that it was only during the hypokinetic phase and thereafter when selective neuronal loss was most apparent. |
T19 | 2528-2631 | DRI_Background | denotes | Regions of neurodegeneration and loss included the striatum, cerebral cortex, thalamus and hippocampus. |
T20 | 2632-2712 | DRI_Background | denotes | TUNEL staining indicated an apoptotic mode of cell death in these brain regions. |
T21 | 2713-2880 | DRI_Outcome | denotes | Comparative neuronal counts after Nissl staining showed as much as 20% loss of small and medium neurons in the striatum in mice at the hypokinetic and akinetic stages. |
T22 | 2881-2955 | DRI_Background | denotes | Reactive astrocytosis accompanied the areas of neurodegeneration and loss. |
T23 | 2956-3188 | DRI_Background | denotes | Polyglutamine aggregates in the form of neuronal intranuclear inclusions and diffuse nuclear and perinuclear aggregations were found in a small percentage of neurons, including those in brain regions that are typically spared in HD. |
T24 | 3189-3296 | DRI_Outcome | denotes | This observation suggests that polyglutamine aggregates may not be sufficient to cause neuronal loss in HD. |
T25 | 3297-3534 | DRI_Outcome | denotes | In both behavioural and neuropathological analyses, wild-type and transgenic animals with 16 CAG repeats were indistinguishable from each other and do not exhibit the changes observed for mice carrying the 48 and 89 CAG repeat mutations. |
T26 | 3535-3769 | DRI_Challenge | denotes | Thus, animals expressing the CAG repeat expansions appear to represent clinically analogous models for HD pathogenesis, and may also provide insights into the underlying pathophysiological mechanisms of other triplet repeat disorders. |