PMC:509305 / 21801-23349 JSONTXT 5 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T13555 0-5 EX denotes There
T13556 6-8 VBZ denotes is
T13557 9-21 VBG denotes accumulating
T13558 22-30 NN denotes evidence
T13559 31-35 IN denotes that
T13561 36-46 NN denotes background
T13562 47-52 NNS denotes genes
T13563 53-56 MD denotes may
T13560 57-66 VB denotes influence
T13564 67-70 DT denotes the
T13565 71-81 NN denotes expression
T13566 82-84 IN denotes of
T13567 85-97 NN denotes autoimmunity
T13568 98-100 IN denotes in
T13569 101-105 NN denotes gene
T13571 105-106 HYPH denotes -
T13570 106-114 VBN denotes targeted
T13572 115-119 NNS denotes mice
T13573 119-120 . denotes .
T13574 120-280 sentence denotes Here we report what is to our knowledge the first systematic study that has examined this in the 129 and C57BL/6 mouse strains, widely used for gene targeting.
T13575 121-125 RB denotes Here
T13577 126-128 PRP denotes we
T13576 129-135 VBP denotes report
T13578 136-140 WP denotes what
T13579 141-143 VBZ denotes is
T13580 144-146 IN denotes to
T13581 147-150 PRP$ denotes our
T13582 151-160 NN denotes knowledge
T13583 161-164 DT denotes the
T13585 165-170 JJ denotes first
T13586 171-181 JJ denotes systematic
T13584 182-187 NN denotes study
T13587 188-192 WDT denotes that
T13589 193-196 VBZ denotes has
T13588 197-205 VBN denotes examined
T13590 206-210 DT denotes this
T13591 211-213 IN denotes in
T13592 214-217 DT denotes the
T13594 218-221 CD denotes 129
T13595 222-225 CC denotes and
T13596 226-231 NN denotes C57BL
T13597 231-232 HYPH denotes /
T13598 232-233 CD denotes 6
T13599 234-239 NN denotes mouse
T13593 240-247 NNS denotes strains
T13600 247-249 , denotes ,
T13601 249-255 RB denotes widely
T13602 256-260 VBN denotes used
T13603 261-264 IN denotes for
T13604 265-269 NN denotes gene
T13605 270-279 NN denotes targeting
T13606 279-280 . denotes .
T13607 280-480 sentence denotes Our results demonstrate interacting loci between 129 and C57BL/6 mice that can cause the expression of a powerful autoimmune phenotype in these animals, in the absence of any gene-targeted mutations.
T13608 281-284 PRP$ denotes Our
T13609 285-292 NNS denotes results
T13610 293-304 VBP denotes demonstrate
T13611 305-316 VBG denotes interacting
T13612 317-321 NNS denotes loci
T13613 322-329 IN denotes between
T13614 330-333 CD denotes 129
T13616 334-337 CC denotes and
T13617 338-343 NN denotes C57BL
T13618 343-344 HYPH denotes /
T13619 344-345 CD denotes 6
T13615 346-350 NNS denotes mice
T13620 351-355 WDT denotes that
T13622 356-359 MD denotes can
T13621 360-365 VB denotes cause
T13623 366-369 DT denotes the
T13624 370-380 NN denotes expression
T13625 381-383 IN denotes of
T13626 384-385 DT denotes a
T13628 386-394 JJ denotes powerful
T13629 395-405 JJ denotes autoimmune
T13627 406-415 NN denotes phenotype
T13630 416-418 IN denotes in
T13631 419-424 DT denotes these
T13632 425-432 NNS denotes animals
T13633 432-434 , denotes ,
T13634 434-436 IN denotes in
T13635 437-440 DT denotes the
T13636 441-448 NN denotes absence
T13637 449-451 IN denotes of
T13638 452-455 DT denotes any
T13640 456-460 NN denotes gene
T13642 460-461 HYPH denotes -
T13641 461-469 VBN denotes targeted
T13639 470-479 NNS denotes mutations
T13643 479-480 . denotes .
T13644 480-675 sentence denotes We also developed a congenic mouse strain bearing a portion of 129 Chromosome 1 on a C57BL/6 background and showed that this wild-type congenic line expressed striking anti-nuclear autoimmunity.
T13645 481-483 PRP denotes We
T13647 484-488 RB denotes also
T13646 489-498 VBD denotes developed
T13648 499-500 DT denotes a
T13650 501-509 JJ denotes congenic
T13651 510-515 NN denotes mouse
T13649 516-522 NN denotes strain
T13652 523-530 VBG denotes bearing
T13653 531-532 DT denotes a
T13654 533-540 NN denotes portion
T13655 541-543 IN denotes of
T13656 544-547 CD denotes 129
T13657 548-558 NN denotes Chromosome
T13658 559-560 CD denotes 1
T13659 561-563 IN denotes on
T13660 564-565 DT denotes a
T13662 566-571 NN denotes C57BL
T13663 571-572 HYPH denotes /
T13664 572-573 CD denotes 6
T13661 574-584 NN denotes background
T13665 585-588 CC denotes and
T13666 589-595 VBD denotes showed
T13667 596-600 IN denotes that
T13669 601-605 DT denotes this
T13671 606-610 JJ denotes wild
T13673 610-611 HYPH denotes -
T13672 611-615 NN denotes type
T13674 616-624 JJ denotes congenic
T13670 625-629 NN denotes line
T13668 630-639 VBD denotes expressed
T13675 640-648 JJ denotes striking
T13677 649-661 JJ denotes anti-nuclear
T13676 662-674 NN denotes autoimmunity
T13678 674-675 . denotes .
T13679 675-1034 sentence denotes By comparing this Chromosome 1 congenic strain with matched congenic mice lacking the Apcs gene, we demonstrated that serum amyloid P component deficiency influences the severity of glomerulonephritis, but is not the prime mover in the induction of anti-nuclear autoimmunity, contrary to our own original interpretation of our data (Bickerstaff et al. 1999).
T13680 676-678 IN denotes By
T13682 679-688 VBG denotes comparing
T13683 689-693 DT denotes this
T13685 694-704 NN denotes Chromosome
T13686 705-706 CD denotes 1
T13687 707-715 JJ denotes congenic
T13684 716-722 NN denotes strain
T13688 723-727 IN denotes with
T13689 728-735 VBN denotes matched
T13691 736-744 JJ denotes congenic
T13690 745-749 NNS denotes mice
T13692 750-757 VBG denotes lacking
T13693 758-761 DT denotes the
T13695 762-766 NN denotes Apcs
T13694 767-771 NN denotes gene
T13696 771-773 , denotes ,
T13697 773-775 PRP denotes we
T13681 776-788 VBD denotes demonstrated
T13698 789-793 IN denotes that
T13700 794-799 NN denotes serum
T13702 800-807 NN denotes amyloid
T13703 808-809 NN denotes P
T13701 810-819 NN denotes component
T13704 820-830 NN denotes deficiency
T13699 831-841 VBZ denotes influences
T13705 842-845 DT denotes the
T13706 846-854 NN denotes severity
T13707 855-857 IN denotes of
T13708 858-876 NN denotes glomerulonephritis
T13709 876-878 , denotes ,
T13710 878-881 CC denotes but
T13711 882-884 VBZ denotes is
T13712 885-888 RB denotes not
T13713 889-892 DT denotes the
T13715 893-898 JJ denotes prime
T13714 899-904 NN denotes mover
T13716 905-907 IN denotes in
T13717 908-911 DT denotes the
T13718 912-921 NN denotes induction
T13719 922-924 IN denotes of
T13720 925-937 JJ denotes anti-nuclear
T13721 938-950 NN denotes autoimmunity
T13722 950-952 , denotes ,
T13723 952-960 JJ denotes contrary
T13724 961-963 IN denotes to
T13725 964-967 PRP$ denotes our
T13727 968-971 JJ denotes own
T13728 972-980 JJ denotes original
T13726 981-995 NN denotes interpretation
T13729 996-998 IN denotes of
T13730 999-1002 PRP$ denotes our
T13731 1003-1007 NNS denotes data
T13732 1008-1009 -LRB- denotes (
T13733 1009-1020 NNP denotes Bickerstaff
T13734 1021-1023 FW denotes et
T13735 1024-1027 FW denotes al.
T13736 1028-1032 CD denotes 1999
T13737 1032-1033 -RRB- denotes )
T13738 1033-1034 . denotes .
T13739 1034-1349 sentence denotes The same consideration applies to other genes located in the same Chromosome 1 region that have been implicated in the development of SLE when inactivated by gene-targeting in 129 embryonic stem cells and then backcrossed onto a pure genetic background (Bolland and Ravetch 2000; Miwa et al. 2002; Wu et al. 2002).
T13740 1035-1038 DT denotes The
T13742 1039-1043 JJ denotes same
T13741 1044-1057 NN denotes consideration
T13743 1058-1065 VBZ denotes applies
T13744 1066-1068 IN denotes to
T13745 1069-1074 JJ denotes other
T13746 1075-1080 NNS denotes genes
T13747 1081-1088 VBN denotes located
T13748 1089-1091 IN denotes in
T13749 1092-1095 DT denotes the
T13751 1096-1100 JJ denotes same
T13752 1101-1111 NN denotes Chromosome
T13753 1112-1113 CD denotes 1
T13750 1114-1120 NN denotes region
T13754 1121-1125 WDT denotes that
T13756 1126-1130 VBP denotes have
T13757 1131-1135 VBN denotes been
T13755 1136-1146 VBN denotes implicated
T13758 1147-1149 IN denotes in
T13759 1150-1153 DT denotes the
T13760 1154-1165 NN denotes development
T13761 1166-1168 IN denotes of
T13762 1169-1172 NN denotes SLE
T13763 1173-1177 WRB denotes when
T13764 1178-1189 VBN denotes inactivated
T13765 1190-1192 IN denotes by
T13766 1193-1197 NN denotes gene
T13767 1197-1198 HYPH denotes -
T13768 1198-1207 VBG denotes targeting
T13769 1208-1210 IN denotes in
T13770 1211-1214 CD denotes 129
T13772 1215-1224 JJ denotes embryonic
T13773 1225-1229 NN denotes stem
T13771 1230-1235 NNS denotes cells
T13774 1236-1239 CC denotes and
T13775 1240-1244 RB denotes then
T13776 1245-1256 VBD denotes backcrossed
T13777 1257-1261 IN denotes onto
T13778 1262-1263 DT denotes a
T13780 1264-1268 JJ denotes pure
T13781 1269-1276 JJ denotes genetic
T13779 1277-1287 NN denotes background
T13782 1288-1289 -LRB- denotes (
T13783 1289-1296 NNP denotes Bolland
T13784 1297-1300 CC denotes and
T13785 1301-1308 NNP denotes Ravetch
T13786 1309-1313 CD denotes 2000
T13787 1313-1314 : denotes ;
T13788 1315-1319 NNP denotes Miwa
T13789 1320-1322 FW denotes et
T13790 1323-1326 FW denotes al.
T13791 1327-1331 CD denotes 2002
T13792 1331-1332 : denotes ;
T13793 1333-1335 NNP denotes Wu
T13794 1336-1338 FW denotes et
T13795 1339-1342 FW denotes al.
T13796 1343-1347 CD denotes 2002
T13797 1347-1348 -RRB- denotes )
T13798 1348-1349 . denotes .
T13799 1349-1548 sentence denotes For each, there has to be a question as to whether the anti-nuclear autoimmunity is due to the gene-targeted mutant gene or to the normal 129 genes expressed in the same region as the targeted gene.
T13800 1350-1353 IN denotes For
T13802 1354-1358 DT denotes each
T13803 1358-1360 , denotes ,
T13804 1360-1365 EX denotes there
T13801 1366-1369 VBZ denotes has
T13805 1370-1372 TO denotes to
T13806 1373-1375 VB denotes be
T13807 1376-1377 DT denotes a
T13808 1378-1386 NN denotes question
T13809 1387-1389 IN denotes as
T13810 1390-1392 IN denotes to
T13811 1393-1400 IN denotes whether
T13813 1401-1404 DT denotes the
T13815 1405-1417 JJ denotes anti-nuclear
T13814 1418-1430 NN denotes autoimmunity
T13812 1431-1433 VBZ denotes is
T13816 1434-1437 IN denotes due
T13817 1438-1440 IN denotes to
T13818 1441-1444 DT denotes the
T13820 1445-1449 NN denotes gene
T13822 1449-1450 HYPH denotes -
T13821 1450-1458 VBN denotes targeted
T13823 1459-1465 NN denotes mutant
T13819 1466-1470 NN denotes gene
T13824 1471-1473 CC denotes or
T13825 1474-1476 IN denotes to
T13826 1477-1480 DT denotes the
T13828 1481-1487 JJ denotes normal
T13829 1488-1491 CD denotes 129
T13827 1492-1497 NNS denotes genes
T13830 1498-1507 VBN denotes expressed
T13831 1508-1510 IN denotes in
T13832 1511-1514 DT denotes the
T13834 1515-1519 JJ denotes same
T13833 1520-1526 NN denotes region
T13835 1527-1529 IN denotes as
T13836 1530-1533 DT denotes the
T13838 1534-1542 VBN denotes targeted
T13837 1543-1547 NN denotes gene
T13839 1547-1548 . denotes .
R3040 T13555 T13556 expl There,is
R3042 T13557 T13558 amod accumulating,evidence
R3044 T13558 T13556 attr evidence,is
R3045 T13559 T13560 mark that,influence
R3046 T13560 T13558 acl influence,evidence
R3048 T13561 T13562 compound background,genes
R3049 T13562 T13560 nsubj genes,influence
R3050 T13563 T13560 aux may,influence
R3051 T13564 T13565 det the,expression
R3052 T13565 T13560 dobj expression,influence
R3053 T13566 T13565 prep of,expression
R3054 T13567 T13566 pobj autoimmunity,of
R3055 T13568 T13560 prep in,influence
R3056 T13569 T13570 npadvmod gene,targeted
R3057 T13570 T13572 amod targeted,mice
R3058 T13571 T13570 punct -,targeted
R3059 T13572 T13568 pobj mice,in
R3060 T13573 T13556 punct .,is
R3061 T13575 T13576 advmod Here,report
R3062 T13577 T13576 nsubj we,report
R3063 T13578 T13579 dep what,is
R3064 T13579 T13576 ccomp is,report
R3066 T13580 T13579 prep to,is
R3067 T13581 T13582 poss our,knowledge
R3068 T13582 T13580 pobj knowledge,to
R3069 T13583 T13584 det the,study
R3070 T13584 T13579 attr study,is
R3071 T13585 T13584 amod first,study
R3072 T13586 T13584 amod systematic,study
R3073 T13587 T13588 dep that,examined
R3074 T13588 T13584 relcl examined,study
R3075 T13589 T13588 aux has,examined
R3076 T13590 T13588 dobj this,examined
R3077 T13591 T13588 prep in,examined
R3078 T13592 T13593 det the,strains
R3079 T13593 T13591 pobj strains,in
R3080 T13594 T13593 nummod 129,strains
R3081 T13595 T13594 cc and,129
R3082 T13596 T13594 conj C57BL,129
R3083 T13600 T13593 punct ", ",strains
R3084 T13597 T13596 punct /,C57BL
R3085 T13601 T13602 advmod widely,used
R3086 T13602 T13593 acl used,strains
R3087 T13598 T13596 nummod 6,C57BL
R3088 T13603 T13602 prep for,used
R3089 T13604 T13605 compound gene,targeting
R3090 T13605 T13603 pobj targeting,for
R3091 T13599 T13593 compound mouse,strains
R3092 T13606 T13576 punct .,report
R3093 T13608 T13609 poss Our,results
R3094 T13706 T13699 dobj severity,influences
R3095 T13609 T13610 nsubj results,demonstrate
R3096 T13611 T13612 amod interacting,loci
R3097 T13707 T13706 prep of,severity
R3098 T13612 T13610 dobj loci,demonstrate
R3099 T13613 T13612 prep between,loci
R3100 T13614 T13615 nummod 129,mice
R3101 T13708 T13707 pobj glomerulonephritis,of
R3102 T13615 T13613 pobj mice,between
R3103 T13616 T13614 cc and,129
R3104 T13709 T13699 punct ", ",influences
R3105 T13617 T13614 conj C57BL,129
R3106 T13618 T13617 punct /,C57BL
R3107 T13619 T13617 nummod 6,C57BL
R3108 T13710 T13699 cc but,influences
R3109 T13620 T13621 dep that,cause
R3110 T13621 T13612 relcl cause,loci
R3111 T13622 T13621 aux can,cause
R3112 T13711 T13699 conj is,influences
R3113 T13623 T13624 det the,expression
R3114 T13624 T13621 dobj expression,cause
R3115 T13625 T13624 prep of,expression
R3116 T13712 T13711 neg not,is
R3117 T13626 T13627 det a,phenotype
R3118 T13627 T13625 pobj phenotype,of
R3119 T13713 T13714 det the,mover
R3120 T13628 T13627 amod powerful,phenotype
R3121 T13629 T13627 amod autoimmune,phenotype
R3122 T13630 T13621 prep in,cause
R3123 T13714 T13711 attr mover,is
R3124 T13631 T13632 det these,animals
R3125 T13632 T13630 pobj animals,in
R3126 T13633 T13621 punct ", ",cause
R3127 T13715 T13714 amod prime,mover
R3128 T13634 T13621 prep in,cause
R3129 T13716 T13711 prep in,is
R3130 T13717 T13718 det the,induction
R3131 T13635 T13636 det the,absence
R3132 T13636 T13634 pobj absence,in
R3133 T13718 T13716 pobj induction,in
R3134 T13637 T13636 prep of,absence
R3135 T13638 T13639 det any,mutations
R3136 T13639 T13637 pobj mutations,of
R3137 T13640 T13641 npadvmod gene,targeted
R3138 T13641 T13639 amod targeted,mutations
R3139 T13642 T13641 punct -,targeted
R3140 T13719 T13718 prep of,induction
R3141 T13643 T13610 punct .,demonstrate
R3142 T13720 T13721 amod anti-nuclear,autoimmunity
R3143 T13645 T13646 nsubj We,developed
R3144 T13647 T13646 advmod also,developed
R3145 T13721 T13719 pobj autoimmunity,of
R3146 T13648 T13649 det a,strain
R3147 T13649 T13646 dobj strain,developed
R3148 T13722 T13711 punct ", ",is
R3149 T13650 T13649 amod congenic,strain
R3150 T13651 T13649 compound mouse,strain
R3151 T13652 T13649 acl bearing,strain
R3152 T13723 T13711 advcl contrary,is
R3153 T13653 T13654 det a,portion
R3154 T13654 T13652 dobj portion,bearing
R3155 T13655 T13654 prep of,portion
R3156 T13724 T13723 prep to,contrary
R3157 T13656 T13657 nummod 129,Chromosome
R3158 T13657 T13655 pobj Chromosome,of
R3159 T13725 T13726 poss our,interpretation
R3160 T13658 T13657 nummod 1,Chromosome
R3161 T13659 T13652 prep on,bearing
R3162 T13660 T13661 det a,background
R3163 T13726 T13724 pobj interpretation,to
R3164 T13661 T13659 pobj background,on
R3165 T13662 T13661 nmod C57BL,background
R3166 T13663 T13662 punct /,C57BL
R3167 T13727 T13726 amod own,interpretation
R3168 T13664 T13662 nummod 6,C57BL
R3169 T13728 T13726 amod original,interpretation
R3170 T13665 T13646 cc and,developed
R3171 T13666 T13646 conj showed,developed
R3172 T13667 T13668 mark that,expressed
R3173 T13668 T13666 ccomp expressed,showed
R3174 T13729 T13726 prep of,interpretation
R3175 T13669 T13670 det this,line
R3176 T13670 T13668 nsubj line,expressed
R3177 T13671 T13672 amod wild,type
R3178 T13672 T13670 nmod type,line
R3179 T13730 T13731 poss our,data
R3180 T13673 T13672 punct -,type
R3181 T13674 T13670 amod congenic,line
R3182 T13675 T13676 amod striking,autoimmunity
R3183 T13731 T13729 pobj data,of
R3184 T13676 T13668 dobj autoimmunity,expressed
R3185 T13677 T13676 amod anti-nuclear,autoimmunity
R3186 T13678 T13646 punct .,developed
R3187 T13680 T13681 prep By,demonstrated
R3188 T13732 T13733 punct (,Bickerstaff
R3189 T13682 T13680 pcomp comparing,By
R3190 T13683 T13684 det this,strain
R3191 T13684 T13682 dobj strain,comparing
R3192 T13733 T13711 meta Bickerstaff,is
R3193 T13685 T13684 nmod Chromosome,strain
R3194 T13686 T13685 nummod 1,Chromosome
R3195 T13687 T13684 amod congenic,strain
R3196 T13734 T13733 nmod et,Bickerstaff
R3197 T13688 T13682 prep with,comparing
R3198 T13689 T13690 amod matched,mice
R3199 T13690 T13688 pobj mice,with
R3200 T13735 T13733 nmod al.,Bickerstaff
R3201 T13691 T13690 amod congenic,mice
R3202 T13692 T13690 acl lacking,mice
R3203 T13693 T13694 det the,gene
R3204 T13736 T13733 nummod 1999,Bickerstaff
R3205 T13694 T13692 dobj gene,lacking
R3206 T13695 T13694 compound Apcs,gene
R3207 T13696 T13681 punct ", ",demonstrated
R3208 T13737 T13733 punct ),Bickerstaff
R3209 T13697 T13681 nsubj we,demonstrated
R3210 T13698 T13699 mark that,influences
R3211 T13738 T13681 punct .,demonstrated
R3212 T13699 T13681 ccomp influences,demonstrated
R3213 T13700 T13701 compound serum,component
R3214 T13701 T13704 compound component,deficiency
R3215 T13740 T13741 det The,consideration
R3216 T13702 T13701 compound amyloid,component
R3217 T13703 T13701 compound P,component
R3218 T13704 T13699 nsubj deficiency,influences
R3219 T13705 T13706 det the,severity
R3220 T13741 T13743 nsubj consideration,applies
R3221 T13742 T13741 amod same,consideration
R3222 T13744 T13743 prep to,applies
R3223 T13745 T13746 amod other,genes
R3224 T13812 T13810 pcomp is,to
R3225 T13813 T13814 det the,autoimmunity
R3226 T13746 T13744 pobj genes,to
R3227 T13814 T13812 nsubj autoimmunity,is
R3228 T13815 T13814 amod anti-nuclear,autoimmunity
R3229 T13816 T13812 prep due,is
R3230 T13747 T13746 acl located,genes
R3231 T13817 T13816 prep to,due
R3232 T13818 T13819 det the,gene
R3233 T13748 T13747 prep in,located
R3234 T13819 T13817 pobj gene,to
R3235 T13820 T13821 npadvmod gene,targeted
R3236 T13821 T13819 amod targeted,gene
R3237 T13749 T13750 det the,region
R3238 T13822 T13821 punct -,targeted
R3239 T13823 T13819 compound mutant,gene
R3240 T13824 T13817 cc or,to
R3241 T13825 T13817 conj to,to
R3242 T13826 T13827 det the,genes
R3243 T13827 T13825 pobj genes,to
R3244 T13750 T13748 pobj region,in
R3245 T13828 T13827 amod normal,genes
R3246 T13829 T13827 nummod 129,genes
R3247 T13830 T13827 acl expressed,genes
R3248 T13751 T13750 amod same,region
R3249 T13831 T13830 prep in,expressed
R3250 T13832 T13833 det the,region
R3251 T13833 T13831 pobj region,in
R3252 T13752 T13750 nmod Chromosome,region
R3253 T13834 T13833 amod same,region
R3254 T13835 T13833 prep as,region
R3255 T13753 T13752 nummod 1,Chromosome
R3256 T13836 T13837 det the,gene
R3257 T13837 T13835 pobj gene,as
R3258 T13838 T13837 amod targeted,gene
R3259 T13754 T13755 dep that,implicated
R3260 T13839 T13801 punct .,has
R3261 T13755 T13746 relcl implicated,genes
R3264 T13756 T13755 aux have,implicated
R3267 T13757 T13755 auxpass been,implicated
R3271 T13758 T13755 prep in,implicated
R3275 T13759 T13760 det the,development
R3278 T13760 T13758 pobj development,in
R3282 T13761 T13760 prep of,development
R3285 T13762 T13761 pobj SLE,of
R3289 T13763 T13764 advmod when,inactivated
R3295 T13764 T13755 advcl inactivated,implicated
R3299 T13765 T13764 agent by,inactivated
R3301 T13766 T13765 pobj gene,by
R3304 T13767 T13766 punct -,gene
R3308 T13768 T13766 amod targeting,gene
R3312 T13769 T13764 prep in,inactivated
R3316 T13770 T13771 nummod 129,cells
R3320 T13771 T13769 pobj cells,in
R3323 T13772 T13771 amod embryonic,cells
R3324 T13773 T13771 compound stem,cells
R3328 T13774 T13764 cc and,inactivated
R3331 T13775 T13776 advmod then,backcrossed
R3334 T13776 T13764 conj backcrossed,inactivated
R3338 T13777 T13776 prep onto,backcrossed
R3341 T13778 T13779 det a,background
R3347 T13779 T13777 pobj background,onto
R3349 T13780 T13779 amod pure,background
R3353 T13781 T13779 amod genetic,background
R3356 T13782 T13783 punct (,Bolland
R3360 T13783 T13764 meta Bolland,inactivated
R3362 T13784 T13783 cc and,Bolland
R3363 T13785 T13783 conj Ravetch,Bolland
R3364 T13786 T13785 nummod 2000,Ravetch
R3367 T13787 T13785 punct ;,Ravetch
R3371 T13788 T13785 conj Miwa,Ravetch
R3374 T13789 T13788 nmod et,Miwa
R3378 T13790 T13788 nmod al.,Miwa
R3382 T13791 T13788 nummod 2002,Miwa
R3385 T13792 T13788 punct ;,Miwa
R3389 T13793 T13788 conj Wu,Miwa
R3391 T13794 T13793 nmod et,Wu
R3392 T13795 T13793 nmod al.,Wu
R3398 T13796 T13793 nummod 2002,Wu
R3401 T13797 T13793 punct ),Wu
R3403 T13798 T13743 punct .,applies
R3407 T13800 T13801 prep For,has
R3412 T13802 T13800 pobj each,For
R3417 T13803 T13801 punct ", ",has
R3421 T13804 T13801 expl there,has
R3425 T13805 T13806 aux to,be
R3429 T13806 T13801 xcomp be,has
R3433 T13807 T13808 det a,question
R3437 T13808 T13806 attr question,be
R3439 T13809 T13808 prep as,question
R3440 T13810 T13809 prep to,as
R3443 T13811 T13812 mark whether,is