PMC:3585731 / 29720-30779 JSONTXT

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    testone

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    pmc-enju-pas

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L929 cells were stably infected with empty MSCV retrovirus or viruses encoding Myr-Akt or the catalytically inactive Myr-Akt K179M. Necroptosis was induced by the addition of zVAD.fmk under serum free conditions (A) or serum or serum free conditions with Nec-1 (B). Viability assays were performed after 24 hr. (C) Myr-Akt and Myr-Akt K179M cells were treated with zVAD.fmk and/or Nec-1 under serum free conditions for 9 hr, followed by western blot using the indicated antibodies. Endogenous Akt (∼) and Myr-Akt (*) bands are indicated. (D) L929 cells, stably infected with Myr-Akt and Myr-Akt K179KM, were stimulated with zVAD.fmk for 9 hr under serum free conditions. TNFα mRNA levels were determined by qRT-PCR and normalized using mouse 18S RNA. (E-G) L929 cells expressing Myr-Akt and Ala and Asp mutants of Thr308 and Ser473 were treated with zVAD.fmk under serum free conditions, followed by viability assay at 24 hr (E), western blot at 9 hr (F), or evaluation of TNFα mRNA levels by qRT-PCR at 9 hrs (G). In all graphs, average±SD was plotted."}

    bionlp-st-ge-2016-test-proteins

    {"project":"bionlp-st-ge-2016-test-proteins","denotations":[{"id":"T31196","span":{"begin":979,"end":983},"obj":"Protein"},{"id":"T31195","span":{"begin":748,"end":751},"obj":"Protein"},{"id":"T31194","span":{"begin":677,"end":681},"obj":"Protein"}],"namespaces":[{"prefix":"_base","uri":"http://bionlp.dbcls.jp/ontology/ge.owl#"}],"text":"(A,B) L929 cells were stably infected with empty MSCV retrovirus or viruses encoding Myr-Akt or the catalytically inactive Myr-Akt K179M. Necroptosis was induced by the addition of zVAD.fmk under serum free conditions (A) or serum or serum free conditions with Nec-1 (B). Viability assays were performed after 24 hr. (C) Myr-Akt and Myr-Akt K179M cells were treated with zVAD.fmk and/or Nec-1 under serum free conditions for 9 hr, followed by western blot using the indicated antibodies. Endogenous Akt (∼) and Myr-Akt (*) bands are indicated. (D) L929 cells, stably infected with Myr-Akt and Myr-Akt K179KM, were stimulated with zVAD.fmk for 9 hr under serum free conditions. TNFα mRNA levels were determined by qRT-PCR and normalized using mouse 18S RNA. (E-G) L929 cells expressing Myr-Akt and Ala and Asp mutants of Thr308 and Ser473 were treated with zVAD.fmk under serum free conditions, followed by viability assay at 24 hr (E), western blot at 9 hr (F), or evaluation of TNFα mRNA levels by qRT-PCR at 9 hrs (G). In all graphs, average±SD was plotted."}

    bionlp-st-ge-2016-uniprot

    {"project":"bionlp-st-ge-2016-uniprot","denotations":[{"id":"T31465","span":{"begin":979,"end":983},"obj":"http://www.uniprot.org/uniprot/P01375"},{"id":"T31464","span":{"begin":677,"end":681},"obj":"http://www.uniprot.org/uniprot/P01375"},{"id":"T31463","span":{"begin":789,"end":792},"obj":"http://www.uniprot.org/uniprot/Q9Y243"},{"id":"T31462","span":{"begin":597,"end":600},"obj":"http://www.uniprot.org/uniprot/Q9Y243"},{"id":"T31461","span":{"begin":585,"end":588},"obj":"http://www.uniprot.org/uniprot/Q9Y243"},{"id":"T31460","span":{"begin":515,"end":518},"obj":"http://www.uniprot.org/uniprot/Q9Y243"},{"id":"T31459","span":{"begin":499,"end":502},"obj":"http://www.uniprot.org/uniprot/Q9Y243"},{"id":"T31458","span":{"begin":337,"end":340},"obj":"http://www.uniprot.org/uniprot/Q9Y243"},{"id":"T31457","span":{"begin":325,"end":328},"obj":"http://www.uniprot.org/uniprot/Q9Y243"},{"id":"T31456","span":{"begin":127,"end":130},"obj":"http://www.uniprot.org/uniprot/Q9Y243"},{"id":"T31455","span":{"begin":89,"end":92},"obj":"http://www.uniprot.org/uniprot/Q9Y243"},{"id":"T31453","span":{"begin":789,"end":792},"obj":"http://www.uniprot.org/uniprot/P31751"},{"id":"T31452","span":{"begin":597,"end":600},"obj":"http://www.uniprot.org/uniprot/P31751"},{"id":"T31451","span":{"begin":585,"end":588},"obj":"http://www.uniprot.org/uniprot/P31751"},{"id":"T31450","span":{"begin":515,"end":518},"obj":"http://www.uniprot.org/uniprot/P31751"},{"id":"T31449","span":{"begin":499,"end":502},"obj":"http://www.uniprot.org/uniprot/P31751"},{"id":"T31448","span":{"begin":337,"end":340},"obj":"http://www.uniprot.org/uniprot/P31751"},{"id":"T31447","span":{"begin":325,"end":328},"obj":"http://www.uniprot.org/uniprot/P31751"},{"id":"T31446","span":{"begin":127,"end":130},"obj":"http://www.uniprot.org/uniprot/P31751"},{"id":"T31445","span":{"begin":89,"end":92},"obj":"http://www.uniprot.org/uniprot/P31751"},{"id":"T31443","span":{"begin":789,"end":792},"obj":"http://www.uniprot.org/uniprot/P31749"},{"id":"T31442","span":{"begin":597,"end":600},"obj":"http://www.uniprot.org/uniprot/P31749"},{"id":"T31441","span":{"begin":585,"end":588},"obj":"http://www.uniprot.org/uniprot/P31749"},{"id":"T31440","span":{"begin":515,"end":518},"obj":"http://www.uniprot.org/uniprot/P31749"},{"id":"T31439","span":{"begin":499,"end":502},"obj":"http://www.uniprot.org/uniprot/P31749"},{"id":"T31438","span":{"begin":337,"end":340},"obj":"http://www.uniprot.org/uniprot/P31749"},{"id":"T31437","span":{"begin":325,"end":328},"obj":"http://www.uniprot.org/uniprot/P31749"},{"id":"T31436","span":{"begin":127,"end":130},"obj":"http://www.uniprot.org/uniprot/P31749"},{"id":"T31435","span":{"begin":89,"end":92},"obj":"http://www.uniprot.org/uniprot/P31749"}],"namespaces":[{"prefix":"_base","uri":"http://www.uniprot.org/uniprot/"}],"text":"(A,B) L929 cells were stably infected with empty MSCV retrovirus or viruses encoding Myr-Akt or the catalytically inactive Myr-Akt K179M. Necroptosis was induced by the addition of zVAD.fmk under serum free conditions (A) or serum or serum free conditions with Nec-1 (B). Viability assays were performed after 24 hr. (C) Myr-Akt and Myr-Akt K179M cells were treated with zVAD.fmk and/or Nec-1 under serum free conditions for 9 hr, followed by western blot using the indicated antibodies. Endogenous Akt (∼) and Myr-Akt (*) bands are indicated. (D) L929 cells, stably infected with Myr-Akt and Myr-Akt K179KM, were stimulated with zVAD.fmk for 9 hr under serum free conditions. TNFα mRNA levels were determined by qRT-PCR and normalized using mouse 18S RNA. (E-G) L929 cells expressing Myr-Akt and Ala and Asp mutants of Thr308 and Ser473 were treated with zVAD.fmk under serum free conditions, followed by viability assay at 24 hr (E), western blot at 9 hr (F), or evaluation of TNFα mRNA levels by qRT-PCR at 9 hrs (G). In all graphs, average±SD was plotted."}

    UBERON-AE

    {"project":"UBERON-AE","denotations":[{"id":"T31183","span":{"begin":871,"end":876},"obj":"http://purl.obolibrary.org/obo/UBERON_0001977"},{"id":"T31182","span":{"begin":654,"end":659},"obj":"http://purl.obolibrary.org/obo/UBERON_0001977"},{"id":"T31181","span":{"begin":399,"end":404},"obj":"http://purl.obolibrary.org/obo/UBERON_0001977"},{"id":"T31180","span":{"begin":234,"end":239},"obj":"http://purl.obolibrary.org/obo/UBERON_0001977"},{"id":"T31179","span":{"begin":225,"end":230},"obj":"http://purl.obolibrary.org/obo/UBERON_0001977"},{"id":"T31178","span":{"begin":196,"end":201},"obj":"http://purl.obolibrary.org/obo/UBERON_0001977"}],"text":"(A,B) L929 cells were stably infected with empty MSCV retrovirus or viruses encoding Myr-Akt or the catalytically inactive Myr-Akt K179M. Necroptosis was induced by the addition of zVAD.fmk under serum free conditions (A) or serum or serum free conditions with Nec-1 (B). Viability assays were performed after 24 hr. (C) Myr-Akt and Myr-Akt K179M cells were treated with zVAD.fmk and/or Nec-1 under serum free conditions for 9 hr, followed by western blot using the indicated antibodies. Endogenous Akt (∼) and Myr-Akt (*) bands are indicated. (D) L929 cells, stably infected with Myr-Akt and Myr-Akt K179KM, were stimulated with zVAD.fmk for 9 hr under serum free conditions. TNFα mRNA levels were determined by qRT-PCR and normalized using mouse 18S RNA. (E-G) L929 cells expressing Myr-Akt and Ala and Asp mutants of Thr308 and Ser473 were treated with zVAD.fmk under serum free conditions, followed by viability assay at 24 hr (E), western blot at 9 hr (F), or evaluation of TNFα mRNA levels by qRT-PCR at 9 hrs (G). In all graphs, average±SD was plotted."}

    GO-BP

    {"project":"GO-BP","denotations":[{"id":"T31200","span":{"begin":138,"end":149},"obj":"http://purl.obolibrary.org/obo/GO_0097528"},{"id":"T31198","span":{"begin":138,"end":149},"obj":"http://purl.obolibrary.org/obo/GO_0070266"}],"text":"(A,B) L929 cells were stably infected with empty MSCV retrovirus or viruses encoding Myr-Akt or the catalytically inactive Myr-Akt K179M. Necroptosis was induced by the addition of zVAD.fmk under serum free conditions (A) or serum or serum free conditions with Nec-1 (B). Viability assays were performed after 24 hr. (C) Myr-Akt and Myr-Akt K179M cells were treated with zVAD.fmk and/or Nec-1 under serum free conditions for 9 hr, followed by western blot using the indicated antibodies. Endogenous Akt (∼) and Myr-Akt (*) bands are indicated. (D) L929 cells, stably infected with Myr-Akt and Myr-Akt K179KM, were stimulated with zVAD.fmk for 9 hr under serum free conditions. TNFα mRNA levels were determined by qRT-PCR and normalized using mouse 18S RNA. (E-G) L929 cells expressing Myr-Akt and Ala and Asp mutants of Thr308 and Ser473 were treated with zVAD.fmk under serum free conditions, followed by viability assay at 24 hr (E), western blot at 9 hr (F), or evaluation of TNFα mRNA levels by qRT-PCR at 9 hrs (G). In all graphs, average±SD was plotted."}

    GO-MF

    {"project":"GO-MF","denotations":[{"id":"T31201","span":{"begin":476,"end":486},"obj":"http://purl.obolibrary.org/obo/GO_0003823"}],"text":"(A,B) L929 cells were stably infected with empty MSCV retrovirus or viruses encoding Myr-Akt or the catalytically inactive Myr-Akt K179M. Necroptosis was induced by the addition of zVAD.fmk under serum free conditions (A) or serum or serum free conditions with Nec-1 (B). Viability assays were performed after 24 hr. (C) Myr-Akt and Myr-Akt K179M cells were treated with zVAD.fmk and/or Nec-1 under serum free conditions for 9 hr, followed by western blot using the indicated antibodies. Endogenous Akt (∼) and Myr-Akt (*) bands are indicated. (D) L929 cells, stably infected with Myr-Akt and Myr-Akt K179KM, were stimulated with zVAD.fmk for 9 hr under serum free conditions. TNFα mRNA levels were determined by qRT-PCR and normalized using mouse 18S RNA. (E-G) L929 cells expressing Myr-Akt and Ala and Asp mutants of Thr308 and Ser473 were treated with zVAD.fmk under serum free conditions, followed by viability assay at 24 hr (E), western blot at 9 hr (F), or evaluation of TNFα mRNA levels by qRT-PCR at 9 hrs (G). In all graphs, average±SD was plotted."}

    GO-CC

    {"project":"GO-CC","denotations":[{"id":"T31207","span":{"begin":476,"end":486},"obj":"http://purl.obolibrary.org/obo/GO_0042571"},{"id":"T31206","span":{"begin":476,"end":486},"obj":"http://purl.obolibrary.org/obo/GO_0019815"},{"id":"T31205","span":{"begin":768,"end":773},"obj":"http://purl.obolibrary.org/obo/GO_0005623"},{"id":"T31204","span":{"begin":553,"end":558},"obj":"http://purl.obolibrary.org/obo/GO_0005623"},{"id":"T31203","span":{"begin":347,"end":352},"obj":"http://purl.obolibrary.org/obo/GO_0005623"},{"id":"T31202","span":{"begin":11,"end":16},"obj":"http://purl.obolibrary.org/obo/GO_0005623"}],"text":"(A,B) L929 cells were stably infected with empty MSCV retrovirus or viruses encoding Myr-Akt or the catalytically inactive Myr-Akt K179M. Necroptosis was induced by the addition of zVAD.fmk under serum free conditions (A) or serum or serum free conditions with Nec-1 (B). Viability assays were performed after 24 hr. (C) Myr-Akt and Myr-Akt K179M cells were treated with zVAD.fmk and/or Nec-1 under serum free conditions for 9 hr, followed by western blot using the indicated antibodies. Endogenous Akt (∼) and Myr-Akt (*) bands are indicated. (D) L929 cells, stably infected with Myr-Akt and Myr-Akt K179KM, were stimulated with zVAD.fmk for 9 hr under serum free conditions. TNFα mRNA levels were determined by qRT-PCR and normalized using mouse 18S RNA. (E-G) L929 cells expressing Myr-Akt and Ala and Asp mutants of Thr308 and Ser473 were treated with zVAD.fmk under serum free conditions, followed by viability assay at 24 hr (E), western blot at 9 hr (F), or evaluation of TNFα mRNA levels by qRT-PCR at 9 hrs (G). In all graphs, average±SD was plotted."}

    sentences

    {"project":"sentences","denotations":[{"id":"T31190","span":{"begin":1021,"end":1059},"obj":"Sentence"},{"id":"T31189","span":{"begin":677,"end":1020},"obj":"Sentence"},{"id":"T31188","span":{"begin":488,"end":676},"obj":"Sentence"},{"id":"T31187","span":{"begin":272,"end":487},"obj":"Sentence"},{"id":"T31186","span":{"begin":138,"end":271},"obj":"Sentence"},{"id":"T31185","span":{"begin":0,"end":137},"obj":"Sentence"},{"id":"T187","span":{"begin":0,"end":137},"obj":"Sentence"},{"id":"T188","span":{"begin":138,"end":271},"obj":"Sentence"},{"id":"T189","span":{"begin":272,"end":487},"obj":"Sentence"},{"id":"T190","span":{"begin":488,"end":676},"obj":"Sentence"},{"id":"T191","span":{"begin":677,"end":1020},"obj":"Sentence"},{"id":"T192","span":{"begin":1021,"end":1059},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"(A,B) L929 cells were stably infected with empty MSCV retrovirus or viruses encoding Myr-Akt or the catalytically inactive Myr-Akt K179M. Necroptosis was induced by the addition of zVAD.fmk under serum free conditions (A) or serum or serum free conditions with Nec-1 (B). Viability assays were performed after 24 hr. (C) Myr-Akt and Myr-Akt K179M cells were treated with zVAD.fmk and/or Nec-1 under serum free conditions for 9 hr, followed by western blot using the indicated antibodies. Endogenous Akt (∼) and Myr-Akt (*) bands are indicated. (D) L929 cells, stably infected with Myr-Akt and Myr-Akt K179KM, were stimulated with zVAD.fmk for 9 hr under serum free conditions. TNFα mRNA levels were determined by qRT-PCR and normalized using mouse 18S RNA. (E-G) L929 cells expressing Myr-Akt and Ala and Asp mutants of Thr308 and Ser473 were treated with zVAD.fmk under serum free conditions, followed by viability assay at 24 hr (E), western blot at 9 hr (F), or evaluation of TNFα mRNA levels by qRT-PCR at 9 hrs (G). In all graphs, average±SD was plotted."}

    simple1

    {"project":"simple1","denotations":[{"id":"T31213","span":{"begin":979,"end":983},"obj":"Protein"},{"id":"T31212","span":{"begin":748,"end":751},"obj":"Protein"},{"id":"T31211","span":{"begin":677,"end":681},"obj":"Protein"}],"text":"(A,B) L929 cells were stably infected with empty MSCV retrovirus or viruses encoding Myr-Akt or the catalytically inactive Myr-Akt K179M. Necroptosis was induced by the addition of zVAD.fmk under serum free conditions (A) or serum or serum free conditions with Nec-1 (B). Viability assays were performed after 24 hr. (C) Myr-Akt and Myr-Akt K179M cells were treated with zVAD.fmk and/or Nec-1 under serum free conditions for 9 hr, followed by western blot using the indicated antibodies. Endogenous Akt (∼) and Myr-Akt (*) bands are indicated. (D) L929 cells, stably infected with Myr-Akt and Myr-Akt K179KM, were stimulated with zVAD.fmk for 9 hr under serum free conditions. TNFα mRNA levels were determined by qRT-PCR and normalized using mouse 18S RNA. (E-G) L929 cells expressing Myr-Akt and Ala and Asp mutants of Thr308 and Ser473 were treated with zVAD.fmk under serum free conditions, followed by viability assay at 24 hr (E), western blot at 9 hr (F), or evaluation of TNFα mRNA levels by qRT-PCR at 9 hrs (G). In all graphs, average±SD was plotted."}

    BioNLP16_DUT

    {"project":"BioNLP16_DUT","denotations":[{"id":"T31433","span":{"begin":687,"end":693},"obj":"Transcription"},{"id":"T31432","span":{"begin":979,"end":983},"obj":"Protein"},{"id":"T31431","span":{"begin":748,"end":751},"obj":"Protein"},{"id":"T31430","span":{"begin":677,"end":681},"obj":"Protein"}],"relations":[{"id":"R21761","pred":"themeOf","subj":"T31430","obj":"T31433"}],"text":"(A,B) L929 cells were stably infected with empty MSCV retrovirus or viruses encoding Myr-Akt or the catalytically inactive Myr-Akt K179M. Necroptosis was induced by the addition of zVAD.fmk under serum free conditions (A) or serum or serum free conditions with Nec-1 (B). Viability assays were performed after 24 hr. (C) Myr-Akt and Myr-Akt K179M cells were treated with zVAD.fmk and/or Nec-1 under serum free conditions for 9 hr, followed by western blot using the indicated antibodies. Endogenous Akt (∼) and Myr-Akt (*) bands are indicated. (D) L929 cells, stably infected with Myr-Akt and Myr-Akt K179KM, were stimulated with zVAD.fmk for 9 hr under serum free conditions. TNFα mRNA levels were determined by qRT-PCR and normalized using mouse 18S RNA. (E-G) L929 cells expressing Myr-Akt and Ala and Asp mutants of Thr308 and Ser473 were treated with zVAD.fmk under serum free conditions, followed by viability assay at 24 hr (E), western blot at 9 hr (F), or evaluation of TNFα mRNA levels by qRT-PCR at 9 hrs (G). In all graphs, average±SD was plotted."}

    BioNLP16_Messiy

    {"project":"BioNLP16_Messiy","denotations":[{"id":"T31704","span":{"begin":979,"end":983},"obj":"Protein"},{"id":"T31703","span":{"begin":748,"end":751},"obj":"Protein"},{"id":"T31702","span":{"begin":677,"end":681},"obj":"Protein"}],"text":"(A,B) L929 cells were stably infected with empty MSCV retrovirus or viruses encoding Myr-Akt or the catalytically inactive Myr-Akt K179M. Necroptosis was induced by the addition of zVAD.fmk under serum free conditions (A) or serum or serum free conditions with Nec-1 (B). Viability assays were performed after 24 hr. (C) Myr-Akt and Myr-Akt K179M cells were treated with zVAD.fmk and/or Nec-1 under serum free conditions for 9 hr, followed by western blot using the indicated antibodies. Endogenous Akt (∼) and Myr-Akt (*) bands are indicated. (D) L929 cells, stably infected with Myr-Akt and Myr-Akt K179KM, were stimulated with zVAD.fmk for 9 hr under serum free conditions. TNFα mRNA levels were determined by qRT-PCR and normalized using mouse 18S RNA. (E-G) L929 cells expressing Myr-Akt and Ala and Asp mutants of Thr308 and Ser473 were treated with zVAD.fmk under serum free conditions, followed by viability assay at 24 hr (E), western blot at 9 hr (F), or evaluation of TNFα mRNA levels by qRT-PCR at 9 hrs (G). In all graphs, average±SD was plotted."}

    DLUT931

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976","pred":"nummod","subj":"T31683","obj":"T31684"},{"id":"R21977","pred":"pobj","subj":"T31684","obj":"T31682"},{"id":"R21978","pred":"punct","subj":"T31685","obj":"T31686"},{"id":"R21979","pred":"appos","subj":"T31686","obj":"T31684"},{"id":"R21980","pred":"punct","subj":"T31687","obj":"T31684"},{"id":"R21981","pred":"punct","subj":"T31688","obj":"T31646"},{"id":"R21982","pred":"prep","subj":"T31689","obj":"T31697"},{"id":"R21983","pred":"det","subj":"T31690","obj":"T31691"},{"id":"R21984","pred":"pobj","subj":"T31691","obj":"T31689"},{"id":"R21985","pred":"punct","subj":"T31692","obj":"T31697"},{"id":"R21986","pred":"amod","subj":"T31693","obj":"T31694"},{"id":"R21987","pred":"compound","subj":"T31694","obj":"T31695"},{"id":"R21988","pred":"nsubjpass","subj":"T31695","obj":"T31697"},{"id":"R21989","pred":"auxpass","subj":"T31696","obj":"T31697"},{"id":"R21990","pred":"ROOT","subj":"T31697","obj":"T31697"},{"id":"R21991","pred":"punct","subj":"T31698","obj":"T31697"}],"text":"(A,B) L929 cells were stably infected with empty MSCV retrovirus or viruses encoding Myr-Akt or the catalytically inactive Myr-Akt K179M. Necroptosis was induced by the addition of zVAD.fmk under serum free conditions (A) or serum or serum free conditions with Nec-1 (B). Viability assays were performed after 24 hr. (C) Myr-Akt and Myr-Akt K179M cells were treated with zVAD.fmk and/or Nec-1 under serum free conditions for 9 hr, followed by western blot using the indicated antibodies. Endogenous Akt (∼) and Myr-Akt (*) bands are indicated. (D) L929 cells, stably infected with Myr-Akt and Myr-Akt K179KM, were stimulated with zVAD.fmk for 9 hr under serum free conditions. TNFα mRNA levels were determined by qRT-PCR and normalized using mouse 18S RNA. (E-G) L929 cells expressing Myr-Akt and Ala and Asp mutants of Thr308 and Ser473 were treated with zVAD.fmk under serum free conditions, followed by viability assay at 24 hr (E), western blot at 9 hr (F), or evaluation of TNFα mRNA levels by qRT-PCR at 9 hrs (G). In all graphs, average±SD was plotted."}

    bionlp-st-ge-2016-test-tees

    {"project":"bionlp-st-ge-2016-test-tees","denotations":[{"id":"T31721","span":{"begin":774,"end":784},"obj":"Gene_expression"},{"id":"T31720","span":{"begin":979,"end":988},"obj":"Protein"},{"id":"T31719","span":{"begin":785,"end":792},"obj":"Protein"},{"id":"T31718","span":{"begin":742,"end":755},"obj":"Protein"},{"id":"T31717","span":{"begin":677,"end":686},"obj":"Protein"},{"id":"T31716","span":{"begin":630,"end":638},"obj":"Protein"},{"id":"T31715","span":{"begin":593,"end":607},"obj":"Protein"},{"id":"T31714","span":{"begin":581,"end":588},"obj":"Protein"},{"id":"T31713","span":{"begin":515,"end":518},"obj":"Protein"},{"id":"T31712","span":{"begin":511,"end":514},"obj":"Protein"},{"id":"T31711","span":{"begin":371,"end":379},"obj":"Protein"},{"id":"T31710","span":{"begin":337,"end":340},"obj":"Protein"},{"id":"T31709","span":{"begin":333,"end":336},"obj":"Protein"},{"id":"T31708","span":{"begin":325,"end":328},"obj":"Protein"},{"id":"T31707","span":{"begin":321,"end":324},"obj":"Protein"},{"id":"T31706","span":{"begin":123,"end":136},"obj":"Protein"},{"id":"T31705","span":{"begin":85,"end":92},"obj":"Protein"}],"relations":[{"id":"R21992","pred":"themeOf","subj":"T31719","obj":"T31721"}],"text":"(A,B) L929 cells were stably infected with empty MSCV retrovirus or viruses encoding Myr-Akt or the catalytically inactive Myr-Akt K179M. Necroptosis was induced by the addition of zVAD.fmk under serum free conditions (A) or serum or serum free conditions with Nec-1 (B). Viability assays were performed after 24 hr. (C) Myr-Akt and Myr-Akt K179M cells were treated with zVAD.fmk and/or Nec-1 under serum free conditions for 9 hr, followed by western blot using the indicated antibodies. Endogenous Akt (∼) and Myr-Akt (*) bands are indicated. (D) L929 cells, stably infected with Myr-Akt and Myr-Akt K179KM, were stimulated with zVAD.fmk for 9 hr under serum free conditions. TNFα mRNA levels were determined by qRT-PCR and normalized using mouse 18S RNA. (E-G) L929 cells expressing Myr-Akt and Ala and Asp mutants of Thr308 and Ser473 were treated with zVAD.fmk under serum free conditions, followed by viability assay at 24 hr (E), western blot at 9 hr (F), or evaluation of TNFα mRNA levels by qRT-PCR at 9 hrs (G). In all graphs, average±SD was plotted."}

    test3

    {"project":"test3","denotations":[{"id":"T31176","span":{"begin":979,"end":983},"obj":"Protein"},{"id":"T31175","span":{"begin":774,"end":784},"obj":"Gene_expression"},{"id":"T31174","span":{"begin":748,"end":751},"obj":"Protein"},{"id":"T31173","span":{"begin":677,"end":681},"obj":"Protein"},{"id":"T31172","span":{"begin":154,"end":161},"obj":"Positive_regulation"},{"id":"T31171","span":{"begin":979,"end":983},"obj":"Protein"},{"id":"T31170","span":{"begin":748,"end":751},"obj":"Protein"},{"id":"T31169","span":{"begin":677,"end":681},"obj":"Protein"}],"text":"(A,B) L929 cells were stably infected with empty MSCV retrovirus or viruses encoding Myr-Akt or the catalytically inactive Myr-Akt K179M. Necroptosis was induced by the addition of zVAD.fmk under serum free conditions (A) or serum or serum free conditions with Nec-1 (B). Viability assays were performed after 24 hr. (C) Myr-Akt and Myr-Akt K179M cells were treated with zVAD.fmk and/or Nec-1 under serum free conditions for 9 hr, followed by western blot using the indicated antibodies. Endogenous Akt (∼) and Myr-Akt (*) bands are indicated. (D) L929 cells, stably infected with Myr-Akt and Myr-Akt K179KM, were stimulated with zVAD.fmk for 9 hr under serum free conditions. TNFα mRNA levels were determined by qRT-PCR and normalized using mouse 18S RNA. (E-G) L929 cells expressing Myr-Akt and Ala and Asp mutants of Thr308 and Ser473 were treated with zVAD.fmk under serum free conditions, followed by viability assay at 24 hr (E), western blot at 9 hr (F), or evaluation of TNFα mRNA levels by qRT-PCR at 9 hrs (G). In all graphs, average±SD was plotted."}