# |
PMID |
Sentence |
1 |
17982689
|
Lysosomal hydrolase cathepsin B (CB) is involved in the apoptotic process and has a key role in breast cancer cell programmed death through the activation of a pro-apoptotic protein BID.
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2 |
17982689
|
Truncated BID participates in the mitochondrial apoptotic pathway that involves the activation of pro-caspase 9.
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3 |
17982689
|
Expression of CB, BID and pro-caspase 9 was determined by Western blotting.
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4 |
17982689
|
The apoptosis of T24 and MB49 cell lines was mediated by activation of pro-caspase 9 and BID, both proteins are involved in mitochondrial apoptosis.
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5 |
17982689
|
Apoptosis and activation of pro-caspase 9 and BID were inhibited by CA-074Me (CA), a cell permeable CB inhibitor.
|
6 |
17982689
|
Lysosomal hydrolase cathepsin B (CB) is involved in the apoptotic process and has a key role in breast cancer cell programmed death through the activation of a pro-apoptotic protein BID.
|
7 |
17982689
|
Truncated BID participates in the mitochondrial apoptotic pathway that involves the activation of pro-caspase 9.
|
8 |
17982689
|
Expression of CB, BID and pro-caspase 9 was determined by Western blotting.
|
9 |
17982689
|
The apoptosis of T24 and MB49 cell lines was mediated by activation of pro-caspase 9 and BID, both proteins are involved in mitochondrial apoptosis.
|
10 |
17982689
|
Apoptosis and activation of pro-caspase 9 and BID were inhibited by CA-074Me (CA), a cell permeable CB inhibitor.
|
11 |
17982689
|
Lysosomal hydrolase cathepsin B (CB) is involved in the apoptotic process and has a key role in breast cancer cell programmed death through the activation of a pro-apoptotic protein BID.
|
12 |
17982689
|
Truncated BID participates in the mitochondrial apoptotic pathway that involves the activation of pro-caspase 9.
|
13 |
17982689
|
Expression of CB, BID and pro-caspase 9 was determined by Western blotting.
|
14 |
17982689
|
The apoptosis of T24 and MB49 cell lines was mediated by activation of pro-caspase 9 and BID, both proteins are involved in mitochondrial apoptosis.
|
15 |
17982689
|
Apoptosis and activation of pro-caspase 9 and BID were inhibited by CA-074Me (CA), a cell permeable CB inhibitor.
|
16 |
17982689
|
Lysosomal hydrolase cathepsin B (CB) is involved in the apoptotic process and has a key role in breast cancer cell programmed death through the activation of a pro-apoptotic protein BID.
|
17 |
17982689
|
Truncated BID participates in the mitochondrial apoptotic pathway that involves the activation of pro-caspase 9.
|
18 |
17982689
|
Expression of CB, BID and pro-caspase 9 was determined by Western blotting.
|
19 |
17982689
|
The apoptosis of T24 and MB49 cell lines was mediated by activation of pro-caspase 9 and BID, both proteins are involved in mitochondrial apoptosis.
|
20 |
17982689
|
Apoptosis and activation of pro-caspase 9 and BID were inhibited by CA-074Me (CA), a cell permeable CB inhibitor.
|
21 |
17982689
|
Lysosomal hydrolase cathepsin B (CB) is involved in the apoptotic process and has a key role in breast cancer cell programmed death through the activation of a pro-apoptotic protein BID.
|
22 |
17982689
|
Truncated BID participates in the mitochondrial apoptotic pathway that involves the activation of pro-caspase 9.
|
23 |
17982689
|
Expression of CB, BID and pro-caspase 9 was determined by Western blotting.
|
24 |
17982689
|
The apoptosis of T24 and MB49 cell lines was mediated by activation of pro-caspase 9 and BID, both proteins are involved in mitochondrial apoptosis.
|
25 |
17982689
|
Apoptosis and activation of pro-caspase 9 and BID were inhibited by CA-074Me (CA), a cell permeable CB inhibitor.
|
26 |
25443632
|
SHARPIN regulates immune signaling and contributes to full transcriptional activity and prevention of cell death in response to TNF in vitro.
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27 |
25443632
|
The inactivating mouse Sharpin cpdm mutation causes TNF-dependent multi-organ inflammation, characterized by dermatitis, liver inflammation, splenomegaly, and loss of Peyer's patches.
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28 |
25443632
|
TNFR1-induced apoptosis can proceed through caspase-8 and BID, but reduction in or loss of these players generally did not suppress inflammation, although Casp8 heterozygosity significantly delayed dermatitis.
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29 |
25443632
|
Ripk3 or Mlkl deficiency partially ameliorated the multi-organ phenotype, and combined Ripk3 deletion and Casp8 heterozygosity almost completely suppressed it, even restoring Peyer's patches.
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30 |
25443632
|
Unexpectedly, Sharpin, Ripk3 and Casp8 triple deficiency caused perinatal lethality.
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