Id |
Subject |
Object |
Predicate |
Lexical cue |
T108 |
0-100 |
Sentence |
denotes |
Spontaneous mutations of the Sharpin (SHANK-associated RH domain-interacting protein, other aliases: |
T3 |
0-100 |
Sentence |
denotes |
Spontaneous mutations of the Sharpin (SHANK-associated RH domain-interacting protein, other aliases: |
T109 |
101-283 |
Sentence |
denotes |
Rbckl1, Sipl1) gene in mice result in systemic inflammation that is characterized by chronic proliferative dermatitis and dysregulated secretion of T helper1 (Th1) and Th2 cytokines. |
T4 |
101-283 |
Sentence |
denotes |
Rbckl1, Sipl1) gene in mice result in systemic inflammation that is characterized by chronic proliferative dermatitis and dysregulated secretion of T helper1 (Th1) and Th2 cytokines. |
T110 |
284-376 |
Sentence |
denotes |
The cellular and molecular mechanisms underlying this inflammatory phenotype remain elusive. |
T5 |
284-376 |
Sentence |
denotes |
The cellular and molecular mechanisms underlying this inflammatory phenotype remain elusive. |
T111 |
377-547 |
Sentence |
denotes |
Dendritic cells may contribute to the initiation and progression of the phenotype of SHARPIN-deficient mice because of their pivotal role in innate and adaptive immunity. |
T6 |
377-547 |
Sentence |
denotes |
Dendritic cells may contribute to the initiation and progression of the phenotype of SHARPIN-deficient mice because of their pivotal role in innate and adaptive immunity. |
T112 |
548-674 |
Sentence |
denotes |
Here we show by flow cytometry that SHARPIN- deficiency did not alter the distribution of different DC subtypes in the spleen. |
T7 |
548-674 |
Sentence |
denotes |
Here we show by flow cytometry that SHARPIN- deficiency did not alter the distribution of different DC subtypes in the spleen. |
T113 |
675-909 |
Sentence |
denotes |
In response to TOLL-like receptor (TLR) agonists LPS and poly I:C, cultured bone marrow-derived dendritic cells (BMDC) from WT and mutant mice exhibited similar increases in expression of co-stimulatory molecules CD40, CD80, and CD86. |
T8 |
675-909 |
Sentence |
denotes |
In response to TOLL-like receptor (TLR) agonists LPS and poly I:C, cultured bone marrow-derived dendritic cells (BMDC) from WT and mutant mice exhibited similar increases in expression of co-stimulatory molecules CD40, CD80, and CD86. |
T114 |
910-1061 |
Sentence |
denotes |
However, stimulated SHARPIN-deficient BMDC had reduced transcription and secretion of pro-inflammatory mediators IL6, IL12P70, GMCSF, and nitric oxide. |
T9 |
910-1061 |
Sentence |
denotes |
However, stimulated SHARPIN-deficient BMDC had reduced transcription and secretion of pro-inflammatory mediators IL6, IL12P70, GMCSF, and nitric oxide. |
T115 |
1062-1234 |
Sentence |
denotes |
Mutant BMDC had defective activation of NF-κB signaling, whereas the MAPK1/3 (ERK1/2) and MAPK11/12/13/14 (p38 MAP kinase isoforms) and TBK1 signaling pathways were intact. |
T10 |
1062-1234 |
Sentence |
denotes |
Mutant BMDC had defective activation of NF-κB signaling, whereas the MAPK1/3 (ERK1/2) and MAPK11/12/13/14 (p38 MAP kinase isoforms) and TBK1 signaling pathways were intact. |
T116 |
1235-1411 |
Sentence |
denotes |
A mixed lymphocyte reaction showed that mutant BMDC only induced a weak Th1 immune response but stimulated increased Th2 cytokine production from allogeneic naïve CD4+ T cells. |
T11 |
1235-1411 |
Sentence |
denotes |
A mixed lymphocyte reaction showed that mutant BMDC only induced a weak Th1 immune response but stimulated increased Th2 cytokine production from allogeneic naïve CD4+ T cells. |
T117 |
1412-1591 |
Sentence |
denotes |
In conclusion, loss of Sharpin in mice significantly affects the immune function of DC and this may partially account for the systemic inflammation and Th2-biased immune response. |
T12 |
1412-1591 |
Sentence |
denotes |
In conclusion, loss of Sharpin in mice significantly affects the immune function of DC and this may partially account for the systemic inflammation and Th2-biased immune response. |