# |
PMID |
Sentence |
1 |
25637015
|
Smad4 promotes differentiation of effector and circulating memory CD8 T cells but is dispensable for tissue-resident memory CD8 T cells.
|
2 |
25637015
|
In contrast, circulating memory CD8 T cells have no requirement for TGF-β but show signs of arrested development in the absence of Smad4, including aberrant CD103 expression.
|
3 |
25637015
|
Our data show that Smad4 is required for normal differentiation of multiple subsets of virus-specific CD8 T cells.
|
4 |
25637015
|
Smad4 promotes differentiation of effector and circulating memory CD8 T cells but is dispensable for tissue-resident memory CD8 T cells.
|
5 |
25637015
|
In contrast, circulating memory CD8 T cells have no requirement for TGF-β but show signs of arrested development in the absence of Smad4, including aberrant CD103 expression.
|
6 |
25637015
|
Our data show that Smad4 is required for normal differentiation of multiple subsets of virus-specific CD8 T cells.
|
7 |
25637015
|
Smad4 promotes differentiation of effector and circulating memory CD8 T cells but is dispensable for tissue-resident memory CD8 T cells.
|
8 |
25637015
|
In contrast, circulating memory CD8 T cells have no requirement for TGF-β but show signs of arrested development in the absence of Smad4, including aberrant CD103 expression.
|
9 |
25637015
|
Our data show that Smad4 is required for normal differentiation of multiple subsets of virus-specific CD8 T cells.
|
10 |
26185420
|
Pancreatic adenocarcinoma is characterized by several germline or acquired genetic mutations, the most common being KRAS (90%), CDK2NA (90%), TP53 (75%-90%), DPC4/SMAD4 (50%).
|
11 |
26185420
|
Recent reports note activity with immunotherapies such as CD40 agonists, CCR2 inhibitors, cancer vaccines, and novel combinations against the immunosuppressive tumor milieu are ongoing.
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