Gene name: phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma
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25387834
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Proline-rich tyrosine kinase 2 controls PI3-kinase activation downstream of the T cell antigen receptor in human T cells.
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25387834
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Proline-rich tyrosine kinase 2 controls PI3-kinase activation downstream of the T cell antigen receptor in human T cells.
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25387834
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Proline-rich tyrosine kinase 2 controls PI3-kinase activation downstream of the T cell antigen receptor in human T cells.
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25387834
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Proline-rich tyrosine kinase 2 controls PI3-kinase activation downstream of the T cell antigen receptor in human T cells.
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25387834
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Proline-rich tyrosine kinase 2 controls PI3-kinase activation downstream of the T cell antigen receptor in human T cells.
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25387834
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We have previously shown that Pyk2 is activated downstream of the TCR in a PI3K-independent manner.
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25387834
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We have previously shown that Pyk2 is activated downstream of the TCR in a PI3K-independent manner.
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25387834
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We have previously shown that Pyk2 is activated downstream of the TCR in a PI3K-independent manner.
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25387834
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We have previously shown that Pyk2 is activated downstream of the TCR in a PI3K-independent manner.
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25387834
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We have previously shown that Pyk2 is activated downstream of the TCR in a PI3K-independent manner.
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25387834
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We observed that Pyk2 localized with the p85 regulatory subunit of PI3K at the LAT complex and that PI3K-dependent signaling was impaired in Pyk2-deficient T cells.
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25387834
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We observed that Pyk2 localized with the p85 regulatory subunit of PI3K at the LAT complex and that PI3K-dependent signaling was impaired in Pyk2-deficient T cells.
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25387834
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We observed that Pyk2 localized with the p85 regulatory subunit of PI3K at the LAT complex and that PI3K-dependent signaling was impaired in Pyk2-deficient T cells.
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25387834
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We observed that Pyk2 localized with the p85 regulatory subunit of PI3K at the LAT complex and that PI3K-dependent signaling was impaired in Pyk2-deficient T cells.
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25387834
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We observed that Pyk2 localized with the p85 regulatory subunit of PI3K at the LAT complex and that PI3K-dependent signaling was impaired in Pyk2-deficient T cells.
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25387834
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Likewise, functions downstream of PI3K, including IFN-γ production and proliferation, were also suppressed in human T cells deficient in Pyk2.
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25387834
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Likewise, functions downstream of PI3K, including IFN-γ production and proliferation, were also suppressed in human T cells deficient in Pyk2.
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25387834
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Likewise, functions downstream of PI3K, including IFN-γ production and proliferation, were also suppressed in human T cells deficient in Pyk2.
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25387834
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Likewise, functions downstream of PI3K, including IFN-γ production and proliferation, were also suppressed in human T cells deficient in Pyk2.
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25387834
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Likewise, functions downstream of PI3K, including IFN-γ production and proliferation, were also suppressed in human T cells deficient in Pyk2.
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25387834
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Collectively, these data demonstrate that Pyk2 is a critical regulator of PI3K function downstream of the TCR.
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25387834
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Collectively, these data demonstrate that Pyk2 is a critical regulator of PI3K function downstream of the TCR.
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25387834
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Collectively, these data demonstrate that Pyk2 is a critical regulator of PI3K function downstream of the TCR.
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25387834
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Collectively, these data demonstrate that Pyk2 is a critical regulator of PI3K function downstream of the TCR.
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25387834
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Collectively, these data demonstrate that Pyk2 is a critical regulator of PI3K function downstream of the TCR.
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