PI3Kδ Forms Distinct Multiprotein Complexes at the TCR Signalosome in Naïve and Differentiated CD4+ T Cells.

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Title: PI3Kδ Forms Distinct Multiprotein Complexes at the TCR Signalosome in Naïve and Differentiated CD4+ T Cells.
Authors: Luff DH; Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, Cambridge, United Kingdom., Wojdyla K; Mass Spectrometry Facility, The Babraham Institute, Cambridge, United Kingdom.; Signalling Programme, The Babraham Institute, Cambridge, United Kingdom., Oxley D; Mass Spectrometry Facility, The Babraham Institute, Cambridge, United Kingdom., Chessa T; Signalling Programme, The Babraham Institute, Cambridge, United Kingdom., Hudson K; Bioscience, Oncology R&D, AstraZeneca, Cambridge, United Kingdom., Hawkins PT; Signalling Programme, The Babraham Institute, Cambridge, United Kingdom., Stephens LR; Signalling Programme, The Babraham Institute, Cambridge, United Kingdom., Barry ST; Bioscience, Oncology R&D, AstraZeneca, Cambridge, United Kingdom., Okkenhaug K; Department of Pathology, University of Cambridge, Cambridge, United Kingdom.
Source: Frontiers in immunology [Front Immunol] 2021 Mar 08; Vol. 12, pp. 631271. Date of Electronic Publication: 2021 Mar 08 (Print Publication: 2021).
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101560960 Publication Model: eCollection Cited Medium: Internet ISSN: 1664-3224 (Electronic) Linking ISSN: 16643224 NLM ISO Abbreviation: Front Immunol Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: PI3Kδ Forms Distinct Multiprotein Complexes at the TCR Signalosome in Naïve and Differentiated CD4<superscript>+</superscript> T Cells.
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  Data: <searchLink fieldCode="AU" term="%22Luff+DH%22">Luff DH</searchLink>; Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Wojdyla+K%22">Wojdyla K</searchLink>; Mass Spectrometry Facility, The Babraham Institute, Cambridge, United Kingdom.; Signalling Programme, The Babraham Institute, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Oxley+D%22">Oxley D</searchLink>; Mass Spectrometry Facility, The Babraham Institute, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Chessa+T%22">Chessa T</searchLink>; Signalling Programme, The Babraham Institute, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Hudson+K%22">Hudson K</searchLink>; Bioscience, Oncology R&D, AstraZeneca, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Hawkins+PT%22">Hawkins PT</searchLink>; Signalling Programme, The Babraham Institute, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Stephens+LR%22">Stephens LR</searchLink>; Signalling Programme, The Babraham Institute, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Barry+ST%22">Barry ST</searchLink>; Bioscience, Oncology R&D, AstraZeneca, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Okkenhaug+K%22">Okkenhaug K</searchLink>; Department of Pathology, University of Cambridge, Cambridge, United Kingdom.
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  Data: <searchLink fieldCode="JN" term="%22101560960%22">Frontiers in immunology</searchLink> [Front Immunol] 2021 Mar 08; Vol. 12, pp. 631271. <i>Date of Electronic Publication: </i>2021 Mar 08 (<i>Print Publication: </i>2021).
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Frontiers+Research+Foundation]%22">Frontiers Research Foundation] </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101560960 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Internet <i>ISSN: </i>1664-3224 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2216643224%22">16643224 </searchLink><i>NLM ISO Abbreviation: </i>Front Immunol <i>Subsets: </i>MEDLINE
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        Value: 10.3389/fimmu.2021.631271
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        Text: English
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      – TitleFull: PI3Kδ Forms Distinct Multiprotein Complexes at the TCR Signalosome in Naïve and Differentiated CD4+ T Cells.
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              Text: 2021 Mar 08
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