CTLA-4 (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "CTLA-4" in French language version.

refsWebsite
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cell.com

  • Tivol EA, Borriello F, Schweitzer AN, Lynch WP, Bluestone JA, Sharpe AH, « Loss of CTLA-4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA-4 », Immunity, vol. 3, no 5,‎ , p. 541–7 (PMID 7584144, DOI 10.1016/1074-7613(95)90125-6, lire en ligne)

doi.org

dx.doi.org

  • (en) Nicholas L Syn, Michele W L Teng, Tony S K Mok et Ross A Soo, « De-novo and acquired resistance to immune checkpoint targeting », The Lancet Oncology, vol. 18, no 12,‎ , e731–e741 (PMID 29208439, DOI 10.1016/s1470-2045(17)30607-1, lire en ligne)
  • Brunet JF, Denizot F, Luciani MF, Roux-Dosseto M, Suzan M, Mattei MG, Golstein P, « A new member of the immunoglobulin superfamily--CTLA-4 », Nature, vol. 328, no 6127,‎ , p. 267–70 (PMID 3496540, DOI 10.1038/328267a0)
  • Dariavach P, Mattéi MG, Golstein P, Lefranc MP, « Human Ig superfamily CTLA-4 gene: chromosomal localization and identity of protein sequence between murine and human CTLA-4 cytoplasmic domains », Eur. J. Immunol., vol. 18, no 12,‎ , p. 1901–5 (PMID 3220103, DOI 10.1002/eji.1830181206)
  • Waterhouse P, Penninger JM, Timms E, Wakeham A, Shahinian A, Lee KP, Thompson CB, Griesser H, Mak TW, « Lymphoproliferative disorders with early lethality in mice deficient in Ctla-4 », Science, vol. 270, no 5238,‎ , p. 985–8 (PMID 7481803, DOI 10.1126/science.270.5238.985, JSTOR 2888113)
  • Tivol EA, Borriello F, Schweitzer AN, Lynch WP, Bluestone JA, Sharpe AH, « Loss of CTLA-4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA-4 », Immunity, vol. 3, no 5,‎ , p. 541–7 (PMID 7584144, DOI 10.1016/1074-7613(95)90125-6, lire en ligne)
  • Krummel MF, Allison JP, « CD28 and CTLA-4 have opposing effects on the response of T cells to stimulation », J. Exp. Med., vol. 182, no 2,‎ , p. 459–65 (PMID 7543139, PMCID 2192127, DOI 10.1084/jem.182.2.459)
  • Walunas TL, Bakker CY, Bluestone JA, « CTLA-4 ligation blocks CD28-dependent T cell activation », J. Exp. Med., vol. 183, no 6,‎ , p. 2541–50 (PMID 8676075, PMCID 2192609, DOI 10.1084/jem.183.6.2541)
  • Walunas TL, Lenschow DJ, Bakker CY, Linsley PS, Freeman GJ, Green JM, Thompson CB, Bluestone JA, « CTLA-4 can function as a negative regulator of T cell activation », Immunity, vol. 1, no 5,‎ , p. 405–13 (PMID 7882171, DOI 10.1016/1074-7613(94)90071-x)
  • Harding FA, McArthur JG, Gross JA, Raulet DH, Allison JP, « CD28-mediated signalling co-stimulates murine T cells and prevents induction of anergy in T-cell clones », Nature, vol. 356, no 6370,‎ , p. 607–9 (PMID 1313950, DOI 10.1038/356607a0)
  • Magistrelli G, Jeannin P, Herbault N, Benoit De Coignac A, Gauchat JF, Bonnefoy JY, Delneste Y, « A soluble form of CTLA-4 generated by alternative splicing is expressed by nonstimulated human T cells », Eur. J. Immunol., vol. 29, no 11,‎ , p. 3596–602 (PMID 10556814, DOI 10.1002/(SICI)1521-4141(199911)29:11<3596::AID-IMMU3596>3.0.CO;2-Y)
  • Lee KM, Chuang E, Griffin M, Khattri R, Hong DK, Zhang W, Straus D, Samelson LE, Thompson CB, Bluestone JA, « Molecular basis of T cell inactivation by CTLA-4 », Science, vol. 282, no 5397,‎ , p. 2263–6 (PMID 9856951, DOI 10.1126/science.282.5397.2263)
  • Qureshi OS, Zheng Y, Nakamura K, Attridge K, Manzotti C, Schmidt EM, Baker J, Jeffery LE, Kaur S, Briggs Z, Hou TZ, Futter CE, Anderson G, Walker LS, Sansom DM, « Trans-endocytosis of CD80 and CD86: a molecular basis for the cell-extrinsic function of CTLA-4 », Science, vol. 332, no 6029,‎ , p. 600–3 (PMID 21474713, PMCID 3198051, DOI 10.1126/science.1202947)
  • Chen J, Ganguly A, Mucsi AD, Meng J, Yan J, Detampel P, Munro F, Zhang Z, Wu M, Hari A, Stenner MD, Zheng W, Kubes P, Xia T, Amrein MW, Qi H, Shi Y, « Strong adhesion by regulatory T cells induces dendritic cell cytoskeletal polarization and contact-dependent lethargy », The Journal of Experimental Medicine, vol. 214, no 2,‎ , p. 327–338 (PMID 28082358, PMCID 5294852, DOI 10.1084/jem.20160620)

elsevier.com

linkinghub.elsevier.com

ensembl.org

May2017.archive.ensembl.org

jstor.org

  • Waterhouse P, Penninger JM, Timms E, Wakeham A, Shahinian A, Lee KP, Thompson CB, Griesser H, Mak TW, « Lymphoproliferative disorders with early lethality in mice deficient in Ctla-4 », Science, vol. 270, no 5238,‎ , p. 985–8 (PMID 7481803, DOI 10.1126/science.270.5238.985, JSTOR 2888113)

nih.gov

ncbi.nlm.nih.gov

  • « Publications PubMed pour l'Homme », sur National Center for Biotechnology Information, U.S. National Library of Medicine
  • « Publications PubMed pour la Souris », sur National Center for Biotechnology Information, U.S. National Library of Medicine
  • (en) Nicholas L Syn, Michele W L Teng, Tony S K Mok et Ross A Soo, « De-novo and acquired resistance to immune checkpoint targeting », The Lancet Oncology, vol. 18, no 12,‎ , e731–e741 (PMID 29208439, DOI 10.1016/s1470-2045(17)30607-1, lire en ligne)
  • Brunet JF, Denizot F, Luciani MF, Roux-Dosseto M, Suzan M, Mattei MG, Golstein P, « A new member of the immunoglobulin superfamily--CTLA-4 », Nature, vol. 328, no 6127,‎ , p. 267–70 (PMID 3496540, DOI 10.1038/328267a0)
  • Dariavach P, Mattéi MG, Golstein P, Lefranc MP, « Human Ig superfamily CTLA-4 gene: chromosomal localization and identity of protein sequence between murine and human CTLA-4 cytoplasmic domains », Eur. J. Immunol., vol. 18, no 12,‎ , p. 1901–5 (PMID 3220103, DOI 10.1002/eji.1830181206)
  • Waterhouse P, Penninger JM, Timms E, Wakeham A, Shahinian A, Lee KP, Thompson CB, Griesser H, Mak TW, « Lymphoproliferative disorders with early lethality in mice deficient in Ctla-4 », Science, vol. 270, no 5238,‎ , p. 985–8 (PMID 7481803, DOI 10.1126/science.270.5238.985, JSTOR 2888113)
  • Tivol EA, Borriello F, Schweitzer AN, Lynch WP, Bluestone JA, Sharpe AH, « Loss of CTLA-4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA-4 », Immunity, vol. 3, no 5,‎ , p. 541–7 (PMID 7584144, DOI 10.1016/1074-7613(95)90125-6, lire en ligne)
  • Krummel MF, Allison JP, « CD28 and CTLA-4 have opposing effects on the response of T cells to stimulation », J. Exp. Med., vol. 182, no 2,‎ , p. 459–65 (PMID 7543139, PMCID 2192127, DOI 10.1084/jem.182.2.459)
  • Walunas TL, Bakker CY, Bluestone JA, « CTLA-4 ligation blocks CD28-dependent T cell activation », J. Exp. Med., vol. 183, no 6,‎ , p. 2541–50 (PMID 8676075, PMCID 2192609, DOI 10.1084/jem.183.6.2541)
  • Walunas TL, Lenschow DJ, Bakker CY, Linsley PS, Freeman GJ, Green JM, Thompson CB, Bluestone JA, « CTLA-4 can function as a negative regulator of T cell activation », Immunity, vol. 1, no 5,‎ , p. 405–13 (PMID 7882171, DOI 10.1016/1074-7613(94)90071-x)
  • Harding FA, McArthur JG, Gross JA, Raulet DH, Allison JP, « CD28-mediated signalling co-stimulates murine T cells and prevents induction of anergy in T-cell clones », Nature, vol. 356, no 6370,‎ , p. 607–9 (PMID 1313950, DOI 10.1038/356607a0)
  • Magistrelli G, Jeannin P, Herbault N, Benoit De Coignac A, Gauchat JF, Bonnefoy JY, Delneste Y, « A soluble form of CTLA-4 generated by alternative splicing is expressed by nonstimulated human T cells », Eur. J. Immunol., vol. 29, no 11,‎ , p. 3596–602 (PMID 10556814, DOI 10.1002/(SICI)1521-4141(199911)29:11<3596::AID-IMMU3596>3.0.CO;2-Y)
  • Lee KM, Chuang E, Griffin M, Khattri R, Hong DK, Zhang W, Straus D, Samelson LE, Thompson CB, Bluestone JA, « Molecular basis of T cell inactivation by CTLA-4 », Science, vol. 282, no 5397,‎ , p. 2263–6 (PMID 9856951, DOI 10.1126/science.282.5397.2263)
  • Qureshi OS, Zheng Y, Nakamura K, Attridge K, Manzotti C, Schmidt EM, Baker J, Jeffery LE, Kaur S, Briggs Z, Hou TZ, Futter CE, Anderson G, Walker LS, Sansom DM, « Trans-endocytosis of CD80 and CD86: a molecular basis for the cell-extrinsic function of CTLA-4 », Science, vol. 332, no 6029,‎ , p. 600–3 (PMID 21474713, PMCID 3198051, DOI 10.1126/science.1202947)
  • Chen J, Ganguly A, Mucsi AD, Meng J, Yan J, Detampel P, Munro F, Zhang Z, Wu M, Hari A, Stenner MD, Zheng W, Kubes P, Xia T, Amrein MW, Qi H, Shi Y, « Strong adhesion by regulatory T cells induces dendritic cell cytoskeletal polarization and contact-dependent lethargy », The Journal of Experimental Medicine, vol. 214, no 2,‎ , p. 327–338 (PMID 28082358, PMCID 5294852, DOI 10.1084/jem.20160620)