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Blood
Volumn 115, Issue 25, 2010, Pages 5125-5126
Somatic ALPS: A FAScinating condition
Author keywords

[No Author keywords available]
Indexed keywords

CASPASE 10; FAS ANTIBODY; FAS ANTIGEN; FAS LIGAND; T LYMPHOCYTE RECEPTOR ALPHA CHAIN; T LYMPHOCYTE RECEPTOR BETA CHAIN;
EID: 77956535878     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2010-04-278465     Document Type: Note
Times cited : (2)
References (7)
  • 1
    • 77954661589 scopus 로고    scopus 로고
    • Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndrome
    • Dowdell KC, Niemela JE, Price S, et al. Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndrome. Blood. 2010;115(25):5164-5169.
    • (2010) Blood , vol.115 , Issue.25 , pp. 5164-5169
    • Dowdell, K.C.1    Niemela, J.E.2    Price, S.3
  • 3
    • 77950368803 scopus 로고    scopus 로고
    • Using biomarkers to predict the presence of FAS mutations in patients with features of the autoimmune lymphoproliferative syndrome
    • Caminha I, Fleisher TA, Hornung RL, et al. Using biomarkers to predict the presence of FAS mutations in patients with features of the autoimmune lymphoproliferative syndrome. J Allergy Clin Immunol. 2010;125(4):946-949.
    • (2010) J Allergy Clin Immunol , vol.125 , Issue.4 , pp. 946-949
    • Caminha, I.1    Fleisher, T.A.2    Hornung, R.L.3
  • 4
    • 77950416383 scopus 로고    scopus 로고
    • Identifying autoimmune lymphoproliferative syndrome in children with Evans syndrome: A multi-institutional study
    • Seif AE, Manno CS, Sheen C, Grupp SA, Teachey DT. Identifying autoimmune lymphoproliferative syndrome in children with Evans syndrome: a multi-institutional study. Blood. 2010;115(11):2142-2145.
    • (2010) Blood , vol.115 , Issue.11 , pp. 2142-2145
    • Seif, A.E.1    Manno, C.S.2    Sheen, C.3    Grupp, S.A.4    Teachey, D.T.5
  • 5
    • 64049096371 scopus 로고    scopus 로고
    • FAS-L, IL-10, and double-negative CD4- CD8-TCR alpha/beta+ T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function
    • Magerus-Chatinet A, Stolzenberg MC, Loffredo MS, et al. FAS-L, IL-10, and double-negative CD4- CD8-TCR alpha/beta+ T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function. Blood. 2009;113(13):3027-3030.
    • (2009) Blood , vol.113 , Issue.13 , pp. 3027-3030
    • Magerus-Chatinet, A.1    Stolzenberg, M.C.2    Loffredo, M.S.3
  • 6
    • 61949157161 scopus 로고    scopus 로고
    • Treatment with sirolimus results in complete responses in patients with autoimmune lymphoproliferative syndrome
    • Teachey DT, Greiner R, Seif A, et al. Treatment with sirolimus results in complete responses in patients with autoimmune lymphoproliferative syndrome. Br J Haematol. 2009;145(1):101-106.
    • (2009) Br J Haematol , vol.145 , Issue.1 , pp. 101-106
    • Teachey, D.T.1    Greiner, R.2    Seif, A.3
  • 7
    • 70449719356 scopus 로고    scopus 로고
    • Human TCR-alpha beta+ CD4- CD8-T cells can derive from CD8+ T cells and display an inflammatory effector phenotype
    • Crispin JC, Tsokos GC. Human TCR-alpha beta+ CD4- CD8-T cells can derive from CD8+ T cells and display an inflammatory effector phenotype. J Immunol. 2009;183(7):4675-4681.
    • (2009) J Immunol , vol.183 , Issue.7 , pp. 4675-4681
    • Crispin, J.C.1    Tsokos, G.C.2

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.