These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
240 related articles for article (PubMed ID: 21083659)
1. X-linked lymphoproliferative syndrome: a genetic condition typified by the triad of infection, immunodeficiency and lymphoma. Rezaei N; Mahmoudi E; Aghamohammadi A; Das R; Nichols KE Br J Haematol; 2011 Jan; 152(1):13-30. PubMed ID: 21083659 [TBL] [Abstract][Full Text] [Related]
2. Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP). Brandau O; Schuster V; Weiss M; Hellebrand H; Fink FM; Kreczy A; Friedrich W; Strahm B; Niemeyer C; Belohradsky BH; Meindl A Hum Mol Genet; 1999 Dec; 8(13):2407-13. PubMed ID: 10556288 [TBL] [Abstract][Full Text] [Related]
3. Study of SH2D1A gene mutation in paediatric patients with B-cell lymphoma. Koochakzadeh L; Hosseinverdi S; Hedayat M; Farahani F; Tofighi A; Eghbali M; Bidoki AZ; Izadyar M; Rahiminejad MS; Ramyar A; Aghamohammadi A; Rezaei N Allergol Immunopathol (Madr); 2015; 43(6):568-70. PubMed ID: 25982576 [TBL] [Abstract][Full Text] [Related]
4. Molecular pathogenesis of EBV susceptibility in XLP as revealed by analysis of female carriers with heterozygous expression of SAP. Palendira U; Low C; Chan A; Hislop AD; Ho E; Phan TG; Deenick E; Cook MC; Riminton DS; Choo S; Loh R; Alvaro F; Booth C; Gaspar HB; Moretta A; Khanna R; Rickinson AB; Tangye SG PLoS Biol; 2011 Nov; 9(11):e1001187. PubMed ID: 22069374 [TBL] [Abstract][Full Text] [Related]
5. Natural killer T cells and X-linked lymphoproliferative syndrome. Latour S Curr Opin Allergy Clin Immunol; 2007 Dec; 7(6):510-4. PubMed ID: 17989527 [TBL] [Abstract][Full Text] [Related]
6. X-linked lymphoproliferative disease: a progressive immunodeficiency. Morra M; Howie D; Grande MS; Sayos J; Wang N; Wu C; Engel P; Terhorst C Annu Rev Immunol; 2001; 19():657-82. PubMed ID: 11244050 [TBL] [Abstract][Full Text] [Related]
7. X-linked lymphoproliferative disease is caused by deficiency of a novel SH2 domain-containing signal transduction adaptor protein. Schuster V; Kreth HW Immunol Rev; 2000 Dec; 178():21-8. PubMed ID: 11213803 [TBL] [Abstract][Full Text] [Related]
8. Distinct interactions of the X-linked lymphoproliferative syndrome gene product SAP with cytoplasmic domains of members of the CD2 receptor family. Lewis J; Eiben LJ; Nelson DL; Cohen JI; Nichols KE; Ochs HD; Notarangelo LD; Duckett CS Clin Immunol; 2001 Jul; 100(1):15-23. PubMed ID: 11414741 [TBL] [Abstract][Full Text] [Related]
9. X-linked lymphoproliferative syndrome in mainland China: review of clinical, genetic, and immunological characteristic. Xu T; Zhao Q; Li W; Chen X; Xue X; Chen Z; Du X; Bai X; Zhao Q; Zhou L; Tang X; Yang X; Kanegane H; Zhao X Eur J Pediatr; 2020 Feb; 179(2):327-338. PubMed ID: 31754776 [TBL] [Abstract][Full Text] [Related]
10. XLP: clinical features and molecular etiology due to mutations in SH2D1A encoding SAP. Tangye SG J Clin Immunol; 2014 Oct; 34(7):772-9. PubMed ID: 25085526 [TBL] [Abstract][Full Text] [Related]
12. Follicular lymphoma in a X-linked lymphoproliferative syndrome carrier female. Woon ST; Ameratunga R; Croxson M; Taylor G; Neas K; Edkins E; Browett P; Gane E; Munn S Scand J Immunol; 2008 Aug; 68(2):153-8. PubMed ID: 18702745 [TBL] [Abstract][Full Text] [Related]
13. Activation-dependent T cell expression of the X-linked lymphoproliferative disease gene product SLAM-associated protein and its assessment for patient detection. Shinozaki K; Kanegane H; Matsukura H; Sumazaki R; Tsuchida M; Makita M; Kimoto Y; Kanai R; Tsumura K; Kondoh T; Moriuchi H; Miyawaki T Int Immunol; 2002 Oct; 14(10):1215-23. PubMed ID: 12356686 [TBL] [Abstract][Full Text] [Related]
14. XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome. Rigaud S; Fondanèche MC; Lambert N; Pasquier B; Mateo V; Soulas P; Galicier L; Le Deist F; Rieux-Laucat F; Revy P; Fischer A; de Saint Basile G; Latour S Nature; 2006 Nov; 444(7115):110-4. PubMed ID: 17080092 [TBL] [Abstract][Full Text] [Related]
15. X-linked lymphoproliferative syndromes and related autosomal recessive disorders. Veillette A; Pérez-Quintero LA; Latour S Curr Opin Allergy Clin Immunol; 2013 Dec; 13(6):614-22. PubMed ID: 24113228 [TBL] [Abstract][Full Text] [Related]
16. Hypogammaglobulinemia and exacerbated CD8 T-cell-mediated immunopathology in SAP-deficient mice with chronic LCMV infection mimics human XLP disease. Crotty S; McCausland MM; Aubert RD; Wherry EJ; Ahmed R Blood; 2006 Nov; 108(9):3085-93. PubMed ID: 16788096 [TBL] [Abstract][Full Text] [Related]
17. [Genetic and proteinic analysis of a Chinese boy with X-linked lymphoproliferative disease and his maternal relatives]. Yang X; Wang J; An YF; Kanegane H; Miyawaki T; Zhao XD Zhonghua Er Ke Za Zhi; 2011 Jun; 49(6):416-20. PubMed ID: 21924052 [TBL] [Abstract][Full Text] [Related]
18. Using flow cytometry to screen patients for X-linked lymphoproliferative disease due to SAP deficiency and XIAP deficiency. Marsh RA; Bleesing JJ; Filipovich AH J Immunol Methods; 2010 Oct; 362(1-2):1-9. PubMed ID: 20816973 [TBL] [Abstract][Full Text] [Related]
19. [Two families of X-linked lymphoproliferative disease type 1 characterized by agammaglobulinemia]. Li WY; Chen JS; Zhao Q; Dai RX; Wang YP; Zhao HY; Chen XM; Xue XH; Sun XY; Tang XM; Zhang Y; Ding Y; Zhao XD; Zhang ZY Zhonghua Er Ke Za Zhi; 2017 May; 55(5):377-382. PubMed ID: 28482391 [No Abstract] [Full Text] [Related]