162 related articles for article (PubMed ID: 16720836)
1. Variations of the perforin gene in patients with autoimmunity/lymphoproliferation and defective Fas function.
Clementi R; Chiocchetti A; Cappellano G; Cerutti E; Ferretti M; Orilieri E; Dianzani I; Ferrarini M; Bregni M; Danesino C; Bozzi V; Putti MC; Cerutti F; Cometa A; Locatelli F; Maccario R; Ramenghi U; Dianzani U
Blood; 2006 Nov; 108(9):3079-84. PubMed ID: 16720836
[TBL] [Abstract][Full Text] [Related]
2. High levels of osteopontin associated with polymorphisms in its gene are a risk factor for development of autoimmunity/lymphoproliferation.
Chiocchetti A; Indelicato M; Bensi T; Mesturini R; Giordano M; Sametti S; Castelli L; Bottarel F; Mazzarino MC; Garbarini L; Giacopelli F; Valesini G; Santoro C; Dianzani I; Ramenghi U; Dianzani U
Blood; 2004 Feb; 103(4):1376-82. PubMed ID: 14592838
[TBL] [Abstract][Full Text] [Related]
3. Variations of the UNC13D gene in patients with autoimmune lymphoproliferative syndrome.
Aricò M; Boggio E; Cetica V; Melensi M; Orilieri E; Clemente N; Cappellano G; Buttini S; Soluri MF; Comi C; Dufour C; Pende D; Dianzani I; Ellis SR; Pagliano S; Marcenaro S; Ramenghi U; Chiocchetti A; Dianzani U
PLoS One; 2013; 8(7):e68045. PubMed ID: 23840885
[TBL] [Abstract][Full Text] [Related]
4. Variations of the perforin gene in patients with type 1 diabetes.
Orilieri E; Cappellano G; Clementi R; Cometa A; Ferretti M; Cerutti E; Cadario F; Martinetti M; Larizza D; Calcaterra V; D'Annunzio G; Lorini R; Cerutti F; Bruno G; Chiocchetti A; Dianzani U
Diabetes; 2008 Apr; 57(4):1078-83. PubMed ID: 18198357
[TBL] [Abstract][Full Text] [Related]
5. Clincal, immunologic, and genetic features of an autoimmune lymphoproliferative syndrome associated with abnormal lymphocyte apoptosis.
Sneller MC; Wang J; Dale JK; Strober W; Middelton LA; Choi Y; Fleisher TA; Lim MS; Jaffe ES; Puck JM; Lenardo MJ; Straus SE
Blood; 1997 Feb; 89(4):1341-8. PubMed ID: 9028957
[TBL] [Abstract][Full Text] [Related]
6. Identification of new Fas mutations in a patient with autoimmune lymphoproliferative syndrome (ALPS) and eosinophilia.
Aspinall AI; Pinto A; Auer IA; Bridges P; Luider J; Dimnik L; Patel KD; Jorgenson K; Woodman RC
Blood Cells Mol Dis; 1999; 25(3-4):227-38. PubMed ID: 10575548
[TBL] [Abstract][Full Text] [Related]
7. Inherited perforin and Fas mutations in a patient with autoimmune lymphoproliferative syndrome and lymphoma.
Clementi R; Dagna L; Dianzani U; Dupré L; Dianzani I; Ponzoni M; Cometa A; Chiocchetti A; Sabbadini MG; Rugarli C; Ciceri F; Maccario R; Locatelli F; Danesino C; Ferrarini M; Bregni M
N Engl J Med; 2004 Sep; 351(14):1419-24. PubMed ID: 15459303
[TBL] [Abstract][Full Text] [Related]
8. Co-inherited mutations of Fas and caspase-10 in development of the autoimmune lymphoproliferative syndrome.
Cerutti E; Campagnoli MF; Ferretti M; Garelli E; Crescenzio N; Rosolen A; Chiocchetti A; Lenardo MJ; Ramenghi U; Dianzani U
BMC Immunol; 2007 Nov; 8():28. PubMed ID: 17999750
[TBL] [Abstract][Full Text] [Related]
9. Role of inherited defects decreasing Fas function in autoimmunity.
Dianzani U; Chiocchetti A; Ramenghi U
Life Sci; 2003 May; 72(25):2803-24. PubMed ID: 12697265
[TBL] [Abstract][Full Text] [Related]
10. A functional analysis of the putative polymorphisms A91V and N252S and 22 missense perforin mutations associated with familial hemophagocytic lymphohistiocytosis.
Voskoboinik I; Thia MC; Trapani JA
Blood; 2005 Jun; 105(12):4700-6. PubMed ID: 15755897
[TBL] [Abstract][Full Text] [Related]
11. Mutations in apoptosis genes: a pathogenetic factor for human disease.
Müllauer L; Gruber P; Sebinger D; Buch J; Wohlfart S; Chott A
Mutat Res; 2001 Jul; 488(3):211-31. PubMed ID: 11397650
[TBL] [Abstract][Full Text] [Related]
12. Expression in transgenic mice of dominant interfering Fas mutations: a model for human autoimmune lymphoproliferative syndrome.
Choi Y; Ramnath VR; Eaton AS; Chen A; Simon-Stoos KL; Kleiner DE; Erikson J; Puck JM
Clin Immunol; 1999 Oct; 93(1):34-45. PubMed ID: 10497009
[TBL] [Abstract][Full Text] [Related]
13. Autoimmune lymphoproliferative syndrome with defective Fas: genotype influences penetrance.
Jackson CE; Fischer RE; Hsu AP; Anderson SM; Choi Y; Wang J; Dale JK; Fleisher TA; Middelton LA; Sneller MC; Lenardo MJ; Straus SE; Puck JM
Am J Hum Genet; 1999 Apr; 64(4):1002-14. PubMed ID: 10090885
[TBL] [Abstract][Full Text] [Related]
14. The -346T polymorphism of the SH2D1A gene is a risk factor for development of autoimmunity/lymphoproliferation in males with defective Fas function.
Boggio E; Melensi M; Bocca S; Chiocchetti A; Comi C; Clemente N; Orilieri E; Soluri MF; D'Alfonso S; Mechelli R; Gentile G; Poggi A; Salvetti M; Ramenghi U; Dianzani U
Hum Immunol; 2012 May; 73(5):585-92. PubMed ID: 22425739
[TBL] [Abstract][Full Text] [Related]
15. IL-17 protects T cells from apoptosis and contributes to development of ALPS-like phenotypes.
Boggio E; Clemente N; Mondino A; Cappellano G; Orilieri E; Gigliotti CL; Toth E; Ramenghi U; Dianzani U; Chiocchetti A
Blood; 2014 Feb; 123(8):1178-86. PubMed ID: 24363402
[TBL] [Abstract][Full Text] [Related]
16. Autoimmune lymphoproliferative syndrome (ALPS) in a patient with a new germline Fas gene mutation.
Del-Rey MJ; Manzanares J; Bosque A; Aguiló JI; Gómez-Rial J; Roldan E; Serrano A; Anel A; Paz-Artal E; Allende LM
Immunobiology; 2007; 212(2):73-83. PubMed ID: 17336828
[TBL] [Abstract][Full Text] [Related]
17. Familial haemophagocytic lymphohistiocytosis in patients who are heterozygous for the A91V perforin variation is often associated with other genetic defects.
Zhang K; Johnson JA; Biroschak J; Villanueva J; Lee SM; Bleesing JJ; Risma KA; Wenstrup RJ; Filipovich AH
Int J Immunogenet; 2007 Aug; 34(4):231-3. PubMed ID: 17627755
[No Abstract] [Full Text] [Related]
18. Perforin: more than just an effector molecule.
Stepp SE; Mathew PA; Bennett M; de Saint Basile G; Kumar V
Immunol Today; 2000 Jun; 21(6):254-6. PubMed ID: 10825735
[No Abstract] [Full Text] [Related]
19. A genetic disorder of lymphocyte apoptosis involving the fas pathway: the autoimmune lymphoproliferative syndrome.
Fleisher TA; Straus SE; Bleesing JJ
Curr Allergy Asthma Rep; 2001 Nov; 1(6):534-40. PubMed ID: 11895618
[TBL] [Abstract][Full Text] [Related]
20. Deficiency of the Fas apoptosis pathway without Fas gene mutations is a familial trait predisposing to development of autoimmune diseases and cancer.
Ramenghi U; Bonissoni S; Migliaretti G; DeFranco S; Bottarel F; Gambaruto C; DiFranco D; Priori R; Conti F; Dianzani I; Valesini G; Merletti F; Dianzani U
Blood; 2000 May; 95(10):3176-82. PubMed ID: 10807785
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
