-
1
-
-
27144454119
-
CD8+ T-cell lymphocytopenia and lack of EVER mutations in a patient with clinically and virologically typical epidermodysplasia verruciformis
-
Azzimonti B, Mondini M, De Andrea M, Gioia D, Dianzani U, Mesturini R et al. (2005) CD8+ T-cell lymphocytopenia and lack of EVER mutations in a patient with clinically and virologically typical epidermodysplasia verruciformis. Arch Dermatol 141:1323-5
-
(2005)
Arch Dermatol
, vol.141
, pp. 1323-1325
-
-
Azzimonti, B.1
Mondini, M.2
De Andrea, M.3
Gioia, D.4
Dianzani, U.5
Mesturini, R.6
-
2
-
-
0034880940
-
Concerted action of the FasL/Fas and perforin/granzyme A and B pathways is mandatory for the development of early viral hepatitis but not for recovery from viral infection
-
Balkow S, Kersten A, Tran TT, Stehle T, Grosse P, Museteanu C et al. (2001) Concerted action of the FasL/Fas and perforin/granzyme A and B pathways is mandatory for the development of early viral hepatitis but not for recovery from viral infection. J Virol 75:8781-91
-
(2001)
J Virol
, vol.75
, pp. 8781-8791
-
-
Balkow, S.1
Kersten, A.2
Tran, T.T.3
Stehle, T.4
Grosse, P.5
Museteanu, C.6
-
3
-
-
33751187119
-
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 et al. (2006) Variations of the perforin gene in patients with autoimmunity/lymphoproliferation and defective Fas function. Blood 108:3079-84
-
(2006)
Blood
, vol.108
, pp. 3079-3084
-
-
Clementi, R.1
Chiocchetti, A.2
Cappellano, G.3
Cerutti, E.4
Ferretti, M.5
Orilieri, E.6
-
4
-
-
4644229431
-
Inherited perforin and Fas mutations in a patient with autoimmune lymphoproliferative syndrome and lymphoma
-
Clementi R, Dagna L, Dianzani U, Dupre L, Dianzani I, Ponzoni M et al. (2004) Inherited perforin and Fas mutations in a patient with autoimmune lymphoproliferative syndrome and lymphoma. N Engl J Med 351:1419-24
-
(2004)
N Engl J Med
, vol.351
, pp. 1419-1424
-
-
Clementi, R.1
Dagna, L.2
Dianzani, U.3
Dupre, L.4
Dianzani, I.5
Ponzoni, M.6
-
6
-
-
17144433746
-
Deficiency of the Fas apoptosis pathway without Fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation
-
Dianzani U, Bragardo M, DiFranco D, Alliaudi C, Scagni P, Buonfiglio D et al. (1997) Deficiency of the Fas apoptosis pathway without Fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation. Blood 89:2871-9
-
(1997)
Blood
, vol.89
, pp. 2871-2879
-
-
Dianzani, U.1
Bragardo, M.2
DiFranco, D.3
Alliaudi, C.4
Scagni, P.5
Buonfiglio, D.6
-
7
-
-
0037427370
-
Role of inherited defects decreasing Fas function in autoimmunity
-
Dianzani U, Chiocchetti A, Ramenghi U (2003) Role of inherited defects decreasing Fas function in autoimmunity. Life Sci 72:2803-24
-
(2003)
Life Sci
, vol.72
, pp. 2803-2824
-
-
Dianzani, U.1
Chiocchetti, A.2
Ramenghi, U.3
-
8
-
-
0028219791
-
Cytotoxicity mediated by T cells and natural killer cells is greatly impaired in perforin-deficient mice
-
Kagi D, Ledermann B, Burki K, Seiler P, Odermatt B, Olsen KJ et al. (1994) Cytotoxicity mediated by T cells and natural killer cells is greatly impaired in perforin-deficient mice. Nature 369:31-7
-
(1994)
Nature
, vol.369
, pp. 31-37
-
-
Kagi, D.1
Ledermann, B.2
Burki, K.3
Seiler, P.4
Odermatt, B.5
Olsen, K.J.6
-
9
-
-
4444379717
-
Primary immunodeficiency diseases: An update
-
Notarangelo L, Casanova JL, Fischer A, Puck J, Rosen F, Seger R et al. (2004) Primary immunodeficiency diseases: an update. J Allergy Clin Immunol 114:677-87
-
(2004)
J Allergy Clin Immunol
, vol.114
, pp. 677-687
-
-
Notarangelo, L.1
Casanova, J.L.2
Fischer, A.3
Puck, J.4
Rosen, F.5
Seger, R.6
-
10
-
-
33749430257
-
Genetics of epidermodysplasia verruciformis: Insights into host defense against papillomaviruses
-
Orth G (2006) Genetics of epidermodysplasia verruciformis: insights into host defense against papillomaviruses. Semin Immunol 18:362-74
-
(2006)
Semin Immunol
, vol.18
, pp. 362-374
-
-
Orth, G.1
-
11
-
-
18744369886
-
Mutations in two adjacent novel genes are associated with epidermodysplasia verruciformis
-
Ramoz N, Rueda LA, Bouadjar B, Montoya LS, Orth G, Favre M (2002) Mutations in two adjacent novel genes are associated with epidermodysplasia verruciformis. Nat Genet 32:579-81
-
(2002)
Nat Genet
, vol.32
, pp. 579-581
-
-
Ramoz, N.1
Rueda, L.A.2
Bouadjar, B.3
Montoya, L.S.4
Orth, G.5
Favre, M.6
-
12
-
-
0345059209
-
An inherited disorder of lymphocyte apoptosis: The autoimmune lymphoproliferative syndrome
-
Straus SE, Sneller M, Lenardo MJ, Puck JM, Strober W (1999) An inherited disorder of lymphocyte apoptosis: the autoimmune lymphoproliferative syndrome. Ann Intern Med 130:591-601
-
(1999)
Ann Intern Med
, vol.130
, pp. 591-601
-
-
Straus, S.E.1
Sneller, M.2
Lenardo, M.J.3
Puck, J.M.4
Strober, W.5
-
13
-
-
33645067636
-
Autoimmune lymphoproliferative syndrome: Molecular basis of disease and clinical phenotype
-
Worth A, Thrasher AJ, Gaspar HB (2006) Autoimmune lymphoproliferative syndrome: molecular basis of disease and clinical phenotype. Br J Haematol 133:124-40
-
(2006)
Br J Haematol
, vol.133
, pp. 124-140
-
-
Worth, A.1
Thrasher, A.J.2
Gaspar, H.B.3
|