-
1
-
-
37149022518
-
Human primary immunodeficiency diseases
-
Fischer, A. 2007. Human primary immunodeficiency diseases. Immunity 27: 835-845.
-
(2007)
Immunity
, vol.27
, pp. 835-845
-
-
Fischer, A.1
-
2
-
-
0347089095
-
The human model: a genetic dissection of immunity to infection in natural conditions
-
Casanova, J.-L. & L. Abel. 2004. The human model: a genetic dissection of immunity to infection in natural conditions. Nat. Rev. Immunol. 4: 55-66.
-
(2004)
Nat. Rev. Immunol.
, vol.4
, pp. 55-66
-
-
Casanova, J.-L.1
Abel, L.2
-
3
-
-
84918792751
-
Prevention of infections during primary immunodeficiency
-
Aguilar, C. et al. 2014. Prevention of infections during primary immunodeficiency. Clin. Infect. Dis. 59: 1462-1470.
-
(2014)
Clin. Infect. Dis.
, vol.59
, pp. 1462-1470
-
-
Aguilar, C.1
-
4
-
-
84974696069
-
Epstein-Barr virus
-
In. D.M. Knipe & P.M. Howley, Eds.: Lippincott Williams & Wilkins.
-
Longnecker, R.M., E. Kieff & J.I. Cohen. 2013. "Epstein-Barr virus." In Fields Virology. D.M. Knipe & P.M. Howley, Eds.: Vol. 2: 1898-1959. Lippincott Williams & Wilkins.
-
(2013)
Fields Virology
, vol.2
, pp. 1898-1959
-
-
Longnecker, R.M.1
Kieff, E.2
Cohen, J.I.3
-
6
-
-
84927652740
-
The immunology of Epstein-Barr virus-induced disease
-
Taylor, G.S., H.M. Long, J.M. Brooks, et al. 2014. The immunology of Epstein-Barr virus-induced disease. Annu. Rev. Immunol. 33: 787-821.
-
(2014)
Annu. Rev. Immunol.
, vol.33
, pp. 787-821
-
-
Taylor, G.S.1
Long, H.M.2
Brooks, J.M.3
-
7
-
-
84897438282
-
Cellular immune controls over Epstein-Barr virus infection: new lessons from the clinic and the laboratory
-
Rickinson, A.B., H.M. Long, U. Palendira, et al. 2014. Cellular immune controls over Epstein-Barr virus infection: new lessons from the clinic and the laboratory. Trends Immunol. 35: 159-169.
-
(2014)
Trends Immunol.
, vol.35
, pp. 159-169
-
-
Rickinson, A.B.1
Long, H.M.2
Palendira, U.3
-
8
-
-
1642334164
-
Persistence of the Epstein-Barr virus and the origins of associated lymphomas
-
Thorley-Lawson, D.A. & A. Gross. 2004. Persistence of the Epstein-Barr virus and the origins of associated lymphomas. N. Engl. J. Med. 350: 1328-1337.
-
(2004)
N. Engl. J. Med.
, vol.350
, pp. 1328-1337
-
-
Thorley-Lawson, D.A.1
Gross, A.2
-
10
-
-
84928018253
-
Epstein-Barr virus latent genes
-
Kang, M.-S. & E. Kieff. 2015. Epstein-Barr virus latent genes. Exp. Mol. Med. 47: e131.
-
(2015)
Exp. Mol. Med.
, vol.47
, pp. e131
-
-
Kang, M.-S.1
Kieff, E.2
-
11
-
-
0033680735
-
EBV-infected B cells in infectious mononucleosis: viral strategies for spreading in the B cell compartment and establishing latency
-
Kurth, J. et al. 2000. EBV-infected B cells in infectious mononucleosis: viral strategies for spreading in the B cell compartment and establishing latency. Immunity 13: 485-495.
-
(2000)
Immunity
, vol.13
, pp. 485-495
-
-
Kurth, J.1
-
12
-
-
0035496101
-
Epstein-Barr virus: exploiting the immune system
-
Thorley-Lawson, D.A. 2001. Epstein-Barr virus: exploiting the immune system. Nat. Rev. Immunol. 1: 75-82.
-
(2001)
Nat. Rev. Immunol.
, vol.1
, pp. 75-82
-
-
Thorley-Lawson, D.A.1
-
13
-
-
0142197627
-
B cells under influence: transformation of B cells by Epstein-Barr virus
-
Küppers, R. 2003. B cells under influence: transformation of B cells by Epstein-Barr virus. Nat. Rev. Immunol. 3: 801-812.
-
(2003)
Nat. Rev. Immunol.
, vol.3
, pp. 801-812
-
-
Küppers, R.1
-
14
-
-
84863682989
-
Epstein-Barr virus infection of naïve B cells in vitro frequently selects clones with mutated immunoglobulin genotypes: implications for virus biology
-
Heath, E. et al. 2012. Epstein-Barr virus infection of naïve B cells in vitro frequently selects clones with mutated immunoglobulin genotypes: implications for virus biology. PLoS Pathog. 8: e1002697.
-
(2012)
PLoS Pathog.
, vol.8
, pp. e1002697
-
-
Heath, E.1
-
15
-
-
84872981290
-
Behavioral, virologic, and immunologic factors associated with acquisition and severity of primary Epstein-Barr virus infection in university students
-
Balfour, H.H. et al. 2013. Behavioral, virologic, and immunologic factors associated with acquisition and severity of primary Epstein-Barr virus infection in university students. J. Infect. Dis. 207: 80-88.
-
(2013)
J. Infect. Dis.
, vol.207
, pp. 80-88
-
-
Balfour, H.H.1
-
16
-
-
0036534769
-
Epitope-specific evolution of human CD8(+) T cell responses from primary to persistent phases of Epstein-Barr virus infection
-
Hislop, A.D., N.E. Annels, N.H. Gudgeon, et al. 2002. Epitope-specific evolution of human CD8(+) T cell responses from primary to persistent phases of Epstein-Barr virus infection. J. Exp. Med. 195: 893-905.
-
(2002)
J. Exp. Med.
, vol.195
, pp. 893-905
-
-
Hislop, A.D.1
Annels, N.E.2
Gudgeon, N.H.3
-
17
-
-
13644262179
-
+ immunodominance among Epstein-Barr virus lytic cycle antigens directly reflects the efficiency of antigen presentation in lytically infected cells
-
+ immunodominance among Epstein-Barr virus lytic cycle antigens directly reflects the efficiency of antigen presentation in lytically infected cells. J. Exp. Med. 201: 349-360.
-
(2005)
J. Exp. Med.
, vol.201
, pp. 349-360
-
-
Pudney, V.A.1
Leese, A.M.2
Rickinson, A.B.3
Hislop, A.D.4
-
18
-
-
0141449970
-
+ T cell response to Epstein-Barr virus during primary and persistent infection
-
+ T cell response to Epstein-Barr virus during primary and persistent infection. J. Exp. Med. 198: 903-911.
-
(2003)
J. Exp. Med.
, vol.198
, pp. 903-911
-
-
Amyes, E.1
-
19
-
-
79960409791
-
+ T cell responses to EBV contrast with CD8 responses in breadth of lytic cycle antigen choice and in lytic cycle recognition
-
+ T cell responses to EBV contrast with CD8 responses in breadth of lytic cycle antigen choice and in lytic cycle recognition. J. Immunol. 187: 92-101.
-
(2011)
J. Immunol.
, vol.187
, pp. 92-101
-
-
Long, H.M.1
-
20
-
-
84908147824
-
Role for early-differentiated natural killer cells in infectious mononucleosis
-
Azzi, T. et al. 2014. Role for early-differentiated natural killer cells in infectious mononucleosis. Blood 124: 2533-2543.
-
(2014)
Blood
, vol.124
, pp. 2533-2543
-
-
Azzi, T.1
-
21
-
-
84890973428
-
Human natural killer cells prevent infectious mononucleosis features by targeting lytic Epstein-Barr virus infection
-
Chijioke, O. et al. 2013. Human natural killer cells prevent infectious mononucleosis features by targeting lytic Epstein-Barr virus infection. Cell Rep. 5: 1489-1498.
-
(2013)
Cell Rep.
, vol.5
, pp. 1489-1498
-
-
Chijioke, O.1
-
22
-
-
33846044017
-
The switch from latent to productive infection in Epstein-Barr virus-infected B cells is associated with sensitization to NK cell killing
-
Pappworth, I.Y., E.C. Wang & M. Rowe. 2007. The switch from latent to productive infection in Epstein-Barr virus-infected B cells is associated with sensitization to NK cell killing. J. Virol. 81: 474-482.
-
(2007)
J. Virol.
, vol.81
, pp. 474-482
-
-
Pappworth, I.Y.1
Wang, E.C.2
Rowe, M.3
-
23
-
-
84891550264
-
Innate immune control of EBV-infected B cells by invariant natural killer T cells
-
Chung, B.K. et al. 2013. Innate immune control of EBV-infected B cells by invariant natural killer T cells. Blood 122: 2600-2608.
-
(2013)
Blood
, vol.122
, pp. 2600-2608
-
-
Chung, B.K.1
-
24
-
-
70350227251
-
+ NKT cells suppress tumorigenesis by EBV-associated malignancies
-
+ NKT cells suppress tumorigenesis by EBV-associated malignancies. Cancer Res. 69: 7935-7944.
-
(2009)
Cancer Res.
, vol.69
, pp. 7935-7944
-
-
Yuling, H.1
-
25
-
-
85047688685
-
EBV-induced human CD8(+) NKT cells synergize CD4(+) NKT cells suppressing EBV-associated tumors upon induction of Th1 bias
-
Xiao, W. et al. 2011. EBV-induced human CD8(+) NKT cells synergize CD4(+) NKT cells suppressing EBV-associated tumors upon induction of Th1 bias. Cell. Mol. Immunol. 8: 368.
-
(2011)
Cell. Mol. Immunol.
, vol.8
, pp. 368
-
-
Xiao, W.1
-
26
-
-
84907996988
-
Targeted activation of human Vγ9Vδ2-T cells controls Epstein-Barr virus-induced B cell lymphoproliferative disease
-
Xiang, Z. et al. 2014. Targeted activation of human Vγ9Vδ2-T cells controls Epstein-Barr virus-induced B cell lymphoproliferative disease. Cancer Cell 26: 565-576.
-
(2014)
Cancer Cell
, vol.26
, pp. 565-576
-
-
Xiang, Z.1
-
27
-
-
80052742108
-
Lymphoproliferative disorders after solid organ transplantation-classification, incidence, risk factors, early detection and treatment options
-
Végso, G., M. Hajdu & A. Sebestyén. 2011. Lymphoproliferative disorders after solid organ transplantation-classification, incidence, risk factors, early detection and treatment options. Pathol. Oncol. Res. 17: 443-454.
-
(2011)
Pathol. Oncol. Res
, vol.17
, pp. 443-454
-
-
Végso, G.1
Hajdu, M.2
Sebestyén, A.3
-
28
-
-
84893792563
-
EBV-induced post transplant lymphoproliferative disorders: a persisting challenge in allogeneic hematopoetic SCT
-
Rasche, L., M. Kapp, H. Einsele & S. Mielke. 2014. EBV-induced post transplant lymphoproliferative disorders: a persisting challenge in allogeneic hematopoetic SCT. Bone Marrow Transplant. 49: 163-167.
-
(2014)
Bone Marrow Transplant.
, vol.49
, pp. 163-167
-
-
Rasche, L.1
Kapp, M.2
Einsele, H.3
Mielke, S.4
-
29
-
-
84901822724
-
Co-infections, inflammation and oncogenesis: future directions for EBV research
-
Rickinson, A.B. 2014. Co-infections, inflammation and oncogenesis: future directions for EBV research. Semin. Cancer Biol. 26: 99-115.
-
(2014)
Semin. Cancer Biol.
, vol.26
, pp. 99-115
-
-
Rickinson, A.B.1
-
30
-
-
84865688046
-
T-cell therapy in the treatment of post-transplant lymphoproliferative disease
-
Bollard, C.M., C.M. Rooney & H.E. Heslop. 2012. T-cell therapy in the treatment of post-transplant lymphoproliferative disease. Nat. Rev. Clin. Oncol. 9: 510-519.
-
(2012)
Nat. Rev. Clin. Oncol.
, vol.9
, pp. 510-519
-
-
Bollard, C.M.1
Rooney, C.M.2
Heslop, H.E.3
-
31
-
-
34548025068
-
Allogeneic cytotoxic T-cell therapy for EBV-positive posttransplantation lymphoproliferative disease: results of a phase 2 multicenter clinical trial
-
Haque, T. et al. 2007. Allogeneic cytotoxic T-cell therapy for EBV-positive posttransplantation lymphoproliferative disease: results of a phase 2 multicenter clinical trial. Blood 110: 1123-1131.
-
(2007)
Blood
, vol.110
, pp. 1123-1131
-
-
Haque, T.1
-
32
-
-
34548825933
-
+ natural killer cell subpopulations
-
+ natural killer cell subpopulations. Blood 110: 1530-1539.
-
(2007)
Blood
, vol.110
, pp. 1530-1539
-
-
Wang, H.1
-
33
-
-
10744222779
-
Natural killer cells in HIV-1 infection: dichotomous effects of viremia on inhibitory and activating receptors and their functional correlates
-
Mavilio, D. et al. 2003. Natural killer cells in HIV-1 infection: dichotomous effects of viremia on inhibitory and activating receptors and their functional correlates. Proc. Natl. Acad. Sci. U. S. A. 100: 15011-15016.
-
(2003)
Proc. Natl. Acad. Sci. U. S. A.
, vol.100
, pp. 15011-15016
-
-
Mavilio, D.1
-
34
-
-
20044391050
-
Characterization of CD56-/16+ NK cells
-
Mavilio, D. et al. 2005. Characterization of CD56-/16+ NK cells. Proc. Natl. Acad. Sci. U. S. A. 102: 2886-2891.
-
(2005)
Proc. Natl. Acad. Sci. U. S. A.
, vol.102
, pp. 2886-2891
-
-
Mavilio, D.1
-
35
-
-
84865466629
-
Sarcomas other than Kaposi sarcoma occurring in immunodeficiency: interpretations from a systematic literature review
-
Bhatia, K., M.S. Shiels, A. Berg & E.A. Engels. 2012 Sarcomas other than Kaposi sarcoma occurring in immunodeficiency: interpretations from a systematic literature review. Curr. Opin. Oncol. 24: 537-546.
-
(2012)
Curr. Opin. Oncol.
, vol.24
, pp. 537-546
-
-
Bhatia, K.1
Shiels, M.S.2
Berg, A.3
Engels, E.A.4
-
37
-
-
84900846113
-
Primary immunodeficiency diseases: an update on the classification from the International Union of immunological societies expert committee for primary immunodeficiency
-
Al-Herz, W. et al. 2014. Primary immunodeficiency diseases: an update on the classification from the International Union of immunological societies expert committee for primary immunodeficiency. Front. Immunol. 5: 1-33.
-
(2014)
Front. Immunol.
, vol.5
, pp. 1-33
-
-
Al-Herz, W.1
-
38
-
-
78650984696
-
X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease
-
Booth, C. et al. 2011. X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease. Blood 117: 53-62.
-
(2011)
Blood
, vol.117
, pp. 53-62
-
-
Booth, C.1
-
39
-
-
0016772968
-
X-linked recessive progressive combined variable immunodeficiency (Duncan's disease)
-
Purtilo, D.T. et al. 1975. X-linked recessive progressive combined variable immunodeficiency (Duncan's disease). Lancet 305: 935-941.
-
(1975)
Lancet
, vol.305
, pp. 935-941
-
-
Purtilo, D.T.1
-
40
-
-
0016772146
-
Acquired agammaglobulinemia after a life-threatening illness with clinical and laboratory features of infectious mononucleosis in three related male children
-
Provisor, A. et al. 1975. Acquired agammaglobulinemia after a life-threatening illness with clinical and laboratory features of infectious mononucleosis in three related male children. N. Engl. J. Med. 293: 62-65.
-
(1975)
N. Engl. J. Med.
, vol.293
, pp. 62-65
-
-
Provisor, A.1
-
41
-
-
0016391672
-
Fatal infectious mononucleosis in a family
-
Bar, R.S. et al. 1974. Fatal infectious mononucleosis in a family. N. Engl. J. Med. 290: 363-367.
-
(1974)
N. Engl. J. Med.
, vol.290
, pp. 363-367
-
-
Bar, R.S.1
-
42
-
-
84930898417
-
XLP: clinical features and molecular etiology due to mutations in SH2D1A encoding SAP
-
Tangye, S.G. 2014. XLP: clinical features and molecular etiology due to mutations in SH2D1A encoding SAP. J. Clin. Immunol. 34: 772-779.
-
(2014)
J. Clin. Immunol.
, vol.34
, pp. 772-779
-
-
Tangye, S.G.1
-
43
-
-
0035817326
-
NTB-A, a novel SH2D1A-associated surface molecule contributing to the inability of natural killer cells to kill Epstein-Barr virus-infected B cells in X-linked lymphoproliferative disease
-
Bottino, C. et al. 2001. NTB-A, a novel SH2D1A-associated surface molecule contributing to the inability of natural killer cells to kill Epstein-Barr virus-infected B cells in X-linked lymphoproliferative disease. J. Exp. Med. 194: 235-246.
-
(2001)
J. Exp. Med.
, vol.194
, pp. 235-246
-
-
Bottino, C.1
-
44
-
-
0034618065
-
X-linked lymphoproliferative disease. 2B4 molecules displaying inhibitory rather than activating function are responsible for the inability of natural killer cells to kill Epstein-Barr virus-infected cells
-
Parolini, S. et al. 2000. X-linked lymphoproliferative disease. 2B4 molecules displaying inhibitory rather than activating function are responsible for the inability of natural killer cells to kill Epstein-Barr virus-infected cells. J. Exp. Med. 192: 337-346.
-
(2000)
J. Exp. Med.
, vol.192
, pp. 337-346
-
-
Parolini, S.1
-
45
-
-
82455175808
-
Molecular pathogenesis of EBV susceptibility in XLP as revealed by analysis of female carriers with heterozygous expression of SAP
-
Palendira, U. et al. 2011. Molecular pathogenesis of EBV susceptibility in XLP as revealed by analysis of female carriers with heterozygous expression of SAP. PLoS Biol. 9: e1001187.
-
(2011)
PLoS Biol
, vol.9
, pp. e1001187
-
-
Palendira, U.1
-
46
-
-
78049368414
-
+ T-cell function in X-linked lymphoproliferative disease is restricted to SLAM family-positive B-cell targets
-
+ T-cell function in X-linked lymphoproliferative disease is restricted to SLAM family-positive B-cell targets. Blood 116: 3249-3257.
-
(2010)
Blood
, vol.116
, pp. 3249-3257
-
-
Hislop, A.D.1
-
47
-
-
70349678683
-
Restimulation-induced apoptosis of T cells is impaired in patients with X-linked lymphoproliferative disease caused by SAP deficiency
-
Snow, A.L. et al. 2009. Restimulation-induced apoptosis of T cells is impaired in patients with X-linked lymphoproliferative disease caused by SAP deficiency. J. Clin. Invest. 119: 2976-2989.
-
(2009)
J. Clin. Invest.
, vol.119
, pp. 2976-2989
-
-
Snow, A.L.1
-
48
-
-
84863794143
-
+ T cells in patients with X-linked lymphoproliferative disease caused by selective pressure from Epstein-Barr virus
-
+ T cells in patients with X-linked lymphoproliferative disease caused by selective pressure from Epstein-Barr virus. J. Exp. Med. 209: 913-924.
-
(2012)
J. Exp. Med.
, vol.209
, pp. 913-924
-
-
Palendira, U.1
-
49
-
-
78149356369
-
X-linked lymphoproliferative syndromes: brothers or distant cousins
-
Filipovich, A.H., K. Zhang, A.L. Snow & R.A. Marsh. 2010. X-linked lymphoproliferative syndromes: brothers or distant cousins? Blood 116: 3398-3408.
-
(2010)
Blood
, vol.116
, pp. 3398-3408
-
-
Filipovich, A.H.1
Zhang, K.2
Snow, A.L.3
Marsh, R.A.4
-
50
-
-
79551644967
-
Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)
-
Schmid, J.P. et al. 2011. Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency). Blood 117: 1522-1529.
-
(2011)
Blood
, vol.117
, pp. 1522-1529
-
-
Schmid, J.P.1
-
51
-
-
33750597717
-
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
-
Rigaud, S. et al. 2006. XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome. Nature 444: 110-114.
-
(2006)
Nature
, vol.444
, pp. 110-114
-
-
Rigaud, S.1
-
52
-
-
77956508441
-
XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease
-
Marsh, R.A. et al. 2010. XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease. Blood 116: 1079-1082.
-
(2010)
Blood
, vol.116
, pp. 1079-1082
-
-
Marsh, R.A.1
-
53
-
-
84904612262
-
X-linked inhibitor of apoptosis protein - a critical death resistance regulator and therapeutic target for personalized cancer therapy
-
Obexer, P. & M.J. Ausserlechner. 2014. X-linked inhibitor of apoptosis protein - a critical death resistance regulator and therapeutic target for personalized cancer therapy. Front. Oncol. 4: 1-9.
-
(2014)
Front. Oncol.
, vol.4
, pp. 1-9
-
-
Obexer, P.1
Ausserlechner, M.J.2
-
54
-
-
84873035362
-
Human iNKT and MAIT cells exhibit a PLZF-dependent proapoptotic propensity that is counterbalanced by XIAP
-
Stephane, G. et al. 2013. Human iNKT and MAIT cells exhibit a PLZF-dependent proapoptotic propensity that is counterbalanced by XIAP. Blood 121: 614-623.
-
(2013)
Blood
, vol.121
, pp. 614-623
-
-
Stephane, G.1
-
55
-
-
84908669884
-
A mutation in X-linked inhibitor of apoptosis (G466X) leads to memory inflation of Epstein-Barr virus-specific T cells
-
Lopez-granados, E. et al. 2014. A mutation in X-linked inhibitor of apoptosis (G466X) leads to memory inflation of Epstein-Barr virus-specific T cells. Clin. Exp. Immunol. 178: 470-482.
-
(2014)
Clin. Exp. Immunol.
, vol.178
, pp. 470-482
-
-
Lopez-granados, E.1
-
56
-
-
84874537855
-
Combined immunodeficiency with life-threatening EBV-associated lymphoproliferative disorder in patients lacking functional CD27
-
Salzer, E. et al. 2013. Combined immunodeficiency with life-threatening EBV-associated lymphoproliferative disorder in patients lacking functional CD27. Haematologica 98: 473-478.
-
(2013)
Haematologica
, vol.98
, pp. 473-478
-
-
Salzer, E.1
-
57
-
-
84857800335
-
CD27 deficiency is associated with combined immunodeficiency and persistent symptomatic EBV viremia
-
Van Montfrans, J.M. et al. 2012. CD27 deficiency is associated with combined immunodeficiency and persistent symptomatic EBV viremia. J. Allergy Clin. Immunol. 129: 787-793.e6.
-
(2012)
J. Allergy Clin. Immunol.
, vol.129
, pp. 787-793e6
-
-
Van Montfrans, J.M.1
-
58
-
-
84941188919
-
Novel mutations in TNFRSF7/CD27: clinical, immunologic, and genetic characterization of human CD27 deficiency
-
e10.
-
Alkhairy, O.K. et al. 2015. Novel mutations in TNFRSF7/CD27: clinical, immunologic, and genetic characterization of human CD27 deficiency. J. Allergy Clin. Immunol. 136: 703-712.e10.
-
(2015)
J. Allergy Clin. Immunol.
, vol.136
, pp. 703-712
-
-
Alkhairy, O.K.1
-
59
-
-
79951822440
-
Role of CD27/CD70 pathway of activation in immunity and tolerance
-
Denoeud, J. & M. Moser. 2011. Role of CD27/CD70 pathway of activation in immunity and tolerance. J. Leukoc. Biol. 89: 195-203.
-
(2011)
J. Leukoc. Biol.
, vol.89
, pp. 195-203
-
-
Denoeud, J.1
Moser, M.2
-
60
-
-
74949120423
-
CD27 sustains survival of CTLs in virus-infected nonlymphoid tissue in mice by inducing autocrine IL-2 production
-
Peperzak, V., Y. Xiao, E.A.M. Veraar & J. Borst. 2010. CD27 sustains survival of CTLs in virus-infected nonlymphoid tissue in mice by inducing autocrine IL-2 production. J. Clin. Invest. 120: 168-178.
-
(2010)
J. Clin. Invest.
, vol.120
, pp. 168-178
-
-
Peperzak, V.1
Xiao, Y.2
Veraar, E.A.M.3
Borst, J.4
-
61
-
-
84872827286
-
The CD27 and CD70 costimulatory pathway inhibits effector function of T helper 17 cells and attenuates associated autoimmunity
-
Coquet, J.M. et al. 2013. The CD27 and CD70 costimulatory pathway inhibits effector function of T helper 17 cells and attenuates associated autoimmunity. Immunity 38: 53-65.
-
(2013)
Immunity
, vol.38
, pp. 53-65
-
-
Coquet, J.M.1
-
62
-
-
0021838877
-
Distinctions between endemic and sporadic forms of Epstein-Barr virus-positive Burkitt's lymphoma
-
Rowe, M. et al. 1985. Distinctions between endemic and sporadic forms of Epstein-Barr virus-positive Burkitt's lymphoma. Int. J. Cancer 35: 435-441.
-
(1985)
Int. J. Cancer
, vol.35
, pp. 435-441
-
-
Rowe, M.1
-
63
-
-
84884376772
-
Inherited human OX40 deficiency underlying classic Kaposi sarcoma of childhood
-
Byun, M. et al. 2013. Inherited human OX40 deficiency underlying classic Kaposi sarcoma of childhood. J. Exp. Med. 210: 1743-1759.
-
(2013)
J. Exp. Med.
, vol.210
, pp. 1743-1759
-
-
Byun, M.1
-
64
-
-
84899050112
-
2+ regulation of immunity against Epstein-Barr virus
-
2+ regulation of immunity against Epstein-Barr virus. Blood 123: 2148-2152.
-
(2014)
Blood
, vol.123
, pp. 2148-2152
-
-
Li, F.-Y.1
-
65
-
-
79960915373
-
2+ revealed by human T-cell immunodeficiency
-
2+ revealed by human T-cell immunodeficiency. Nature 475: 471-476.
-
(2011)
Nature
, vol.475
, pp. 471-476
-
-
Li, F.-Y.1
-
66
-
-
84880283279
-
2+ regulates cytotoxic functions of NK and CD8 T cells in chronic EBV infection through NKG2D
-
2+ regulates cytotoxic functions of NK and CD8 T cells in chronic EBV infection through NKG2D. Science 341: 186-191.
-
(2013)
Science
, vol.341
, pp. 186-191
-
-
Chaigne-Delalande, B.1
-
68
-
-
84860772152
-
Loss-of-function mutations within the IL-2 inducible kinase ITK in patients with EBV-associated lymphoproliferative diseases
-
Linka, R.M. et al. 2012. Loss-of-function mutations within the IL-2 inducible kinase ITK in patients with EBV-associated lymphoproliferative diseases. Leukemia 26: 963-971.
-
(2012)
Leukemia
, vol.26
, pp. 963-971
-
-
Linka, R.M.1
-
69
-
-
79952335915
-
IL-2-inducible T-cell kinase deficiency: clinical presentation and therapeutic approach
-
Stepensky, P. et al. 2011. IL-2-inducible T-cell kinase deficiency: clinical presentation and therapeutic approach. Haematologica 96: 472-476.
-
(2011)
Haematologica
, vol.96
, pp. 472-476
-
-
Stepensky, P.1
-
70
-
-
66449085077
-
Girls homozygous for an IL-2- inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation
-
Huck, K. et al. 2009. Girls homozygous for an IL-2- inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation. J. Clin. Invest. 119: 1350-1358.
-
(2009)
J. Clin. Invest.
, vol.119
, pp. 1350-1358
-
-
Huck, K.1
-
71
-
-
84904872011
-
+ T-cell lymphopenia
-
+ T-cell lymphopenia. Blood 124: 655-657.
-
(2014)
Blood
, vol.124
, pp. 655-657
-
-
Serwas, N.K.1
-
72
-
-
84912042007
-
Interleukin-2-inducible T-cell kinase (ITK) deficiency-clinical and molecular aspects
-
Ghosh, S., K. Bienemann, K. Boztug & A. Borkhardt. 2014. Interleukin-2-inducible T-cell kinase (ITK) deficiency-clinical and molecular aspects. J. Clin. Immunol. 34: 892-899.
-
(2014)
J. Clin. Immunol.
, vol.34
, pp. 892-899
-
-
Ghosh, S.1
Bienemann, K.2
Boztug, K.3
Borkhardt, A.4
-
73
-
-
84879686304
-
On guard: coronin proteins in innate and adaptive immunity
-
Pieters, J., P. Müller & R. Jayachandran. 2013. On guard: coronin proteins in innate and adaptive immunity. Nat. Rev. Immunol. 13: 510-518.
-
(2013)
Nat. Rev. Immunol.
, vol.13
, pp. 510-518
-
-
Pieters, J.1
Müller, P.2
Jayachandran, R.3
-
74
-
-
54549117897
-
The actin regulator coronin 1A is mutant in a thymic egress-deficient mouse strain and in a patient with severe combined immunodeficiency
-
Shiow, L.R. et al. 2008. The actin regulator coronin 1A is mutant in a thymic egress-deficient mouse strain and in a patient with severe combined immunodeficiency. Nat. Immunol. 9: 1307-1315.
-
(2008)
Nat. Immunol.
, vol.9
, pp. 1307-1315
-
-
Shiow, L.R.1
-
76
-
-
63249106283
-
Severe combined immunodeficiency (SCID) and attention deficit hyperactivity disorder (ADHD) associated with a coronin-1A mutation and a chromosome 16p11.2 deletion
-
Shiow, L.R. et al. 2009. Severe combined immunodeficiency (SCID) and attention deficit hyperactivity disorder (ADHD) associated with a coronin-1A mutation and a chromosome 16p11.2 deletion. Clin. Immunol. 131: 24-30.
-
(2009)
Clin. Immunol.
, vol.131
, pp. 24-30
-
-
Shiow, L.R.1
-
77
-
-
84878550216
-
Whole-exome sequencing identifies coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation
-
Moshous, D. et al. 2013. Whole-exome sequencing identifies coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation. J. Allergy Clin. Immunol. 131: 1594-1603.
-
(2013)
J. Allergy Clin. Immunol.
, vol.131
, pp. 1594-1603
-
-
Moshous, D.1
-
78
-
-
84939874248
-
Compound heterozygous CORO1A mutations in siblings with a mucocutaneous-immunodeficiency syndrome of epidermodysplasia verruciformis-HPV, molluscum contagiosum and granulomatous tuberculoid leprosy
-
Stray-Pedersen, A. et al. 2014. Compound heterozygous CORO1A mutations in siblings with a mucocutaneous-immunodeficiency syndrome of epidermodysplasia verruciformis-HPV, molluscum contagiosum and granulomatous tuberculoid leprosy. J. Clin. Immunol. 34: 871-890.
-
(2014)
J. Clin. Immunol.
, vol.34
, pp. 871-890
-
-
Stray-Pedersen, A.1
-
79
-
-
0029892132
-
Natural killer (NK) cell deficiency associated with an epitope-deficient Fc receptor type IIIA (CD16-II)
-
Jawahar, S. et al. 1996. Natural killer (NK) cell deficiency associated with an epitope-deficient Fc receptor type IIIA (CD16-II). Clin. Exp. Immunol. 103: 408-413.
-
(1996)
Clin. Exp. Immunol.
, vol.103
, pp. 408-413
-
-
Jawahar, S.1
-
80
-
-
0029859088
-
Identification of an unusual Fc gamma receptor IIIa (CD16) on natural killer cells in a patient with recurrent infections
-
De Vries, E. et al. 1996. Identification of an unusual Fc gamma receptor IIIa (CD16) on natural killer cells in a patient with recurrent infections. Blood 88: 3022-3027.
-
(1996)
Blood
, vol.88
, pp. 3022-3027
-
-
De Vries, E.1
-
81
-
-
84867177624
-
Human immunode ciency-causing mutation denes CD16 in spontaneous NK cell cytotoxicity
-
Grier, J.T. et al. 2012. Human immunode ciency-causing mutation denes CD16 in spontaneous NK cell cytotoxicity. J. Clin. Invest. 122: 3769-3780.
-
(2012)
J. Clin. Invest.
, vol.122
, pp. 3769-3780
-
-
Grier, J.T.1
-
82
-
-
0038549067
-
PI3K in lymphocyte development, differentiation and activation
-
Okkenhaug, K. & B. Vanhaesebroeck. 2003. PI3K in lymphocyte development, differentiation and activation. Nat. Rev. Immunol. 3: 317-330.
-
(2003)
Nat. Rev. Immunol.
, vol.3
, pp. 317-330
-
-
Okkenhaug, K.1
Vanhaesebroeck, B.2
-
83
-
-
84887824378
-
Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damage
-
Angulo, I. et al. 2013. Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damage. Science 342: 866-871.
-
(2013)
Science
, vol.342
, pp. 866-871
-
-
Angulo, I.1
-
84
-
-
84891030577
-
Dominant-activating germline mutations in the gene encoding the PI (3) K catalytic subunit p110 δ result in T cell senescence and human immunodeficiency
-
Lucas, C.L. et al. 2014. Dominant-activating germline mutations in the gene encoding the PI (3) K catalytic subunit p110 δ result in T cell senescence and human immunodeficiency. Nat. Immunol. 15: 88-97.
-
(2014)
Nat. Immunol.
, vol.15
, pp. 88-97
-
-
Lucas, C.L.1
-
85
-
-
84921847830
-
Heterozygous splice mutation in PIK3R1 causes human immunodeficiency with lymphoproliferation due to dominant activation of PI3K
-
Lucas, C.L. et al. 2014. Heterozygous splice mutation in PIK3R1 causes human immunodeficiency with lymphoproliferation due to dominant activation of PI3K. J. Exp. Med. 211: 2537-2547.
-
(2014)
J. Exp. Med.
, vol.211
, pp. 2537-2547
-
-
Lucas, C.L.1
-
86
-
-
84860359332
-
Agammaglobulinemia and absent B lineage cells in a patient lacking the p85 subunit of PI3K
-
Conley, M.E. et al. 2012. Agammaglobulinemia and absent B lineage cells in a patient lacking the p85 subunit of PI3K. J. Exp. Med. 209: 463-470.
-
(2012)
J. Exp. Med.
, vol.209
, pp. 463-470
-
-
Conley, M.E.1
-
87
-
-
84907008346
-
A human immunodeficiency caused by mutations in the PIK3R1 gene
-
Deau, M.-C. et al. 2014. A human immunodeficiency caused by mutations in the PIK3R1 gene. J. Clin. Invest. 124: 3923-3928.
-
(2014)
J. Clin. Invest.
, vol.124
, pp. 3923-3928
-
-
Deau, M.-C.1
-
88
-
-
84900848952
-
The critical role of IL-15-PI3K-mTOR pathway in natural killer cell effector functions
-
Nandagopal, N., A.K. Ali, A.K. Komal & S.H. Lee. 2014. The critical role of IL-15-PI3K-mTOR pathway in natural killer cell effector functions. Front. Immunol. 5: 1-12.
-
(2014)
Front. Immunol.
, vol.5
, pp. 1-12
-
-
Nandagopal, N.1
Ali, A.K.2
Komal, A.K.3
Lee, S.H.4
-
89
-
-
84859837132
-
The phenotype of human STK4 deficiency
-
Abdollahpour, H. et al. 2012. The phenotype of human STK4 deficiency. Blood 119: 3450-3457.
-
(2012)
Blood
, vol.119
, pp. 3450-3457
-
-
Abdollahpour, H.1
-
90
-
-
84859875061
-
MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival
-
Nehme, N.T. et al. 2012. MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival. Blood 119: 3458-3468.
-
(2012)
Blood
, vol.119
, pp. 3458-3468
-
-
Nehme, N.T.1
-
91
-
-
84865429528
-
Inherited MST1 deficiency underlies susceptibility to EV-HPV infections
-
Crequer, A. et al. 2012. Inherited MST1 deficiency underlies susceptibility to EV-HPV infections. PLoS One 7: e44010.
-
(2012)
PLoS One
, vol.7
, pp. e44010
-
-
Crequer, A.1
-
92
-
-
57049172523
-
Clinical heterogeneity can hamper the diagnosis of patients with ZAP70 deficiency
-
Turul, T. et al. 2009. Clinical heterogeneity can hamper the diagnosis of patients with ZAP70 deficiency. Eur. J. Pediatr. 168: 87-93.
-
(2009)
Eur. J. Pediatr.
, vol.168
, pp. 87-93
-
-
Turul, T.1
-
93
-
-
79551500391
-
Diffuse large B-cell lymphoma as presenting feature of Zap-70 deficiency
-
Newell, A. et al. 2011. Diffuse large B-cell lymphoma as presenting feature of Zap-70 deficiency. J. Allergy Clin. Immunol. 127: 517-520.
-
(2011)
J. Allergy Clin. Immunol.
, vol.127
, pp. 517-520
-
-
Newell, A.1
-
94
-
-
84902342846
-
CTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferation
-
Martin, E. et al. 2014. CTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferation. Nature 510: 288-292.
-
(2014)
Nature
, vol.510
, pp. 288-292
-
-
Martin, E.1
-
95
-
-
84900450280
-
Reprint of "The clinical impact of deficiency in DNA non-homologous end-joining
-
Woodbine, L., A.R. Gennery & P.A. Jeggo. 2014. Reprint of "The clinical impact of deficiency in DNA non-homologous end-joining". DNA Repair (Amst) 17: 9-20.
-
(2014)
DNA Repair (Amst)
, vol.17
, pp. 9-20
-
-
Woodbine, L.1
Gennery, A.R.2
Jeggo, P.A.3
-
96
-
-
0037312006
-
Partial T and B lymphocyte immunodeficiency and predisposition to lymphoma in patients with hypomorphic mutations in Artemis
-
Moshous, D. et al. 2003. Partial T and B lymphocyte immunodeficiency and predisposition to lymphoma in patients with hypomorphic mutations in Artemis. J. Clin. Invest. 111: 381-387.
-
(2003)
J. Clin. Invest.
, vol.111
, pp. 381-387
-
-
Moshous, D.1
-
97
-
-
77953544834
-
Chronic inflammatory bowel disease as key manifestation of atypical ARTEMIS deficiency
-
Rohr, J. et al. 2010. Chronic inflammatory bowel disease as key manifestation of atypical ARTEMIS deficiency. J. Clin. Immunol. 30: 314-320.
-
(2010)
J. Clin. Immunol.
, vol.30
, pp. 314-320
-
-
Rohr, J.1
-
98
-
-
84881086382
-
Atypical combined immunodeficiency due to Artemis defect: a case presenting as hyperimmunoglobulin M syndrome and with LGLL
-
Bajin, I˙.Y. et al. 2013. Atypical combined immunodeficiency due to Artemis defect: a case presenting as hyperimmunoglobulin M syndrome and with LGLL. Mol. Immunol. 56: 354-357.
-
(2013)
Mol. Immunol.
, vol.56
, pp. 354-357
-
-
Bajin, I.1
-
99
-
-
33645785057
-
A severe form of human combined immunodeficiency due to mutations in DNA ligase IV
-
Enders, A. et al. 2006. A severe form of human combined immunodeficiency due to mutations in DNA ligase IV. J. Immunol. 176: 5060-5068.
-
(2006)
J. Immunol.
, vol.176
, pp. 5060-5068
-
-
Enders, A.1
-
100
-
-
0033166623
-
Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient
-
Riballo, E. et al. 1999. Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient. Curr. Biol. 9: 699-702.
-
(1999)
Curr. Biol.
, vol.9
, pp. 699-702
-
-
Riballo, E.1
-
101
-
-
84872865986
-
Identification of the DNA repair defects in a case of Dubowitz syndrome
-
Yue, J. et al. 2013. Identification of the DNA repair defects in a case of Dubowitz syndrome. PLoS One 8: e54389.
-
(2013)
PLoS One
, vol.8
, pp. e54389
-
-
Yue, J.1
-
102
-
-
30944455282
-
Severe combined immunodeficiency and microcephaly in siblings with hypomorphic mutations in DNA ligase IV
-
Buck, D. et al. 2006. Severe combined immunodeficiency and microcephaly in siblings with hypomorphic mutations in DNA ligase IV. Eur. J. Immunol. 36: 224-235.
-
(2006)
Eur. J. Immunol.
, vol.36
, pp. 224-235
-
-
Buck, D.1
-
103
-
-
18244362081
-
DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency
-
O'Driscoll, M. et al. 2001. DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency. Mol. Cell 8: 1175-1185.
-
(2001)
Mol. Cell
, vol.8
, pp. 1175-1185
-
-
O'Driscoll, M.1
-
104
-
-
31044446450
-
+ severe combined immunodeficiency caused by a LIG4 mutation
-
+ severe combined immunodeficiency caused by a LIG4 mutation. J. Clin. Invest. 116: 137-145.
-
(2006)
J. Clin. Invest.
, vol.116
, pp. 137-145
-
-
Van Der Burg, M.1
-
105
-
-
57149133526
-
Omenn syndrome is associated with mutations in DNA ligase IV
-
Grunebaum, E., A. Bates & C.M. Roifman. 2008. Omenn syndrome is associated with mutations in DNA ligase IV. J. Allergy Clin. Immunol. 122: 1219-1220.
-
(2008)
J. Allergy Clin. Immunol.
, vol.122
, pp. 1219-1220
-
-
Grunebaum, E.1
Bates, A.2
Roifman, C.M.3
-
106
-
-
24344461251
-
A patient with mutations in DNA Ligase IV: clinical features and overlap with Nijmegen breakage syndrome
-
Ben-Omran, T.I., K. Cerosaletti, P. Concannon, et al. 2005. A patient with mutations in DNA Ligase IV: clinical features and overlap with Nijmegen breakage syndrome. Am. J. Med. Genet. A 137A: 283-287.
-
(2005)
Am. J. Med. Genet A.
, vol.137A
, pp. 283-287
-
-
Ben-Omran, T.I.1
Cerosaletti, K.2
Concannon, P.3
-
107
-
-
34247248708
-
Epstein-Barr virus-associated B-cell lymphoma in a patient with DNA ligase IV (LIG4) syndrome
-
Toita, N. et al. 2007. Epstein-Barr virus-associated B-cell lymphoma in a patient with DNA ligase IV (LIG4) syndrome. Am. J. Med. Genet. A 143A: 742-745.
-
(2007)
Am. J. Med. Genet. A
, vol.143A
, pp. 742-745
-
-
Toita, N.1
-
109
-
-
84878262930
-
Mutations in GATA2 cause human NK cell deficiency with specific loss of the CD56 bright subset
-
Mace, E.M. et al. 2013. Mutations in GATA2 cause human NK cell deficiency with specific loss of the CD56 bright subset. Blood 121: 2669-2677.
-
(2013)
Blood
, vol.121
, pp. 2669-2677
-
-
Mace, E.M.1
-
110
-
-
84894095710
-
GATA2 deficiency: a protean disorder of hematopoiesis, lymphatics, and immunity
-
Spinner, M.A. et al. 2014. GATA2 deficiency: a protean disorder of hematopoiesis, lymphatics, and immunity. Blood 123: 809-821.
-
(2014)
Blood
, vol.123
, pp. 809-821
-
-
Spinner, M.A.1
-
111
-
-
0024315206
-
Severe herpesvirus infections in an adolescent without natural killer cells
-
Biron, C.A., K.S. Byron & J.L. Sullivan. 1989. Severe herpesvirus infections in an adolescent without natural killer cells. N. Engl. J. Med. 320: 1731-1735.
-
(1989)
N. Engl. J. Med.
, vol.320
, pp. 1731-1735
-
-
Biron, C.A.1
Byron, K.S.2
Sullivan, J.L.3
-
112
-
-
84857875264
-
MCM4 mutation causes adrenal failure, short stature, and natural killer cell deficiency in humans
-
Hughes, C.R. et al. 2012. MCM4 mutation causes adrenal failure, short stature, and natural killer cell deficiency in humans. J. Clin. Invest. 122: 814-820.
-
(2012)
J. Clin. Invest.
, vol.122
, pp. 814-820
-
-
Hughes, C.R.1
-
113
-
-
84857815874
-
Partial MCM4 deficiency in patients with growth retardation, adrenal insufficiency, and natural killer cell deficiency
-
Gineau, L. et al. 2012. Partial MCM4 deficiency in patients with growth retardation, adrenal insufficiency, and natural killer cell deficiency. J. Clin. Invest. 122: 821-832.
-
(2012)
J. Clin. Invest.
, vol.122
, pp. 821-832
-
-
Gineau, L.1
-
114
-
-
33645467271
-
A novel primary immunodeficiency with specific natural-killer cell deficiency maps to the centromeric region of chromosome 8
-
Dunne, J. et al. 2006. A novel primary immunodeficiency with specific natural-killer cell deficiency maps to the centromeric region of chromosome 8. Am. J. Hum. Genet. 78: 721-727.
-
(2006)
Am. J. Hum. Genet.
, vol.78
, pp. 721-727
-
-
Dunne, J.1
-
116
-
-
0031929550
-
Molecular genetics of the Hermansky-Pudlak and Chediak-Higashi syndromes
-
Spritz, R.A. 1998. Molecular genetics of the Hermansky-Pudlak and Chediak-Higashi syndromes. Platelets 9: 21-29.
-
(1998)
Platelets
, vol.9
, pp. 21-29
-
-
Spritz, R.A.1
-
117
-
-
0018868919
-
A new immunodeficiency disorder in humans involving NK cells
-
284
-
Roder J.C. et al. 1980. A new immunodeficiency disorder in humans involving NK cells. Nature 284: 553-555.
-
(1980)
Nature
, pp. 553-555
-
-
Roder, J.C.1
-
118
-
-
80055087431
-
Subtle differences in CTL cytotoxicity determine susceptibility to hemophagocytic lymphohistiocytosis in mice and humans with Chediak-Higashi syndrome
-
Jessen, B. et al. 2011. Subtle differences in CTL cytotoxicity determine susceptibility to hemophagocytic lymphohistiocytosis in mice and humans with Chediak-Higashi syndrome. Blood 118: 4620-4629.
-
(2011)
Blood
, vol.118
, pp. 4620-4629
-
-
Jessen, B.1
-
119
-
-
0022635084
-
Anti-Epstein-Barr virus memory T cell response in Chediak-Higashi syndrome patients
-
Merino, F., M. Pauza & D.T. Purtilo. 1986. Anti-Epstein-Barr virus memory T cell response in Chediak-Higashi syndrome patients. Immunol. Lett. 12: 51-54.
-
(1986)
Immunol. Lett.
, vol.12
, pp. 51-54
-
-
Merino, F.1
Pauza, M.2
Purtilo, D.T.3
-
120
-
-
84881504826
-
Clinical characteristics and outcomes of Chediak-Higashi syndrome. A nationwide survey of Japan
-
Nagai, K., F. Ochi, K. Terui, et al. 2013. Clinical characteristics and outcomes of Chediak-Higashi syndrome. A nationwide survey of Japan. Pediatr. Blood Cancer 60: 1582-1586.
-
(2013)
Pediatr. Blood Cancer
, vol.60
, pp. 1582-1586
-
-
Nagai, K.1
Ochi, F.2
Terui, K.3
-
121
-
-
0031887486
-
Genetic defects in Chediak-Higashi syndrome and the beige mouse
-
Spritz, R.A. 1998. Genetic defects in Chediak-Higashi syndrome and the beige mouse. J. Clin. Immunol. 18: 97-105.
-
(1998)
J. Clin. Immunol.
, vol.18
, pp. 97-105
-
-
Spritz, R.A.1
-
122
-
-
0034131028
-
A review of Epstein-Barr virus infection in patients with immunodeficiency disorders
-
Okano, M. & T.G. Gross. 2000. A review of Epstein-Barr virus infection in patients with immunodeficiency disorders. Am. J. Med. Sci. 319: 392-396.
-
(2000)
Am. J. Med. Sci
, vol.319
, pp. 392-396
-
-
Okano, M.1
Gross, T.G.2
-
123
-
-
0022887134
-
Chronic active Epstein-Barr virus infection in patients with Chediak-Higashi syndrome
-
Merino, F., W. Henle & P. Ramírez-Duque. 1986. Chronic active Epstein-Barr virus infection in patients with Chediak-Higashi syndrome. J. Clin. Immunol. 6: 299-305.
-
(1986)
J. Clin. Immunol
, vol.6
, pp. 299-305
-
-
Merino, F.1
Henle, W.2
Ramírez-Duque, P.3
-
124
-
-
79961181036
-
Rituximab and cyclosporine therapy for accelerated phase Chediak-Higashi syndrome
-
Ogimi, C. et al. 2011. Rituximab and cyclosporine therapy for accelerated phase Chediak-Higashi syndrome. Pediatr. Blood Cancer 57: 677-680.
-
(2011)
Pediatr. Blood Cancer
, vol.57
, pp. 677-680
-
-
Ogimi, C.1
-
125
-
-
77649153819
-
WASP: a key immunological multitasker
-
Thrasher, A.J. & S.O. Burns. 2010. WASP: a key immunological multitasker. Nat. Rev. Immunol. 10: 182-192.
-
(2010)
Nat. Rev. Immunol.
, vol.10
, pp. 182-192
-
-
Thrasher, A.J.1
Burns, S.O.2
-
128
-
-
0027729408
-
Epstein-Barr virus-related lymphomagenesis in a child with Wiskott-Aldrich syndrome
-
Gulley, M.L., C.L. Chen & N. Raab-Traub. 1993. Epstein-Barr virus-related lymphomagenesis in a child with Wiskott-Aldrich syndrome. Hematol. Oncol. 11: 139-145.
-
(1993)
Hematol. Oncol.
, vol.11
, pp. 139-145
-
-
Gulley, M.L.1
Chen, C.L.2
Raab-Traub, N.3
-
129
-
-
0031020518
-
Epstein-Barr virus-associated malignant lymphoma with macroamylasemia and monoclonal gammopathy in a patient with Wiskott-Aldrich syndrome
-
Yoshida, K. et al. 1997. Epstein-Barr virus-associated malignant lymphoma with macroamylasemia and monoclonal gammopathy in a patient with Wiskott-Aldrich syndrome. Pediatr. Hematol. Oncol. 14: 85-89.
-
(1997)
Pediatr. Hematol. Oncol.
, vol.14
, pp. 85-89
-
-
Yoshida, K.1
-
130
-
-
0027216739
-
Distinct clonotypic Epstein-Barr virus-induced fatal lymphoproliferative disorder in a patient with Wiskott-Aldrich syndrome
-
Nakanishi, M. et al. 1993. Distinct clonotypic Epstein-Barr virus-induced fatal lymphoproliferative disorder in a patient with Wiskott-Aldrich syndrome. Cancer 72: 1376-1381.
-
(1993)
Cancer
, vol.72
, pp. 1376-1381
-
-
Nakanishi, M.1
-
131
-
-
79955021525
-
Hodgkin's and non-Hodgkin's lymphomas occurring in two brothers with Wiskott-Aldrich syndrome and review of the literature
-
Du, S. et al. 2011. Hodgkin's and non-Hodgkin's lymphomas occurring in two brothers with Wiskott-Aldrich syndrome and review of the literature. Pediatr. Dev. Pathol. 14: 64-70.
-
(2011)
Pediatr. Dev. Pathol.
, vol.14
, pp. 64-70
-
-
Du, S.1
-
132
-
-
0035210857
-
Epstein-Barr virus-associated Hodgkin's disease in a patient with Wiskott-Aldrich syndrome
-
Sasahara, Y. et al. 2001. Epstein-Barr virus-associated Hodgkin's disease in a patient with Wiskott-Aldrich syndrome. Acta Paediatr. 90: 1348-1351.
-
(2001)
Acta Paediatr
, vol.90
, pp. 1348-1351
-
-
Sasahara, Y.1
-
133
-
-
0043122921
-
Malignant B cell non-Hodgkin's lymphoma of the larynx in children with Wiskott-Aldrich syndrome
-
Palenzuela, G., F. Bernard, Q. Gardiner & M. Mondain. 2003. Malignant B cell non-Hodgkin's lymphoma of the larynx in children with Wiskott-Aldrich syndrome. Int. J. Pediatr. Otorhinolaryngol. 67: 989-993.
-
(2003)
Int. J. Pediatr. Otorhinolaryngol.
, vol.67
, pp. 989-993
-
-
Palenzuela, G.1
Bernard, F.2
Gardiner, Q.3
Mondain, M.4
-
134
-
-
0038006199
-
Isolated EBV lymphoproliferative disease in a child with Wiskott-Aldrich syndrome manifesting as cutaneous lymphomatoid granulomatosis and responsive to anti-CD20 immunotherapy
-
Sebire, N.J., S. Haselden, M. Malone, et al. 2003. Isolated EBV lymphoproliferative disease in a child with Wiskott-Aldrich syndrome manifesting as cutaneous lymphomatoid granulomatosis and responsive to anti-CD20 immunotherapy. J. Clin. Pathol. 56: 555-557.
-
(2003)
J. Clin. Pathol.
, vol.56
, pp. 555-557
-
-
Sebire, N.J.1
Haselden, S.2
Malone, M.3
-
135
-
-
84924384551
-
Mechanisms of ATM activation
-
Paull, T.T. 2015. Mechanisms of ATM activation. Annu. Rev. Biochem. 84: 711-738.
-
(2015)
Annu. Rev. Biochem.
, vol.84
, pp. 711-738
-
-
Paull, T.T.1
-
136
-
-
84897944709
-
Immune deficiency in ataxia-telangiectasia: a longitudinal study of 44 patients
-
Chopra, C. et al. 2014. Immune deficiency in ataxia-telangiectasia: a longitudinal study of 44 patients. Clin. Exp. Immunol. 176: 275-282.
-
(2014)
Clin. Exp. Immunol.
, vol.176
, pp. 275-282
-
-
Chopra, C.1
-
137
-
-
84874698238
-
Reply to "testing for herpesvirus infection is essential in children with chromosomal-instability syndromes
-
Kulinski, J.M. & V.L. Tarakanova. 2013. Reply to "testing for herpesvirus infection is essential in children with chromosomal-instability syndromes." J. Virol. 87: 3618.
-
(2013)
J. Virol.
, vol.87
, pp. 3618
-
-
Kulinski, J.M.1
Tarakanova, V.L.2
-
138
-
-
84920983463
-
Incidence, presentation, and prognosis of malignancies in ataxia-telangiectasia: a report from the French National Registry of Primary Immune Deficiencies
-
Suarez, F. et al. 2014. Incidence, presentation, and prognosis of malignancies in ataxia-telangiectasia: a report from the French National Registry of Primary Immune Deficiencies. J. Clin. Oncol. 33: 202-208.
-
(2014)
J. Clin. Oncol.
, vol.33
, pp. 202-208
-
-
Suarez, F.1
-
139
-
-
84897531867
-
Natural history of autoimmune lymphoproliferative syndrome associated with FAS gene mutations
-
Price, S. et al. 2014. Natural history of autoimmune lymphoproliferative syndrome associated with FAS gene mutations. Blood 123: 1989-1999.
-
(2014)
Blood
, vol.123
, pp. 1989-1999
-
-
Price, S.1
-
140
-
-
0035412359
-
The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosis
-
Straus, S.E. et al. 2001. The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosis. Blood 98: 194-200.
-
(2001)
Blood
, vol.98
, pp. 194-200
-
-
Straus, S.E.1
-
141
-
-
84949104129
-
Autoimmune lymphoproliferative syndrome and Epstein-Barr virus-associated lymphoma: an adjunctive diagnostic role for monitoring EBV viremia
-
Pace, R. & D.C. Vinh. 2013. Autoimmune lymphoproliferative syndrome and Epstein-Barr virus-associated lymphoma: an adjunctive diagnostic role for monitoring EBV viremia? Case Reports Immunol. 2013: 245893.
-
(2013)
Case Reports Immunol
, vol.2013
, pp. 245893
-
-
Pace, R.1
Vinh, D.C.2
-
143
-
-
0032903411
-
X-Linked agammaglobulinemia patients are not infected with Epstein-Barr virus: implications for the biology of the virus
-
Faulkner, G.C. et al. 1999. X-Linked agammaglobulinemia patients are not infected with Epstein-Barr virus: implications for the biology of the virus. J. Virol. 73: 1555-1564.
-
(1999)
J. Virol.
, vol.73
, pp. 1555-1564
-
-
Faulkner, G.C.1
-
144
-
-
84874260436
-
Human complement receptor type 1/CD35 is an Epstein-Barr virus receptor
-
Ogembo, J.G. et al. 2013. Human complement receptor type 1/CD35 is an Epstein-Barr virus receptor. Cell Rep. 3: 371-385.
-
(2013)
Cell Rep.
, vol.3
, pp. 371-385
-
-
Ogembo, J.G.1
-
145
-
-
23844541961
-
Epstein-Barr virus can establish infection in the absence of a classical memory B-cell population
-
Conacher, M. et al. 2005. Epstein-Barr virus can establish infection in the absence of a classical memory B-cell population. J. Virol. 79: 11128-11134.
-
(2005)
J. Virol.
, vol.79
, pp. 11128-11134
-
-
Conacher, M.1
-
147
-
-
0036284601
-
Asymptomatic deficiency in the peptide transporter associated to antigen processing (TAP)
-
De la Salle, H. et al. 2002. Asymptomatic deficiency in the peptide transporter associated to antigen processing (TAP). Clin. Exp. Immunol. 128: 525-531.
-
(2002)
Clin. Exp. Immunol.
, vol.128
, pp. 525-531
-
-
De la Salle, H.1
-
148
-
-
84887628703
-
Transporter associated with antigen processing deficiency syndrome: case report of an adolescent with chronic perforated granulomatous skin lesions due to TAP2 mutation
-
Konstantinou, P. et al. 2013. Transporter associated with antigen processing deficiency syndrome: case report of an adolescent with chronic perforated granulomatous skin lesions due to TAP2 mutation. Pediatr. Dermatol. 30: e223-e225.
-
(2013)
Pediatr. Dermatol.
, vol.30
, pp. e223-e225
-
-
Konstantinou, P.1
-
150
-
-
0035886881
-
Processing of a multiple membrane spanning Epstein-Barr virus protein for CD8(+)T cell recognition reveals a proteasome-dependent, transporter associated with antigen processing-independent pathway
-
Lautscham, G. et al. 2001. Processing of a multiple membrane spanning Epstein-Barr virus protein for CD8(+)T cell recognition reveals a proteasome-dependent, transporter associated with antigen processing-independent pathway. J. Exp. Med. 194: 1053-1068.
-
(2001)
J. Exp. Med.
, vol.194
, pp. 1053-1068
-
-
Lautscham, G.1
-
151
-
-
0037386520
-
TAP-independent antigen presentation on MHC class I molecules: lessons from Epstein-Barr virus
-
Lautscham, G., A. Rickinson & N. Blake. 2003. TAP-independent antigen presentation on MHC class I molecules: lessons from Epstein-Barr virus. Microbes Infect. 5: 291-299.
-
(2003)
Microbes Infect
, vol.5
, pp. 291-299
-
-
Lautscham, G.1
Rickinson, A.2
Blake, N.3
-
152
-
-
84875635224
-
Importance of TAP-independent processing pathways
-
Oliveira, C.C. & T. Van Hall. 2013. Importance of TAP-independent processing pathways. Mol. Immunol. 55: 113-116.
-
(2013)
Mol. Immunol.
, vol.55
, pp. 113-116
-
-
Oliveira, C.C.1
Van Hall, T.2
-
153
-
-
81055126777
-
Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients
-
Ouederni, M. et al. 2011. Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients. Blood 118: 5108-5118.
-
(2011)
Blood
, vol.118
, pp. 5108-5118
-
-
Ouederni, M.1
-
154
-
-
34547110512
-
Epstein-Barr virus entry
-
Hutt-Fletcher, L.M. 2007. Epstein-Barr virus entry. J. Virol. 81: 7825-7832.
-
(2007)
J. Virol.
, vol.81
, pp. 7825-7832
-
-
Hutt-Fletcher, L.M.1
-
155
-
-
84880301748
-
B-cell lymphoma in a patient with complete interferon gamma receptor 1 deficiency
-
Bax, H.I. et al. 2013. B-cell lymphoma in a patient with complete interferon gamma receptor 1 deficiency. J. Clin. Immunol. 33: 1062-1066.
-
(2013)
J. Clin. Immunol.
, vol.33
, pp. 1062-1066
-
-
Bax, H.I.1
-
156
-
-
78649351360
-
Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries
-
De Beaucoudrey, L. et al. 2010. Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries. Medicine (Baltimore) 89: 381-402.
-
(2010)
Medicine (Baltimore)
, vol.89
, pp. 381-402
-
-
De Beaucoudrey, L.1
-
157
-
-
0022353117
-
Replication of Epstein-Barr virus within the epithelial cells of oral 'hairy' leukoplakia, an AIDS-associated lesion
-
Greenspan, J.S. et al. 1985. Replication of Epstein-Barr virus within the epithelial cells of oral 'hairy' leukoplakia, an AIDS-associated lesion. N. Engl. J. Med. 313: 1564-1571.
-
(1985)
N. Engl. J. Med.
, vol.313
, pp. 1564-1571
-
-
Greenspan, J.S.1
-
159
-
-
84862983486
-
SAP signaling: a dual mechanism of action
-
Le Borgne, M. & A.S. Shaw. 2012. SAP signaling: a dual mechanism of action. Immunity 36: 899-901.
-
(2012)
Immunity
, vol.36
, pp. 899-901
-
-
Le Borgne, M.1
Shaw, A.S.2
|