-
1
-
-
0016772968
-
X-linked recessive progressive combined variable immunodeficiency (Duncan’s disease)
-
PID: 48119, COI: 1:STN:280:CSqC2MrhsVQ%3D
-
Purtilo DT, Cassel CK, Yang JP, Harper R: X-linked recessive progressive combined variable immunodeficiency (Duncan’s disease). Lancet 1975, 1:935–940. DOI: 10.1016/S0140-6736(75)92004-8
-
(1975)
Lancet
, vol.1
, pp. 935-940
-
-
Purtilo, D.T.1
Cassel, C.K.2
Yang, J.P.3
Harper, R.4
-
2
-
-
0029161779
-
X-linked lymphoproliferative disease: twenty-five years after the discovery
-
PID: 8559596, COI: 1:STN:280:BymD1MfntFc%3D
-
Seemayer TA, Gross TG, Egeler RM, et al.: X-linked lymphoproliferative disease: twenty-five years after the discovery. Pediatr Res 1995, 38:471–478. DOI: 10.1203/00006450-199510000-00001
-
(1995)
Pediatr Res
, vol.38
, pp. 471-478
-
-
Seemayer, T.A.1
Gross, T.G.2
Egeler, R.M.3
-
3
-
-
0018821254
-
X-linked lymphoproliferative syndrome registry report
-
PID: 7188959, COI: 1:STN:280:Bi%2BC3sblvFc%3D
-
Hamilton JK, Paquin LA, Sullivan JL, et al.: X-linked lymphoproliferative syndrome registry report. J Pediatr 1980, 96:669–673. DOI: 10.1016/S0022-3476(80)80735-9
-
(1980)
J Pediatr
, vol.96
, pp. 669-673
-
-
Hamilton, J.K.1
Paquin, L.A.2
Sullivan, J.L.3
-
4
-
-
0027382845
-
X-linked lymphoproliferative disease
-
PID: 8237920, COI: 1:STN:280:ByuD2MnivF0%3D
-
Seemayer TA, Grierson H, Pirruccello SJ, et al.: X-linked lymphoproliferative disease. Am J Dis Child 1993, 147:1242–1245.
-
(1993)
Am J Dis Child
, vol.147
, pp. 1242-1245
-
-
Seemayer, T.A.1
Grierson, H.2
Pirruccello, S.J.3
-
5
-
-
0035469882
-
Alterations of the X-linked lymphoproliferative disease gene SH2D1A in common variable immunodeficiency syndrome
-
PID: 11520777, COI: 1:CAS:528:DC%2BD3MXmvFGjtr0%3D, Reports on six patients diaged with common variable immunodeficiency subsequently found to have mutations the SAP gene. Four of six died of infection or complications of infections
-
Morra M, Silander O, Calpe S, et al.: Alterations of the X-linked lymphoproliferative disease gene SH2D1A in common variable immunodeficiency syndrome. Blood 2001, 98:1321–1325. Reports on six patients diagnosed with common variable immunodeficiency subsequently found to have mutations in the SAP gene. Four of six died of infection or complications of infections. DOI: 10.1182/blood.V98.5.1321
-
(2001)
Blood
, vol.98
, pp. 1321-1325
-
-
Morra, M.1
Silander, O.2
Calpe, S.3
-
6
-
-
0034780947
-
X-linked lymphoproliferative disease: three atypical cases
-
PID: 11678908, COI: 1:STN:280:DC%2BD3MrntFWgtw%3D%3D, Describes three patients diaged with common variable immunodeficiency with no SAP expression. The index patient went on to develop fatal fulminant infectious mononucleosis
-
Nistala K, Gilmour KC, Cranston T, et al.: X-linked lymphoproliferative disease: three atypical cases. Clin Exp Immunol 2001, 126:126–130. Describes three patients diagnosed with common variable immunodeficiency with no SAP expression. The index patient went on to develop fatal fulminant infectious mononucleosis. DOI: 10.1046/j.1365-2249.2001.01599.x
-
(2001)
Clin Exp Immunol
, vol.126
, pp. 126-130
-
-
Nistala, K.1
Gilmour, K.C.2
Cranston, T.3
-
7
-
-
0035883052
-
SH2D1A mutations in Japanese males with severe Epstein-Barr virus--associated illnesses
-
PID: 11493483, COI: 1:CAS:528:DC%2BD3MXmtFeit7c%3D, The authors studied 40 males with severe EBV-associated disease, and identified 10 who had SAP mutations. Nine had fulminant infectious mononucleosis and one an EBV-positive lymphoma
-
Sumazaki R, Kanegane H, Osaki M, et al.: SH2D1A mutations in Japanese males with severe Epstein-Barr virus--associated illnesses. Blood 2001, 98:1268–1270. The authors studied 40 males with severe EBV-associated disease, and identified 10 who had SAP mutations. Nine had fulminant infectious mononucleosis and one an EBV-positive lymphoma. DOI: 10.1182/blood.V98.4.1268
-
(2001)
Blood
, vol.98
, pp. 1268-1270
-
-
Sumazaki, R.1
Kanegane, H.2
Osaki, M.3
-
8
-
-
0035865529
-
Hemophagocytic lymphohistiocytosis due to germline mutations in SH2D1A, the X-linked lymphoproliferative disease gene
-
PID: 11159547, COI: 1:CAS:528:DC%2BD3MXht1Gis70%3D, A study reporting that four of 25 patients with apparently sporadic hemophagocytic lymphohistiocytosis secondary to EBV had muations SAP
-
Arico M, Imashuku S, Clementi R, et al.: Hemophagocytic lymphohistiocytosis due to germline mutations in SH2D1A, the X-linked lymphoproliferative disease gene. Blood 2001, 97:1131–1133. A study reporting that four of 25 patients with apparently sporadic hemophagocytic lymphohistiocytosis secondary to EBV had muations in SAP. DOI: 10.1182/blood.V97.4.1131
-
(2001)
Blood
, vol.97
, pp. 1131-1133
-
-
Arico, M.1
Imashuku, S.2
Clementi, R.3
-
9
-
-
0028873285
-
Epstein-Barr virus--an old dog with new tricks
-
PID: 7990868, COI: 1:STN:280:ByqD1c3osVY%3D
-
Liebowitz D: Epstein-Barr virus--an old dog with new tricks. N Engl J Med 1995, 332:55–57. DOI: 10.1056/NEJM199501053320112
-
(1995)
N Engl J Med
, vol.332
, pp. 55-57
-
-
Liebowitz, D.1
-
10
-
-
0030761670
-
Epstein-Barr virus and the immune system. Hide and seek
-
PID: 9256227, COI: 1:STN:280:ByiA1Mfjt10%3D
-
Cohen JI: Epstein-Barr virus and the immune system. Hide and seek. JAMA 1997, 278:510–513. DOI: 10.1001/jama.278.6.510
-
(1997)
JAMA
, vol.278
, pp. 510-513
-
-
Cohen, J.I.1
-
11
-
-
0035879367
-
Prevalence of antibodies to four herpesviruses among adults with glioma and controls
-
PID: 11447050, COI: 1:STN:280:DC%2BD3MvhsFCqsQ%3D%3D
-
Wrensch M, Weinberg A, Wiencke J, et al.: Prevalence of antibodies to four herpesviruses among adults with glioma and controls. Am J Epidemiol 2001, 154:161–165. DOI: 10.1093/aje/154.2.161
-
(2001)
Am J Epidemiol
, vol.154
, pp. 161-165
-
-
Wrensch, M.1
Weinberg, A.2
Wiencke, J.3
-
12
-
-
0025990587
-
The X-linked lymphoproliferative disease: from autopsy toward cloning the gene 1975–1990
-
PID: 1660601, COI: 1:STN:280:By2D1c%2FksFM%3D
-
Purtilo DT, Grierson HL, Davis JR, Okano M: The X-linked lymphoproliferative disease: from autopsy toward cloning the gene 1975–1990. Pediatr Pathol 1991, 11:685–710.
-
(1991)
Pediatr Pathol
, vol.11
, pp. 685-710
-
-
Purtilo, D.T.1
Grierson, H.L.2
Davis, J.R.3
Okano, M.4
-
13
-
-
0034218889
-
Advances in the management of hemophagocytic lymphohistiocytosis
-
PID: 10979202, COI: 1:STN:280:DC%2BD3cvpt1GitQ%3D%3D
-
Imashuku S: Advances in the management of hemophagocytic lymphohistiocytosis. Int J Hematol 2000, 72:1–11.
-
(2000)
Int J Hematol
, vol.72
, pp. 1-11
-
-
Imashuku, S.1
-
14
-
-
0034331249
-
Correlation of mutations of the SH2D1A gene and epstein-barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative disease
-
PID: 11049992, COI: 1:CAS:528:DC%2BD3cXnslGnt7o%3D
-
Sumegi J, Huang D, Lanyi A, et al.: Correlation of mutations of the SH2D1A gene and epstein-barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative disease. Blood 2000, 96:3118–3125.
-
(2000)
Blood
, vol.96
, pp. 3118-3125
-
-
Sumegi, J.1
Huang, D.2
Lanyi, A.3
-
15
-
-
0020385375
-
Immune deficiency in the X-linked lymphoproliferative syndrome. I. Epstein-Barr virus-specific defects
-
PID: 6292290, COI: 1:STN:280:BiyD2MfgtFM%3D
-
Harada S, Sakamoto K, Seeley JK, et al.: Immune deficiency in the X-linked lymphoproliferative syndrome. I. Epstein-Barr virus-specific defects. J Immunol 1982, 129:2532–2535.
-
(1982)
J Immunol
, vol.129
, pp. 2532-2535
-
-
Harada, S.1
Sakamoto, K.2
Seeley, J.K.3
-
16
-
-
0025860510
-
Immunoglobulin class and subclass deficiencies prior to Epstein-Barr virus infection in males with X-linked lymphoproliferative disease
-
PID: 1683154, COI: 1:STN:280:By2D2MbhtlQ%3D
-
Grierson HL, Skare J, Hawk J, et al.: Immunoglobulin class and subclass deficiencies prior to Epstein-Barr virus infection in males with X-linked lymphoproliferative disease. Am J Med Genet 1991, 40:294–297. DOI: 10.1002/ajmg.1320400309
-
(1991)
Am J Med Genet
, vol.40
, pp. 294-297
-
-
Grierson, H.L.1
Skare, J.2
Hawk, J.3
-
17
-
-
0032976666
-
Common variable immunodeficiency: clinical and immunological features of 248 patients
-
PID: 10413651, COI: 1:STN:280:DyaK1Mzktl2nuw%3D%3D
-
Cunningham-Rundles C, Bodian C: Common variable immunodeficiency: clinical and immunological features of 248 patients. Clin Immunol 1999, 92:34–48. DOI: 10.1006/clim.1999.4725
-
(1999)
Clin Immunol
, vol.92
, pp. 34-48
-
-
Cunningham-Rundles, C.1
Bodian, C.2
-
18
-
-
0023146287
-
Malignant lymphoma in the X-linked lymphoproliferative syndrome
-
PID: 3815312, COI: 1:STN:280:BiiC3s%2FmtFc%3D
-
Harrington DS, Weisenburger DD, Purtilo DT: Malignant lymphoma in the X-linked lymphoproliferative syndrome. Cancer 1987, 59:1419–1429. DOI: 10.1002/1097-0142(19870415)59:8<1419::AID-CNCR2820590807>3.0.CO;2-P
-
(1987)
Cancer
, vol.59
, pp. 1419-1429
-
-
Harrington, D.S.1
Weisenburger, D.D.2
Purtilo, D.T.3
-
19
-
-
0032756539
-
Epstein-Barr virusnegative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP)
-
PID: 10556288, COI: 1:CAS:528:DyaK1MXnvFKrtbs%3D
-
Brandau O, Schuster V, Weiss M, et al.: Epstein-Barr virusnegative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP). Hum Mol Genet 1999, 8:2407–2413. DOI: 10.1093/hmg/8.13.2407
-
(1999)
Hum Mol Genet
, vol.8
, pp. 2407-2413
-
-
Brandau, O.1
Schuster, V.2
Weiss, M.3
-
20
-
-
4243693554
-
Absence of SH2D1A point mutations in 62 Burkitts lymphoma cell lines
-
Yin L, Toccco T, Pauly S, et al.: Absence of SH2D1A point mutations in 62 Burkitts lymphoma cell lines. Am J Hum Genet 1999, 65(Suppl):A331.
-
(1999)
Am J Hum Genet
, vol.65
, pp. A331
-
-
Yin, L.1
Toccco, T.2
Pauly, S.3
-
21
-
-
0032730874
-
Immune-deficient bronchiectasis associated with X-linked lymphoproliferative disease
-
PID: 10475441, COI: 1:STN:280:DyaK1Mvgt1ChtA%3D%3D
-
Mehta VK, Massad MG, Tripathi SP, et al.: Immune-deficient bronchiectasis associated with X-linked lymphoproliferative disease. Ann Thorac Surg 1999, 68:578–580. DOI: 10.1016/S0003-4975(99)00603-7
-
(1999)
Ann Thorac Surg
, vol.68
, pp. 578-580
-
-
Mehta, V.K.1
Massad, M.G.2
Tripathi, S.P.3
-
22
-
-
0035171816
-
Lymphocytic vasculitis in X-linked lymphoproliferative disease
-
PID: 11133747, COI: 1:CAS:528:DC%2BD3MXis1equw%3D%3D
-
Dutz JP, Benoit L, Wang X, et al.: Lymphocytic vasculitis in X-linked lymphoproliferative disease. Blood 2001, 97:95–100. DOI: 10.1182/blood.V97.1.95
-
(2001)
Blood
, vol.97
, pp. 95-100
-
-
Dutz, J.P.1
Benoit, L.2
Wang, X.3
-
23
-
-
0021828975
-
Necrotizing lymphoid vasculitis in X-linked lymphoproliferative syndrome
-
PID: 2986573, COI: 1:STN:280:BiqC1Mfjt1w%3D
-
Loeffel S, Chang CH, Heyn R, et al.: Necrotizing lymphoid vasculitis in X-linked lymphoproliferative syndrome. Arch Pathol Lab Med 1985, 109:546–550.
-
(1985)
Arch Pathol Lab Med
, vol.109
, pp. 546-550
-
-
Loeffel, S.1
Chang, C.H.2
Heyn, R.3
-
24
-
-
0028219556
-
Retinal necrosis in X-linked lymphoproliferative disease
-
PID: 8152766, COI: 1:STN:280:ByuB3czmt1c%3D
-
Grossniklaus HE, Aaberg TM, Purnell EW, et al.: Retinal necrosis in X-linked lymphoproliferative disease. Ophthalmology 1994, 101:705–709.
-
(1994)
Ophthalmology
, vol.101
, pp. 705-709
-
-
Grossniklaus, H.E.1
Aaberg, T.M.2
Purnell, E.W.3
-
25
-
-
0020067594
-
Abnormal anti-Epstein Barr virus antibodies in carriers of the X-linked lymphoproliferative syndrome and in females at risk
-
PID: 6274962, COI: 1:STN:280:Bi2D1MbkslM%3D
-
Sakamoto K, Seeley JK, Lindsten T, et al.: Abnormal anti-Epstein Barr virus antibodies in carriers of the X-linked lymphoproliferative syndrome and in females at risk. J Immunol 1982, 128:904–907.
-
(1982)
J Immunol
, vol.128
, pp. 904-907
-
-
Sakamoto, K.1
Seeley, J.K.2
Lindsten, T.3
-
26
-
-
0030937079
-
HLH-94: a treatment protocol for hemophagocytic lymphohistiocytosis. HLH study group of the Histiocyte Society
-
PID: 9121398, COI: 1:STN:280:ByiB2M3ptF0%3D
-
Henter JI, Arico M, Egeler RM, et al.: HLH-94: a treatment protocol for hemophagocytic lymphohistiocytosis. HLH study group of the Histiocyte Society. Med Pediatr Oncol 1997, 28:342–347. DOI: 10.1002/(SICI)1096-911X(199705)28:5<342::AID-MPO3>3.0.CO;2-H
-
(1997)
Med Pediatr Oncol
, vol.28
, pp. 342-347
-
-
Henter, J.I.1
Arico, M.2
Egeler, R.M.3
-
27
-
-
0022920982
-
Allogeneic bone marrow transplantation for X-linked lymphoproliferative syndrome
-
PID: 3526660, COI: 1:STN:280:BimB1M%2Flslw%3D
-
Filipovich AH, Blazar BR, Ramsay NK, et al.: Allogeneic bone marrow transplantation for X-linked lymphoproliferative syndrome. Transplantation 1986, 42:222–224.
-
(1986)
Transplantation
, vol.42
, pp. 222-224
-
-
Filipovich, A.H.1
Blazar, B.R.2
Ramsay, N.K.3
-
28
-
-
0028346730
-
Successful bone marrow transplantation in a boy with X-linked lymphoproliferative syndrome and acute severe infectious mononucleosis
-
PID: 8054918, COI: 1:STN:280:ByuA3s3gsl0%3D
-
Pracher E, Panzer-Grumayer ER, et al.: Successful bone marrow transplantation in a boy with X-linked lymphoproliferative syndrome and acute severe infectious mononucleosis. Bone Marrow Transplant 1994, 13:655–658.
-
(1994)
Bone Marrow Transplant
, vol.13
, pp. 655-658
-
-
Pracher, E.1
Panzer-Grumayer, E.R.2
-
29
-
-
0029947122
-
Cure of X-linked lymphoproliferative disease (XLP) with allogeneic hematopoietic stem cell transplantation (HSCT): report from the XLP registry
-
PID: 8733691, COI: 1:STN:280:BymA3Mzps1c%3D
-
Gross TG, Filipovich AH, Conley ME, et al.: Cure of X-linked lymphoproliferative disease (XLP) with allogeneic hematopoietic stem cell transplantation (HSCT): report from the XLP registry. Bone Marrow Transplant 1996, 17:741–744.
-
(1996)
Bone Marrow Transplant
, vol.17
, pp. 741-744
-
-
Gross, T.G.1
Filipovich, A.H.2
Conley, M.E.3
-
30
-
-
0036464666
-
Hematopoietic stem cell transplantation for severe combined immunodeficiency in the neonatal period leads to superior thymic output and improved survival
-
PID: 11806989, COI: 1:CAS:528:DC%2BD38XhtValsb8%3D
-
Myers LA, Patel DD, Puck JM, Buckley RH: Hematopoietic stem cell transplantation for severe combined immunodeficiency in the neonatal period leads to superior thymic output and improved survival. Blood 2002, 99:872–878. DOI: 10.1182/blood.V99.3.872
-
(2002)
Blood
, vol.99
, pp. 872-878
-
-
Myers, L.A.1
Patel, D.D.2
Puck, J.M.3
Buckley, R.H.4
-
31
-
-
0027367461
-
Brief report: correction of X-linked lymphoproliferative disease by transplantation of cord-blood stem cells
-
PID: 8232431, COI: 1:STN:280:ByuD2M%2FgtVQ%3D
-
Vowels MR, Tang RL, Berdoukas V, et al.: Brief report: correction of X-linked lymphoproliferative disease by transplantation of cord-blood stem cells. N Engl J Med 1993, 329:1623–1625. DOI: 10.1056/NEJM199311253292205
-
(1993)
N Engl J Med
, vol.329
, pp. 1623-1625
-
-
Vowels, M.R.1
Tang, R.L.2
Berdoukas, V.3
-
32
-
-
0034724857
-
Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease
-
PID: 10784449, COI: 1:CAS:528:DC%2BD3cXivFGhtbc%3D
-
Cavazzana-Calvo M, Hacein-Bey S, de Saint Basile G, et al.: Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease. Science 2000, 288:669–672. DOI: 10.1126/science.288.5466.669
-
(2000)
Science
, vol.288
, pp. 669-672
-
-
Cavazzana-Calvo, M.1
Hacein-Bey, S.2
de Saint Basile, G.3
-
33
-
-
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
-
PID: 10934222, COI: 1:CAS:528:DC%2BD3cXlsFygt78%3D
-
Parolini S, Bottino C, Falco M, et al.: 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 2000, 192:337–346. DOI: 10.1084/jem.192.3.337
-
(2000)
J Exp Med
, vol.192
, pp. 337-346
-
-
Parolini, S.1
Bottino, C.2
Falco, M.3
-
34
-
-
0035817326
-
NTB-A [correction of GNTB-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
-
PID: 11489943, COI: 1:CAS:528:DC%2BD3MXlvFShurc%3D
-
Bottino C, Falco M, Parolini S, et al.: NTB-A [correction of GNTB-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 2001, 194:235–246. DOI: 10.1084/jem.194.3.235
-
(2001)
J Exp Med
, vol.194
, pp. 235-246
-
-
Bottino, C.1
Falco, M.2
Parolini, S.3
-
35
-
-
0019255923
-
Deficient natural killer cell activity in x-linked lymphoproliferative syndrome
-
PID: 6158759, COI: 1:STN:280:Bi6D3sznsFc%3D
-
Sullivan JL, Byron KS, Brewster FE, Purtilo DT: Deficient natural killer cell activity in x-linked lymphoproliferative syndrome. Science 1980, 210:543–545. DOI: 10.1126/science.6158759
-
(1980)
Science
, vol.210
, pp. 543-545
-
-
Sullivan, J.L.1
Byron, K.S.2
Brewster, F.E.3
Purtilo, D.T.4
-
36
-
-
0022460495
-
Defective natural killing activity but retention of lymphocyte-mediated antibody-dependent cellular cytotoxicity in patients with the X-linked lymphoproliferative syndrome
-
PID: 3742598, COI: 1:STN:280:BimB1MfktFQ%3D
-
Argov S, Johnson DR, Collins M, et al.: Defective natural killing activity but retention of lymphocyte-mediated antibody-dependent cellular cytotoxicity in patients with the X-linked lymphoproliferative syndrome. Cell Immunol 1986, 100:1–9. DOI: 10.1016/0008-8749(86)90001-8
-
(1986)
Cell Immunol
, vol.100
, pp. 1-9
-
-
Argov, S.1
Johnson, D.R.2
Collins, M.3
-
37
-
-
0032190081
-
The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM
-
PID: 9774102, COI: 1:CAS:528:DyaK1cXms1amsrg%3D
-
Sayos J, Wu C, Morra M, et al.: The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM. Nature 1998, 395:462–469. DOI: 10.1038/26683
-
(1998)
Nature
, vol.395
, pp. 462-469
-
-
Sayos, J.1
Wu, C.2
Morra, M.3
-
38
-
-
17344372694
-
Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene
-
PID: 9771704, COI: 1:CAS:528:DyaK1cXms1amsb8%3D
-
Coffey AJ, Brooksbank RA, Brandau O, et al.: Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene. Nat Genet 1998, 20:129–135. DOI: 10.1038/2424
-
(1998)
Nat Genet
, vol.20
, pp. 129-135
-
-
Coffey, A.J.1
Brooksbank, R.A.2
Brandau, O.3
-
39
-
-
13144278345
-
Inactivating mutations in an SH2 domain-encoding gene in X-linked lymphoproliferative syndrome
-
PID: 9811875, COI: 1:CAS:528:DyaK1cXnsVGgsbw%3D
-
Nichols KE, Harkin DP, Levitz S, et al.: Inactivating mutations in an SH2 domain-encoding gene in X-linked lymphoproliferative syndrome. Proc Natl Acad Sci U S A 1998, 95:13765–13770. DOI: 10.1073/pnas.95.23.13765
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 13765-13770
-
-
Nichols, K.E.1
Harkin, D.P.2
Levitz, S.3
-
40
-
-
0034521222
-
Potential pathways for regulation of NK and T cell responses: differential X-linked lymphoproliferative syndrome gene product SAP interactions with SLAM and 2B4
-
PID: 11099315, COI: 1:CAS:528:DC%2BD3MXpvVCh
-
Sayos J, Nguyen KB, Wu C, et al.: Potential pathways for regulation of NK and T cell responses: differential X-linked lymphoproliferative syndrome gene product SAP interactions with SLAM and 2B4. Int Immunol 2000, 12:1749–1757. DOI: 10.1093/intimm/12.12.1749
-
(2000)
Int Immunol
, vol.12
, pp. 1749-1757
-
-
Sayos, J.1
Nguyen, K.B.2
Wu, C.3
-
41
-
-
0033212986
-
Crystal structures of the XLP protein SAP reveal a class of SH2 domains with extended, phosphotyrosine-independent sequence recognition
-
PID: 10549287, COI: 1:CAS:528:DyaK1MXntFCgsLs%3D
-
Poy F, Yaffe MB, Sayos J, et al.: Crystal structures of the XLP protein SAP reveal a class of SH2 domains with extended, phosphotyrosine-independent sequence recognition. Mol Cell 1999, 4:555–561. DOI: 10.1016/S1097-2765(00)80206-3
-
(1999)
Mol Cell
, vol.4
, pp. 555-561
-
-
Poy, F.1
Yaffe, M.B.2
Sayos, J.3
-
42
-
-
0035965317
-
Characterization of SH2D1A missense mutations identified in X-linked lymphoproliferative disease patients
-
PID: 11477068, COI: 1:CAS:528:DC%2BD3MXnt1yru7w%3D
-
Morra M, Simarro-Grande M, Martin M, et al.: Characterization of SH2D1A missense mutations identified in X-linked lymphoproliferative disease patients. J Biol Chem 2001, 276:36809–36816. DOI: 10.1074/jbc.M101305200
-
(2001)
J Biol Chem
, vol.276
, pp. 36809-36816
-
-
Morra, M.1
Simarro-Grande, M.2
Martin, M.3
-
43
-
-
0035554933
-
SAP controls T cell responses to virus and terminal differentiation of TH2 cells
-
PID: 11323694, COI: 1:CAS:528:DC%2BD3MXjtlShtL0%3D
-
Wu C, Nguyen KB, Pien GC, et al.: SAP controls T cell responses to virus and terminal differentiation of TH2 cells. Nat Immunol 2001, 2:410–414. DOI: 10.1038/ni0901-823
-
(2001)
Nat Immunol
, vol.2
, pp. 410-414
-
-
Wu, C.1
Nguyen, K.B.2
Pien, G.C.3
-
44
-
-
0035912823
-
Altered lymphocyte responses and cytokine production in mice deficient in the X-linked lymphoproliferative disease gene SH2D1A/DSHP/ SAP
-
PID: 11404475, COI: 1:CAS:528:DC%2BD3MXkslWlsr4%3D
-
Czar MJ, Kersh EN, Mijares LA, et al.: Altered lymphocyte responses and cytokine production in mice deficient in the X-linked lymphoproliferative disease gene SH2D1A/DSHP/ SAP. Proc Natl Acad Sci U S A 2001, 98:7449–7454. DOI: 10.1073/pnas.131193098
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 7449-7454
-
-
Czar, M.J.1
Kersh, E.N.2
Mijares, L.A.3
-
45
-
-
0035063939
-
X-linked lymphoproliferative disease: a progressive immunodeficiency
-
PID: 11244050, COI: 1:CAS:528:DC%2BD3MXivFKgu7w%3D
-
Morra M, Howie D, Grande MS, et al.: X-linked lymphoproliferative disease: a progressive immunodeficiency. Annu Rev Immunol 2001, 19:657–682. DOI: 10.1146/annurev.immunol.19.1.657
-
(2001)
Annu Rev Immunol
, vol.19
, pp. 657-682
-
-
Morra, M.1
Howie, D.2
Grande, M.S.3
-
46
-
-
0033564638
-
Cutting edge: human 2B4, an activating NK cell receptor, recruits the protein tyrosine phosphatase SHP-2 and the adaptor signaling protein SAP
-
PID: 10358138, COI: 1:CAS:528:DyaK1MXktF2itLw%3D
-
Tangye SG, Lazetic S, Woollatt E, et al.: Cutting edge: human 2B4, an activating NK cell receptor, recruits the protein tyrosine phosphatase SHP-2 and the adaptor signaling protein SAP. J Immunol 1999, 162:6981–6985.
-
(1999)
J Immunol
, vol.162
, pp. 6981-6985
-
-
Tangye, S.G.1
Lazetic, S.2
Woollatt, E.3
-
47
-
-
0034294836
-
Defective NK cell activation in X-linked lymphoproliferative disease
-
PID: 11034354, COI: 1:CAS:528:DC%2BD3cXntVyjur0%3D
-
Benoit L, Wang X, Pabst HF, et al.: Defective NK cell activation in X-linked lymphoproliferative disease. J Immunol 2000, 165:3549–3553.
-
(2000)
J Immunol
, vol.165
, pp. 3549-3553
-
-
Benoit, L.1
Wang, X.2
Pabst, H.F.3
-
48
-
-
0034889004
-
Regulation of SLAMmediated signal transduction by SAP, the X-linked lymphoproliferative gene product
-
PID: 11477403, COI: 1:CAS:528:DC%2BD3MXlslGjtb4%3D, This study Identified a potentially new role for SAP intracellular signaling. SAP can change the conformation of the intracellular portion of SLAM, allowing recruitment of the Fyn tyrosine kinase
-
Latour S, Gish G, Helgason CD, et al.: Regulation of SLAMmediated signal transduction by SAP, the X-linked lymphoproliferative gene product. Nat Immunol 2001, 2:681–690. This study Identified a potentially new role for SAP in intracellular signaling. SAP can change the conformation of the intracellular portion of SLAM, allowing recruitment of the Fyn tyrosine kinase. DOI: 10.1038/90615
-
(2001)
Nat Immunol
, vol.2
, pp. 681-690
-
-
Latour, S.1
Gish, G.2
Helgason, C.D.3
-
49
-
-
0034691123
-
The X-linked lymphoproliferative syndrome gene product SH2D1A associates with p62dok (Dok1) and activates NF-kappa B
-
PID: 10852966, COI: 1:CAS:528:DC%2BD3cXksVKhs74%3D, This report demonstrated an association of SAP with p62dok, and showed that SAP can activate NK-_B. This further expands the number of pathways which SAP is apparently involved
-
Sylla BS, Murphy K, Cahir-McFarland E, et al.: The X-linked lymphoproliferative syndrome gene product SH2D1A associates with p62dok (Dok1) and activates NF-kappa B. Proc Natl Acad Sci U S A 2000, 97:7470–7475. This report demonstrated an association of SAP with p62dok, and showed that SAP can activate NK-_B. This further expands the number of pathways in which SAP is apparently involved. DOI: 10.1073/pnas.130193097
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 7470-7475
-
-
Sylla, B.S.1
Murphy, K.2
Cahir-McFarland, E.3
|