-
1
-
-
0025812810
-
Reexamination of the blood lymphocyte transformation test in the diagnosis of chronic beryllium disease
-
Mroz MM, Kreiss K, Lezotte DC, Campbell PA, Newman LS. Reexamination of the blood lymphocyte transformation test in the diagnosis of chronic beryllium disease. J Allergy Clin Immunol 1991 : 88 : 54 60.
-
(1991)
J Allergy Clin Immunol
, vol.88
, pp. 54-60
-
-
Mroz, M.M.1
Kreiss, K.2
Lezotte, D.C.3
Campbell, P.A.4
Newman, L.S.5
-
2
-
-
0029827397
-
Significance of the blood beryllium lymphocyte proliferation test
-
Newman LS. Significance of the blood beryllium lymphocyte proliferation test. Environ Health Perspect 1996 : 104 (Suppl 5 953 6.
-
(1996)
Environ Health Perspect
, vol.104
, Issue.5
, pp. 953-6
-
-
Newman, L.S.1
-
3
-
-
0024501760
-
Maintenance of alveolitis in patients with chronic beryllium disease by beryllium-specific helper T cells
-
Saltini C, Winestock K, Kirby M, Pinkston P, Crystal RG. Maintenance of alveolitis in patients with chronic beryllium disease by beryllium-specific helper T cells. N Engl J Med 1989 : 320 : 1103 9.
-
(1989)
N Engl J Med
, vol.320
, pp. 1103-9
-
-
Saltini, C.1
Winestock, K.2
Kirby, M.3
Pinkston, P.4
Crystal, R.G.5
-
4
-
-
10744224113
-
Influence of MHC class II in susceptibility to beryllium sensitization and chronic beryllium disease
-
Maier LA, McGrath DS, Sato H et al. Influence of MHC class II in susceptibility to beryllium sensitization and chronic beryllium disease. J Immunol 2003 : 171 : 6910 8.
-
(2003)
J Immunol
, vol.171
, pp. 6910-8
-
-
Maier, L.A.1
McGrath, D.S.2
Sato, H.3
-
6
-
-
0032879738
-
Regulation of alveolar macrophage-T cell interactions during Th1-type sarcoid inflammatory process
-
Agostini C, Trentin L, Perin A et al. Regulation of alveolar macrophage-T cell interactions during Th1-type sarcoid inflammatory process. Am J Physiol 1999 : 277 (Pt 1 L240 50.
-
(1999)
Am J Physiol
, vol.277
, Issue.1
-
-
Agostini, C.1
Trentin, L.2
Perin, A.3
-
7
-
-
33744914590
-
BTNL2, a butyrophilin-like molecule that functions to inhibit T cell activation
-
Nguyen T, Liu XK, Zhang Y, Dong C. BTNL2, a butyrophilin-like molecule that functions to inhibit T cell activation. J Immunol 2006 : 176 : 7354 60.
-
(2006)
J Immunol
, vol.176
, pp. 7354-60
-
-
Nguyen, T.1
Liu, X.K.2
Zhang, Y.3
Dong, C.4
-
8
-
-
23944435405
-
The BTNL2 gene and sarcoidosis susceptibility in African Americans and Whites
-
Rybicki BA, Walewski JL, Maliarik MJ, Kian H, Iannuzzi MC. The BTNL2 gene and sarcoidosis susceptibility in African Americans and Whites. Am J Hum Genet 2005 : 77 : 491 9.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 491-9
-
-
Rybicki, B.A.1
Walewski, J.L.2
Maliarik, M.J.3
Kian, H.4
Iannuzzi, M.C.5
-
9
-
-
20144388906
-
Sarcoidosis is associated with a truncating splice site mutation in BTNL2
-
Valentonyte R, Hampe J, Huse K et al. Sarcoidosis is associated with a truncating splice site mutation in BTNL2. Nat Genet 2005 : 37 : 357 64.
-
(2005)
Nat Genet
, vol.37
, pp. 357-64
-
-
Valentonyte, R.1
Hampe, J.2
Huse, K.3
-
10
-
-
33646272188
-
Analysis of a functional BTNL2 polymorphism in type 1 diabetes, rheumatoid arthritis, and systemic lupus erythematosus
-
Orozco G, Eerligh P, Sanchez E et al. Analysis of a functional BTNL2 polymorphism in type 1 diabetes, rheumatoid arthritis, and systemic lupus erythematosus. Hum Immunol 2005 : 66 : 1235 41.
-
(2005)
Hum Immunol
, vol.66
, pp. 1235-41
-
-
Orozco, G.1
Eerligh, P.2
Sanchez, E.3
-
11
-
-
11144229674
-
Beryllium sensitization progresses to chronic beryllium disease: A longitudinal study of disease risk
-
Newman LS, Mroz MM, Balkissoon R, Maier LA. Beryllium sensitization progresses to chronic beryllium disease: a longitudinal study of disease risk. Am J Respir Crit Care Med 2005 : 171 : 54 60.
-
(2005)
Am J Respir Crit Care Med
, vol.171
, pp. 54-60
-
-
Newman, L.S.1
Mroz, M.M.2
Balkissoon, R.3
Maier, L.A.4
-
12
-
-
0032906574
-
Angiotensin-1 converting enzyme polymorphisms in chronic beryllium disease
-
Maier LA, Raynolds MV, Young DA, Barker EA, Newman LS. Angiotensin-1 converting enzyme polymorphisms in chronic beryllium disease. Am J Respir Crit Care Med 1999 : 159 (Pt 1 1342 50.
-
(1999)
Am J Respir Crit Care Med
, vol.159
, Issue.1
, pp. 1342-50
-
-
Maier, L.A.1
Raynolds, M.V.2
Young, D.A.3
Barker, E.A.4
Newman, L.S.5
-
13
-
-
0029618012
-
Phototyping: Comprehensive DNA typing for HLA-A, B, C, DRB1, DRB3, DRB4, DRB5 & DQB1 by PCR with 144 primer mixes utilizing sequence-specific primers (PCR-SSP)
-
Bunce M, O'Neill CM, Barnardo MC et al. Phototyping: comprehensive DNA typing for HLA-A, B, C, DRB1, DRB3, DRB4, DRB5 & DQB1 by PCR with 144 primer mixes utilizing sequence-specific primers (PCR-SSP). Tissue Antigens 1995 : 46 : 355 67.
-
(1995)
Tissue Antigens
, vol.46
, pp. 355-67
-
-
Bunce, M.1
O'Neill, C.M.2
Barnardo, M.C.3
-
14
-
-
0033301923
-
Molecular typing for the MHC with PCR-SSP
-
Welsh K, Bunce M. Molecular typing for the MHC with PCR-SSP. Rev Immunogenet 1999 : 1 : 157 76.
-
(1999)
Rev Immunogenet
, vol.1
, pp. 157-76
-
-
Welsh, K.1
Bunce, M.2
-
15
-
-
0035071957
-
A new statistical method for haplotype reconstruction from population data
-
Stephens M, Smith NJ, Donnelly P. A new statistical method for haplotype reconstruction from population data. Am J Hum Genet 2001 : 68 : 978 89.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 978-89
-
-
Stephens, M.1
Smith, N.J.2
Donnelly, P.3
-
16
-
-
0035756443
-
A web-based tool to retrieve human genome polymorphisms from public databases
-
Riva A, Kohane IS. A web-based tool to retrieve human genome polymorphisms from public databases. Proc AMIA Symp 2001 : 558 62.
-
(2001)
Proc AMIA Symp
, pp. 558-62
-
-
Riva, A.1
Kohane, I.S.2
-
17
-
-
26244450874
-
Identification of HLA-DRPhebeta47 as the susceptibility marker of hypersensitivity to beryllium in individuals lacking the berylliosis-associated supratypic marker HLA-DPGlubeta69
-
Amicosante M, Berretta F, Rossman M et al. Identification of HLA-DRPhebeta47 as the susceptibility marker of hypersensitivity to beryllium in individuals lacking the berylliosis-associated supratypic marker HLA-DPGlubeta69. Respir Res 2005 : 6 : 94.
-
(2005)
Respir Res
, vol.6
, pp. 94
-
-
Amicosante, M.1
Berretta, F.2
Rossman, M.3
-
18
-
-
0030755675
-
Interaction of genetic and exposure factors in the prevalence of berylliosis
-
Richeldi L, Kreiss K, Mroz MM, Zhen B, Tartoni P, Saltini C. Interaction of genetic and exposure factors in the prevalence of berylliosis. Am J Ind Med 1997 : 32 : 337 40.
-
(1997)
Am J Ind Med
, vol.32
, pp. 337-40
-
-
Richeldi, L.1
Kreiss, K.2
Mroz, M.M.3
Zhen, B.4
Tartoni, P.5
Saltini, C.6
-
19
-
-
0037086022
-
Human leukocyte antigen Class II amino acid epitopes: Susceptibility and progression markers for beryllium hypersensitivity
-
Rossman MD, Stubbs J, Lee CW, Argyris E, Magira E, Monos D. Human leukocyte antigen Class II amino acid epitopes: susceptibility and progression markers for beryllium hypersensitivity. Am J Respir Crit Care Med 2002 : 165 : 788 94.
-
(2002)
Am J Respir Crit Care Med
, vol.165
, pp. 788-94
-
-
Rossman, M.D.1
Stubbs, J.2
Lee, C.W.3
Argyris, E.4
Magira, E.5
Monos, D.6
-
20
-
-
27944456858
-
Role of the berylliosis-associated HLA-DPGlu69 supratypic variant in determining the response to beryllium in a blood T-cells beryllium-stimulated proliferation test
-
Amicosante M, Deubner D, Saltini C. Role of the berylliosis-associated HLA-DPGlu69 supratypic variant in determining the response to beryllium in a blood T-cells beryllium-stimulated proliferation test. Sarcoidosis Vasc Diffuse Lung Dis 2005 : 22 : 175 9.
-
(2005)
Sarcoidosis Vasc Diffuse Lung Dis
, vol.22
, pp. 175-9
-
-
Amicosante, M.1
Deubner, D.2
Saltini, C.3
-
21
-
-
0027430877
-
HLA-DPB1 glutamate 69: A genetic marker of beryllium disease
-
Richeldi L, Sorrentino R, Saltini C. HLA-DPB1 glutamate 69: a genetic marker of beryllium disease. Science 1993 : 262 : 242 4.
-
(1993)
Science
, vol.262
, pp. 242-4
-
-
Richeldi, L.1
Sorrentino, R.2
Saltini, C.3
-
22
-
-
0033178964
-
Differential susceptibilities to chronic beryllium disease contributed by different Glu69 HLA-DPB1 and -DPA1 alleles
-
Wang Z, White PS, Petrovic M et al. Differential susceptibilities to chronic beryllium disease contributed by different Glu69 HLA-DPB1 and -DPA1 alleles. J Immunol 1999 : 163 : 1647 53.
-
(1999)
J Immunol
, vol.163
, pp. 1647-53
-
-
Wang, Z.1
White, P.S.2
Petrovic, M.3
-
23
-
-
0033741884
-
Beryllium presentation to CD4+ T cells underlies disease-susceptibility HLA-DP alleles in chronic beryllium disease
-
Fontenot AP, Torres M, Marshall WH, Newman LS, Kotzin BL. Beryllium presentation to CD4+ T cells underlies disease-susceptibility HLA-DP alleles in chronic beryllium disease. Proc Natl Acad Sci U S A 2000 : 97 : 12717 22.
-
(2000)
Proc Natl Acad Sci U S a
, vol.97
, pp. 12717-22
-
-
Fontenot, A.P.1
Torres, M.2
Marshall, W.H.3
Newman, L.S.4
Kotzin, B.L.5
-
24
-
-
33748796075
-
Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves' disease appears to be secondary to DRB1 exon 2 position beta74
-
Simmonds MJ, Heward JM, Barrett JC, Franklyn JA, Gough SC. Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves' disease appears to be secondary to DRB1 exon 2 position beta74. Clin Endocrinol (Oxf) 2006 : 65 : 429 32.
-
(2006)
Clin Endocrinol (Oxf)
, vol.65
, pp. 429-32
-
-
Simmonds, M.J.1
Heward, J.M.2
Barrett, J.C.3
Franklyn, J.A.4
Gough, S.C.5
-
25
-
-
29644442440
-
Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15
-
Traherne JA, Barcellos LF, Sawcer SJ et al. Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15. Hum Mol Genet 2006 : 15 : 155 61.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 155-61
-
-
Traherne, J.A.1
Barcellos, L.F.2
Sawcer, S.J.3
-
26
-
-
27744454605
-
Beryllium presentation to CD4+ T cells is dependent on a single amino acid residue of the MHC class II beta-chain
-
Bill JR, Mack DG, Falta MT et al. Beryllium presentation to CD4+ T cells is dependent on a single amino acid residue of the MHC class II beta-chain. J Immunol 2005 : 175 : 7029 37.
-
(2005)
J Immunol
, vol.175
, pp. 7029-37
-
-
Bill, J.R.1
MacK, D.G.2
Falta, M.T.3
|