-
1
-
-
0026650944
-
Human T-cell activation deficiencies
-
Arnaiz-Villena A, Timon M, Gallego CR, Blas MP, Correl A, Villa JMM, Regueiro JR (1992): Human T-cell activation deficiencies. Immunol Today 13:259-265.
-
(1992)
Immunol Today
, vol.13
, pp. 259-265
-
-
Arnaiz-Villena, A.1
Timon, M.2
Gallego, C.R.3
Blas, M.P.4
Correl, A.5
Villa, J.M.M.6
Regueiro, J.R.7
-
2
-
-
0027216789
-
Dyskeratosis congenita: Three additional families show linkage to a locus in Xq28
-
Arngrimsson R, Dokal I, Luzzatto L, Connor JM (1993): Dyskeratosis congenita: Three additional families show linkage to a locus in Xq28. J Med Genet 30:618-619.
-
(1993)
J Med Genet
, vol.30
, pp. 618-619
-
-
Arngrimsson, R.1
Dokal, I.2
Luzzatto, L.3
Connor, J.M.4
-
3
-
-
0025233576
-
Genetic and mutational analysis of the T-cell antigen receptor
-
Ashwell JD, Klausner RD (1990): Genetic and mutational analysis of the T-cell antigen receptor. Annu Rev Immunol 8:139-167.
-
(1990)
Annu Rev Immunol
, vol.8
, pp. 139-167
-
-
Ashwell, J.D.1
Klausner, R.D.2
-
4
-
-
0026598252
-
Molecular associations between the T-lymphocyte antigen receptor complex and the surface antigens CD2, CD4, or CDS and CDS
-
Beyers AD, Spruyt LL, Williams AF (1992): Molecular associations between the T-lymphocyte antigen receptor complex and the surface antigens CD2, CD4, or CDS and CDS. Proc Natl Acad Sci USA 89: 2945-2949.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 2945-2949
-
-
Beyers, A.D.1
Spruyt, L.L.2
Williams, A.F.3
-
5
-
-
0025599933
-
Primary combined immunodeficiency resulting from defective transcription of multiple T-cell lymphokine genes
-
Chatila T, Castigli E, Pahwa R, Pahwa S, Chirmule N, Oyaizu N, Good RA, Geha RS (1990): Primary combined immunodeficiency resulting from defective transcription of multiple T-cell lymphokine genes. Proc Natl Acad Sci USA 87:10033-10037.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 10033-10037
-
-
Chatila, T.1
Castigli, E.2
Pahwa, R.3
Pahwa, S.4
Chirmule, N.5
Oyaizu, N.6
Good, R.A.7
Geha, R.S.8
-
6
-
-
0026691858
-
Molecular approaches to analysis of X-linked immunodeficiencies
-
Conley ME (1992): Molecular approaches to analysis of X-linked immunodeficiencies. Annu Rev Immunol 10:215-238.
-
(1992)
Annu Rev Immunol
, vol.10
, pp. 215-238
-
-
Conley, M.E.1
-
7
-
-
0022477628
-
Assignment of the gene for dyskeratosis congenita to Xq28
-
Conner JM, Gatherer D, Gray FC, Pirrit LA, Affara NA (1986): Assignment of the gene for dyskeratosis congenita to Xq28. Hum Genet 72:348-351.
-
(1986)
Hum Genet
, vol.72
, pp. 348-351
-
-
Conner, J.M.1
Gatherer, D.2
Gray, F.C.3
Pirrit, L.A.4
Affara, N.A.5
-
8
-
-
2742543634
-
Primary immunodeficiency diseases: Severe combined immunodeficiency diseases (SCIDs)
-
Paul WE (ed): New York: Raven Press
-
Cooper MD, Butler JL (1989): Primary immunodeficiency diseases: Severe combined immunodeficiency diseases (SCIDs). In Paul WE (ed): "Fundamental Immunology." New York: Raven Press, pp 1034-1039.
-
(1989)
Fundamental Immunology
, pp. 1034-1039
-
-
Cooper, M.D.1
Butler, J.L.2
-
10
-
-
0025779736
-
Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome)
-
De Saint-Basile G, Le Deist F, de Vilartay JP, Cerf-Bensussan N, Jourdet O, Brousse N, Griscelli C, Fischer A (1991): Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome). J Clin Invest 87:1352-1359.
-
(1991)
J Clin Invest
, vol.87
, pp. 1352-1359
-
-
De Saint-Basile, G.1
Le Deist, F.2
De Vilartay, J.P.3
Cerf-Bensussan, N.4
Jourdet, O.5
Brousse, N.6
Griscelli, C.7
Fischer, A.8
-
11
-
-
0021926097
-
Dyskeratosis congenita with hypoplastic anemia and stem cell defect
-
Friedland M, Lutton JD, Spitzer R, Leverk RD (1985): Dyskeratosis congenita with hypoplastic anemia and stem cell defect. Am J Hematol 20:85-87.
-
(1985)
Am J Hematol
, vol.20
, pp. 85-87
-
-
Friedland, M.1
Lutton, J.D.2
Spitzer, R.3
Leverk, R.D.4
-
12
-
-
0027506211
-
Transmembrane signaling and T-cell immunodeficiency
-
Gelfand EW (1993): Transmembrane signaling and T-cell immunodeficiency. Pediatr Res 33:16-19.
-
(1993)
Pediatr Res
, vol.33
, pp. 16-19
-
-
Gelfand, E.W.1
-
13
-
-
0021068521
-
Diagnosis and Classification of Severe Combined Immunodeficiency Disease
-
New York: Alan R. Liss, Inc., for the National Foundation-March of Dimes
-
Gelfand EW, Dosch HM (1983): Diagnosis and Classification of Severe Combined Immunodeficiency Disease. New York: Alan R. Liss, Inc., for the National Foundation-March of Dimes. BD:OAS XIX(3):65-72.
-
(1983)
BD:OAS
, vol.19
, Issue.3
, pp. 65-72
-
-
Gelfand, E.W.1
Dosch, H.M.2
-
14
-
-
84944282145
-
X-linked dyskeratosis congenita with pancytopenia
-
Gutman A, Frumkin A, Adam A, Bloch-Schtacher N, Rozenszajn LA (1978): X-linked dyskeratosis congenita with pancytopenia. Arch Dermatol 114:1667-1671.
-
(1978)
Arch Dermatol
, vol.114
, pp. 1667-1671
-
-
Gutman, A.1
Frumkin, A.2
Adam, A.3
Bloch-Schtacher, N.4
Rozenszajn, L.A.5
-
15
-
-
0024469727
-
Associations of the skeletal and immune system
-
Hong R (1989): Associations of the skeletal and immune system. Am J Med Genet 34:55-59.
-
(1989)
Am J Med Genet
, vol.34
, pp. 55-59
-
-
Hong, R.1
-
16
-
-
0025971630
-
T cell antigen receptor activation pathways: The tyrosine kinase connection
-
Klausner RD, Samelson LE (1991): T cell antigen receptor activation pathways: The tyrosine kinase connection. Cell 64:875-878.
-
(1991)
Cell
, vol.64
, pp. 875-878
-
-
Klausner, R.D.1
Samelson, L.E.2
-
17
-
-
0026507198
-
T cell immunodeficiency in dyskeratosis congenita
-
Lee BW, Yap HK, Quah TC, Chong A, Seah CC (1992): T cell immunodeficiency in dyskeratosis congenita. Arch Dis Child 67:524-526.
-
(1992)
Arch Dis Child
, vol.67
, pp. 524-526
-
-
Lee, B.W.1
Yap, H.K.2
Quah, T.C.3
Chong, A.4
Seah, C.C.5
-
18
-
-
0021972279
-
The gene encoding the human interleukin-2 receptor is located on chromosome 10
-
Leonard WJ, Donlon TA, Lebo RB, Greene WC (1985): The gene encoding the human interleukin-2 receptor is located on chromosome 10. Science 228:1547-1549.
-
(1985)
Science
, vol.228
, pp. 1547-1549
-
-
Leonard, W.J.1
Donlon, T.A.2
Lebo, R.B.3
Greene, W.C.4
-
19
-
-
0026799821
-
Progress in primary immunodeficiency
-
Matsumoto S, Sakiyama Y, Ariga T, Gallagher R, Taguchi Y (1992): Progress in primary immunodeficiency. Immunol Today 13:4-5.
-
(1992)
Immunol Today
, vol.13
, pp. 4-5
-
-
Matsumoto, S.1
Sakiyama, Y.2
Ariga, T.3
Gallagher, R.4
Taguchi, Y.5
-
20
-
-
0027403374
-
Interleukin-2 receptor y chain mutation results in X-linked severe combined immunodeficiency in humans
-
Noguchi M, Yi H, Rosenblatt HM, Filipovich AH, Adelstein S, Modi WS, McBride OW, Leonard WJ (1993): Interleukin-2 receptor y chain mutation results in X-linked severe combined immunodeficiency in humans. Cell 73:147-157.
-
(1993)
Cell
, vol.73
, pp. 147-157
-
-
Noguchi, M.1
Yi, H.2
Rosenblatt, H.M.3
Filipovich, A.H.4
Adelstein, S.5
Modi, W.S.6
McBride, O.W.7
Leonard, W.J.8
-
21
-
-
0015427342
-
Congenital dyskeratosis: Zinner-Engman-Cole syndrome with thymic dysplasia and aplastic anemia
-
Ortega JA, Swanson VL, Landig BH, Hammond GD (1972): Congenital dyskeratosis: Zinner-Engman-Cole syndrome with thymic dysplasia and aplastic anemia. Am J Dis Child 124:701-704.
-
(1972)
Am J Dis Child
, vol.124
, pp. 701-704
-
-
Ortega, J.A.1
Swanson, V.L.2
Landig, B.H.3
Hammond, G.D.4
-
22
-
-
0024492985
-
Etiologic heterogeneity in dyskeratosis congenita
-
Pai GS, Morgan S, Whetsell C (1989): Etiologic heterogeneity in dyskeratosis congenita. Am J Med Genet 32:63-66.
-
(1989)
Am J Med Genet
, vol.32
, pp. 63-66
-
-
Pai, G.S.1
Morgan, S.2
Whetsell, C.3
-
23
-
-
18744436873
-
New and old immunodeficiencies
-
Stiehm ER (1993): New and old immunodeficiencies. Pediatr Res 33: 2-8.
-
(1993)
Pediatr Res
, vol.33
, pp. 2-8
-
-
Stiehm, E.R.1
-
24
-
-
0020084060
-
Dyskeratosis congenita: An autosomal dominant disorder
-
Tchou PK, Kohn T (1982): Dyskeratosis congenita: An autosomal dominant disorder. J Am Acad Dermatol 6:1034-1039.
-
(1982)
J Am Acad Dermatol
, vol.6
, pp. 1034-1039
-
-
Tchou, P.K.1
Kohn, T.2
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