-
2
-
-
0011375574
-
Adrenal autoimmunity and autoimmune polyglandular syndromes
-
Rose N.R. and Mackay I.R., (eds) Academic Press, Orlando
-
Maclaren N.K., Blizzard R.M. 1985. Adrenal autoimmunity and autoimmune polyglandular syndromes. In The autoimmune disease. Rose N.R. and Mackay I.R., (eds) Academic Press, Orlando, pp. 201-225
-
(1985)
The Autoimmune Disease
, pp. 201-225
-
-
Maclaren, N.K.1
Blizzard, R.M.2
-
3
-
-
0019811879
-
Two types of autoimmune Addison's disease associated with different polyglandular autoimmune (PGA) syndromes
-
Neufeld M., Maclaren N.K., Blizzard R.M. 1981. Two types of autoimmune Addison's disease associated with different polyglandular autoimmune (PGA) syndromes. Medicine 60: 355-362
-
(1981)
Medicine
, vol.60
, pp. 355-362
-
-
Neufeld, M.1
Maclaren, N.K.2
Blizzard, R.M.3
-
5
-
-
0021807826
-
Autoimmune polyendocrinopathy-candidosis-ectodermal dystrophy (APECED): Autosomal recessive inheritance
-
Ahonen P. 1985. Autoimmune polyendocrinopathy-candidosis-ectodermal dystrophy (APECED): Autosomal recessive inheritance. Clin. Genet. 27: 535-542
-
(1985)
Clin. Genet.
, vol.27
, pp. 535-542
-
-
Ahonen, P.1
-
6
-
-
0025295238
-
Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients
-
Ahonen P., Myllarniemi S., Sipila I., Perheentupa J. 1990. Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients. N. Engl. J. Med. 322: 1829-1836
-
(1990)
N. Engl. J. Med.
, vol.322
, pp. 1829-1836
-
-
Ahonen, P.1
Myllarniemi, S.2
Sipila, I.3
Perheentupa, J.4
-
7
-
-
0026481974
-
Polyglandular autoimmune syndrome type 1 among Iranian Jews
-
Zlotogora J., Shapiro M.S. 1992. Polyglandular autoimmune syndrome type 1 among Iranian Jews. J. Med. Genet. 29: 824-826
-
(1992)
J. Med. Genet.
, vol.29
, pp. 824-826
-
-
Zlotogora, J.1
Shapiro, M.S.2
-
8
-
-
0022656450
-
Inherited susceptibility to autoimmune Addison's disease is linked to human leukocyte antigens-DR3 and/or DR4, except when associated with type I autoimmune polyglandular syndrome
-
Maclaren N.K., Riley W.J. 1986. Inherited susceptibility to autoimmune Addison's disease is linked to human leukocyte antigens-DR3 and/or DR4, except when associated with type I autoimmune polyglandular syndrome. J. Cli. Endocr. Metab. 62: 455-459
-
(1986)
J. Cli. Endocr. Metab.
, vol.62
, pp. 455-459
-
-
Maclaren, N.K.1
Riley, W.J.2
-
9
-
-
0028064998
-
An autosomal locus causing autoimmune disease: Autoimmune polyglandular disease type I assigned to chromosome 21
-
Aaltonen J., Bjorses P., Sandkuijl L., Perheentupa J., Peltonen L. 1994. An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21. Nature Genet. 8: 83-87
-
(1994)
Nature Genet.
, vol.8
, pp. 83-87
-
-
Aaltonen, J.1
Bjorses, P.2
Sandkuijl, L.3
Perheentupa, J.4
Peltonen, L.5
-
10
-
-
0029836686
-
Genetic homogeneity of autoimmune polyglandular disease type I
-
Bjorses P., Aaltonen J., Vikman A., Perheentupa J., Ben-Zion G., Chiumello G., Dahl N., Heideman P., Hoorweg-Nijman J.J.G., Mathivon L., Mullis P.E., Pohl M., Ritzen M., Romeo G., Shapiro M.S., Smith C.S., Solyom J., Zlotogora J., Peltonen L. 1996. Genetic homogeneity of autoimmune polyglandular disease type I. Am. J. Hum. Genet. 59: 879-886
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 879-886
-
-
Bjorses, P.1
Aaltonen, J.2
Vikman, A.3
Perheentupa, J.4
Ben-Zion, G.5
Chiumello, G.6
Dahl, N.7
Heideman, P.8
Hoorweg-Nijman, J.J.G.9
Mathivon, L.10
Mullis, P.E.11
Pohl, M.12
Ritzen, M.13
Romeo, G.14
Shapiro, M.S.15
Smith, C.S.16
Solyom, J.17
Zlotogora, J.18
Peltonen, L.19
-
12
-
-
0025847727
-
Dinucleotide repeat polymorphism at the human liver-type 6-phosphofructokinase (PFKL) gene
-
Polymeropoulos W.H., Rath D.S., Xiao H., Merril C.R. 1991. Dinucleotide repeat polymorphism at the human liver-type 6-phosphofructokinase (PFKL) gene. Nucleic Acids Research 19: 2517
-
(1991)
Nucleic Acids Research
, vol.19
, pp. 2517
-
-
Polymeropoulos, W.H.1
Rath, D.S.2
Xiao, H.3
Merril, C.R.4
-
13
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C., Faure S., Fizames C., Samson D., Drouot N., Vignal A., Millasseau P., Marc S., Hazan J., Seboun E., Lathrop M., Gyapay G., Morissette J., Weissenbach J. 1996. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380: 152-154
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
Marc, S.8
Hazan, J.9
Seboun, E.10
Lathrop, M.11
Gyapay, G.12
Morissette, J.13
Weissenbach, J.14
-
14
-
-
0025880312
-
Linkage mapping of D21S171 to the distal long arm of human chromosome 21 using a polymorphic (AC)n dinucleotide repeat
-
Peterson M.B. 1991. Linkage mapping of D21S171 to the distal long arm of human chromosome 21 using a polymorphic (AC)n dinucleotide repeat. Hum. Genet. 87: 401-404
-
(1991)
Hum. Genet.
, vol.87
, pp. 401-404
-
-
Peterson, M.B.1
-
15
-
-
0025284549
-
Distinct mutations in two patients with leukocyte adhesion deficiency and their functional correlates
-
Warklaw A.J., Hibbs M.L., Stacker S.A., Springer T.A. 1990. Distinct mutations in two patients with leukocyte adhesion deficiency and their functional correlates. J. Exp. Med. 172: 335-345
-
(1990)
J. Exp. Med.
, vol.172
, pp. 335-345
-
-
Warklaw, A.J.1
Hibbs, M.L.2
Stacker, S.A.3
Springer, T.A.4
-
16
-
-
0028276422
-
Investigation of the polymorphic AvaII site by a PCR-based assay at the human CD18 gene locus
-
Matsuura S., Kishi F. 1994. Investigation of the polymorphic AvaII site by a PCR-based assay at the human CD18 gene locus. Hum. Genet. 93: 721
-
(1994)
Hum. Genet.
, vol.93
, pp. 721
-
-
Matsuura, S.1
Kishi, F.2
-
17
-
-
0029564587
-
Intrafamilial and case-control association analysis of D2S152 in insulin-dependent diabetes
-
Luo D.F., Maclaren N.K., Huang H.S., Muir A., She J.X. 1995. Intrafamilial and case-control association analysis of D2S152 in insulin-dependent diabetes. Autoimmunity 21: 143-147
-
(1995)
Autoimmunity
, vol.21
, pp. 143-147
-
-
Luo, D.F.1
Maclaren, N.K.2
Huang, H.S.3
Muir, A.4
She, J.X.5
-
20
-
-
0028968329
-
A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci
-
Terwilliger J.D. 1995. A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci. Am. J. Hum. Genet. 56: 777-787
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 777-787
-
-
Terwilliger, J.D.1
-
21
-
-
0030931352
-
High-resolution physical and transcriptional mapping of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy locus on chromosome 21q22.3 by FISH
-
Aaltonen J., Horelli-Kuitunen N., Fan J.B., Bjorses P., Perheentupa J., Myers R., Palotie A., Peltonen L. 1997. High-resolution physical and transcriptional mapping of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy locus on chromosome 21q22.3 by FISH. Genome Research 7: 820-829
-
(1997)
Genome Research
, vol.7
, pp. 820-829
-
-
Aaltonen, J.1
Horelli-Kuitunen, N.2
Fan, J.B.3
Bjorses, P.4
Perheentupa, J.5
Myers, R.6
Palotie, A.7
Peltonen, L.8
-
22
-
-
0031104910
-
SMT3A, a human homologue of the S. cerevisiae SMT3 gene, maps to chromosome 21qter and defines a novel gene family
-
Lapenta V., Chiurazzi P., van der Spek P., Pizzuti A., Hanaoka F., Brahe C. 1997. SMT3A, a human homologue of the S. cerevisiae SMT3 gene, maps to chromosome 21qter and defines a novel gene family. Genomics 40: 362-366
-
(1997)
Genomics
, vol.40
, pp. 362-366
-
-
Lapenta, V.1
Chiurazzi, P.2
Van Der Spek, P.3
Pizzuti, A.4
Hanaoka, F.5
Brahe, C.6
-
23
-
-
0029083423
-
Model for a transcript map of human chromosome 21: Isolation of new coding sequences from exon and enriched cDNa libraries
-
Yaspo M.L., Gellen L., Mott R., Korn B., Nizetic D., Poustka A.M., Lehrach H. 1995. Model for a transcript map of human chromosome 21: isolation of new coding sequences from exon and enriched cDNA libraries. Hum. Mol. Genet. 4: 1291-1304
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1291-1304
-
-
Yaspo, M.L.1
Gellen, L.2
Mott, R.3
Korn, B.4
Nizetic, D.5
Poustka, A.M.6
Lehrach, H.7
-
24
-
-
0028964373
-
Isolation and characterization of a candidate gene for progressive myoclonus epilepsy on 21q22.3
-
Yamakawa K., Mitchell S., Hubert R., Chen X.N., Colbern S., Huo Y.K., Gadomski C., Kim U.J., Korenberg J.R. 1995. Isolation and characterization of a candidate gene for progressive myoclonus epilepsy on 21q22.3. Hum. Mol. Genet. 4: 709-716
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 709-716
-
-
Yamakawa, K.1
Mitchell, S.2
Hubert, R.3
Chen, X.N.4
Colbern, S.5
Huo, Y.K.6
Gadomski, C.7
Kim, U.J.8
Korenberg, J.R.9
-
25
-
-
0028848581
-
Localization of cDNAs to a region poorly represented in the CEPH chromosome 21 YAC contig: Candidate genes for genetic diseases mapped to 21q22.3
-
Gardiner K., Ichikawa H., Ohki M., Patterson D., Cheng J.F. 1995. Localization of cDNAs to a region poorly represented in the CEPH chromosome 21 YAC contig: candidate genes for genetic diseases mapped to 21q22.3. Genomics 30: 376-379
-
(1995)
Genomics
, vol.30
, pp. 376-379
-
-
Gardiner, K.1
Ichikawa, H.2
Ohki, M.3
Patterson, D.4
Cheng, J.F.5
-
26
-
-
0031569841
-
Cloning of a novel homeobox-containing gene, PKNOX1, and mapping to human chromosome 21q22.3
-
Chen H., Rossier C., Nakamura Y., Lynn A., Chakravarti A., Antonarakis S.E. 1997. Cloning of a novel homeobox-containing gene, PKNOX1, and mapping to human chromosome 21q22.3. Genomics 41: 193-200
-
(1997)
Genomics
, vol.41
, pp. 193-200
-
-
Chen, H.1
Rossier, C.2
Nakamura, Y.3
Lynn, A.4
Chakravarti, A.5
Antonarakis, S.E.6
-
27
-
-
0031172067
-
The NNP-1 gene (D21S2056E), which encodes a novel nuclear protein, maps in close proximity to the cystatin B gene within the EPM1 and APECED critical region on 21q22.3
-
Jansen E., Meulemans S.M.P., Orlans I.C.R., Van de Ven W.J.M. 1997. The NNP-1 gene (D21S2056E), which encodes a novel nuclear protein, maps in close proximity to the cystatin B gene within the EPM1 and APECED critical region on 21q22.3. Genomics 42: 336-341
-
(1997)
Genomics
, vol.42
, pp. 336-341
-
-
Jansen, E.1
Meulemans, S.M.P.2
Orlans, I.C.R.3
Van De Ven, W.J.M.4
-
28
-
-
0024353079
-
Th1 and Th2 cells: Different patterns of lymphokine secretion lead to different functional properties
-
Mosmann T.R., Coffman R.L. 1989. Th1 and Th2 cells: different patterns of lymphokine secretion lead to different functional properties. Annu. Rev. Immunol. 7: 145-173
-
(1989)
Annu. Rev. Immunol.
, vol.7
, pp. 145-173
-
-
Mosmann, T.R.1
Coffman, R.L.2
-
29
-
-
0029879015
-
Biological role of Th cell subsets in candidiasis
-
Romani L., Puccetti P., Bistoni F. 1996. Biological role of Th cell subsets in candidiasis. Chem. Immunol. 63: 115-137
-
(1996)
Chem. Immunol.
, vol.63
, pp. 115-137
-
-
Romani, L.1
Puccetti, P.2
Bistoni, F.3
-
30
-
-
0029311227
-
A Th1-Th2-like switch in candidiasis: New perspectives for therapy
-
Puccetti P., Romani L., Bistoni F. 1995. A Th1-Th2-like switch in candidiasis: new perspectives for therapy. Trends Microbiol. 3: 237-240
-
(1995)
Trends Microbiol.
, vol.3
, pp. 237-240
-
-
Puccetti, P.1
Romani, L.2
Bistoni, F.3
-
31
-
-
0028859564
-
Production and function of cytokines in natural and acquired immunity to Candida albicans infection
-
Ashman R.B., Papadimitriou J.M. 1995. Production and function of cytokines in natural and acquired immunity to Candida albicans infection. Microbio. Rev. 59: 646-672
-
(1995)
Microbio. Rev.
, vol.59
, pp. 646-672
-
-
Ashman, R.B.1
Papadimitriou, J.M.2
-
32
-
-
0030018170
-
Chronic mucocutaneous candidiasis. I. Altered antigen-stimulated IL-2, IL-4, IL-6 and interferon-gamma (IFN-gamma) production
-
Lilic D., Cant A.J., Abinun M., Calvert J.E., Spickett G.P. 1996. Chronic mucocutaneous candidiasis. I. Altered antigen-stimulated IL-2, IL-4, IL-6 and interferon-gamma (IFN-gamma) production. Clin. Exp. Immunol. 105: 205-212
-
(1996)
Clin. Exp. Immunol.
, vol.105
, pp. 205-212
-
-
Lilic, D.1
Cant, A.J.2
Abinun, M.3
Calvert, J.E.4
Spickett, G.P.5
-
33
-
-
0029916406
-
Enhanced IgE response to Candida albicans in postoperative invasive candidiasis
-
Savolainen J., Rantala A., Nermes M., Lehtonen L., Viander M. 1996. Enhanced IgE response to Candida albicans in postoperative invasive candidiasis. Clin. Exp. Allergy 26: 452-460
-
(1996)
Clin. Exp. Allergy
, vol.26
, pp. 452-460
-
-
Savolainen, J.1
Rantala, A.2
Nermes, M.3
Lehtonen, L.4
Viander, M.5
-
34
-
-
0346599403
-
An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains
-
The Finnish-German APECED Consortium. 1997. An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains. Nat. Genet. 17: 399-403
-
(1997)
Nat. Genet.
, vol.17
, pp. 399-403
-
-
-
35
-
-
16944367194
-
Positional cloning of the APECED gene
-
Nagamine K., Peterson P., Scott H.S., Kudoh J., Minoshima S., Heino M., Krohn K.J., Lalioti M.D., Mullis P.E., Antonarakis S.E., Asakawa S., Ito F., Shimizu N. 1997. Positional cloning of the APECED gene. Nat. Genet. 17: 393-398
-
(1997)
Nat. Genet.
, vol.17
, pp. 393-398
-
-
Nagamine, K.1
Peterson, P.2
Scott, H.S.3
Kudoh, J.4
Minoshima, S.5
Heino, M.6
Krohn, K.J.7
Lalioti, M.D.8
Mullis, P.E.9
Antonarakis, S.E.10
Asakawa, S.11
Ito, F.12
Shimizu, N.13
|