141 related articles for article (PubMed ID: 18990219)
1. A new 500 kb haplotype associated with high CD8+ T-lymphocyte numbers predicts a less severe expression of hereditary hemochromatosis.
Cruz E; Whittington C; Krikler SH; Mascarenhas C; Lacerda R; Vieira J; Porto G
BMC Med Genet; 2008 Nov; 9():97. PubMed ID: 18990219
[TBL] [Abstract][Full Text] [Related]
2. A study of 82 extended HLA haplotypes in HFE-C282Y homozygous hemochromatosis subjects: relationship to the genetic control of CD8+ T-lymphocyte numbers and severity of iron overload.
Cruz E; Vieira J; Almeida S; Lacerda R; Gartner A; Cardoso CS; Alves H; Porto G
BMC Med Genet; 2006 Mar; 7():16. PubMed ID: 16509978
[TBL] [Abstract][Full Text] [Related]
3. Effects of highly conserved major histocompatibility complex (MHC) extended haplotypes on iron and low CD8+ T lymphocyte phenotypes in HFE C282Y homozygous hemochromatosis patients from three geographically distant areas.
Costa M; Cruz E; Barton JC; Thorstensen K; Morais S; da Silva BM; Pinto JP; Vieira CP; Vieira J; Acton RT; Porto G
PLoS One; 2013; 8(11):e79990. PubMed ID: 24282517
[TBL] [Abstract][Full Text] [Related]
4. Low serum transferrin levels in HFE C282Y homozygous subjects are associated with low CD8(+) T lymphocyte numbers.
Macedo MF; Cruz E; Lacerda R; Porto G; de Sousa M
Blood Cells Mol Dis; 2005; 35(3):319-25. PubMed ID: 16140024
[TBL] [Abstract][Full Text] [Related]
5. Low numbers of CD8+ T lymphocytes in hereditary haemochromatosis are explained by a decrease of the most mature CD8+ effector memory T cells.
Macedo MF; Porto G; Costa M; Vieira CP; Rocha B; Cruz E
Clin Exp Immunol; 2010 Mar; 159(3):363-71. PubMed ID: 20015273
[TBL] [Abstract][Full Text] [Related]
6. The CD8+ T-lymphocyte profile as a modifier of iron overload in HFE hemochromatosis: an update of clinical and immunological data from 70 C282Y homozygous subjects.
Cruz E; Melo G; Lacerda R; Almeida S; Porto G
Blood Cells Mol Dis; 2006; 37(1):33-9. PubMed ID: 16762569
[TBL] [Abstract][Full Text] [Related]
7. Lymphocyte gene expression signatures from patients and mouse models of hereditary hemochromatosis reveal a function of HFE as a negative regulator of CD8+ T-lymphocyte activation and differentiation in vivo.
Costa M; Cruz E; Oliveira S; Benes V; Ivacevic T; Silva MJ; Vieira I; Dias F; Fonseca S; Gonçalves M; Lima M; Leitão C; Muckenthaler MU; Pinto J; Porto G
PLoS One; 2015; 10(4):e0124246. PubMed ID: 25880808
[TBL] [Abstract][Full Text] [Related]
8. Hepatic damage in C282Y homozygotes relates to low numbers of CD8+ cells in the liver lobuli.
Cardoso EM; Hagen K; de Sousa M; Hultcrantz R
Eur J Clin Invest; 2001 Jan; 31(1):45-53. PubMed ID: 11168438
[TBL] [Abstract][Full Text] [Related]
9. T-cell receptor repertoire in hereditary hemochromatosis: a study of 32 hemochromatosis patients and 274 healthy subjects.
Cardoso C; Porto G; Lacerda R; Resende D; Rodrigues P; Bravo F; Oliveira JC; Justiça B; de Sousa M
Hum Immunol; 2001 May; 62(5):488-99. PubMed ID: 11334672
[TBL] [Abstract][Full Text] [Related]
10. Involvement of the major histocompatibility complex region in the genetic regulation of circulating CD8 T-cell numbers in humans.
Cruz E; Vieira J; Gonçalves R; Alves H; Almeida S; Rodrigues P; Lacerda R; Porto G
Tissue Antigens; 2004 Jul; 64(1):25-34. PubMed ID: 15191520
[TBL] [Abstract][Full Text] [Related]
11. A putative gene located at the MHC class I region around the D6S105 marker contributes to the setting of CD8+ T-lymphocyte numbers in humans.
Vieira J; Cardoso CS; Pinto J; Patil K; Brazdil P; Cruz E; Mascarenhas C; Lacerda R; Gartner A; Almeida S; Alves H; Porto G
Int J Immunogenet; 2007 Oct; 34(5):359-67. PubMed ID: 17845307
[TBL] [Abstract][Full Text] [Related]
12. The ancestral hemochromatosis haplotype is associated with a severe phenotype expression in Italian patients.
Piperno A; Arosio C; Fargion S; Roetto A; Nicoli C; Girelli D; Sbaiz L; Gasparini P; Boari G; Sampietro M; Camaschella C
Hepatology; 1996 Jul; 24(1):43-6. PubMed ID: 8707280
[TBL] [Abstract][Full Text] [Related]
13. HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload.
Barton JC; Wiener HW; Acton RT; Go RC
Blood Cells Mol Dis; 2005; 34(1):38-47. PubMed ID: 15607698
[TBL] [Abstract][Full Text] [Related]
14. Clinical and family studies in genetic hemochromatosis: microsatellite and HFE studies in five atypical families.
Adams PC; Campion ML; Gandon G; LeGall JY; David V; Jouanolle AM
Hepatology; 1997 Oct; 26(4):986-90. PubMed ID: 9328324
[TBL] [Abstract][Full Text] [Related]
15. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000).
Martinelli AL; Filho R; Cruz S; Franco R; Tavella M; Secaf M; Ramalho L; Zucoloto S; Rodrigues S; Zago M
Genet Mol Res; 2005 Mar; 4(1):31-8. PubMed ID: 15841433
[TBL] [Abstract][Full Text] [Related]
16. Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis.
de Tayrac M; Roth MP; Jouanolle AM; Coppin H; le Gac G; Piperno A; Férec C; Pelucchi S; Scotet V; Bardou-Jacquet E; Ropert M; Bouvet R; Génin E; Mosser J; Deugnier Y
J Hepatol; 2015 Mar; 62(3):664-72. PubMed ID: 25457201
[TBL] [Abstract][Full Text] [Related]
17. DMT1 genetic variability is not responsible for phenotype variability in hereditary hemochromatosis.
Kelleher T; Ryan E; Barrett S; O'Keane C; Crowe J
Blood Cells Mol Dis; 2004; 33(1):35-9. PubMed ID: 15223008
[TBL] [Abstract][Full Text] [Related]
18. Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE).
Gandon G; Jouanolle AM; Chauvel B; Mauvieux V; le Treut A; Feingold J; Le Gall JY; David V; Yaouanq J
Hum Genet; 1996 Jan; 97(1):103-13. PubMed ID: 8557248
[TBL] [Abstract][Full Text] [Related]
19. Low penetrant hemochromatosis phenotype in eight families: no evidence of modifiers in the MHC region.
Sachot S; Moirand R; Jouanolle AM; Mosser J; Fergelot P; Deugnier Y; Brissot P; le Gall JY; David V
Blood Cells Mol Dis; 2001; 27(2):518-29. PubMed ID: 11500063
[TBL] [Abstract][Full Text] [Related]
20. Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.
Aguilar-Martinez P; Esculié-Coste C; Bismuth M; Giansily-Blaizot M; Larrey D; Schved JF
Blood Cells Mol Dis; 2001; 27(1):290-3. PubMed ID: 11358390
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
