BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

71 related articles for article (PubMed ID: 11500063)

  • 1. 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]  

  • 2. 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]  

  • 3. Unique genetic profile of hereditary hemochromatosis in Russians: high frequency of C282Y mutation in population, but not in patients.
    Potekhina ES; Lavrov AV; Samokhodskaya LM; Efimenko AY; Balatskiy AV; Baev AA; Litvinova MM; Nikitina LA; Shipulin GA; Bochkov NP; Tkachuk VA; Bochkov VN
    Blood Cells Mol Dis; 2005; 35(2):182-8. PubMed ID: 16055358
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Hemochromatosis. Determination of the C282Y mutation frequency in the population of the Czech Republic and sensitivity of hemochromatosis detection using Guthrie cards].
    Zdárský E; Horák J; Stríteský J; Heirler F
    Cas Lek Cesk; 1999 Aug; 138(16):497-9. PubMed ID: 10566227
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Searching for hereditary hemochromatosis.
    Laudicina RJ
    Clin Lab Sci; 2006; 19(3):174-83. PubMed ID: 16910235
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants.
    Pedersen P; Milman N
    Ann Hematol; 2009 Aug; 88(8):775-84. PubMed ID: 19159930
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Early onset hereditary hemochromatosis resulting from a novel TFR2 gene nonsense mutation (R105X) in two siblings of north French descent.
    Le Gac G; Mons F; Jacolot S; Scotet V; Férec C; Frébourg T
    Br J Haematol; 2004 Jun; 125(5):674-8. PubMed ID: 15147384
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hemochromatosis (HFE) and transferrin receptor-1 (TFRC1) genes in sporadic porphyria cutanea tarda (sPCT).
    Lamoril J; Andant C; Gouya L; Malonova E; Grandchamp B; Martásek P; Deybac JC; Puy H
    Cell Mol Biol (Noisy-le-grand); 2002 Feb; 48(1):33-41. PubMed ID: 11929045
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The penetrance of hereditary hemochromatosis.
    Waalen J; Nordestgaard BG; Beutler E
    Best Pract Res Clin Haematol; 2005 Jun; 18(2):203-20. PubMed ID: 15737885
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Was the C282Y mutation an Irish Gaelic mutation that the Vikings helped disseminate? HLA haplotype observations of hemochromatosis from the west coast of Sweden.
    Olsson KS; Konar J; Dufva IH; Ricksten A; Raha-Chowdhury R
    Eur J Haematol; 2011 Jan; 86(1):75-82. PubMed ID: 20946107
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two novel nonsense mutations of HFE gene in five unrelated italian patients with hemochromatosis.
    Piperno A; Arosio C; Fossati L; Viganò M; Trombini P; Vergani A; Mancia G
    Gastroenterology; 2000 Aug; 119(2):441-5. PubMed ID: 10930379
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Analysis of the HFE gene in a large Spanish kindred with hereditary hemochromatosis].
    Roa S; Martín-Oterino JA; Rodríguez RE; García-Berrocal B; Sánchez-Rodríguez A; González-Sarmiento R
    Med Clin (Barc); 2001 Jan; 116(3):100-3. PubMed ID: 11181289
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A recombination event close to HFE gene in hereditary hemochromatosis.
    Roetto A; Sbaiz L; Bosio S; Piperno A; Fargion S; Carella M; Totaro A; Grifa A; Gasparini P; Camaschella C
    Ann Genet; 1997; 40(3):150-3. PubMed ID: 9401103
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Heterogeneity of hemochromatosis in Italy.
    Piperno A; Sampietro M; Pietrangelo A; Arosio C; Lupica L; Montosi G; Vergani A; Fraquelli M; Girelli D; Pasquero P; Roetto A; Gasparini P; Fargion S; Conte D; Camaschella C
    Gastroenterology; 1998 May; 114(5):996-1002. PubMed ID: 9558289
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromosome 6p SNP microhaplotypes and IgG3 levels in hemochromatosis probands with HFE p.C282Y homozygosity.
    Barton JC; Barton JC; Cruz E; Teles MJ; Guimarães JT; Porto G
    Blood Cells Mol Dis; 2020 Nov; 85():102461. PubMed ID: 32623342
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Anonymous marker loci within 400 kb of HLA-A generate haplotypes in linkage disequilibrium with the hemochromatosis gene (HFE).
    Yaouanq J; Perichon M; Chorney M; Pontarotti P; Le Treut A; el Kahloun A; Mauvieux V; Blayau M; Jouanolle AM; Chauvel B
    Am J Hum Genet; 1994 Feb; 54(2):252-63. PubMed ID: 8304342
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A 6p22 reference map of leukocyte DNA: exclusion of rearrangement in four cases of atypical haemochromatosis.
    Wallace DF; Partridge J; Robertson A; Simpson VM; Worwood M; Bomford AB; Volz A; Ziegler A; Dooley JS; Walker AP
    Eur J Hum Genet; 1998; 6(5):523-6. PubMed ID: 9801878
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.