These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

42 related articles for article (PubMed ID: 15749659)

  • 1. Why do humans need two types of transferrin receptor? Lessons from a rare genetic disorder.
    Camaschella C
    Haematologica; 2005 Mar; 90(3):296. PubMed ID: 15749659
    [No Abstract]   [Full Text] [Related]  

  • 2. Two novel mutations, L490R and V561X, in transferrin receptor 2 in Japanese patients with hemochromatosis.
    Bergamaschi G
    Haematologica; 2005 Mar; 90(3):289A. PubMed ID: 15749651
    [No Abstract]   [Full Text] [Related]  

  • 3. New TFR2 mutations in young Italian patients with hemochromatosis.
    Biasiotto G; Camaschella C; Forni GL; Polotti A; Zecchina G; Arosio P
    Haematologica; 2008 Feb; 93(2):309-10. PubMed ID: 18245657
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Transferrin receptor 2 is frequently expressed in human cancer cell lines.
    Calzolari A; Oliviero I; Deaglio S; Mariani G; Biffoni M; Sposi NM; Malavasi F; Peschle C; Testa U
    Blood Cells Mol Dis; 2007; 39(1):82-91. PubMed ID: 17428703
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two novel mutations, L490R and V561X, of the transferrin receptor 2 gene in Japanese patients with hemochromatosis.
    Koyama C; Wakusawa S; Hayashi H; Suzuki R; Yano M; Yoshioka K; Kozuru M; Takayamam Y; Okada T; Mabuchi H
    Haematologica; 2005 Mar; 90(3):302-7. PubMed ID: 15749661
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Transferrin receptor-1 and 2 expression in chronic lymphocytic leukemia.
    Smilevska T; Stamatopoulos K; Samara M; Belessi C; Tsompanakou A; Paterakis G; Stavroyianni N; Athanasiadou I; Chiotoglou I; Hadzidimitriou A; Athanasiadou A; Douka V; Saloum R; Laoutaris N; Anagnostopoulos A; Fassas A; Stathakis N; Kollia P
    Leuk Res; 2006 Feb; 30(2):183-9. PubMed ID: 16054692
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel polymorphism (219G>A) in the transferrin receptor gene.
    Meregalli M; Corbetta N; Pellagatti A; Martinez di Montemuros F; Tavazzi D; Fargion S; Sampietro M
    Hum Mutat; 2000 Apr; 15(4):389. PubMed ID: 10738001
    [No Abstract]   [Full Text] [Related]  

  • 8. Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overload.
    Majore S; Milano F; Binni F; Stuppia L; Cerrone A; Tafuri A; De Bernardo C; Palka G; Grammatico P
    Haematologica; 2006 Aug; 91(8 Suppl):ECR33. PubMed ID: 16923517
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The mechanism of iron release from the transferrin-receptor 1 adduct.
    Hémadi M; Ha-Duong NT; El Hage Chahine JM
    J Mol Biol; 2006 May; 358(4):1125-36. PubMed ID: 16564538
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The molecular mechanism for receptor-stimulated iron release from the plasma iron transport protein transferrin.
    Giannetti AM; Halbrooks PJ; Mason AB; Vogt TM; Enns CA; Björkman PJ
    Structure; 2005 Nov; 13(11):1613-23. PubMed ID: 16271884
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Transferrin receptor 2 mutations in patients with juvenile hemochromatosis phenotype.
    Ravasi G; Rausa M; Pelucchi S; Arosio C; Greni F; Mariani R; Pelloni I; Silvestri L; Pineda P; Camaschella C; Piperno A
    Am J Hematol; 2015 Dec; 90(12):E226-7. PubMed ID: 26408288
    [No Abstract]   [Full Text] [Related]  

  • 12. Inhibition of transferrin receptor 1 transcription by a cell density response element.
    Wang J; Chen G; Pantopoulos K
    Biochem J; 2005 Dec; 392(Pt 2):383-8. PubMed ID: 16092918
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Iron absorption and hepatic iron uptake are increased in a transferrin receptor 2 (Y245X) mutant mouse model of hemochromatosis type 3.
    Drake SF; Morgan EH; Herbison CE; Delima R; Graham RM; Chua AC; Leedman PJ; Fleming RE; Bacon BR; Olynyk JK; Trinder D
    Am J Physiol Gastrointest Liver Physiol; 2007 Jan; 292(1):G323-8. PubMed ID: 16935854
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early-onset haemochromatosis caused by a novel combination of TFR2 mutations(p.R396X/c.1538-2 A>G) in a woman of Italian descent.
    Gérolami V; Le Gac G; Mercier L; Nezri M; Bergé-Lefranc JL; Férec C
    Haematologica; 2008 May; 93(5):e45-6. PubMed ID: 18450729
    [No Abstract]   [Full Text] [Related]  

  • 15. The requirement of iron transport for lymphocyte function.
    Lo B
    Nat Genet; 2016 Jan; 48(1):10-1. PubMed ID: 26711111
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Structure of the glycosylphosphatidylinositol anchor of the Trypanosoma brucei transferrin receptor.
    Mehlert A; Ferguson MA
    Mol Biochem Parasitol; 2007 Feb; 151(2):220-3. PubMed ID: 17140675
    [No Abstract]   [Full Text] [Related]  

  • 17. Transfection of human prostate cancer CA-HPV-10 cells with cytosolic sulfotransferase SULT1E1 affects estrogen signaling and gene transcription.
    Kapoor R; Sheng JJ
    Drug Metab Dispos; 2008 Feb; 36(2):316-21. PubMed ID: 17984287
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Predominantly post-transcriptional regulation of activation molecules in chronic lymphocytic leukemia: the case of transferrin receptors.
    Chiotoglou I; Smilevska T; Samara M; Likousi S; Belessi C; Athanasiadou I; Stavroyianni N; Samara S; Laoutaris N; Vamvakopoulos N; Anagnostopoulos A; Fassas A; Stamatopoulos K; Kollia P
    Blood Cells Mol Dis; 2008; 41(2):203-9. PubMed ID: 18621559
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Detection of hereditary hemochromatosis].
    Saglini V; Lazzaro M; Keller F; Perren A
    Rev Med Suisse; 2007 Sep; 3(123):1952-7. PubMed ID: 17918491
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Secretory IgA mediates retrotranscytosis of intact gliadin peptides via the transferrin receptor in celiac disease.
    Matysiak-Budnik T; Moura IC; Arcos-Fajardo M; Lebreton C; Ménard S; Candalh C; Ben-Khalifa K; Dugave C; Tamouza H; van Niel G; Bouhnik Y; Lamarque D; Chaussade S; Malamut G; Cellier C; Cerf-Bensussan N; Monteiro RC; Heyman M
    J Exp Med; 2008 Jan; 205(1):143-54. PubMed ID: 18166587
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.