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    Results: 1 to 20 of 74

    1.

    Iranian hereditary hemochromatosis patients: baseline characteristics, laboratory data and gene mutations.

    Zamani F, Bagheri Z, Bayat M, Fereshtehnejad SM, Basi A, Najmabadi H, Ajdarkosh H.

    Med Sci Monit. 2012 Oct;18(10):CR622-9.

    PMID:
    23018356
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    2.

    Type 3 hereditary hemochromatosis in a patient from sub-Saharan Africa: is there a link between African iron overload and TFR2 dysfunction?

    Majore S, Ricerca BM, Radio FC, Binni F, Cosentino I, Gallusi G, De Bernardo C, Morrone A, Grammatico P.

    Blood Cells Mol Dis. 2013 Jan;50(1):31-2. doi: 10.1016/j.bcmd.2012.08.007. Epub 2012 Sep 11. No abstract available.

    PMID:
    22981443
    [PubMed - indexed for MEDLINE]
    3.

    Smad6 and Smad7 are co-regulated with hepcidin in mouse models of iron overload.

    Vujić Spasić M, Sparla R, Mleczko-Sanecka K, Migas MC, Breitkopf-Heinlein K, Dooley S, Vaulont S, Fleming RE, Muckenthaler MU.

    Biochim Biophys Acta. 2013 Jan;1832(1):76-84. doi: 10.1016/j.bbadis.2012.08.013. Epub 2012 Aug 31.

    PMID:
    22960056
    [PubMed - indexed for MEDLINE]
    4.

    Clinicopathological study of Japanese patients with genetic iron overload syndromes.

    Hattori A, Miyajima H, Tomosugi N, Tatsumi Y, Hayashi H, Wakusawa S.

    Pathol Int. 2012 Sep;62(9):612-8. doi: 10.1111/j.1440-1827.2012.02848.x.

    PMID:
    22924847
    [PubMed - indexed for MEDLINE]
    5.

    Mutations in the HFE, TFR2, and SLC40A1 genes in patients with hemochromatosis.

    Del-Castillo-Rueda A, Moreno-Carralero MI, Cuadrado-Grande N, Alvarez-Sala-Walther LA, Enríquez-de-Salamanca R, Méndez M, Morán-Jiménez MJ.

    Gene. 2012 Oct 15;508(1):15-20. doi: 10.1016/j.gene.2012.07.069. Epub 2012 Aug 4.

    PMID:
    22890139
    [PubMed - indexed for MEDLINE]
    6.

    Mild iron overload in an African American man with SLC40A1 D270V.

    Lee PL, Gaasterland T, Barton JC.

    Acta Haematol. 2012;128(1):28-32. doi: 10.1159/000337034. Epub 2012 May 15.

    PMID:
    22584997
    [PubMed - indexed for MEDLINE]
    7.

    Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits.

    Ding K, Shameer K, Jouni H, Masys DR, Jarvik GP, Kho AN, Ritchie MD, McCarty CA, Chute CG, Manolio TA, Kullo IJ.

    Mayo Clin Proc. 2012 May;87(5):461-74. doi: 10.1016/j.mayocp.2012.01.016.

    PMID:
    22560525
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    8.

    TMPRSS6, but not TF, TFR2 or BMP2 variants are associated with increased risk of iron-deficiency anemia.

    An P, Wu Q, Wang H, Guan Y, Mu M, Liao Y, Zhou D, Song P, Wang C, Meng L, Man Q, Li L, Zhang J, Wang F.

    Hum Mol Genet. 2012 May 1;21(9):2124-31. doi: 10.1093/hmg/dds028. Epub 2012 Feb 8.

    PMID:
    22323359
    [PubMed - indexed for MEDLINE]
    Free Article
    9.

    Identification of a novel mutation in the HAMP gene that causes non-detectable hepcidin molecules in a Japanese male patient with juvenile hemochromatosis.

    Hattori A, Tomosugi N, Tatsumi Y, Suzuki A, Hayashi K, Katano Y, Inagaki Y, Ishikawa T, Hayashi H, Goto H, Wakusawa S.

    Blood Cells Mol Dis. 2012 Mar 15;48(3):179-82. doi: 10.1016/j.bcmd.2012.01.002. Epub 2012 Jan 30.

    PMID:
    22297252
    [PubMed - indexed for MEDLINE]
    10.

    Iron excess limits HHIPL-2 gene expression and decreases osteoblastic activity in human MG-63 cells.

    Doyard M, Fatih N, Monnier A, Island ML, Aubry M, Leroyer P, Bouvet R, Chalès G, Mosser J, Loréal O, Guggenbuhl P.

    Osteoporos Int. 2012 Oct;23(10):2435-45. doi: 10.1007/s00198-011-1871-z. Epub 2012 Jan 12.

    PMID:
    22237814
    [PubMed - indexed for MEDLINE]
    11.

    Characterization of glyceraldehyde-3-phosphate dehydrogenase as a novel transferrin receptor.

    Kumar S, Sheokand N, Mhadeshwar MA, Raje CI, Raje M.

    Int J Biochem Cell Biol. 2012 Jan;44(1):189-99. doi: 10.1016/j.biocel.2011.10.016. Epub 2011 Nov 2.

    PMID:
    22062951
    [PubMed - indexed for MEDLINE]
    12.

    Non-HFE hepatic iron overload.

    Pietrangelo A, Caleffi A, Corradini E.

    Semin Liver Dis. 2011 Aug;31(3):302-18. doi: 10.1055/s-0031-1286061. Epub 2011 Sep 7. Review.

    PMID:
    21901660
    [PubMed - indexed for MEDLINE]
    13.

    The molecular pathogenesis of hereditary hemochromatosis.

    Babitt JL, Lin HY.

    Semin Liver Dis. 2011 Aug;31(3):280-92. doi: 10.1055/s-0031-1286059. Epub 2011 Sep 7. Review.

    PMID:
    21901658
    [PubMed - indexed for MEDLINE]
    14.

    Hereditary hemochromatosis and transferrin receptor 2.

    Chen J, Enns CA.

    Biochim Biophys Acta. 2012 Mar;1820(3):256-63. doi: 10.1016/j.bbagen.2011.07.015. Epub 2011 Aug 16. Review.

    PMID:
    21864651
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    15.

    Iron disorders of genetic origin: a changing world.

    Brissot P, Bardou-Jacquet E, Jouanolle AM, Loréal O.

    Trends Mol Med. 2011 Dec;17(12):707-13. doi: 10.1016/j.molmed.2011.07.004. Epub 2011 Aug 20. Review.

    PMID:
    21862411
    [PubMed - indexed for MEDLINE]
    16.

    Hepatocytes internalize trophic receptors at large endocytic "Hot Spots".

    Cao H, Krueger EW, McNiven MA.

    Hepatology. 2011 Nov;54(5):1819-29. doi: 10.1002/hep.24572.

    PMID:
    21793030
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    17.

    Mutations in HFE and TFR2 genes in a Spanish patient with hemochromatosis.

    Rueda Adel C, Grande NC, Fernández EA, Enríquez de Salamanca R, Sala LA, Jiménez MJ.

    Rev Esp Enferm Dig. 2011 Jul;103(7):379-82. English, Spanish.

    PMID:
    21770687
    [PubMed - indexed for MEDLINE]
    Free Article
    18.

    [Signaling in iron metabolism via transferrin receptor 2: significance in erythropoiesis].

    Kawabata H.

    Rinsho Ketsueki. 2011 Jun;52(6):399-405. Review. No abstract available.

    PMID:
    21737992
    [PubMed - indexed for MEDLINE]
    19.

    Changes in iron-regulatory gene expression occur in human cell culture models of Parkinson's disease.

    Carroll CB, Zeissler ML, Chadborn N, Gibson K, Williams G, Zajicek JP, Morrison KE, Hanemann CO.

    Neurochem Int. 2011 Aug;59(1):73-80. doi: 10.1016/j.neuint.2011.05.006. Epub 2011 Jun 6.

    PMID:
    21672570
    [PubMed - indexed for MEDLINE]
    20.

    The A Allele of the -576G>A polymorphism of the transferrin gene is associated with the increased risk of age-related macular degeneration in smokers.

    Wysokinski D, Szaflik J, Sklodowska A, Kolodziejska U, Dorecka M, Romaniuk D, Wozniak K, Blasiak J, Szaflik JP.

    Tohoku J Exp Med. 2011;223(4):253-61.

    PMID:
    21422745
    [PubMed - indexed for MEDLINE]
    Free Article

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