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Journal Abstract Search

217 related items for PubMed ID: 29928945

  • 1. The role of TMPRSS6 gene variants in iron-related hematological parameters in Turkish patients with iron deficiency anemia.
    Batar B, Bavunoglu I, Hacioglu Y, Cengiz M, Mutlu T, Yavuzer S, Yavuzer H, Cuhadar Ercelebi D, Erhan D, Unal S, Tunckale A, Guven M.
    Gene; 2018 Oct 05; 673():201-205. PubMed ID: 29928945
    [Abstract] [Full Text] [Related]

  • 2. An investigation of the relationship between TMPRSS6 gene expression, genetic variants and clinical findings in breast cancer.
    Mete M, Trabulus DC, Talu CK, Ozoran E, Mutlu T, Tekin B, Guven M.
    Mol Biol Rep; 2020 Jun 05; 47(6):4225-4231. PubMed ID: 32385772
    [Abstract] [Full Text] [Related]

  • 3. Genetic analysis of TMPRSS6 gene in Saudi female patients with iron deficiency anemia.
    Al-Jamea LH, Woodman A, Heiba NM, Elshazly SA, Khalaf NB, Fathallah DM, Al-Nashmi ME, Quiambao JV, Deifalla AH.
    Hematol Oncol Stem Cell Ther; 2021 Mar 05; 14(1):41-50. PubMed ID: 32446932
    [Abstract] [Full Text] [Related]

  • 4. 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 01; 21(9):2124-31. PubMed ID: 22323359
    [Abstract] [Full Text] [Related]

  • 5. The role of TMPRSS6 polymorphisms in iron deficiency anemia partially responsive to oral iron treatment.
    Poggiali E, Andreozzi F, Nava I, Consonni D, Graziadei G, Cappellini MD.
    Am J Hematol; 2015 Apr 01; 90(4):306-9. PubMed ID: 25557470
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  • 8. A child with severe iron-deficiency anemia and a complex TMPRSS6 genotype.
    Capra AP, Ferro E, Cannavò L, La Rosa MA, Zirilli G.
    Hematology; 2017 Oct 01; 22(9):559-564. PubMed ID: 28447549
    [Abstract] [Full Text] [Related]

  • 9. The role of TMPRSS6 and HFE variants in iron deficiency anemia in celiac disease.
    De Falco L, Tortora R, Imperatore N, Bruno M, Capasso M, Girelli D, Castagna A, Caporaso N, Iolascon A, Rispo A.
    Am J Hematol; 2018 Mar 01; 93(3):383-393. PubMed ID: 29194702
    [Abstract] [Full Text] [Related]

  • 10. TMPRSS6 rs855791 polymorphism influences the susceptibility to iron deficiency anemia in women at reproductive age.
    Pei SN, Ma MC, You HL, Fu HC, Kuo CY, Rau KM, Wang MC, Lee CT.
    Int J Med Sci; 2014 Mar 01; 11(6):614-9. PubMed ID: 24782651
    [Abstract] [Full Text] [Related]

  • 11. Transferrin Saturation/Hepcidin Ratio Discriminates TMPRSS6-Related Iron Refractory Iron Deficiency Anemia from Patients with Multi-Causal Iron Deficiency Anemia.
    van der Staaij H, Donker AE, Bakkeren DL, Salemans JMJI, Mignot-Evers LAA, Bongers MY, Dieleman JP, Galesloot TE, Laarakkers CM, Klaver SM, Swinkels DW.
    Int J Mol Sci; 2022 Feb 08; 23(3):. PubMed ID: 35163840
    [Abstract] [Full Text] [Related]

  • 12. The Association of TMPRSS6 Gene Polymorphism and Iron Intake with Iron Status among Under-Two-Year-Old Children in Lombok, Indonesia.
    Shinta D, Asmarinah0000-0001-6417-2942Department of Medical Biology, Faculty of Medicine, Universitas Indonesia, Jakarta 10430, Indonesia. asmarinah.si@gmx.de., Adhiyanto C, Htet MK, Fahmida U.
    Nutrients; 2019 Apr 19; 11(4):. PubMed ID: 31010126
    [Abstract] [Full Text] [Related]

  • 13. TMPRSS6 rs855791 Polymorphism Status in Children with Celiac Disease and Anemia.
    Urbaszek K, Drabińska N, Szaflarska-Popławska A, Jarocka-Cyrta E.
    Nutrients; 2021 Aug 13; 13(8):. PubMed ID: 34444942
    [Abstract] [Full Text] [Related]

  • 14. Association of TMPRSS6 polymorphisms with ferritin, hemoglobin, and type 2 diabetes risk in a Chinese Han population.
    Gan W, Guan Y, Wu Q, An P, Zhu J, Lu L, Jing L, Yu Y, Ruan S, Xie D, Makrides M, Gibson RA, Anderson GJ, Li H, Lin X, Wang F.
    Am J Clin Nutr; 2012 Mar 13; 95(3):626-32. PubMed ID: 22301935
    [Abstract] [Full Text] [Related]

  • 15. Role of TMPRSS6 rs855791 (T > C) polymorphism in reproductive age women with iron deficiency anemia from Lahore, Pakistan.
    Lone NM, Shah SHS, Farooq M, Arif M, Younis S, Riaz S.
    Saudi J Biol Sci; 2021 Jan 13; 28(1):748-753. PubMed ID: 33424363
    [Abstract] [Full Text] [Related]

  • 16. A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron.
    Melis MA, Cau M, Congiu R, Sole G, Barella S, Cao A, Westerman M, Cazzola M, Galanello R.
    Haematologica; 2008 Oct 13; 93(10):1473-9. PubMed ID: 18603562
    [Abstract] [Full Text] [Related]

  • 17. Associations of Common Variants in HFE and TMPRSS6 Genes with Hepcidin-25 and Iron Status Parameters in Patients with End-Stage Renal Disease.
    Dopsaj V, Topić A, Savković M, Milinković N, Novaković I, Ćujić D, Simić-Ogrizović S.
    Dis Markers; 2019 Oct 13; 2019():4864370. PubMed ID: 30984307
    [Abstract] [Full Text] [Related]

  • 18. Functional and clinical impact of novel TMPRSS6 variants in iron-refractory iron-deficiency anemia patients and genotype-phenotype studies.
    De Falco L, Silvestri L, Kannengiesser C, Morán E, Oudin C, Rausa M, Bruno M, Aranda J, Argiles B, Yenicesu I, Falcon-Rodriguez M, Yilmaz-Keskin E, Kocak U, Beaumont C, Camaschella C, Iolascon A, Grandchamp B, Sanchez M.
    Hum Mutat; 2014 Nov 13; 35(11):1321-9. PubMed ID: 25156943
    [Abstract] [Full Text] [Related]

  • 19. The A736V TMPRSS6 polymorphism influences hepcidin and iron metabolism in chronic hemodialysis patients: TMPRSS6 and hepcidin in hemodialysis.
    Pelusi S, Girelli D, Rametta R, Campostrini N, Alfieri C, Traglia M, Dongiovanni P, Como G, Toniolo D, Camaschella C, Messa P, Fargion S, Valenti L.
    BMC Nephrol; 2013 Feb 22; 14():48. PubMed ID: 23433094
    [Abstract] [Full Text] [Related]

  • 20. [Identification and characterization of clinical features and gene mutation in a patient with iron refractory iron deficiency anemia (IRIDA)].
    Xiong Y, Yang W, Li Y, Peng G, Li Y, Fan H, Ye L, Song L, Zhao X, Li J, Jing L, Zhang L, Zhou K, Xu Y, Zhang F.
    Zhonghua Xue Ye Xue Za Zhi; 2014 Jun 22; 35(6):486-90. PubMed ID: 24985168
    [Abstract] [Full Text] [Related]

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