BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

271 related articles for article (PubMed ID: 26633544)

  • 1. The global prevalence of HFE and non-HFE hemochromatosis estimated from analysis of next-generation sequencing data.
    Wallace DF; Subramaniam VN
    Genet Med; 2016 Jun; 18(6):618-26. PubMed ID: 26633544
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of novel mutations in HFE, HFE2, TfR2, and SLC40A1 genes in Chinese patients affected by hereditary hemochromatosis.
    Wang Y; Du Y; Liu G; Guo S; Hou B; Jiang X; Han B; Chang Y; Nie G
    Int J Hematol; 2017 Apr; 105(4):521-525. PubMed ID: 27896572
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genes.
    Radio FC; Majore S; Aurizi C; Sorge F; Biolcati G; Bernabini S; Giotti I; Torricelli F; Giannarelli D; De Bernardo C; Grammatico P
    Blood Cells Mol Dis; 2015 Jun; 55(1):71-5. PubMed ID: 25976471
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of novel mutations in hemochromatosis genes by targeted next generation sequencing in Italian patients with unexplained iron overload.
    Badar S; Busti F; Ferrarini A; Xumerle L; Bozzini P; Capelli P; Pozzi-Mucelli R; Campostrini N; De Matteis G; Marin Vargas S; Giorgetti A; Delledonne M; Olivieri O; Girelli D
    Am J Hematol; 2016 Jun; 91(4):420-5. PubMed ID: 26799139
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients.
    Santos PC; Cançado RD; Pereira AC; Schettert IT; Soares RA; Pagliusi RA; Hirata RD; Hirata MH; Teixeira AC; Figueiredo MS; Chiattone CS; Krieger JE; Guerra-Shinohara EM
    Blood Cells Mol Dis; 2011 Apr; 46(4):302-7. PubMed ID: 21411349
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Next-generation sequencing of hereditary hemochromatosis-related genes: Novel likely pathogenic variants found in the Portuguese population.
    Faria R; Silva B; Silva C; Loureiro P; Queiroz A; Fraga S; Esteves J; Mendes D; Fleming R; Vieira L; Gonçalves J; Faustino P
    Blood Cells Mol Dis; 2016 Oct; 61():10-5. PubMed ID: 27667161
    [TBL] [Abstract][Full Text] [Related]  

  • 7. New Mutations in
    Hernández G; Ferrer-Cortès X; Venturi V; Musri M; Pilquil MF; Torres PMM; Rodríguez IH; Mínguez MÀR; Kelleher NJ; Pelucchi S; Piperno A; Alberca EP; Ricós GG; Giró EC; Pérez-Montero S; Tornador C; Villà-Freixa J; Sánchez M
    Genes (Basel); 2021 Dec; 12(12):. PubMed ID: 34946929
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The mechanisms of systemic iron homeostasis and etiology, diagnosis, and treatment of hereditary hemochromatosis.
    Kawabata H
    Int J Hematol; 2018 Jan; 107(1):31-43. PubMed ID: 29134618
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Causes of iron overload in blood donors - a clinical study.
    Laursen AH; Bjerrum OW; Friis-Hansen L; Hansen TO; Marott JL; Magnussen K
    Vox Sang; 2018 Feb; 113(2):110-119. PubMed ID: 29230833
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotypic analysis of hemochromatosis subtypes reveals variations in severity of iron overload and clinical disease.
    Sandhu K; Flintoff K; Chatfield MD; Dixon JL; Ramm LE; Ramm GA; Powell LW; Subramaniam VN; Wallace DF
    Blood; 2018 Jul; 132(1):101-110. PubMed ID: 29743178
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of Novel Mutations by Targeted NGS Panel in Patients with Hyperferritinemia.
    Ravasi G; Pelucchi S; Bertola F; Capelletti MM; Mariani R; Piperno A
    Genes (Basel); 2021 Nov; 12(11):. PubMed ID: 34828384
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Correlation of genotype and phenotype in 32 patients with hereditary hemochromatosis in China.
    Wu L; Zhang W; Li Y; Zhou D; Zhang B; Xu A; Wu Z; Wu L; Li S; Wang X; Zhao X; Wang Q; Li M; Wang Y; You H; Huang J; Ou X; Jia J
    Orphanet J Rare Dis; 2021 Sep; 16(1):398. PubMed ID: 34583728
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular pathogenesis of hereditary hemochromatosis.
    Liu J; Pu C; Lang L; Qiao L; Abdullahi MA; Jiang C
    Histol Histopathol; 2016 Aug; 31(8):833-40. PubMed ID: 27031690
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Non-
    Lv T; Zhang W; Xu A; Li Y; Zhou D; Zhang B; Li X; Zhao X; Wang Y; Wang X; Duan W; Wang Q; Xu H; Zheng J; Zhao R; Zhu L; Dong Y; Lu L; Chen Y; Long J; Zheng S; Wang W; You H; Jia J; Ou X; Huang J
    J Med Genet; 2018 Oct; 55(10):650-660. PubMed ID: 30166352
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Non-HFE haemochromatosis.
    Wallace DF; Subramaniam VN
    World J Gastroenterol; 2007 Sep; 13(35):4690-8. PubMed ID: 17729390
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Non-HFE-related hereditary iron overload].
    Aguilar-Martinez P
    Presse Med; 2007 Sep; 36(9 Pt 2):1279-91. PubMed ID: 17540536
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 508(1):15-20. PubMed ID: 22890139
    [TBL] [Abstract][Full Text] [Related]  

  • 18. HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening.
    Barton JC; Acton RT; Leiendecker-Foster C; Lovato L; Adams PC; McLaren GD; Eckfeldt JH; McLaren CE; Reboussin DM; Gordeuk VR; Speechley MR; Reiss JA; Press RD; Dawkins FW;
    Genet Test; 2007; 11(3):269-75. PubMed ID: 17949288
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Non-HFE hemochromatosis.
    Pietrangelo A
    Semin Liver Dis; 2005 Nov; 25(4):450-60. PubMed ID: 16315138
    [TBL] [Abstract][Full Text] [Related]  

  • 20. DENND3 p.L708V activating variant is involved in the pathogenesis of hereditary hemochromatosis via the RAB12/TFR2 signaling pathway.
    Li Y; Xu A; Ouyang Q; Zhang W; Zhang C; Chen Z; Zhou D; Zhang B; Duan W; Zhao X; Wang X; You H; Ou X; Jia J; Huang J
    Hepatol Int; 2023 Jun; 17(3):648-661. PubMed ID: 36729283
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.