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3. Consequences of expressing mutants of the hemochromatosis gene (HFE) into a human neuronal cell line lacking endogenous HFE. Lee SY; Patton SM; Henderson RJ; Connor JR FASEB J; 2007 Feb; 21(2):564-76. PubMed ID: 17194693 [TBL] [Abstract][Full Text] [Related]
4. Expression of the HFE allelic variant H63D in SH-SY5Y cells affects tau phosphorylation at serine residues. Hall EC; Lee SY; Mairuae N; Simmons Z; Connor JR Neurobiol Aging; 2011 Aug; 32(8):1409-19. PubMed ID: 19775775 [TBL] [Abstract][Full Text] [Related]
5. Prolyl-peptidyl isomerase, Pin1, phosphorylation is compromised in association with the expression of the HFE polymorphic allele, H63D. Hall EC; Lee SY; Simmons Z; Neely EB; Nandar W; Connor JR Biochim Biophys Acta; 2010 Apr; 1802(4):389-95. PubMed ID: 20060900 [TBL] [Abstract][Full Text] [Related]
6. Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis. Lawless MW; White M; Mankan AK; O'Dwyer MJ; Norris S Tissue Antigens; 2007 Oct; 70(4):294-300. PubMed ID: 17767550 [TBL] [Abstract][Full Text] [Related]
7. Mutant HFE H63D protein is associated with prolonged endoplasmic reticulum stress and increased neuronal vulnerability. Liu Y; Lee SY; Neely E; Nandar W; Moyo M; Simmons Z; Connor JR J Biol Chem; 2011 Apr; 286(15):13161-70. PubMed ID: 21349849 [TBL] [Abstract][Full Text] [Related]
8. HFE gene variants affect iron in the brain. Nandar W; Connor JR J Nutr; 2011 Apr; 141(4):729S-739S. PubMed ID: 21346098 [TBL] [Abstract][Full Text] [Related]
9. The effects of okra (Abelmoschus esculentus Linn.) on the cellular events associated with Alzheimer's disease in a stably expressed HFE neuroblastoma SH-SY5Y cell line. Mairuae N; Connor JR; Lee SY; Cheepsunthorn P; Tongjaroenbuangam W Neurosci Lett; 2015 Aug; 603():6-11. PubMed ID: 26170247 [TBL] [Abstract][Full Text] [Related]
10. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis. Gottschalk R; Seidl C; Schilling S; Braner A; Seifried E; Hoelzer D; Kaltwasser JP Eur J Immunogenet; 2000 Jun; 27(3):129-34. PubMed ID: 10940080 [TBL] [Abstract][Full Text] [Related]
11. Effect of HFE variants on sphingolipid expression by SH-SY5Y human neuroblastoma cells. Ali-Rahmani F; Hengst JA; Connor JR; Schengrund CL Neurochem Res; 2011 Sep; 36(9):1687-96. PubMed ID: 21243428 [TBL] [Abstract][Full Text] [Related]
12. A mutation in the HFE gene is associated with altered brain iron profiles and increased oxidative stress in mice. Nandar W; Neely EB; Unger E; Connor JR Biochim Biophys Acta; 2013 Jun; 1832(6):729-41. PubMed ID: 23429074 [TBL] [Abstract][Full Text] [Related]
13. Expression of hereditary hemochromatosis C282Y HFE protein in HEK293 cells activates specific endoplasmic reticulum stress responses. Lawless MW; Mankan AK; White M; O'Dwyer MJ; Norris S BMC Cell Biol; 2007 Jul; 8():30. PubMed ID: 17650303 [TBL] [Abstract][Full Text] [Related]
14. C282Y-HFE gene variant affects cholesterol metabolism in human neuroblastoma cells. Ali-Rahmani F; Huang MA; Schengrund CL; Connor JR; Lee SY PLoS One; 2014; 9(2):e88724. PubMed ID: 24533143 [TBL] [Abstract][Full Text] [Related]
15. Effects of C282Y, H63D, and S65C HFE gene mutations, diet, and life-style factors on iron status in a general Mediterranean population from Tarragona, Spain. Aranda N; Viteri FE; Montserrat C; Arija V Ann Hematol; 2010 Aug; 89(8):767-73. PubMed ID: 20107990 [TBL] [Abstract][Full Text] [Related]
16. HFE polymorphisms influence the response to chemotherapeutic agents via induction of p16INK4A. Lee SY; Liu S; Mitchell RM; Slagle-Webb B; Hong YS; Sheehan JM; Connor JR Int J Cancer; 2011 Nov; 129(9):2104-14. PubMed ID: 21190189 [TBL] [Abstract][Full Text] [Related]
17. Relationships and distinctions in iron-regulatory networks responding to interrelated signals. Muckenthaler M; Richter A; Gunkel N; Riedel D; Polycarpou-Schwarz M; Hentze S; Falkenhahn M; Stremmel W; Ansorge W; Hentze MW Blood; 2003 May; 101(9):3690-8. PubMed ID: 12393473 [TBL] [Abstract][Full Text] [Related]
18. Diagnostic utility of HFE variants in Spanish patients: association with HLA alleles and role in susceptibility to acute lymphoblastic leukemia. Rodríguez-López R; Donoso M; Fernández-Cavada M; González LM; Margallo A; Corral C; Gallego M; García de Cáceres MT; Herrera T; González C; Vagace JM; Gervasini G Gene; 2013 Feb; 514(1):31-5. PubMed ID: 23178241 [TBL] [Abstract][Full Text] [Related]
19. Sample-to-SNP kit: a reliable, easy and fast tool for the detection of HFE p.H63D and p.C282Y variations associated to hereditary hemochromatosis. Nielsen PB; Petersen MS; Ystaas V; Andersen RV; Hansen KM; Blaabjerg V; Refstrup M Gene; 2012 Oct; 507(1):79-84. PubMed ID: 22735619 [TBL] [Abstract][Full Text] [Related]
20. Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population. Kucinskas L; Juzenas S; Sventoraityte J; Cedaviciute R; Vitkauskiene A; Kalibatas V; Kondrackiene J; Kupcinskas L Ann Hematol; 2012 Apr; 91(4):491-5. PubMed ID: 21947086 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]