Crossref journal-article
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The FASEB Journal (311)
Bibliography

Lee, S. Y., Patton, S. M., Henderson, R. J., & Connor, J. R. (2006). Consequences of expressing mutants of the hemochromatosis gene ( HFE ) into a human neuronal cell line lacking endogenous HFE. The FASEB Journal, 21(2), 564–576. Portico.

Authors 4
  1. Sang Y. Lee (first)
  2. Stephanie M. Patton (additional)
  3. Rebecca J. Henderson (additional)
  4. James R. Connor (additional)
References 59 Referenced 50
  1. {'key': 'e_1_2_6_2_1', 'article-title': 'Haemochromatosis and the liver', 'author': 'Niederau C.', 'year': '1999', 'journal-title': 'J. Hepatol. 30 (Suppl'} / J. Hepatol. 30 (Suppl / Haemochromatosis and the liver by Niederau C. (1999)
  2. 10.1016/S0016-5085(99)70244-1
  3. 10.1089/10906570050114902
  4. 10.1006/bcmd.1998.0211
  5. 10.1111/j.1399-0039.1998.tb03076.x
  6. {'key': 'e_1_2_6_7_1', 'first-page': '315', 'article-title': 'Haemochromatosis mutation analysis in a normal Irish population', 'volume': '57', 'author': 'Ryan F.', 'year': '2000', 'journal-title': 'Br. J. Biomed. Sci'} / Br. J. Biomed. Sci / Haemochromatosis mutation analysis in a normal Irish population by Ryan F. (2000)
  7. {'key': 'e_1_2_6_8_1', 'first-page': '127', 'article-title': 'Genetic hemochromatosis, a Celtic disease: is it now time for population screening? Genet', 'volume': '5', 'author': 'Byrnes V.', 'year': '2001', 'journal-title': 'Test'} / Test / Genetic hemochromatosis, a Celtic disease: is it now time for population screening? Genet by Byrnes V. (2001)
  8. 10.1038/ng0896-399
  9. 10.1034/j.1399-0004.2001.600111.x
  10. 10.1006/bcmd.2001.0451
  11. 10.1038/ng1196-251
  12. 10.1038/ng1196-249
  13. 10.1016/S0168-8278(00)80415-8
  14. 10.1002/1096-8628(20000703)93:1<58::AID-AJMG10>3.0.CO;2-L
  15. {'key': 'e_1_2_6_16_1', 'article-title': 'Erratum: are hereditary hemochromatosis mutations involved in alzheimer disease? Am', 'author': 'Moalem S.', 'year': '2000', 'journal-title': 'J. Med. Genet'} / J. Med. Genet / Erratum: are hereditary hemochromatosis mutations involved in alzheimer disease? Am by Moalem S. (2000)
  16. 10.1016/S0197-4580(01)00219-6
  17. 10.1159/000068480
  18. 10.1002/ajmg.b.10069 / Am. J. Med. Genet. B. Neuropsychiatr. Genet / Association of HFE mutations with neurodegeneration and oxidative stress in Alzheimer's disease and correlation with APOE by Pulliam J. F. (2003)
  19. 10.1093/jnci/95.2.154
  20. 10.1016/j.jns.2004.08.003
  21. {'key': 'e_1_2_6_22_1', 'article-title': "HFE mutations and Alzheimer's disease", 'author': 'Connor J. R.', 'year': '2006', 'journal-title': 'J. Alzheimers Dis'} / J. Alzheimers Dis / HFE mutations and Alzheimer's disease by Connor J. R. (2006)
  22. 10.1016/j.neurobiolaging.2003.06.008
  23. 10.1016/S0047-6374(03)00031-9
  24. 10.1136/jmg.2003.015552
  25. 10.1212/01.WNL.0000123114.04644.CC
  26. 10.1006/abio.1996.0032
  27. 10.1006/abio.1997.2126
  28. 10.1016/j.neurobiolaging.2004.08.006
  29. 10.1196/annals.1306.001
  30. 10.1016/j.bbamcr.2004.09.032
  31. 10.1073/pnas.85.7.2171
  32. 10.1002/(SICI)1097-4547(19990315)55:6<674::AID-JNR3>3.0.CO;2-J
  33. 10.1002/glia.20235
  34. 10.1046/j.1365-2249.2001.01707.x
  35. 10.1016/S0006-8993(97)01543-6
  36. 10.1002/(SICI)1097-4547(19990415)56:2<166::AID-JNR6>3.0.CO;2-S
  37. {'key': 'e_1_2_6_38_1', 'first-page': '709', 'article-title': "Iron as a vulnerability factor in nigrostriatal degeneration in aging and Parkinson's disease", 'volume': '46', 'author': 'Floor E.', 'year': '2000', 'journal-title': 'Cell. Mol. Biol. (Noisy‐le‐grand)'} / Cell. Mol. Biol. (Noisy‐le‐grand) / Iron as a vulnerability factor in nigrostriatal degeneration in aging and Parkinson's disease by Floor E. (2000)
  38. 10.3233/JAD-2001-3506
  39. 10.1016/S0014-5793(00)02173-6
  40. 10.1074/jbc.273.34.22068
  41. 10.1182/blood.V94.11.3915
  42. 10.1016/S0014-5793(99)01330-7
  43. 10.1016/S0167-4889(01)00075-1
  44. 10.1042/BJ20021607
  45. 10.1002/jnr.490370405
  46. 10.1002/jcp.10056
  47. 10.1111/j.1572-0241.2003.07222.x
  48. 10.1006/bbrc.1999.1554
  49. 10.1016/j.molbrainres.2003.10.013
  50. 10.1046/j.1471-4159.2001.00231.x
  51. 10.1073/pnas.94.24.13198
  52. 10.1073/pnas.95.4.1472
  53. {'key': 'e_1_2_6_54_1', 'first-page': '682', 'article-title': 'Increased expression of mitochondrial peroxiredoxin‐3 (thioredoxin peroxidase‐2) protects cancer cells against hypoxia and drug‐induced hydrogen peroxide‐dependent apoptosis', 'volume': '1', 'author': 'Nonn L.', 'year': '2003', 'journal-title': 'Mol. Cancer Res'} / Mol. Cancer Res / Increased expression of mitochondrial peroxiredoxin‐3 (thioredoxin peroxidase‐2) protects cancer cells against hypoxia and drug‐induced hydrogen peroxide‐dependent apoptosis by Nonn L. (2003)
  54. 10.1212/01.wnl.0000176032.94434.d4
  55. 10.1002/ijc.21331 / Int. J. Cancer / Hemochromatosis gene mutations among Finnish male breast and prostate cancer patients by Syrjakoski K. (2005)
  56. 10.1158/1055-9965.EPI-03-0188
  57. 10.1016/S1542-3565(03)00132-0
  58. {'key': 'e_1_2_6_59_1', 'first-page': '5902', 'article-title': 'Hypermethylation‐associated inactivation of the cellular retinol binding‐protein 1 gene in human cancer', 'volume': '62', 'author': 'Esteller M.', 'year': '2002', 'journal-title': 'Cancer Res'} / Cancer Res / Hypermethylation‐associated inactivation of the cellular retinol binding‐protein 1 gene in human cancer by Esteller M. (2002)
  59. 10.1073/pnas.242614699
Dates
Type When
Created 18 years, 8 months ago (Dec. 28, 2006, 8:12 p.m.)
Deposited 3 years, 10 months ago (Oct. 29, 2021, 4:58 p.m.)
Indexed 3 months, 1 week ago (May 19, 2025, 4:25 a.m.)
Issued 18 years, 8 months ago (Dec. 27, 2006)
Published 18 years, 8 months ago (Dec. 27, 2006)
Published Online 18 years, 8 months ago (Dec. 27, 2006)
Published Print 18 years, 6 months ago (Feb. 1, 2007)
Funders 2
  1. Alzheimer's Association 10.13039/100000957

    Region: Americas

    gov (Associations and societies (private and public))

    Labels3
    1. Alzheimer's Disease and Related Disorders Association, Inc.
    2. Alzheimer's Disease & Related Disorders Association, Inc.
    3. AA
  2. Muscular Dystrophy Association 10.13039/100005202

    Region: Americas

    gov (Associations and societies (private and public))

    Labels2
    1. Muscular Dystrophy Association, Inc.
    2. MDA

@article{Lee_2006, title={Consequences of expressing mutants of the hemochromatosis gene ( HFE ) into a human neuronal cell line lacking endogenous HFE}, volume={21}, ISSN={1530-6860}, url={http://dx.doi.org/10.1096/fj.06-6397com}, DOI={10.1096/fj.06-6397com}, number={2}, journal={The FASEB Journal}, publisher={Wiley}, author={Lee, Sang Y. and Patton, Stephanie M. and Henderson, Rebecca J. and Connor, James R.}, year={2006}, month=dec, pages={564–576} }