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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1983 1
1984 1
1985 2
1986 2
1987 2
1988 2
1991 3
1992 1
1996 2
1999 1
2000 2
2001 2
2004 1
2006 1
2007 1
2008 2
2010 1
2012 1
2013 1
2014 1
2023 1
2024 0

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PubMed (cited) for id: 134770

29 results

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Page 1
Heterozygous nonsense variants in the ferritin heavy-chain gene FTH1 cause a neuroferritinopathy.
Shieh JT, Tintos-Hernandez JA, Murali CN, Penon-Portmann M, Flores-Mendez M, Santana A, Bulos JA, Du K, Dupuis L, Damseh N, Mendoza-Londoño R, Berera C, Lee JC, Phillips JJ, Alves CAPF, Dmochowski IJ, Ortiz-González XR. Shieh JT, et al. HGG Adv. 2023 Oct 12;4(4):100236. doi: 10.1016/j.xhgg.2023.100236. Epub 2023 Sep 3. HGG Adv. 2023. PMID: 37660254 Free PMC article.
Binding and uptake of H-ferritin are mediated by human transferrin receptor-1.
Li L, Fang CJ, Ryan JC, Niemi EC, Lebrón JA, Björkman PJ, Arase H, Torti FM, Torti SV, Nakamura MC, Seaman WE. Li L, et al. Proc Natl Acad Sci U S A. 2010 Feb 23;107(8):3505-10. doi: 10.1073/pnas.0913192107. Epub 2010 Feb 4. Proc Natl Acad Sci U S A. 2010. PMID: 20133674 Free PMC article.
29 results