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Transferrin receptor 1 is a cellular receptor for human heme-albumin.
Jennifer B, Berg V, Modak M, Puck A, Seyerl-Jiresch M, Künig S, Zlabinger GJ, Steinberger P, Chou J, Geha RS, Öhler L, Yachie A, Choe H, Kraller M, Stockinger H, Stöckl J. Jennifer B, et al. Among authors: yachie a. Commun Biol. 2020 Oct 27;3(1):621. doi: 10.1038/s42003-020-01294-5. Commun Biol. 2020. PMID: 33110194 Free PMC article.
Corticosteroid enhances heme oxygenase-1 production by circulating monocytes by up-regulating hemoglobin scavenger receptor and amplifying the receptor-mediated uptake of hemoglobin-haptoglobin complex.
Yamazaki H, Ohta K, Tsukiji H, Toma T, Hashida Y, Ishizaki A, Saito T, Arai S, Koizumi S, Yachie A. Yamazaki H, et al. Among authors: yachie a. Biochem Biophys Res Commun. 2007 Jun 29;358(2):506-12. doi: 10.1016/j.bbrc.2007.04.136. Epub 2007 Apr 30. Biochem Biophys Res Commun. 2007. PMID: 17490617
Heme Oxygenase-1 Deficiency and Oxidative Stress: A Review of 9 Independent Human Cases and Animal Models.
Yachie A. Yachie A. Int J Mol Sci. 2021 Feb 3;22(4):1514. doi: 10.3390/ijms22041514. Int J Mol Sci. 2021. PMID: 33546372 Free PMC article. Review.
Since Yachie et al. reported the first description of human heme oxygenase (HO)-1 deficiency more than 20 years ago, few additional human cases have been reported in the literature. ...In this regard, therapy to induce HO-1 production by pharmacological intervention repres …
Since Yachie et al. reported the first description of human heme oxygenase (HO)-1 deficiency more than 20 years ago, few additional h …
Structural evidence of genomic exon-deletion mediated by Alu-Alu recombination in a human case with heme oxygenase-1 deficiency.
Saikawa Y, Kaneda H, Yue L, Shimura S, Toma T, Kasahara Y, Yachie A, Koizumi S. Saikawa Y, et al. Among authors: yachie a. Hum Mutat. 2000 Aug;16(2):178-9. doi: 10.1002/1098-1004(200008)16:2<178::AID-HUMU16>3.0.CO;2-X. Hum Mutat. 2000. PMID: 10923045
We previously reported a family affected by heme oxygenase-1 (HO-1) deficiency [Yachie et al., 1999]. The proband was a compound heterozygote for a complete loss of exon 2 (the maternal allele) and a two-nucleotide deletion within exon 3 (the pa …
We previously reported a family affected by heme oxygenase-1 (HO-1) deficiency [Yachie et al., 1999]. The proband was a …
[Heme oxygenase 1 deficiency].
Yachie A, Koizumi S. Yachie A, et al. Ryoikibetsu Shokogun Shirizu. 2001;(33):796-7. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462691 Review. Japanese. No abstract available.
398 results