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Results: 1 to 20 of 25

Cited In for PubMed (Select 5675426)

1.

Ceruloplasmin has two nearly identical sites that bind myeloperoxidase.

Bakhautdin B, Goksoy Bakhautdin E, Fox PL.

Biochem Biophys Res Commun. 2014 Oct 31;453(4):722-7. doi: 10.1016/j.bbrc.2014.09.134. Epub 2014 Oct 6.

PMID:
25301560
2.

Haemolysis and perturbations in the systemic iron metabolism of suckling, copper-deficient mosaic mutant mice - an animal model of Menkes disease.

Lenartowicz M, Starzyński RR, Krzeptowski W, Grzmil P, Bednarz A, Ogórek M, Pierzchała O, Staroń R, Gajowiak A, Lipiński P.

PLoS One. 2014 Sep 23;9(9):e107641. doi: 10.1371/journal.pone.0107641. eCollection 2014.

3.

Molecular mediators governing iron-copper interactions.

Gulec S, Collins JF.

Annu Rev Nutr. 2014;34:95-116. doi: 10.1146/annurev-nutr-071812-161215. Epub 2014 Jun 2. Review.

4.

Transcription factors Sp1 and Hif2α mediate induction of the copper-transporting ATPase (Atp7a) gene in intestinal epithelial cells during hypoxia.

Xie L, Collins JF.

J Biol Chem. 2013 Aug 16;288(33):23943-52. doi: 10.1074/jbc.M113.489500. Epub 2013 Jun 28.

5.
6.

Protective role of macrophage-derived ceruloplasmin in inflammatory bowel disease.

Bakhautdin B, Febbraio M, Goksoy E, de la Motte CA, Gulen MF, Childers EP, Hazen SL, Li X, Fox PL.

Gut. 2013 Feb;62(2):209-19. doi: 10.1136/gutjnl-2011-300694. Epub 2012 Feb 16.

7.

Impact of copper limitation on expression and function of multicopper oxidases (ferroxidases).

Prohaska JR.

Adv Nutr. 2011 Mar;2(2):89-95. doi: 10.3945/an.110.000208. Epub 2011 Mar 10. Review.

8.

Hepcidin and ferroportin: the new players in iron metabolism.

De Domenico I, Ward DM, Kaplan J.

Semin Liver Dis. 2011 Aug;31(3):272-9. doi: 10.1055/s-0031-1286058. Epub 2011 Sep 7. Review.

9.

Metabolic crossroads of iron and copper.

Collins JF, Prohaska JR, Knutson MD.

Nutr Rev. 2010 Mar;68(3):133-47. doi: 10.1111/j.1753-4887.2010.00271.x. Review.

10.

Anemic copper-deficient rats, but not mice, display low hepcidin expression and high ferroportin levels.

Jenkitkasemwong S, Broderius M, Nam H, Prohaska JR, Knutson MD.

J Nutr. 2010 Apr;140(4):723-30. doi: 10.3945/jn.109.117077. Epub 2010 Feb 17.

11.

Role of the syncytium in placenta-mediated complications of preeclampsia.

Guller S.

Thromb Res. 2009 Sep;124(4):389-92. doi: 10.1016/j.thromres.2009.05.016. Epub 2009 Jun 16. Review.

12.

Placental expression of ceruloplasmin in pregnancies complicated by severe preeclampsia.

Guller S, Buhimschi CS, Ma YY, Huang ST, Yang L, Kuczynski E, Zambrano E, Lockwood CJ, Buhimschi IA.

Lab Invest. 2008 Oct;88(10):1057-67. doi: 10.1038/labinvest.2008.74. Epub 2008 Aug 4.

13.

Copper-induced ferroportin-1 expression in J774 macrophages is associated with increased iron efflux.

Chung J, Haile DJ, Wessling-Resnick M.

Proc Natl Acad Sci U S A. 2004 Mar 2;101(9):2700-5. Epub 2004 Feb 18.

14.

Zinc suppresses the iron-accumulation phenotype of Saccharomyces cerevisiae lacking the yeast frataxin homologue (Yfh1).

Santos R, Dancis A, Eide D, Camadro JM, Lesuisse E.

Biochem J. 2003 Oct 15;375(Pt 2):247-54.

15.

Induction of the Root Cell Plasma Membrane Ferric Reductase (An Exclusive Role for Fe and Cu).

Cohen CK, Norvell WA, Kochian LV.

Plant Physiol. 1997 Jul;114(3):1061-1069.

16.

Essential role for mammalian copper transporter Ctr1 in copper homeostasis and embryonic development.

Lee J, Prohaska JR, Thiele DJ.

Proc Natl Acad Sci U S A. 2001 Jun 5;98(12):6842-7.

17.

Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux.

Harris ZL, Durley AP, Man TK, Gitlin JD.

Proc Natl Acad Sci U S A. 1999 Sep 14;96(19):10812-7.

18.

Hereditary deficiency of ferroxidase (aka caeruloplasmin)

Logan JI.

J Neurol Neurosurg Psychiatry. 1996 Nov;61(5):431-2. No abstract available.

19.

The Menkes/Wilson disease gene homologue in yeast provides copper to a ceruloplasmin-like oxidase required for iron uptake.

Yuan DS, Stearman R, Dancis A, Dunn T, Beeler T, Klausner RD.

Proc Natl Acad Sci U S A. 1995 Mar 28;92(7):2632-6.

20.

Aceruloplasminemia: molecular characterization of this disorder of iron metabolism.

Harris ZL, Takahashi Y, Miyajima H, Serizawa M, MacGillivray RT, Gitlin JD.

Proc Natl Acad Sci U S A. 1995 Mar 28;92(7):2539-43.

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