Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 29

2.

Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease).

SCHEINBERG IH, GITLIN D.

Science. 1952 Oct 31;116(3018):484-5. No abstract available.

PMID:
12994898
3.

Studies on familial hypotransferrinemia: unique clinical course and molecular pathology.

Hayashi A, Wada Y, Suzuki T, Shimizu A.

Am J Hum Genet. 1993 Jul;53(1):201-13.

4.

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene.

Tanzi RE, Petrukhin K, Chernov I, Pellequer JL, Wasco W, Ross B, Romano DM, Parano E, Pavone L, Brzustowicz LM, et al.

Nat Genet. 1993 Dec;5(4):344-50.

PMID:
8298641
5.

The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene.

Bull PC, Thomas GR, Rommens JM, Forbes JR, Cox DW.

Nat Genet. 1993 Dec;5(4):327-37. Erratum in: Nat Genet 1994 Feb;6(2):214.

PMID:
8298639
6.

The FET3 gene of S. cerevisiae encodes a multicopper oxidase required for ferrous iron uptake.

Askwith C, Eide D, Van Ho A, Bernard PS, Li L, Davis-Kaplan S, Sipe DM, Kaplan J.

Cell. 1994 Jan 28;76(2):403-10.

PMID:
8293473
7.

Molecular characterization of a copper transport protein in S. cerevisiae: an unexpected role for copper in iron transport.

Dancis A, Yuan DS, Haile D, Askwith C, Eide D, Moehle C, Kaplan J, Klausner RD.

Cell. 1994 Jan 28;76(2):393-402.

PMID:
8293472
8.

Isolation and characterization of a human liver cDNA as a candidate gene for Wilson disease.

Yamaguchi Y, Heiny ME, Gitlin JD.

Biochem Biophys Res Commun. 1993 Nov 30;197(1):271-7.

PMID:
8250934
9.

Expression of the Wilson disease gene is deficient in the Long-Evans Cinnamon rat.

Yamaguchi Y, Heiny ME, Shimizu N, Aoki T, Gitlin JD.

Biochem J. 1994 Jul 1;301 ( Pt 1):1-4.

10.

Single-chain structure of human ceruloplasmin: the complete amino acid sequence of the whole molecule.

Takahashi N, Ortel TL, Putnam FW.

Proc Natl Acad Sci U S A. 1984 Jan;81(2):390-4.

11.

Coagulation factors V and VIII and ceruloplasmin constitute a family of structurally related proteins.

Church WR, Jernigan RL, Toole J, Hewick RM, Knopf J, Knutson GJ, Nesheim ME, Mann KG, Fass DN.

Proc Natl Acad Sci U S A. 1984 Nov;81(22):6934-7.

12.

Factors influencing serum ceruloplasmin levels in normal individuals.

Cox DW.

J Lab Clin Med. 1966 Dec;68(6):893-904. No abstract available.

PMID:
5926186
13.

The possible significance of the ferrous oxidase activity of ceruloplasmin in normal human serum.

Osaki S, Johnson DA, Frieden E.

J Biol Chem. 1966 Jun 25;241(12):2746-51. No abstract available.

14.

Iron metabolism in copper-deficient swine.

Lee GR, Nacht S, Lukens JN, Cartwright GE.

J Clin Invest. 1968 Sep;47(9):2058-69.

15.

The mobilization of iron from the perfused mammalian liver by a serum copper enzyme, ferroxidase I.

Osaki S, Johnson DA, Frieden E.

J Biol Chem. 1971 May 10;246(9):3018-23. No abstract available.

16.

The role of ceruloplasmin in iron metabolism.

Roeser HP, Lee GR, Nacht S, Cartwright GE.

J Clin Invest. 1970 Dec;49(12):2408-17.

17.
18.

Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration.

Miyajima H, Nishimura Y, Mizoguchi K, Sakamoto M, Shimizu T, Honda N.

Neurology. 1987 May;37(5):761-7.

PMID:
3574673
19.

Characterization, mapping, and expression of the human ceruloplasmin gene.

Yang F, Naylor SL, Lum JB, Cutshaw S, McCombs JL, Naberhaus KH, McGill JR, Adrian GS, Moore CM, Barnett DR, et al.

Proc Natl Acad Sci U S A. 1986 May;83(10):3257-61.

20.
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk