(Q50335650)

English

Hereditary ceruloplasmin deficiency with hemosiderosis.

scientific article published in June 1996

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

Hereditary ceruloplasmin deficiency with hemosiderosis. (English)

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

author name string

N Okamoto

1

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

S Wada

2

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

T Oga

3

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

Y Kawabata

4

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

Y Baba

5

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

D Habu

6

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

Z Takeda

7

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

Y Wada

8

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

publication date

1 June 1996

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

97

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

6

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

755-758

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

Mapping, cloning and genetic characterization of the region containing the Wilson disease gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ceruloplasmin. A scavenger of superoxide anion radicals

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aceruloplasminemia: molecular characterization of this disorder of iron metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Mobilization of Iron from the Perfused Mammalian Liver by a Serum Copper Enzyme, Ferroxidase I

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of ceruloplasmin on superoxide-dependent iron release from ferritin and lipid peroxidation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete cDNA sequence of human preceruloplasmin

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of a partial candidate gene for Menkes disease by positional cloning

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S004390050132

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

1 reference

Europe PubMed Central

5 March 2018

http://europepmc.org/abstract/MED/8641692

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q50335650&oldid=2144067701"