Wilson's Disease-Crossroads of Genetics, Inflammation and Immunity/Autoimmunity: Clinical and Molecular Issues.

Humans Hepatolenticular Degeneration / genetics Autoimmunity / genetics Inflammation / genetics Animals Copper Copper-Transporting ATPases / genetics Mutation
ATP7B Wilson’s disease autoantibodies autoimmunity copper cuproptosis ferroptosis immunology inflammation oxidative stress

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
20 Aug 2024
Historique:
received: 19 07 2024
revised: 11 08 2024
accepted: 13 08 2024
medline: 31 8 2024
pubmed: 31 8 2024
entrez: 29 8 2024
Statut: epublish

Résumé

Wilson's disease (WD) is a rare, autosomal recessive disorder of copper metabolism caused by pathogenic mutations in the

Identifiants

DOI: 10.3390/ijms25169034 PMID: 39201720
pubmed: 39201720
pii: ijms25169034
doi: 10.3390/ijms25169034
pii:
doi:

Substances chimiques

Copper 789U1901C5
Copper-Transporting ATPases EC 7.2.2.8
ATP7B protein, human EC 7.2.2.8

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Grażyna Gromadzka (G)

Department of Biomedical Sciences, Faculty of Medicine, Collegium Medicum, Cardinal Stefan Wyszynski University, Wóycickiego Street 1/3, 01-938 Warsaw, Poland.
ORCID: 0000-0002-4325-8971

Julia Czerwińska (J)

Students Scientific Association "Immunis", Cardinal Stefan Wyszynski University, Dewajtis Street 5, 01-815 Warsaw, Poland.

Elżbieta Krzemińska (E)

Students Scientific Association "Immunis", Cardinal Stefan Wyszynski University, Dewajtis Street 5, 01-815 Warsaw, Poland.

Adam Przybyłkowski (A)

Department of Gastroenterology and Internal Medicine, Medical University of Warsaw, Banacha 1a, 02-097 Warsaw, Poland.
ORCID: 0000-0002-5851-2856

Tomasz Litwin (T)

Second Department of Neurology, Institute of Psychiatry and Neurology, Sobieskiego Street 9, 02-957 Warsaw, Poland.
ORCID: 0000-0003-2670-9651

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Classifications MeSH

questionsmedicales.fr › Eucaryotes › Animaux › Chordés › Vertébrés › Mammifères › Eutheria › Primates › Haplorhini › Catarrhini › Hominidae › Humains › Wilson's Disease-Crossroads of Genetics,...
questionsmedicales.fr › Maladies métaboliques et nutritionnelles › Maladies métaboliques › Erreurs innées du métabolisme › Erreurs innées du métabolisme des métaux › Dégénérescence hépatolenticulaire › Wilson's Disease-Crossroads of Genetics,...
questionsmedicales.fr › Phénomènes du système immunitaire › Immunité › Auto-immunité › Wilson's Disease-Crossroads of Genetics,...
questionsmedicales.fr › États, signes et symptômes pathologiques › Processus pathologiques › Inflammation › Wilson's Disease-Crossroads of Genetics,...
questionsmedicales.fr › Eucaryotes › Animaux › Wilson's Disease-Crossroads of Genetics,...
questionsmedicales.fr › Produits chimiques inorganiques › Métaux › Métaux lourds › Cuivre › Wilson's Disease-Crossroads of Genetics,...
questionsmedicales.fr › Acides aminés, peptides et protéines › Protéines › Protéines membranaires › Protéines de transport membranaire › P-type ATPases › Copper-transporting ATPases › Wilson's Disease-Crossroads of Genetics,...
questionsmedicales.fr › Phénomènes génétiques › Variation génétique › Mutation › Wilson's Disease-Crossroads of Genetics,...