Profile of plasma microRNAs as a potential biomarker of Wilson's disease.

Wilson's disease (WD) is a rare condition resulting from autosomal recessive mutations in ATP7B, a copper transporter, manifesting with hepatic, neurological, and psychiatric symptoms. Timely diagnosis and appropriate treatment yield a positive prognosis, while delayed identification and/or ins...

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Authors: Sánchez-Monteagudo A, Ripollés E, Murillo O, Domènech S, Álvarez-Sauco M, Girona E, Sastre-Bataller I, Bono A, García-Villarreal L, Tugores A, García-García F, González-Aseguinolaza G, Berenguer M, Espinós C
Format: article
Status:Published version
Publication Date:2024
Country:España
Institution:Centro de Investigación Principe Felipe (CIPF)
Repository:r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
OAI Identifier:oai:cipf.fundanetsuite.com:p4385
Online Access:https://cipf.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=4385
Access Level:Open access
Keyword:Drug monitoring, Prognosis, miR-122-5p, miR-192-5p, miR-885-5p
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spelling Profile of plasma microRNAs as a potential biomarker of Wilson's disease.Sánchez-Monteagudo ARipollés EMurillo ODomènech SÁlvarez-Sauco MGirona ESastre-Bataller IBono AGarcía-Villarreal LTugores AGarcía-García FGonzález-Aseguinolaza GBerenguer MEspinós CDrug monitoring, Prognosis, miR-122-5p, miR-192-5p, miR-885-5pWilson's disease (WD) is a rare condition resulting from autosomal recessive mutations in ATP7B, a copper transporter, manifesting with hepatic, neurological, and psychiatric symptoms. Timely diagnosis and appropriate treatment yield a positive prognosis, while delayed identification and/or insufficient therapy lead to a poor outcome. Our aim was to establish a prognostic method for WD by characterising biomarkers based on circulating microRNAs.SPRINGER JAPAN KK2024info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttps://cipf.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=4385JOURNAL OF GASTROENTEROLOGYISSN: 09441174ISSNe: 14355922reponame:r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)instname:Centro de Investigación Principe Felipe (CIPF)Inglésinfo:eu-repo/semantics/openAccessoai:cipf.fundanetsuite.com:p43852026-06-17T11:19:47Z
dc.title.none.fl_str_mv Profile of plasma microRNAs as a potential biomarker of Wilson's disease.
title Profile of plasma microRNAs as a potential biomarker of Wilson's disease.
spellingShingle Profile of plasma microRNAs as a potential biomarker of Wilson's disease.
Sánchez-Monteagudo A
Drug monitoring, Prognosis, miR-122-5p, miR-192-5p, miR-885-5p
title_short Profile of plasma microRNAs as a potential biomarker of Wilson's disease.
title_full Profile of plasma microRNAs as a potential biomarker of Wilson's disease.
title_fullStr Profile of plasma microRNAs as a potential biomarker of Wilson's disease.
title_full_unstemmed Profile of plasma microRNAs as a potential biomarker of Wilson's disease.
title_sort Profile of plasma microRNAs as a potential biomarker of Wilson's disease.
dc.creator.none.fl_str_mv Sánchez-Monteagudo A
Ripollés E
Murillo O
Domènech S
Álvarez-Sauco M
Girona E
Sastre-Bataller I
Bono A
García-Villarreal L
Tugores A
García-García F
González-Aseguinolaza G
Berenguer M
Espinós C
author Sánchez-Monteagudo A
author_facet Sánchez-Monteagudo A
Ripollés E
Murillo O
Domènech S
Álvarez-Sauco M
Girona E
Sastre-Bataller I
Bono A
García-Villarreal L
Tugores A
García-García F
González-Aseguinolaza G
Berenguer M
Espinós C
author_role author
author2 Ripollés E
Murillo O
Domènech S
Álvarez-Sauco M
Girona E
Sastre-Bataller I
Bono A
García-Villarreal L
Tugores A
García-García F
González-Aseguinolaza G
Berenguer M
Espinós C
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Drug monitoring, Prognosis, miR-122-5p, miR-192-5p, miR-885-5p
topic Drug monitoring, Prognosis, miR-122-5p, miR-192-5p, miR-885-5p
description Wilson's disease (WD) is a rare condition resulting from autosomal recessive mutations in ATP7B, a copper transporter, manifesting with hepatic, neurological, and psychiatric symptoms. Timely diagnosis and appropriate treatment yield a positive prognosis, while delayed identification and/or insufficient therapy lead to a poor outcome. Our aim was to establish a prognostic method for WD by characterising biomarkers based on circulating microRNAs.
publishDate 2024
dc.date.none.fl_str_mv 2024
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://cipf.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=4385
url https://cipf.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=4385
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv SPRINGER JAPAN KK
publisher.none.fl_str_mv SPRINGER JAPAN KK
dc.source.none.fl_str_mv JOURNAL OF GASTROENTEROLOGY
ISSN: 09441174
ISSNe: 14355922
reponame:r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
instname:Centro de Investigación Principe Felipe (CIPF)
instname_str Centro de Investigación Principe Felipe (CIPF)
reponame_str r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
collection r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
repository.name.fl_str_mv
repository.mail.fl_str_mv
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score 15.811543

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