List of works - Nuria Andreu

A novel Wiskott-Aldrich syndrome protein (WASP) complex mutation identified in a WAS patient results in an aberrant product at the C-terminus from two transcripts with unusual polyA signals

scientific article

Behavioral characterization of a mouse model overexpressing DSCR1/ RCAN1.

scientific article

Citizen-science reveals changes in the oral microbiome in Spain through age and lifestyle factors

scientific article published on 19 May 2022

Cloning, mapping and expression analysis of VPS33B, the human orthologue of rat Vps33b

scientific article

Genome and transcriptome analysis of the Mesoamerican common bean and the role of gene duplications in establishing tissue and temporal specialization of genes

scientific article

Genome-wide miR-155 and miR-802 target gene identification in the hippocampus of Ts65Dn Down syndrome mouse model by miRNA sponges

scientific article

Identification and characterization of BTBD1, a novel BTB domain containing gene on human chromosome 15q24

scientific article

Identification and characterization of a novel splice-site mutation in a patient with Wiskott-Aldrich syndrome

scientific article

Identification of C15orf5, a heart-enriched transcript on chromosome 15q23-q24.

scientific article published on July 2001

Increased NR2A expression and prolonged decay of NMDA-induced calcium transient in cerebellum of TgDyrk1A mice, a mouse model of Down syndrome.

scientific article

Novel membrane cell projection defects in Wiskott-Aldrich syndrome B cells

scientific article

Oncolytic adenoviruses armed with thymidine kinase can be traced by PET imaging and show potent antitumoural effects by ganciclovir dosing.

scientific article

PACSIN 3 is a novel SH3 domain cytoplasmic adapter protein of the pacsin-syndapin-FAP52 gene family.

scientific article

PALML, a novel paralemmin-related gene mapping on human chromosome 1p21

scientific journal article

Targeting Dyrk1A with AAVshRNA attenuates motor alterations in TgDyrk1A, a mouse model of Down syndrome.

scientific article

Two novel mutations identified in the Wiskott-Aldrich syndrome protein gene cause Wiskott-Aldrich syndrome and thrombocytopenia

scientific article

Wiskott-Aldrich syndrome in a female with skewed X-chromosome inactivation

scientific article

List of works by Nuria Andreu

A novel Wiskott-Aldrich syndrome protein (WASP) complex mutation identified in a WAS patient results in an aberrant product at the C-terminus from two transcripts with unusual polyA signals

Behavioral characterization of a mouse model overexpressing DSCR1/ RCAN1.

Citizen-science reveals changes in the oral microbiome in Spain through age and lifestyle factors

Cloning, mapping and expression analysis of VPS33B, the human orthologue of rat Vps33b

Genome and transcriptome analysis of the Mesoamerican common bean and the role of gene duplications in establishing tissue and temporal specialization of genes

Genome-wide miR-155 and miR-802 target gene identification in the hippocampus of Ts65Dn Down syndrome mouse model by miRNA sponges

Identification and characterization of BTBD1, a novel BTB domain containing gene on human chromosome 15q24

Identification and characterization of a novel splice-site mutation in a patient with Wiskott-Aldrich syndrome

Identification of C15orf5, a heart-enriched transcript on chromosome 15q23-q24.

Increased NR2A expression and prolonged decay of NMDA-induced calcium transient in cerebellum of TgDyrk1A mice, a mouse model of Down syndrome.

Novel membrane cell projection defects in Wiskott-Aldrich syndrome B cells

Oncolytic adenoviruses armed with thymidine kinase can be traced by PET imaging and show potent antitumoural effects by ganciclovir dosing.

PACSIN 3 is a novel SH3 domain cytoplasmic adapter protein of the pacsin-syndapin-FAP52 gene family.

PALML, a novel paralemmin-related gene mapping on human chromosome 1p21

Targeting Dyrk1A with AAVshRNA attenuates motor alterations in TgDyrk1A, a mouse model of Down syndrome.

Two novel mutations identified in the Wiskott-Aldrich syndrome protein gene cause Wiskott-Aldrich syndrome and thrombocytopenia

Wiskott-Aldrich syndrome in a female with skewed X-chromosome inactivation