Lista de obras - Nuria Andreu - Dominio Público Uruguay

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

artículo científico publicado en 2005

Behavioral characterization of a mouse model overexpressing DSCR1/ RCAN1.

artículo científico publicado en 2011

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

artículo científico publicado en 2022

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

artículo científico publicado en 2000

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

artículo científico publicado en 2016

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

artículo científico publicado en 2015

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

artículo científico publicado en 2001

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

artículo científico publicado en 2003

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

artículo científico publicado en 2001

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

artículo científico publicado en 2008

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

artículo científico publicado en 2007

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

artículo científico publicado en 2011

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

artículo científico publicado en 2001

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.

artículo científico publicado en 2008

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

artículo científico publicado en 2007

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

artículo científico publicado en 2003

Lista de obras de 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