Lista de obras -

Association of an IGHV3-66 gene variant with Kawasaki disease

artículo científico publicado en 2020

CXCL10/IP-10 is a biomarker and mediator for Kawasaki disease

artículo científico publicado en 2015

Endoplasmic reticulum stress-induced caspase-4 activation mediates apoptosis and neurodegeneration in INCL.

artículo científico publicado en 2006

GLUT10 Maintains the Integrity of Major Arteries through Regulation of Redox Homeostasis and Mitochondrial Function.

artículo científico publicado en 2017

Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease

artículo científico publicado en 2011

Genome-wide transcriptome analysis to further understand neutrophil activation and lncRNA transcript profiles in Kawasaki disease

artículo científico publicado en 2019

Glucose transporter 10 modulates adipogenesis via an ascorbic acid-mediated pathway to protect mice against diet-induced metabolic dysregulation

scientific article published on 26 May 2020

Glycogen-branching enzyme deficiency leads to abnormal cardiac development: novel insights into glycogen storage disease IV.

artículo científico publicado en 2010

Identification of Methylation-Driven, Differentially Expressed STXBP6 as a Novel Biomarker in Lung Adenocarcinoma.

artículo científico publicado en 2017

Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study

scientific journal article

Interaction of uteroglobin with lipocalin-1 receptor suppresses cancer cell motility and invasion.

artículo científico publicado en 2006

Interplay between SIN3A and STAT3 mediates chromatin conformational changes and GFAP expression during cellular differentiation

artículo científico publicado en 2011

Knock-in human FGFR3 achondroplasia mutation as a mouse model for human skeletal dysplasia

artículo científico publicado en 2017

Lack of an endogenous anti-inflammatory protein in mice enhances colonization of B16F10 melanoma cells in the lungs.

artículo científico publicado en 2010

Mice lacking uteroglobin are highly susceptible to developing pulmonary fibrosis

artículo científico publicado en 2006

Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome

artículo científico publicado en 2010

Mutations in the SLC2A10 gene cause arterial abnormalities in mice

artículo científico publicado en 2008

Palmitoyl protein thioesterase-1 deficiency impairs synaptic vesicle recycling at nerve terminals, contributing to neuropathology in humans and mice

artículo científico publicado en 2008

Palmitoyl-protein thioesterase-1 deficiency leads to the activation of caspase-9 and contributes to rapid neurodegeneration in INCL.

artículo científico publicado en 2006

Palmitoyl-protein thioesterase-1 deficiency mediates the activation of the unfolded protein response and neuronal apoptosis in INCL

scientific journal article

Production of lysophosphatidylcholine by cPLA2 in the brain of mice lacking PPT1 is a signal for phagocyte infiltration

scientific journal article

RAGE signaling contributes to neuroinflammation in infantile neuronal ceroid lipofuscinosis

artículo científico publicado en 2008

Replication and meta-analysis of GWAS identified susceptibility loci in Kawasaki disease confirm the importance of B lymphoid tyrosine kinase (BLK) in disease susceptibility

artículo científico publicado en 2013

Sugars act as signal molecules and osmotica to regulate the expression of alpha-amylase genes and metabolic activities in germinating cereal grains

scientific article published on 01 March 1996

Tumor suppressor SCUBE2 inhibits breast-cancer cell migration and invasion through the reversal of epithelial-mesenchymal transition

artículo científico publicado en 2013

Twist1 Plays an Anti-apoptotic Role in Mutant Huntingtin Expression Striatal Progenitor Cells

artículo científico publicado en 2019

Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis

artículo científico publicado en 2012

Uteroglobin suppresses allergen-induced TH2 differentiation by down-regulating the expression of serum amyloid A and SOCS-3 genes

artículo científico publicado en 2006

Variant GADL1 and response to lithium therapy in bipolar I disorder

artículo científico publicado en 2013

Lista de obras de

Association of an IGHV3-66 gene variant with Kawasaki disease

CXCL10/IP-10 is a biomarker and mediator for Kawasaki disease

Endoplasmic reticulum stress-induced caspase-4 activation mediates apoptosis and neurodegeneration in INCL.

GLUT10 Maintains the Integrity of Major Arteries through Regulation of Redox Homeostasis and Mitochondrial Function.

Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease

Genome-wide transcriptome analysis to further understand neutrophil activation and lncRNA transcript profiles in Kawasaki disease

Glucose transporter 10 modulates adipogenesis via an ascorbic acid-mediated pathway to protect mice against diet-induced metabolic dysregulation

Glycogen-branching enzyme deficiency leads to abnormal cardiac development: novel insights into glycogen storage disease IV.

Identification of Methylation-Driven, Differentially Expressed STXBP6 as a Novel Biomarker in Lung Adenocarcinoma.

Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study

Interaction of uteroglobin with lipocalin-1 receptor suppresses cancer cell motility and invasion.

Interplay between SIN3A and STAT3 mediates chromatin conformational changes and GFAP expression during cellular differentiation

Knock-in human FGFR3 achondroplasia mutation as a mouse model for human skeletal dysplasia

Lack of an endogenous anti-inflammatory protein in mice enhances colonization of B16F10 melanoma cells in the lungs.

Mice lacking uteroglobin are highly susceptible to developing pulmonary fibrosis

Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome

Mutations in the SLC2A10 gene cause arterial abnormalities in mice

Palmitoyl protein thioesterase-1 deficiency impairs synaptic vesicle recycling at nerve terminals, contributing to neuropathology in humans and mice

Palmitoyl-protein thioesterase-1 deficiency leads to the activation of caspase-9 and contributes to rapid neurodegeneration in INCL.

Palmitoyl-protein thioesterase-1 deficiency mediates the activation of the unfolded protein response and neuronal apoptosis in INCL

Production of lysophosphatidylcholine by cPLA2 in the brain of mice lacking PPT1 is a signal for phagocyte infiltration

RAGE signaling contributes to neuroinflammation in infantile neuronal ceroid lipofuscinosis

Replication and meta-analysis of GWAS identified susceptibility loci in Kawasaki disease confirm the importance of B lymphoid tyrosine kinase (BLK) in disease susceptibility

Sugars act as signal molecules and osmotica to regulate the expression of alpha-amylase genes and metabolic activities in germinating cereal grains

Tumor suppressor SCUBE2 inhibits breast-cancer cell migration and invasion through the reversal of epithelial-mesenchymal transition

Twist1 Plays an Anti-apoptotic Role in Mutant Huntingtin Expression Striatal Progenitor Cells

Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis

Uteroglobin suppresses allergen-induced TH2 differentiation by down-regulating the expression of serum amyloid A and SOCS-3 genes

Variant GADL1 and response to lithium therapy in bipolar I disorder