Lista de obras - Fuencisla Matesanz - Dominio Público Uruguay

A New Risk Variant for Multiple Sclerosis at 11q23.3 Locus Is Associated with Expansion of CXCR5+ Circulating Regulatory T Cells

artículo científico publicado en 2020

A comparison of genomic profiles of complex diseases under different models.

artículo científico publicado en 2016

A cytokine gene screen uncovers SOCS1 as genetic risk factor for multiple sclerosis

artículo científico publicado en 2011

A functional variant that affects exon-skipping and protein expression of SP140 as genetic mechanism predisposing to multiple sclerosis.

artículo científico publicado en 2015

A new cDNA sequence for the murine interleukin-2 gene

artículo científico publicado en 1992

A new risk variant for multiple sclerosis at the immunoglobulin heavy chain locus associates with intrathecal IgG, IgM index and oligoclonal bands

artículo científico publicado en 2014

A splice variant in the ACSL5 gene relates migraine with fatty acid activation in mitochondria

artículo científico publicado en 2016

ANKRD55 and DHCR7 are novel multiple sclerosis risk loci

article

Allelic expression and interleukin-2 polymorphisms in multiple sclerosis.

artículo científico publicado en 2001

Allelic selection of human IL-2 gene

article

Analysis of -631 and -475 interleukin-2 promoter single nucleotide polymorphisms in multiple sclerosis

scientific article published on 01 October 2002

Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients

artículo científico publicado en 2016

CD40: novel association with Crohn's disease and replication in multiple sclerosis susceptibility

artículo científico publicado en 2010

Characterization of the MAL2-positive compartment in oligodendrocytes

artículo científico publicado en 2009

Chitinase 3-like 1 plasma levels are increased in patients with progressive forms of multiple sclerosis

artículo científico publicado en 2011

Closing the case ofAPOEin multiple sclerosis: no association with disease risk in over 29 000 subjects: Figure 1

Correction: CD40: Novel Association with Crohn's Disease and Replication in Multiple Sclerosis Susceptibility

artículo científico publicado en 2010

Differential expression of the H-ras mutated and normal alleles in rabbit dmba-induced keratoacanthomas

Effects of the multiple sclerosis associated -330 promoter polymorphism in IL2 allelic expression

artículo científico publicado en 2004

Existence of at least five interleukin-2 molecules in different mouse strains

artículo científico publicado en 1993

Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease

artículo científico publicado en 2019

Exome sequencing study in patients with multiple sclerosis reveals variants associated with disease course

artículo científico publicado en 2018

Fine mapping and functional analysis of the multiple sclerosis risk gene CD6

artículo científico publicado en 2013

Genome-wide CTCF distribution in vertebrates defines equivalent sites that aid the identification of disease-associated genes.

artículo científico publicado en 2011

Genome-wide association filtering using a highly locus-specific transmission/disequilibrium test

artículo científico publicado en 2010

Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1

artículo científico publicado en 2012

Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk

artículo científico publicado en 2013

Genome-wide significant association with seven novel multiple sclerosis risk loci

artículo científico publicado en 2015

Genomewide study of multiple sclerosis

Glutamine and tetrapeptide repeat variations affect the biological activity of different mouse interleukin-2 alleles

artículo científico publicado en 1996

HERV-W polymorphism in chromosome X is associated with multiple sclerosis risk and with differential expression of MSRV.

artículo científico publicado en 2014

Hexose-6-phosphate dehydrogenase: a new risk gene for multiple sclerosis

artículo científico publicado en 2009

High ACSL5 transcript levels associate with systemic lupus erythematosus and apoptosis in Jurkat T lymphocytes and peripheral blood cells

artículo científico publicado en 2011

High expression in bacteria and purification of polymorphic mouse interleukin 2 molecules.

artículo científico publicado en 1998

Human endogenous retrovirus HERV-Fc1 association with multiple sclerosis susceptibility: a meta-analysis

artículo científico publicado en 2014

IFNAR1 and IFNAR2 polymorphisms confer susceptibility to multiple sclerosis but not to interferon-beta treatment response

artículo científico publicado en 2005

IL2RA/CD25 gene polymorphisms: uneven association with multiple sclerosis (MS) and type 1 diabetes (T1D).

artículo científico publicado en 2009

IL2RA/CD25 polymorphisms contribute to multiple sclerosis susceptibility

artículo científico publicado en 2007

Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis

artículo científico publicado en 2012

In-vivo and in-vitro analysis of retroviral vectors carrying the N-ras oncogene

scientific article published on 01 September 1995

Increasing power by using haplotype similarity in a multimarker transmission/disequilibrium test.

artículo científico publicado en 2012

Induction of Autoantibodies to Different Interleukin-2 Allotypes

artículo científico publicado en 1999

Influence of the LILRA3 Deletion on Multiple Sclerosis Risk: Original Data and Meta-Analysis.

artículo científico publicado en 2015

Interaction of PLP with GFP-MAL2 in the human oligodendroglial cell line HOG

artículo científico publicado en 2011

Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations

artículo científico publicado en 2008

Lack of association between -384 and 114 IL-2 gene polymorphisms and rheumatoid arthritis

article

MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis

artículo científico publicado en 2013

Members 6B and 14 of the TNF receptor superfamily in multiple sclerosis predisposition

article

Multiple sclerosis association study with theTENR-IL2-IL21region in a Spanish population

article

Multiple sclerosis risk variant HLA-DRB1*1501 associates with high expression of DRB1 gene in different human populations

artículo científico publicado en 2012

OAS1 gene haplotype confers susceptibility to multiple sclerosis.

artículo científico publicado en 2006

Polymorphisms in the IL2, IL2RA and IL2RB genes in multiple sclerosis risk

artículo científico publicado en 2010

Protein tyrosine phosphatase gene (PTPN22) polymorphism in multiple sclerosis.

artículo científico publicado en 2005

Replication of top markers of a genome-wide association study in multiple sclerosis in Spain.

artículo científico publicado en 2010

Replication study of 10 genes showing evidence for association with multiple sclerosis: validation of TMEM39A, IL12B and CLBL genes

article

SP140 regulates the expression of immune-related genes associated with multiple sclerosis and other autoimmune diseases by NF-κB inhibition

article

STAT3 locus in inflammatory bowel disease and multiple sclerosis susceptibility

article

Sample reproducibility of genetic association using different multimarker TDTs in genome-wide association studies: characterization and a new approach.

artículo científico publicado en 2012

TNFRSF1A polymorphisms rs1800693 and rs4149584 in patients with multiple sclerosis.

artículo científico publicado en 2013

Tag-SNP analysis of the GFI1-EVI5-RPL5-FAM69 risk locus for multiple sclerosis

artículo científico publicado en 2010

The -174/-597 promoter polymorphisms in the interleukin-6 gene are not associated with susceptibility to multiple sclerosis.

artículo científico publicado en 2001

The 1858T PTPN22 gene variant contributes to a genetic risk of type 1 diabetes in a Ukrainian population.

artículo científico publicado en 2006

The C-terminal domain of the Plasmodium falciparum acyl-CoA synthetases PfACS1 and PfACS3 functions as ligand for ankyrin.

artículo científico publicado en 2003

The Plasmodium falciparum fatty acyl-CoA synthetase family (PfACS) and differential stage-specific expression in infected erythrocytes

artículo científico publicado en 2003

The T244I variant of the interleukin-7 receptor-alpha gene and multiple sclerosis

artículo científico publicado en 2008

The autoimmune disease-associated KIF5A, CD226 and SH2B3 gene variants confer susceptibility for multiple sclerosis

artículo científico publicado en 2010

The cloning and expression of Pfacs1, a Plasmodium falciparum fatty acyl coenzyme A synthetase-1 targeted to the host erythrocyte cytoplasm

artículo científico publicado en 1999

The high producer variant of the Fc-receptor like-3 (FCRL3) gene is involved in protection against multiple sclerosis

artículo científico publicado en 2008

The multiple sclerosis-associated regulatory variant rs10877013 affects expression of CYP27B1 and VDR under inflammatory or vitamin D stimuli.

artículo científico publicado en 2015

Validation of the CD6 and TNFRSF1A loci as risk factors for multiple sclerosis in Spain.

artículo científico publicado en 2010

Lista de obras de Fuencisla Matesanz

A New Risk Variant for Multiple Sclerosis at 11q23.3 Locus Is Associated with Expansion of CXCR5+ Circulating Regulatory T Cells

A comparison of genomic profiles of complex diseases under different models.

A cytokine gene screen uncovers SOCS1 as genetic risk factor for multiple sclerosis

A functional variant that affects exon-skipping and protein expression of SP140 as genetic mechanism predisposing to multiple sclerosis.

A new cDNA sequence for the murine interleukin-2 gene

A new risk variant for multiple sclerosis at the immunoglobulin heavy chain locus associates with intrathecal IgG, IgM index and oligoclonal bands

A splice variant in the ACSL5 gene relates migraine with fatty acid activation in mitochondria

ANKRD55 and DHCR7 are novel multiple sclerosis risk loci

Allelic expression and interleukin-2 polymorphisms in multiple sclerosis.

Allelic selection of human IL-2 gene

Analysis of -631 and -475 interleukin-2 promoter single nucleotide polymorphisms in multiple sclerosis

Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients

CD40: novel association with Crohn's disease and replication in multiple sclerosis susceptibility

Characterization of the MAL2-positive compartment in oligodendrocytes

Chitinase 3-like 1 plasma levels are increased in patients with progressive forms of multiple sclerosis

Closing the case ofAPOEin multiple sclerosis: no association with disease risk in over 29 000 subjects: Figure 1

Correction: CD40: Novel Association with Crohn's Disease and Replication in Multiple Sclerosis Susceptibility

Differential expression of the H-ras mutated and normal alleles in rabbit dmba-induced keratoacanthomas

Effects of the multiple sclerosis associated -330 promoter polymorphism in IL2 allelic expression

Existence of at least five interleukin-2 molecules in different mouse strains

Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease

Exome sequencing study in patients with multiple sclerosis reveals variants associated with disease course

Fine mapping and functional analysis of the multiple sclerosis risk gene CD6

Genome-wide CTCF distribution in vertebrates defines equivalent sites that aid the identification of disease-associated genes.

Genome-wide association filtering using a highly locus-specific transmission/disequilibrium test

Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1

Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk

Genome-wide significant association with seven novel multiple sclerosis risk loci

Genomewide study of multiple sclerosis

Glutamine and tetrapeptide repeat variations affect the biological activity of different mouse interleukin-2 alleles

HERV-W polymorphism in chromosome X is associated with multiple sclerosis risk and with differential expression of MSRV.

Hexose-6-phosphate dehydrogenase: a new risk gene for multiple sclerosis

High ACSL5 transcript levels associate with systemic lupus erythematosus and apoptosis in Jurkat T lymphocytes and peripheral blood cells

High expression in bacteria and purification of polymorphic mouse interleukin 2 molecules.

Human endogenous retrovirus HERV-Fc1 association with multiple sclerosis susceptibility: a meta-analysis

IFNAR1 and IFNAR2 polymorphisms confer susceptibility to multiple sclerosis but not to interferon-beta treatment response

IL2RA/CD25 gene polymorphisms: uneven association with multiple sclerosis (MS) and type 1 diabetes (T1D).

IL2RA/CD25 polymorphisms contribute to multiple sclerosis susceptibility

Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis

In-vivo and in-vitro analysis of retroviral vectors carrying the N-ras oncogene

Increasing power by using haplotype similarity in a multimarker transmission/disequilibrium test.

Induction of Autoantibodies to Different Interleukin-2 Allotypes

Influence of the LILRA3 Deletion on Multiple Sclerosis Risk: Original Data and Meta-Analysis.

Interaction of PLP with GFP-MAL2 in the human oligodendroglial cell line HOG

Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations

Lack of association between -384 and 114 IL-2 gene polymorphisms and rheumatoid arthritis

MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis

Members 6B and 14 of the TNF receptor superfamily in multiple sclerosis predisposition

Multiple sclerosis association study with theTENR-IL2-IL21region in a Spanish population

Multiple sclerosis risk variant HLA-DRB1*1501 associates with high expression of DRB1 gene in different human populations

OAS1 gene haplotype confers susceptibility to multiple sclerosis.

Polymorphisms in the IL2, IL2RA and IL2RB genes in multiple sclerosis risk

Protein tyrosine phosphatase gene (PTPN22) polymorphism in multiple sclerosis.

Replication of top markers of a genome-wide association study in multiple sclerosis in Spain.

Replication study of 10 genes showing evidence for association with multiple sclerosis: validation of TMEM39A, IL12B and CLBL genes

SP140 regulates the expression of immune-related genes associated with multiple sclerosis and other autoimmune diseases by NF-κB inhibition

STAT3 locus in inflammatory bowel disease and multiple sclerosis susceptibility

Sample reproducibility of genetic association using different multimarker TDTs in genome-wide association studies: characterization and a new approach.

TNFRSF1A polymorphisms rs1800693 and rs4149584 in patients with multiple sclerosis.

Tag-SNP analysis of the GFI1-EVI5-RPL5-FAM69 risk locus for multiple sclerosis

The -174/-597 promoter polymorphisms in the interleukin-6 gene are not associated with susceptibility to multiple sclerosis.

The 1858T PTPN22 gene variant contributes to a genetic risk of type 1 diabetes in a Ukrainian population.

The C-terminal domain of the Plasmodium falciparum acyl-CoA synthetases PfACS1 and PfACS3 functions as ligand for ankyrin.

The Plasmodium falciparum fatty acyl-CoA synthetase family (PfACS) and differential stage-specific expression in infected erythrocytes

The T244I variant of the interleukin-7 receptor-alpha gene and multiple sclerosis

The autoimmune disease-associated KIF5A, CD226 and SH2B3 gene variants confer susceptibility for multiple sclerosis

The cloning and expression of Pfacs1, a Plasmodium falciparum fatty acyl coenzyme A synthetase-1 targeted to the host erythrocyte cytoplasm

The high producer variant of the Fc-receptor like-3 (FCRL3) gene is involved in protection against multiple sclerosis

The multiple sclerosis-associated regulatory variant rs10877013 affects expression of CYP27B1 and VDR under inflammatory or vitamin D stimuli.

Validation of the CD6 and TNFRSF1A loci as risk factors for multiple sclerosis in Spain.