Lista de obras - Elena Sanchez - Dominio Público Uruguay

A 3'-untranslated region variant is associated with impaired expression of CD226 in T and natural killer T cells and is associated with susceptibility to systemic lupus erythematosus.

artículo científico publicado en 2010

Absence of COCH mutations in patients with Meniere disease.

artículo científico publicado en 2004

Allelic heterogeneity in NCF2 associated with systemic lupus erythematosus (SLE) susceptibility across four ethnic populations

artículo científico publicado en 2013

Analysis of a GT microsatellite in the promoter of the foxp3/scurfin gene in autoimmune diseases.

artículo científico publicado en 2005

Analysis of a functional BTNL2 polymorphism in type 1 diabetes, rheumatoid arthritis, and systemic lupus erythematosus.

artículo científico publicado en 2005

Analysis of autosomal genes reveals gene-sex interactions and higher total genetic risk in men with systemic lupus erythematosus

artículo científico publicado en 2011

Analysis of interleukin-23 receptor (IL23R) gene polymorphisms in systemic lupus erythematosus

artículo científico publicado en 2007

Analysis of the functional NFKB1 promoter polymorphism in rheumatoid arthritis and systemic lupus erythematosus.

artículo científico publicado en 2005

Association of a functional inducible nitric oxide synthase promoter variant with susceptibility to biopsy-proven giant cell arteritis.

artículo científico publicado en 2005

Association of a functional single-nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with rheumatoid arthritis and systemic lupus erythematosus

artículo científico publicado en 2005

Association of aCD24 gene polymorphism with susceptibility to systemic lupus erythematosus

article

Association of the CT60 marker of the CTLA4 gene with systemic lupus erythematosus

article

Association study of IRAK-M and SIGIRR genes with SLE in a large European-descent population

article

Association study of genetic variants of pro-inflammatory chemokine and cytokine genes in systemic lupus erythematosus

artículo científico publicado en 2006

Compound heterozygous PNPLA6 mutations cause Boucher-Neuhäuser syndrome with late-onset ataxia

artículo científico publicado en 2014

Early disease onset is predicted by a higher genetic risk for lupus and is associated with a more severe phenotype in lupus patients

artículo científico publicado en 2010

Effects of Amerindian Genetic Ancestry on Clinical Variables and Therapy in Patients with Rheumatoid Arthritis

artículo científico publicado en 2017

Evidence for gene-gene epistatic interactions among susceptibility loci for systemic lupus erythematosus

artículo científico publicado en 2012

Evidence of association of macrophage migration inhibitory factor gene polymorphisms with systemic lupus erythematosus

article

Evidence of new risk genetic factor to systemic lupus erythematosus: the UBASH3A gene.

artículo científico publicado en 2013

Fine mapping of Xq28: both MECP2 and IRAK1 contribute to risk for systemic lupus erythematosus in multiple ancestral groups

artículo científico publicado en 2012

Fine-mapping and transethnic genotyping establish IL2/IL21 genetic association with lupus and localize this genetic effect to IL21

artículo científico publicado en 2011

Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus

artículo científico publicado en 2008

Genetically determined Amerindian ancestry correlates with increased frequency of risk alleles for systemic lupus erythematosus

artículo científico publicado en 2010

Genomic Insights into the Ancestry and Demographic History of South America

artículo científico publicado en 2015

Identification of a Large DNAJB2 Deletion in a Family with Spinal Muscular Atrophy and Parkinsonism.

artículo científico publicado en 2016

Identification of a new putative functional IL18 gene variant through an association study in systemic lupus erythematosus

artículo científico publicado en 2009

Identification of novel genetic susceptibility loci in African American lupus patients in a candidate gene association study

artículo científico publicado en 2011

Impact of genetic ancestry and sociodemographic status on the clinical expression of systemic lupus erythematosus in American Indian-European populations

artículo científico publicado en 2012

Impact of interleukin-18 polymorphisms-607 and -137 on clinical characteristics of renal cell carcinoma patients

scientific article published on 12 January 2010

Inducible but not endothelial nitric oxide synthase polymorphism is associated with susceptibility to rheumatoid arthritis in northwest Spain.

artículo científico publicado en 2004

Inducible nitric oxide synthase promoter polymorphism in human brucellosis

artículo científico publicado en 2003

Interleukin 12 (IL12B), interleukin 12 receptor (IL12RB1) and interleukin 23 (IL23A) gene polymorphism in systemic lupus erythematosus.

artículo científico publicado en 2005

Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease

artículo científico publicado en 2014

Investigating the role of CD24 gene polymorphisms in rheumatoid arthritis

article

MYO9B gene polymorphisms are associated with autoimmune diseases in Spanish population

article

Macrophage migration inhibitory factor gene influences the risk of developing tuberculosis in northwestern Colombian population

article

No evidence for genetic association of interferon regulatory factor 3 in systemic lupus erythematosus.

artículo científico publicado en 2009

No primary association of MICA polymorphism with systemic lupus erythematosus

scientific article published on 14 March 2006

Phenotypic associations of genetic susceptibility loci in systemic lupus erythematosus

artículo científico publicado en 2011

Pla2g6 Deficiency in Zebrafish Leads to Dopaminergic Cell Death, Axonal Degeneration, Increased β-Synuclein Expression, and Defects in Brain Functions and Pathways.

artículo científico publicado en 2018

Polymorphisms of the FCRL3 gene in a Spanish population of systemic lupus erythematosus patients

article

Promoter Insertion/Deletion in the IRF5 Gene Is Highly Associated with Susceptibility to Systemic Lupus Erythematosus in Distinct Populations, But Exerts a Modest Effect on Gene Expression in Peripheral Blood Mononuclear Cells

article

Recent findings on genetics of systemic autoimmune diseases

artículo científico publicado en 2010

Replication of the TNFSF4 (OX40L) promoter region association with systemic lupus erythematosus

artículo científico publicado en 2008

SLC22A4, RUNX1, and SUMO4 polymorphisms are not associated with rheumatoid arthritis: a case-control study in a Spanish population

artículo científico publicado en 2006

SORT1 Mutation Resulting in Sortilin Deficiency and p75(NTR) Upregulation in a Family With Essential Tremor.

artículo científico publicado en 2015

Study of a functional polymorphism in the p53 gene in systemic lupus erythematosus: lack of replication in a Spanish population

artículo científico publicado en 2006

Study of two polymorphisms of the MHC2TA gene with systemic lupus erythematosus

article

The TRAF1-C5 region on chromosome 9q33 is associated with multiple autoimmune diseases.

artículo científico publicado en 2009

Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies

artículo científico publicado en 2019

[Common genetic factors in autoimmunity]

artículo científico publicado en 2008

Lista de obras de Elena Sanchez

A 3'-untranslated region variant is associated with impaired expression of CD226 in T and natural killer T cells and is associated with susceptibility to systemic lupus erythematosus.

Absence of COCH mutations in patients with Meniere disease.

Allelic heterogeneity in NCF2 associated with systemic lupus erythematosus (SLE) susceptibility across four ethnic populations

Analysis of a GT microsatellite in the promoter of the foxp3/scurfin gene in autoimmune diseases.

Analysis of a functional BTNL2 polymorphism in type 1 diabetes, rheumatoid arthritis, and systemic lupus erythematosus.

Analysis of autosomal genes reveals gene-sex interactions and higher total genetic risk in men with systemic lupus erythematosus

Analysis of interleukin-23 receptor (IL23R) gene polymorphisms in systemic lupus erythematosus

Analysis of the functional NFKB1 promoter polymorphism in rheumatoid arthritis and systemic lupus erythematosus.

Association of a functional inducible nitric oxide synthase promoter variant with susceptibility to biopsy-proven giant cell arteritis.

Association of a functional single-nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with rheumatoid arthritis and systemic lupus erythematosus

Association of aCD24 gene polymorphism with susceptibility to systemic lupus erythematosus

Association of the CT60 marker of the CTLA4 gene with systemic lupus erythematosus

Association study of IRAK-M and SIGIRR genes with SLE in a large European-descent population

Association study of genetic variants of pro-inflammatory chemokine and cytokine genes in systemic lupus erythematosus

Compound heterozygous PNPLA6 mutations cause Boucher-Neuhäuser syndrome with late-onset ataxia

Early disease onset is predicted by a higher genetic risk for lupus and is associated with a more severe phenotype in lupus patients

Effects of Amerindian Genetic Ancestry on Clinical Variables and Therapy in Patients with Rheumatoid Arthritis

Evidence for gene-gene epistatic interactions among susceptibility loci for systemic lupus erythematosus

Evidence of association of macrophage migration inhibitory factor gene polymorphisms with systemic lupus erythematosus

Evidence of new risk genetic factor to systemic lupus erythematosus: the UBASH3A gene.

Fine mapping of Xq28: both MECP2 and IRAK1 contribute to risk for systemic lupus erythematosus in multiple ancestral groups

Fine-mapping and transethnic genotyping establish IL2/IL21 genetic association with lupus and localize this genetic effect to IL21

Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus

Genetically determined Amerindian ancestry correlates with increased frequency of risk alleles for systemic lupus erythematosus

Genomic Insights into the Ancestry and Demographic History of South America

Identification of a Large DNAJB2 Deletion in a Family with Spinal Muscular Atrophy and Parkinsonism.

Identification of a new putative functional IL18 gene variant through an association study in systemic lupus erythematosus

Identification of novel genetic susceptibility loci in African American lupus patients in a candidate gene association study

Impact of genetic ancestry and sociodemographic status on the clinical expression of systemic lupus erythematosus in American Indian-European populations

Impact of interleukin-18 polymorphisms-607 and -137 on clinical characteristics of renal cell carcinoma patients

Inducible but not endothelial nitric oxide synthase polymorphism is associated with susceptibility to rheumatoid arthritis in northwest Spain.

Inducible nitric oxide synthase promoter polymorphism in human brucellosis

Interleukin 12 (IL12B), interleukin 12 receptor (IL12RB1) and interleukin 23 (IL23A) gene polymorphism in systemic lupus erythematosus.

Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease

Investigating the role of CD24 gene polymorphisms in rheumatoid arthritis

MYO9B gene polymorphisms are associated with autoimmune diseases in Spanish population

Macrophage migration inhibitory factor gene influences the risk of developing tuberculosis in northwestern Colombian population

No evidence for genetic association of interferon regulatory factor 3 in systemic lupus erythematosus.

No primary association of MICA polymorphism with systemic lupus erythematosus

Phenotypic associations of genetic susceptibility loci in systemic lupus erythematosus

Pla2g6 Deficiency in Zebrafish Leads to Dopaminergic Cell Death, Axonal Degeneration, Increased β-Synuclein Expression, and Defects in Brain Functions and Pathways.

Polymorphisms of the FCRL3 gene in a Spanish population of systemic lupus erythematosus patients

Promoter Insertion/Deletion in the IRF5 Gene Is Highly Associated with Susceptibility to Systemic Lupus Erythematosus in Distinct Populations, But Exerts a Modest Effect on Gene Expression in Peripheral Blood Mononuclear Cells

Recent findings on genetics of systemic autoimmune diseases

Replication of the TNFSF4 (OX40L) promoter region association with systemic lupus erythematosus

SLC22A4, RUNX1, and SUMO4 polymorphisms are not associated with rheumatoid arthritis: a case-control study in a Spanish population

SORT1 Mutation Resulting in Sortilin Deficiency and p75(NTR) Upregulation in a Family With Essential Tremor.

Study of a functional polymorphism in the p53 gene in systemic lupus erythematosus: lack of replication in a Spanish population

Study of two polymorphisms of the MHC2TA gene with systemic lupus erythematosus

The TRAF1-C5 region on chromosome 9q33 is associated with multiple autoimmune diseases.

Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies

[Common genetic factors in autoimmunity]