Lista de obras - Justin P Rubio - Dominio Público Uruguay

A DNA resequencing array for genes involved in Parkinson's disease.

artículo científico publicado en 2012

A YAC contig map of Plasmodium falciparum chromosome 4: characterization of a DNA amplification between two recently separated isolates

scientific article published on 01 March 1995

A conserved sorting-associated protein is mutant in chorea-acanthocytosis

artículo científico publicado en 2001

A genome-wide association study in progressive multiple sclerosis

scientific journal article

A genomewide association study of smoking relapse in four European population-based samples

scientific article published on 01 August 2013

A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis

artículo científico publicado en 2010

An 18-kDa translocator protein (TSPO) polymorphism explains differences in binding affinity of the PET radioligand PBR28

artículo científico publicado en 2012

CD127 immunophenotyping suggests altered CD4+ T cell regulation in primary progressive multiple sclerosis

scientific article published on 11 April 2008

Common variation in the MOG gene influences transcript splicing in humans.

artículo científico publicado en 2010

Current status of the Plasmodium falciparum genome project.

artículo científico publicado en 1996

Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe.

artículo científico publicado en 2012

Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data.

artículo científico publicado en 2005

Effects of enzyme inducers efavirenz and tipranavir/ritonavir on the pharmacokinetics of the HIV integrase inhibitor dolutegravir

artículo científico publicado en 2014

Estimation of the Antirelapse Efficacy of Tafenoquine, Using Plasmodium vivax Genotyping.

artículo científico publicado en 2015

Evaluation of the effect of UGT1A1 polymorphisms on dolutegravir pharmacokinetics

artículo científico publicado en 2014

Exome array analysis suggests an increased variant burden in families with schizophrenia.

artículo científico publicado en 2016

Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus.

artículo científico publicado en 2009

Gene expression and genotyping studies implicate the interleukin 7 receptor in the pathogenesis of primary progressive multiple sclerosis

article

Genetic deficiency of plasma lipoprotein-associated phospholipase A2 (PLA2G7 V297F null mutation) and risk of Alzheimer's disease in Japan

artículo científico publicado en 2010

Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis

artículo científico publicado en 2002

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

artículo científico publicado en 2011

Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci

artículo científico publicado en 2011

HLA-DRB1 associations with disease susceptibility and clinical course in Australians with multiple sclerosis.

artículo científico publicado en 2009

Haplotypes of the interleukin 7 receptor alpha gene are correlated with altered expression in whole blood cells in multiple sclerosis.

artículo científico publicado en 2007

Heterogeneity at the HLA-DRB1 allelic variation locus does not influence multiple sclerosis disease severity, brain atrophy or cognition

artículo científico publicado en 2010

Interleukin-2 receptor-α proximal promoter hypomethylation is associated with multiple sclerosis

artículo científico publicado en 2017

Leptin's metabolic and immune functions can be uncoupled at the ligand/receptor interaction level

artículo científico publicado en 2014

Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients

artículo científico publicado en 2010

On the utility of data from the International HapMap Project for Australian association studies.

artículo científico publicado en 2006

Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease

artículo científico publicado en 2007

Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray Studies

artículo científico publicado en 2010

Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism

artículo científico publicado en 2009

Tafenoquine treatment of Plasmodium vivax malaria: suggestive evidence that CYP2D6 reduced metabolism is not associated with relapse in the Phase 2b DETECTIVE trial.

artículo científico publicado en 2016

The ATP-binding cassette (ABC) gene family of Plasmodium falciparum.

artículo científico publicado en 1996

The chorea of McLeod syndrome

artículo científico publicado en 2001

The chromosomal organization of the Plasmodium falciparum var gene family is conserved

scientific article published on 01 July 1997

Validation of linear cerebral atrophy markers in multiple sclerosis

artículo científico publicado en 2008

Variants of ST8SIA1 are associated with risk of developing multiple sclerosis

artículo científico publicado en 2008

Lista de obras de Justin P Rubio

A DNA resequencing array for genes involved in Parkinson's disease.

A YAC contig map of Plasmodium falciparum chromosome 4: characterization of a DNA amplification between two recently separated isolates

A conserved sorting-associated protein is mutant in chorea-acanthocytosis

A genome-wide association study in progressive multiple sclerosis

A genomewide association study of smoking relapse in four European population-based samples

A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis

An 18-kDa translocator protein (TSPO) polymorphism explains differences in binding affinity of the PET radioligand PBR28

CD127 immunophenotyping suggests altered CD4+ T cell regulation in primary progressive multiple sclerosis

Common variation in the MOG gene influences transcript splicing in humans.

Current status of the Plasmodium falciparum genome project.

Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe.

Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data.

Effects of enzyme inducers efavirenz and tipranavir/ritonavir on the pharmacokinetics of the HIV integrase inhibitor dolutegravir

Estimation of the Antirelapse Efficacy of Tafenoquine, Using Plasmodium vivax Genotyping.

Evaluation of the effect of UGT1A1 polymorphisms on dolutegravir pharmacokinetics

Exome array analysis suggests an increased variant burden in families with schizophrenia.

Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus.

Gene expression and genotyping studies implicate the interleukin 7 receptor in the pathogenesis of primary progressive multiple sclerosis

Genetic deficiency of plasma lipoprotein-associated phospholipase A2 (PLA2G7 V297F null mutation) and risk of Alzheimer's disease in Japan

Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci

HLA-DRB1 associations with disease susceptibility and clinical course in Australians with multiple sclerosis.

Haplotypes of the interleukin 7 receptor alpha gene are correlated with altered expression in whole blood cells in multiple sclerosis.

Heterogeneity at the HLA-DRB1 allelic variation locus does not influence multiple sclerosis disease severity, brain atrophy or cognition

Interleukin-2 receptor-α proximal promoter hypomethylation is associated with multiple sclerosis

Leptin's metabolic and immune functions can be uncoupled at the ligand/receptor interaction level

Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients

On the utility of data from the International HapMap Project for Australian association studies.

Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease

Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray Studies

Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism

Tafenoquine treatment of Plasmodium vivax malaria: suggestive evidence that CYP2D6 reduced metabolism is not associated with relapse in the Phase 2b DETECTIVE trial.

The ATP-binding cassette (ABC) gene family of Plasmodium falciparum.

The chorea of McLeod syndrome

The chromosomal organization of the Plasmodium falciparum var gene family is conserved

Validation of linear cerebral atrophy markers in multiple sclerosis

Variants of ST8SIA1 are associated with risk of developing multiple sclerosis