UCP2 and mitochondrial haplogroups as a multiple sclerosis risk factor

No abstract is available for this paper.

• Publication year

  2007

• Venue

  Multiple Sclerosis

• Publication date

  2007-02-09

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1177/1352458506070454PMID 17463068
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Multiple Sclerosis Severity Score: Using disability and disease duration to rate disease severity

  2005cited by this paper
• Association of a common polymorphism in the promoter of UCP2 with susceptibility to multiple sclerosis

  2005cited by this paper
• Mapping gene activity in complex disorders: Integration of expression and genomic scans for multiple sclerosis.

  2005cited by this paper
• Genomics and new targets for multiple sclerosis.

  2005cited by this paper
• Mitochondrial haplogroups in Basque multiple sclerosis patients

  2004cited by this paper
• Uncoupling Protein 2 Promoter Polymorphism −866G/A Affects Its Expression in β-Cells and Modulates Clinical Profiles of Japanese Type 2 Diabetic Patients

  2004cited by this paper
• Uncoupling protein 2 promoter polymorphism -866G/A affects its expression in beta-cells and modulates clinical profiles of Japanese type 2 diabetic patients.

  2004cited by this paper
• The multiple sclerosis severity score

  2003cited by this paper
• Uncoupling protein 2 prevents neuronal death including that occurring during seizures: a mechanism for preconditioning.

  2003cited by this paper
• Mitochondrial uncoupling protein 2 in the central nervous system: neuromodulator and neuroprotector.

  2003cited by this paper
• Multiple sclerosis: Genomic rewards

  2001cited by this paper
• Gene expression profiling of the nervous system in murine experimental autoimmune encephalomyelitis.

  2001cited by this paper
• A common polymorphism in the promoter of UCP2 is associated with decreased risk of obesity in middle-aged humans

  2001cited by this paper
• Recommended diagnostic criteria for multiple sclerosis: Guidelines from the international panel on the diagnosis of multiple sclerosis

  2001cited by this paper
• Human mtDNA haplogroups associated with high or reduced spermatozoa motility.

  2000cited by this paper
• Identification of genetic loci controlling the characteristics and severity of brain and spinal cord lesions in experimental allergic encephalomyelitis.

  2000cited by this paper
• Esclerosis múltiple. Análisis clínico retrospectivo y prospectivo de una serie hospitalaria de base poblacional

  2000cited by this paper
• mtDNA haplogroup J: a contributing factor of optic neuritis

  1999cited by this paper
• Human mitochondrial DNA variation and the origin of Basques

  1995cited by this paper
• Principal component analysis of gene frequencies and the origin of Basques.

  1994cited by this paper
• Increased circulation of T lymphocytes bearing surface thymosin α1 in patients with myasthenia gravis

  1983cited by this paper
• Rating neurologic impairment in multiple sclerosis

  1983cited by this paper
• Multiple Sclerosis and Other Demyelinating Diseases

  1970cited by this paper
• Copyright © American Society for Investigative Pathology DOI: 10.2353/ajpath.2006.051069 Immunopathology and Infectious Diseases Uncoupling Protein 2 Has Protective Function during

  year unknowncited by this paper

• The review of the relationship between UCP2 and obesity: Focusing on inflammatory-obesity

  2021cites this paper
• Risk of Multiple Sclerosis: Analysis of Interactions between Variants of Nuclear and Mitochondrial Genomes

  2021cites this paper
• The effects of glucose and fructose on body weight and some biochemical parameters in rats

  2018cites this paper
• UCP2 up-regulation within the course of autoimmune encephalomyelitis correlates with T-lymphocyte activation.

  2017cites this paper
• Estudio de regiones génicas relacionadas con el estrés oxidativo: papel en la artrosis

  2017cites this paper
• UCP2 866 G/A gene (rs659366) polymorphism associated with diabetes type 2 in Turkish population

  2017cites this paper
• Common UCP2 variants contribute to serum urate concentrations and the risk of hyperuricemia

  2016cites this paper
• Neurogenetic Disorders in the Basque Population

  2015cites this paper
• Transcriptional analysis of the glial cell differentiation in the diseased and normal central nervous system

  2015cites this paper
• Tumor necrosis factor-α impairs oligodendroglial differentiation through a mitochondria-dependent process

  2014cites this paper
• Transcriptomic Meta-Analysis of Multiple Sclerosis and Its Experimental Models

  2014cites this paper
• Stressed cybrids model demyelinated axons in multiple sclerosis

  2013cites this paper
• Proliferation and differentiation of osteoblasts from the mandible of osteoporotic rats

  2012cites this paper
• Association of the UCP2 45-bp insertion/deletion polymorphism with diabetes type 2 and obesity in Saudi population

  2012cites this paper
• Multiple sclerosis as a polygenic disease: An update

  2010cites this paper
• Uncoupling protein 2 polymorphisms as risk factors for NTDs.

  2009cites this paper
• Association between synapsin III gene promoter SNPs and multiple sclerosis in Basque patients

  2009cites this paper
• A Homozygous Genetic Variant of Mitochondrial Uncoupling Protein 4 Exerts Protection Against the Occurrence of Multiple Sclerosis

  2009cites this paper
• Enhanced levels of mitochondrial enzyme 17beta-hydroxysteroid dehydrogenase type 10 in patients with Alzheimer disease and multiple sclerosis.

  2009cites this paper
• Mitochondrial DNA sequence variation and neurodegeneration

  2008influential citation
• The use of a genetic strategy to study the role of modulation of oxidative stress by uncoupling proteins 2 and 3 in the pathogenesis of Type 2 Diabetes.

  2008cites this paper
• Influence of CCR5-Delta32 genotype in Spanish population with multiple sclerosis.

  2007cites this paper
• Influence of CCR5-Δ32 genotype in Spanish population with multiple sclerosis

  2007cites this paper