(Q56112201)

1

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David R Booth

2

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Bruce H Bennetts

3

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Robert N S Heard

4

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Graeme J Stewart

European Journal of Human Genetics

6

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publication date

27 April 2005

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published in

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volume

13

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issue

7

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page(s)

815-822

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cites work

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B-lymphocyte alloantigens associated with multiple sclerosis

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HLA-DR, -DQA1 and -DQB1 associations in Australian multiple sclerosis patients

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Nitric oxide and the immune response

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Activation of the inducible form of nitric oxide synthase in the brains of patients with multiple sclerosis

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Inducible nitric oxide synthase in chronic active multiple sclerosis plaques: distribution, cellular expression and association with myelin damage

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Our shifting understanding of the role of nitric oxide in autoimmune encephalomyelitis: a review

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Genome-wide TDT analysis in a localized population with a high prevalence of multiple sclerosis indicates the importance of a region on chromosome 14q.

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Updated results of the United Kingdom linkage-based genome screen in multiple sclerosis

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Genomewide scan of multiple sclerosis in Finnish multiplex families

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A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

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A whole genome screen for linkage disequilibrium in multiple sclerosis confirms disease associations with regions previously linked to susceptibility

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An extended genome scan in 442 Canadian multiple sclerosis-affected sibships: a report from the Canadian Collaborative Study Group

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Cytokine-mediated transcriptional induction of the human inducible nitric oxide synthase gene requires both activator protein 1 and nuclear factor kappaB-binding sites

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Binding of the transcription factor interferon regulatory factor-1 to the inducible nitric-oxide synthase promoter

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Association of a functional inducible nitric oxide synthase promoter variant with complications in type 2 diabetes

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Inducible nitric oxide synthase gene (NOS2A) haplotypes and the outcome of hepatitis C virus infection

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The CCTTT polymorphism in the NOS2A gene is associated with dementia with Lewy bodies.

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Haplotypic relationship between SNP and microsatellite markers at the NOS2A locus in two populations

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New diagnostic criteria for multiple sclerosis: guidelines for research protocols

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Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools.

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Single nucleotide polymorphism--disease relationships: statistical issues for the performance of association studies

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Functional analysis of human promoter polymorphisms.

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TRANSFAC: an integrated system for gene expression regulation

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Nitric oxide is a potential down-regulating molecule in autoimmune disease: inhibition of nitric oxide production renders PVG rats highly susceptible to EAE.

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Prevention of experimental allergic encephalomyelitis by targeting nitric oxide and peroxynitrite: implications for the treatment of multiple sclerosis

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Inhibition of nitric oxide synthase initiates relapsing remitting experimental autoimmune encephalomyelitis in rats, yet nitric oxide appears to be essential for clinical expression of disease

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A dichotomous role for nitric oxide during acute Toxoplasma gondii infection in mice

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Haplotype tagging for the identification of common disease genes

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Genetic Analysis of Multiple Sclerosis in Europeans

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7 January 2021

Multiple sclerosis, multiple genes

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7 January 2021

Nitric oxide as a secretory product of mammalian cells

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7 January 2021

Nitric oxide metabolite determinations reveal continuous inflammation in multiple sclerosis

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7 January 2021

Nucleotide and haplotypic diversity of the NOS2A promoter region and its relationship to cerebral malaria

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7 January 2021

No linkage or association of the nitric oxide synthase genes to multiple sclerosis

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7 January 2021

No association of inducible nitric oxide synthase gene ( NOS2A ) to multiple sclerosis

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7 January 2021

Detection of single-nucleotide polymorphisms with the WAVE DNA fragment analysis system

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7 January 2021

A genome-wide screen for linkage disequilibrium in Australian HLA-DRB1*1501 positive multiple sclerosis patients

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7 January 2021

Mice with an inactivation of the inducible nitric oxide synthase gene are susceptible to experimental autoimmune encephalomyelitis

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7 January 2021

A novel nitric oxide scavenger in combination with cyclosporine A ameliorates experimental autoimmune encephalomyelitis progression in mice

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7 January 2021

Inducible nitric oxide synthase gene expression and enzyme activity correlate with disease activity in murine experimental autoimmune encephalomyelitis

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7 January 2021

Expression of the inducible isoform of nitric oxide synthase in the central nervous system of mice correlates with the severity of actively induced experimental allergic encephalomyelitis

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201422

7 January 2021

Aminoguanidine, a selective inhibitor of the inducible nitric oxide synthase, has different effects on experimental allergic encephalomyelitis in the induction and progression phase

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7 January 2021