(Q44126855)

30 November 2017

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

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30 November 2017

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1

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30 November 2017

Dominic P. Kwiatkowski

7

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30 November 2017

Rockett K

2

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30 November 2017

Ackerman H

3

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30 November 2017

Hull J

4

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30 November 2017

Usen S

5

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30 November 2017

Pinder M

6

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30 November 2017

1 October 2003

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30 November 2017

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30 November 2017

4

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30 November 2017

506-514

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30 November 2017

7

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https://scigraph.springernature.com/pub.10.1038/sj.gene.6364022

30 November 2017

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The future of genetic studies of complex human diseases

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Linkage disequilibrium and the mapping of complex human traits.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Genetic isolates: separate but equal?

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Chromosome-wide distribution of haplotype blocks and the role of recombination hot spots

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

The structure of linkage disequilibrium at the DBH locus strongly influences the magnitude of association between diallelic markers and plasma dopamine beta-hydroxylase activity

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Nucleotide diversity and haplotype structure of the human angiotensinogen gene in two populations

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

The genetically isolated populations of Finland and Sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Consistent long-range linkage disequilibrium generated by admixture in a Bantu-Semitic hybrid population

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

High-resolution haplotype structure in the human genome

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Linkage disequilibrium between microsatellite markers extends beyond 1 cM on chromosome 20 in Finns

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Transmission of haplotypes of microsatellite markers rather than single marker alleles in the mapping of a putative type 1 diabetes susceptibility gene (IDDM6)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

The critical region for Behçet disease in the human major histocompatibility complex is reduced to a 46-kb segment centromeric of HLA-B, by association analysis using refined microsatellite mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

IL-12p40 is associated with type 1 diabetes in Caucasian-American families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Association mapping of disease loci, by use of a pooled DNA genomic screen

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Global patterns of linkage disequilibrium at the CD4 locus and modern human origins

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human origins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Nitric oxide and infectious diseases

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Inducible nitric oxide synthase: what difference does it make?

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Nitric oxide: mediator, murderer, and medicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Peroxynitrite: a two-faced metabolite of nitric oxide

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Transcriptional regulation of human inducible nitric oxide synthase (NOS2) gene by cytokines: initial analysis of the human NOS2 promoter

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Multiple NF-kappaB enhancer elements regulate cytokine induction of the human inducible nitric oxide synthase gene

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Polymorphism in promoter region of inducible nitric oxide synthase gene and protection against malaria

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Evolution of a homopurine-homopyrimidine pentanucleotide repeat sequence upstream of the human inducible nitric oxide synthase gene.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Inducible nitric oxide synthase polymorphism and fatal cerebral malaria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

A new NOS2 promoter polymorphism associated with increased nitric oxide production and protection from severe malaria in Tanzanian and Kenyan children

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Characterization of single-nucleotide polymorphisms in coding regions of human genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Using mitochondrial and nuclear DNA markers to reconstruct human evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

High resolution of human evolutionary trees with polymorphic microsatellites

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Genetic traces of ancient demography

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Microsatellite spreading in the human genome: evolutionary mechanisms and structural implications

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Alu repeats: a source for the genesis of primate microsatellites.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Characteristics and frequency of germline mutations at microsatellite loci from the human Y chromosome, as revealed by direct observation in father/son pairs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Relative mutation rates at di-, tri-, and tetranucleotide microsatellite loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Mutation of human short tandem repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Microsatellites: consensus and controversy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Evolutionary relationships of human populations from an analysis of nuclear DNA polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Significant association of longer forms of CCTTT Microsatellite repeat in the inducible nitric oxide synthase promoter with severe malaria in Thailand.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Association of respiratory syncytial virus bronchiolitis with the interleukin 8 gene region in UK families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

IFNGR1 gene promoter polymorphisms and susceptibility to cerebral malaria

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Minisatellite diversity supports a recent African origin for modern humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Haplotype tagging for the identification of common disease genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

Prospects for whole-genome linkage disequilibrium mapping of common disease genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

7 January 2021

Linkage disequilibrium mapping of complex disease: fantasy or reality?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

7 January 2021

A look at linkage disequilibrium

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

7 January 2021

The use of a genetic map of biallelic markers in linkage studies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

7 January 2021

Genotyping and functional analysis of a polymorphic (CCTTT)(n) repeat of NOS2A in diabetic retinopathy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

7 January 2021

(CCTTT)n repeat polymorphism in the NOS2 gene promoter is associated with atopy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

7 January 2021

Characterization and functional analysis of the human inducible nitric oxide synthase gene promoter.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

7 January 2021

Identifiers

DOI

10.1038/SJ.GENE.6364022

1 reference

release_sxlsnvh5tjgl3mz3lukmaecnqm

30 November 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/sxlsnvh5tjgl3mz3lukmaecnqm

24 November 2022

mapped directly with Wikidata item

1 reference