Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse - Wikidata - wikimedia - TriplyDB

Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

http://www.wikidata.org/entity/Q34869723

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SNP discovery via 454 transcriptome sequencing The mouse genome sequence--the end of the tail, or just the beginning?Use of a dense single nucleotide polymorphism map for in silico mapping in the mouse ARTS: a web-based tool for the set-up of high-throughput genome-wide mapping panels for the SNP genotyping of mouse mutants.Construction and characterization of a genomic BAC library for the Mus m. musculus mouse subspecies (PWD/Ph inbred strain).Comparative analysis of haplotype association mapping algorithms Host susceptibility to malaria in human and mice: compatible approaches to identify potential resistant genes Mst1 directs Myosin IIa partitioning of low and higher affinity integrins during T cell migration A high-resolution map of segmental DNA copy number variation in the mouse genome The Genetic Architecture of Hearing Impairment in Mice: Evidence for Frequency-Specific Genetic Determinants Phylometabonomic patterns of adaptation to high fat diet feeding in inbred mice Progressive Hearing Loss in Mice Carrying a Mutation in Usp53.Evidence that Cd101 is an autoimmune diabetes gene in nonobese diabetic mice Inositol (1,4,5) trisphosphate 3 kinase B controls positive selection of T cells and modulates Erk activity Identification of three loci affecting HDL-cholesterol levels in a screen for chemically induced recessive mutations in mice Alleles that modulate late life hearing in genetically heterogeneous mice Multivariate analyses reveal common and drug-specific genetic influences on responses to four drugs of abuse.A novel allele of myosin VIIa reveals a critical function for the C-terminal FERM domain for melanosome transport in retinal pigment epithelial cells.A major QTL on chromosome 11 influences psychostimulant and opioid sensitivity in mice Combining data from multiple inbred line crosses improves the power and resolution of quantitative trait loci mapping.Integrating genetic and gene expression data: application to cardiovascular and metabolic traits in mice.Contribution of Asian mouse subspecies Mus musculus molossinus to genomic constitution of strain C57BL/6J, as defined by BAC-end sequence-SNP analysis Complex haplotypes, copy number polymorphisms and coding variation in two recently divergent mouse strains.Sipa1 is a candidate for underlying the metastasis efficiency modifier locus Mtes1.A high-resolution single nucleotide polymorphism genetic map of the mouse genome Mouse SNP Miner: an annotated database of mouse functional single nucleotide polymorphisms.Genome-wide association study for age-related hearing loss (AHL) in the mouse: a meta-analysis A point mutation in Sec61alpha1 leads to diabetes and hepatosteatosis in mice.A simple, bead-based approach for multi-SNP molecular haplotyping Cis-acting expression quantitative trait loci in mice.A high-resolution multistrain haplotype analysis of laboratory mouse genome reveals three distinctive genetic variation patterns.Mapping segmental and sequence variations among laboratory mice using BAC array CGH.Fine mapping reveals that promotion susceptibility locus 1 (Psl1) is a compound locus with multiple genes that modify susceptibility to skin tumor development Identification of quantitative trait loci for locomotor activation and anxiety using closely related inbred strains.A locus mapping to mouse chromosome 7 determines infarct volume in a mouse model of ischemic stroke Variation in IL-1beta gene expression is a major determinant of genetic differences in arthritis aggressivity in mice Confirmation of multiple seizure susceptibility QTLs on chromosome 15 in C57BL/6J and DBA/2J inbred mice.An evolutionarily conserved role for the aryl hydrocarbon receptor in the regulation of movement.A mutant mouse with a highly specific contextual fear-conditioning deficit found in an N-ethyl-N-nitrosourea (ENU) mutagenesis screen.Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

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Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

http://www.wikidata.org/entity/Q34869723

description

2003 nî lūn-bûn

@nan

2003 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2003年の論文

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2003年論文

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2003年論文

@zh-hant

2003年論文

@zh-hk

2003年論文

@zh-mo

2003年論文

@zh-tw

2003年论文

@wuu

name

Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

@ast

Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

@en

Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

@nl

type

label

Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

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Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

@en

Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

@nl

prefLabel

Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

@ast

Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

@en

Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

@nl

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PNAS.0130101100

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

@en

P2093

Andrey Santrosyan

http://www.w3.org/2001/XMLSchema#string

Colin F Fletcher

http://www.w3.org/2001/XMLSchema#string

Francis Kalush

http://www.w3.org/2001/XMLSchema#string

Hua Wu

http://www.w3.org/2001/XMLSchema#string

Kevin Smylie

http://www.w3.org/2001/XMLSchema#string

Lisa M Tarantino

http://www.w3.org/2001/XMLSchema#string

Mark D Adams

http://www.w3.org/2001/XMLSchema#string

Mathew T Pletcher

http://www.w3.org/2001/XMLSchema#string

Michael P Cooke

http://www.w3.org/2001/XMLSchema#string

Richard J Glynne

http://www.w3.org/2001/XMLSchema#string

P2860

A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity

BLAT--the BLAST-like alignment tool

The structure of haplotype blocks in the human genome

Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex

Linkage disequilibrium in the human genome

The Celera Discovery System.

A YAC-based physical map of the mouse genome.

Map Manager QTX, cross-platform software for genetic mapping.

Genealogies of mouse inbred strains.

A genetic linkage map of the mouse: current applications and future prospects.

P304

3380-3385

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scholarly article

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10.1073/PNAS.0130101100

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P407

P433

6

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100

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Neal G. Copeland

Nancy A. Jenkins

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2003-02-28T00:00:00Z

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10878479

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P698

12612341

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single-nucleotide polymorphism

P932

152301

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