Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse. - Wikidata - awgldk - TriplyDB

Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

http://www.wikidata.org/entity/Q34483116

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Cholesterol metabolism is required for intracellular hedgehog signal transduction in vivo The Spontaneous Ataxic Mouse Mutant Tippy is Characterized by a Novel Purkinje Cell Morphogenesis and Degeneration Phenotype.Conserved role of unc-79 in ethanol responses in lightweight mutant mice THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia The IFT-A complex regulates Shh signaling through cilia structure and membrane protein trafficking A novel murine allele of Intraflagellar Transport Protein 172 causes a syndrome including VACTERL-like features with hydrocephalus Lethal skeletal dysplasia in mice and humans lacking the golgin GMAP-210 TRIM28 is required by the mouse KRAB domain protein ZFP568 to control convergent extension and morphogenesis of extra-embryonic tissues Identification of three loci affecting HDL-cholesterol levels in a screen for chemically induced recessive mutations in mice Primary ciliary dyskinesia in mice lacking the novel ciliary protein Pcdp1.Mouse Kif7/Costal2 is a cilia-associated protein that regulates Sonic hedgehog signaling Large-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous system Genetic variation and population substructure in outbred CD-1 mice: implications for genome-wide association studies A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux type Male hypogonadism and germ cell loss caused by a mutation in Polo-like kinase 4.A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype.A high-resolution association mapping panel for the dissection of complex traits in mice Genetic suppression of the circadian Clock mutation by the melatonin biosynthesis pathway Binary trait mapping in experimental crosses with selective genotyping.A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome.Concurrent Lpin1 and Nrcam mouse mutations result in severe peripheral neuropathy with transitory hindlimb paralysis.Confirmation of an epilepsy modifier locus on mouse chromosome 11 and candidate gene analysis by RNA-Seq.A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse.ESCRT-II/Vps25 constrains digit number by endosome-mediated selective modulation of FGF-SHH signaling.A high-resolution single nucleotide polymorphism genetic map of the mouse genome Enhancing genetic mapping of complex genomes through the design of highly-multiplexed SNP arrays: application to the large and unsequenced genomes of white spruce and black spruce Hypersensitivity of primordial germ cells to compromised replication-associated DNA repair involves ATM-p53-p21 signaling ENU Mutagenesis in the Mouse.Fine mapping in 94 inbred mouse strains using a high-density haplotype resource.Genome-wide identification of mouse congenital heart disease loci.Genetic interactions between chromosomes 11 and 18 contribute to airway hyperresponsiveness in mice A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosis A forward genetic screen in mice identifies mutants with abnormal cortical patterning.Angiogenesis QTL on Mouse Chromosome 8 Colocalizes with Differential β-Defensin Expression.De novo exon duplication in a new allele of mouse Glra1 (spasmodic)174delG mutation in mouse MFRP causes photoreceptor degeneration and RPE atrophy.Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse.Variant mapping and mutation discovery in inbred mice using next-generation sequencing Interleukin 22 is a candidate gene for Tmevp3, a locus controlling Theiler's virus-induced neurological diseases ENU mutagenesis in mice identifies candidate genes for hypogonadism

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Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

http://www.wikidata.org/entity/Q34483116

description

2006 nî lūn-bûn

@nan

2006 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2006年の論文

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2006年論文

@yue

2006年論文

@zh-hant

2006年論文

@zh-hk

2006年論文

@zh-mo

2006年論文

@zh-tw

2006年论文

@wuu

name

Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

@ast

Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

@en

Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

@nl

type

label

Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

@ast

Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

@en

Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

@nl

prefLabel

Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

@ast

Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

@en

Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

@nl

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Genome Research

P1476

Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

@en

P2093

Alison Brown

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

Andrew D Bolton

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

Bryan C Bjork

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

Cheng Li

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

Danielle K Manning

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

David J Kwiatkowski

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David R Beier

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Kate Montgomery

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

Martha Hotz Vitaterna

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Noelle D Dwyer

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P2860

Use of a dense single nucleotide polymorphism map for in silico mapping in the mouse

Genome-wide linkage identifies novel modifier loci of aganglionosis in the Sox10Dom model of Hirschsprung disease

Role of insulin-like growth factors in embryonic and postnatal growth

dChipSNP: significance curve and clustering of SNP-array-based loss-of-heterozygosity data.

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

Structure and expression of the hairless gene of mice.

An efficient SNP system for mouse genome scanning and elucidating strain relationships.

In silico genetics: identification of a functional element regulating H2-Ealpha gene expression.

Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis.

MGD: the Mouse Genome Database

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436-440

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scholarly article

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10.1101/GR.4563306

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3

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16

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Jennifer L. Moran

Joseph S. Takahashi

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2006-02-03T00:00:00Z

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7311980

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16461637

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1415208

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