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Mutation in archain 1, a subunit of COPI coatomer complex, causes diluted coat color and Purkinje cell degenerationMice with alopecia, osteoporosis, and systemic amyloidosis due to mutation in Zdhhc13, a gene coding for palmitoyl acyltransferasel7Rn6 encodes a novel protein required for clara cell function in mouse lung developmentMouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics ProjectZfp423 controls proliferation and differentiation of neural precursors in cerebellar vermis formation.A focused and efficient genetic screening strategy in the mouse: identification of mutations that disrupt cortical developmentCongenital heart disease: emerging themes linking genetics and developmentZfp423 Regulates Sonic Hedgehog Signaling via Primary Cilium FunctionHcn1 is a tremorgenic genetic component in a rat model of essential tremorErbb2 is required for cardiac atrial electrical activity during developmentAccelerating aging by mouse reverse genetics: a rational approach to understanding longevityInsertional mutagenesis in mice: new perspectives and toolsA point mutation in the gene for asparagine-linked glycosylation 10B (Alg10b) causes nonsyndromic hearing impairment in mice (Mus musculus).Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental diseaseMutations in the cofilin partner Aip1/Wdr1 cause autoinflammatory disease and macrothrombocytopeniaMutation of l7Rn3 shows that Odz4 is required for mouse gastrulationDissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen.Analysis of mouse embryonic patterning and morphogenesis by forward geneticsENU mutagenesis reveals that Notchless homolog 1 (Drosophila) affects Cdkn1a and several members of the Wnt pathway during murine pre-implantation developmentEpigenetic integration of the developing brain and faceA suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome.Nur7 is a nonsense mutation in the mouse aspartoacylase gene that causes spongy degeneration of the CNSA mouse chromosome 4 balancer ENU-mutagenesis screen isolates eleven lethal lines.The ataxia3 mutation in the N-terminal cytoplasmic domain of sodium channel Na(v)1.6 disrupts intracellular traffickingRandom mutagenesis of proximal mouse chromosome 5 uncovers predominantly embryonic lethal mutationsThe Mammalian Phenotype Ontology as a unifying standard for experimental and high-throughput phenotyping dataCorrelation of microsynteny conservation and disease gene distribution in mammalian genomes.Modeling chromosomes in mouse to explore the function of genes, genomic disorders, and chromosomal organizationGene mutations and genomic rearrangements in the mouse as a result of transposon mobilization from chromosomal concatemersRegional variation in the density of essential genes in mice.The expanding role of mouse genetics for understanding human biology and diseaseDiscovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxin.Suppressor screen in Mpl-/- mice: c-Myb mutation causes supraphysiological production of platelets in the absence of thrombopoietin signaling.Genotype, phenotype, and karyotype correlation in the XO mouse model of Turner Syndrome.Modifier screens in the mouse: time to move forward with reverse genetics.N-ethyl-N-nitrosourea mutagenesis: boarding the mouse mutant express.Lampe1: an ENU-germline mutation causing spontaneous hepatosteatosis identified through targeted exon-enrichment and next-generation sequencing.ENU Mutagenesis in the Mouse.Genome-wide identification of mouse congenital heart disease loci.Sleeping Beauty transposon mutagenesis in rat spermatogonial stem cells.
P2860
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P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
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
Functional genetic analysis of mouse chromosome 11
@ast
Functional genetic analysis of mouse chromosome 11
@en
Functional genetic analysis of mouse chromosome 11
@nl
type
label
Functional genetic analysis of mouse chromosome 11
@ast
Functional genetic analysis of mouse chromosome 11
@en
Functional genetic analysis of mouse chromosome 11
@nl
prefLabel
Functional genetic analysis of mouse chromosome 11
@ast
Functional genetic analysis of mouse chromosome 11
@en
Functional genetic analysis of mouse chromosome 11
@nl
P2093
P50
P3181
P356
P1433
P1476
Functional genetic analysis of mouse chromosome 11
@en
P2093
Allan Bradley
Amander T Clark
Andrew P Salinger
David W Stockton
Hisashi Nakamura
Kathryn E Hentges
Monica J Justice
Randy L Johnson
Richard R Behringer
P2888
P3181
P356
10.1038/NATURE01865
P407
P577
2003-09-04T00:00:00Z
P6179
1022433087