Modifier genes and protective alleles in humans and mice.
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Chipping away at 'stemness'Cartilage-specific deletion of ephrin-B2 in mice results in early developmental defects and an osteoarthritis-like phenotype during aging in vivo.Embryonic fibroblasts from mice lacking Tgif were defective in cell cyclingLamin b1 polymorphism influences morphology of the nuclear envelope, cell cycle progression, and risk of neural tube defects in miceSystematic behavioral evaluation of Huntington's disease transgenic and knock-in mouse models.Overexpression of ALS-associated p.M337V human TDP-43 in mice worsens disease features compared to wild-type human TDP-43 mice.A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death.A pipeline combining multiple strategies for prioritizing heterozygous variants for the identification of candidate genes in exome datasetsInvolvement of the modifier gene of a human Mendelian disorder in a negative selection process.Strain background effects and genetic modifiers of hearing in mice.Mouse genetic background influences the dental phenotype.Epistatic Networks Jointly Influence Phenotypes Related to Metabolic Disease and Gene Expression in Diversity Outbred Mice.Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes.QTL analysis identifies a modifier locus of aganglionosis in the rat model of Hirschsprung disease carrying Ednrb(sl) mutations.Discovery Genetics - The History and Future of Spontaneous Mutation Research.Frequent phosphodiesterase 11A gene (PDE11A) defects in patients with Carney complex (CNC) caused by PRKAR1A mutations: PDE11A may contribute to adrenal and testicular tumors in CNC as a modifier of the phenotype.Allelic variation, aneuploidy, and nongenetic mechanisms suppress a monogenic trait in yeast.The conditional nature of genetic interactions: the consequences of wild-type backgrounds on mutational interactions in a genome-wide modifier screenTechnical approaches for mouse models of human diseaseGenome-wide linkage analysis to identify genetic modifiers of ALK mutation penetrance in familial neuroblastoma.Identification of genetic loci affecting the severity of symptoms of Hirschsprung disease in rats carrying Ednrbsl mutations by quantitative trait locus analysis.Modifier genes and non-genetic factors reshape anatomical deficits in Zfp423-deficient mice.Contrasting genetic architectures in different mouse reference populations used for studying complex traits.Exome Sequencing Identifies a Novel LMNA Splice-Site Mutation and Multigenic Heterozygosity of Potential Modifiers in a Family with Sick Sinus Syndrome, Dilated Cardiomyopathy, and Sudden Cardiac DeathQTL analysis of modifiers for pigmentary disorder in rats carrying Ednrb sl mutations.Genetic modification of the schisis phenotype in a mouse model of X-linked retinoschisisCandidate genetic modifiers of retinitis pigmentosa identified by exploiting natural variation in DrosophilaGenetic factors modifying clinical expression of autosomal dominant RP.Strategies for assessment of botanical action on metabolic syndrome in the mouse and evidence for a genotype-specific effect of Russian tarragon in the regulation of insulin sensitivity.Genetic regulation of plasma von Willebrand factor levels: quantitative trait loci analysis in a mouse model.Genomic consequences of background effects on scalloped mutant expressivity in the wing of Drosophila melanogaster.Independent effects of genetic variations in mannose-binding lectin influence the course of HIV disease: the advantage of heterozygosity for coding mutations.Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.CCL3L1 gene-containing segmental duplications and polymorphisms in CCR5 affect risk of systemic lupus erythaematosus.Next-generation sequencing of vertebrate experimental organisms.Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophyProstate cancer: from the pathophysiologic implications of some genetic risk factors to translation in personalized cancer treatments.Cadherins mediate sequential roles through a hierarchy of mechanisms in the developing mammillary body.ATM and the DNA damage response. Workshop on ataxia-telangiectasia and related syndromes.Systematic genetics swims forward elegantly.
P2860
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P2860
Modifier genes and protective alleles in humans and mice.
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունիսին 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
Modifier genes and protective alleles in humans and mice.
@ast
Modifier genes and protective alleles in humans and mice.
@en
type
label
Modifier genes and protective alleles in humans and mice.
@ast
Modifier genes and protective alleles in humans and mice.
@en
prefLabel
Modifier genes and protective alleles in humans and mice.
@ast
Modifier genes and protective alleles in humans and mice.
@en
P1476
Modifier genes and protective alleles in humans and mice.
@en
P2093
Joseph H Nadeau
P304
P356
10.1016/S0959-437X(03)00061-3
P577
2003-06-01T00:00:00Z