Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics - Wikidata - wikimedia - TriplyDB

Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics

Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics

http://www.wikidata.org/entity/Q30389888

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Integrating Genomic Data Sets for Knowledge Discovery: An Informed Approach to Management of Captive Endangered Species INFRAFRONTIER: a European resource for studying the functional basis of human disease Rapid phenotyping of knockout mice to identify genetic determinants of bone strength The flora phenotype ontology (FLOPO): tool for integrating morphological traits and phenotypes of vascular plants Prevalence of sexual dimorphism in mammalian phenotypic traits Systematic screening for skin, hair, and nail abnormalities in a large-scale knockout mouse program.Aneuploidy screening of embryonic stem cell clones by metaphase karyotyping and droplet digital polymerase chain reaction.Progressive neurologic and somatic disease in a novel mouse model of human mucopolysaccharidosis type IIIC.Translational plasticity facilitates the accumulation of nonsense genetic variants in the human population.The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations.High-throughput discovery of novel developmental phenotypes.Mouse Genome Informatics (MGI) Resource: Genetic, Genomic, and Biological Knowledgebase for the Laboratory Mouse.Addressing reproducibility in single-laboratory phenotyping experiments.Opportunities and challenges in modeling human brain disorders in transgenic primates.A staging system for correct phenotype interpretation of mouse embryos harvested on embryonic day 14 (E14.5).Network-Guided Key Gene Discovery for a Given Cellular Process.How mice are indispensable for understanding obesity and diabetes genetics.A bioimage informatics platform for high-throughput embryo phenotyping.From Peas to Disease: Modifier Genes, Network Resilience, and the Genetics of Health.Modeling human disease in rodents by CRISPR/Cas9 genome editing.Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis.Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Genetic differential calculus.Genetic Background Limits Generalizability of Genotype-Phenotype Relationships.A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.Adipocyte glucocorticoid receptor is important in lipolysis and insulin resistance due to exogenous steroids, but not insulin resistance caused by high fat feeding Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.Emerging and evolving concepts in gene essentiality.Identification of genetic elements in metabolism by high-throughput mouse phenotyping.Do Gametes Woo? Evidence for Their Nonrandom Union at Fertilization.Probability of phenotypically detectable protein damage by ENU-induced mutations in the Mutagenetix database.Fluorescent nanodiamond tracking reveals intraneuronal transport abnormalities induced by brain-disease-related genetic risk factors.Reproducibility and replicability of rodent phenotyping in preclinical studies Mouse phenotyping sheds light on rare disease.Assessing mouse behaviour throughout the light/dark cycle using automated in-cage analysis tools.Seh1 targets GATOR2 and Nup153 to mitotic chromosomes.Placentation defects are highly prevalent in embryonic lethal mouse mutants.Guidelines on severity assessment and classification of genetically altered mouse and rat lines.Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutants.OligoPVP: Phenotype-driven analysis of individual genomic information to prioritize oligogenic disease variants

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P2860

Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics

http://www.wikidata.org/entity/Q30389888

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2015 nî lūn-bûn

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2015 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2015 թվականի հուլիսին հրատարակված գիտական հոդված

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2015年の論文

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Nature Genetics

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Alain Guimond

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Alexander Götz

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Ali Önder Yildirim

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Aline Lux

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André Dierich

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P2860

Understanding mammalian genetic systems: the challenge of phenotyping in the mouse

Rapid-throughput skeletal phenotyping of 100 knockout mice identifies 9 new genes that determine bone strength

A conditional knockout resource for the genome-wide study of mouse gene function

GWAS Central: a comprehensive resource for the comparison and interrogation of genome-wide association studies

Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes

Towards an encyclopaedia of mammalian gene function: the International Mouse Phenotyping Consortium

EuroPhenome: a repository for high-throughput mouse phenotyping data

EuroPhenome and EMPReSS: online mouse phenotyping resource

Applying the ARRIVE Guidelines to an In Vivo Database

Measuring inconsistency in meta-analyses

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10.1038/NG.3360

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Martin Klingenspor

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Martin Hrabě de Angelis

Robert Hoehndorf

Patrick M. Nolan

John M. Hancock

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2015-07-27T00:00:00Z

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