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Innovations in phenotyping of mouse models in the German Mouse Clinic.

Innovations in phenotyping of mouse models in the German Mouse Clinic.

http://www.wikidata.org/entity/Q30485660

about

Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes INFRAFRONTIER: a European resource for studying the functional basis of human disease Viable Ednra Y129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation Generation and Standardized, Systemic Phenotypic Analysis of Pou3f3L423P Mutant Mice A robust and reliable non-invasive test for stress responsivity in mice.Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice.Peroxidasin is essential for eye development in the mouse Novel small-eye allele in paired box gene 6 (Pax6) is caused by a point mutation in intron 7 and creates a new exon.Longitudinal fundus and retinal studies with SD-OCT: a comparison of five mouse inbred strains.Long-term experiment to study the development, interaction, and influencing factors of DEXA parameters.Standardized, systemic phenotypic analysis of Umod(C93F) and Umod(A227T) mutant mice.Cox4i2, Ifit2, and Prdm11 Mutant Mice: Effective Selection of Genes Predisposing to an Altered Airway Inflammatory Response from a Large Compendium of Mutant Mouse Lines.Network Modules of the Cross-Species Genotype-Phenotype Map Reflect the Clinical Severity of Human Diseases High-throughput screening of mouse gene knockouts identifies established and novel skeletal phenotypes.Discovery and characterization of spontaneous mouse models of craniofacial dysmorphology.Clinical Chemistry Reference Intervals for C57BL/6J, C57BL/6N, and C3HeB/FeJ Mice (Mus musculus)Phenotypic comparison of common mouse strains developing high-fat diet-induced hepatosteatosis.Retinal proteome alterations in a mouse model of type 2 diabetes.The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations.Chromosome substitution strains: gene discovery, functional analysis, and systems studies.Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 I27N mutant mice.Endothelial amine oxidase AOC3 transiently contributes to adaptive immune responses in the airways.Defective immuno- and thymoproteasome assembly causes severe immunodeficiency.Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising data.

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P2860

Innovations in phenotyping of mouse models in the German Mouse Clinic.

http://www.wikidata.org/entity/Q30485660

description

2012 nî lūn-bûn

@nan

2012 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի օգոստոսին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

Innovations in phenotyping of mouse models in the German Mouse Clinic.

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Innovations in phenotyping of mouse models in the German Mouse Clinic.

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Innovations in phenotyping of mouse models in the German Mouse Clinic.

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Innovations in phenotyping of mouse models in the German Mouse Clinic.

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Innovations in phenotyping of mouse models in the German Mouse Clinic.

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Innovations in phenotyping of mouse models in the German Mouse Clinic.

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Mammalian Genome

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Innovations in phenotyping of mouse models in the German Mouse Clinic.

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Alexander Götz

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Alexandra M Vernaleken

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Andreas Zimmer

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Anja Hurt

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Anja Schrewe

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Anna Dewert

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Annemarie Wolff-Muscate

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Barbara Fridrich

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Beatrix Naton

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Birgit Rathkolb

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P2860

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits

Neural basis of an inherited speech and language disorder.

Post-stroke inhibition of induced NADPH oxidase type 4 prevents oxidative stress and neurodegeneration

Murine missing in metastasis (MIM) mediates cell polarity and regulates the motility response to growth factors

A forkhead-domain gene is mutated in a severe speech and language disorder

Missing-in-metastasis MIM/MTSS1 promotes actin assembly at intercellular junctions and is required for integrity of kidney epithelia

Loss of the actin remodeler Eps8 causes intestinal defects and improved metabolic status in mice

A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice

Mouse phenotyping.

MausDB: an open source application for phenotype data and mouse colony management in large-scale mouse phenotyping projects.

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9-10

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23

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Martin Klingenspor

Martin Hrabě de Angelis

Valérie Gailus-Durner

Gabriele Möller

Sabine M. Hölter

Ali Önder Yildirim

Julia Calzada-Wack

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2012-08-29T00:00:00Z

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230748019

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