about
Robust and sensitive analysis of mouse knockout phenotypesA common control group - optimising the experiment design to maximise sensitivityGenome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genesOptimising experimental design for high-throughput phenotyping in mice: a case studyMouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics ProjectReporting phenotypes in mouse models when considering body size as a potential confounderApplying the ARRIVE Guidelines to an In Vivo DatabaseHistopathology reveals correlative and unique phenotypes in a high-throughput mouse phenotyping screenAnalysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinicsThe International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping dataA gene expression resource generated by genome-wide lacZ profiling in the mouse.PhenStat: A Tool Kit for Standardized Analysis of High Throughput Phenotypic Data.Recommendations for minimum information for publication of experimental pathology data: MINPEPA guidelines.Protein profiling of human postmortem brain using 2-dimensional fluorescence difference gel electrophoresis (2-D DIGE).Identification of clock genes using difference gel electrophoresis.The role of sex and body weight on the metabolic effects of high-fat diet in C57BL/6N micePrevalence of sexual dimorphism in mammalian phenotypic traitsThe fallacy of ratio correction to address confounding factors.Impact of temporal variation on design and analysis of mouse knockout phenotyping studiesDisruption of the potassium channel regulatory subunit KCNE2 causes iron-deficient anemia.Targeting of Slc25a21 is associated with orofacial defects and otitis media due to disrupted expression of a neighbouring gene.Experimental and husbandry procedures as potential modifiers of the results of phenotyping testsA mouse informatics platform for phenotypic and translational discovery.Deficiency for the ubiquitin ligase UBE3B in a blepharophimosis-ptosis-intellectual-disability syndrome.A high-throughput in vivo micronucleus assay for genome instability screening in miceHigh-fat feeding rapidly induces obesity and lipid derangements in C57BL/6N mice.Design and analysis issues in quantitative proteomics studies.Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole-body energy expenditureStandardized Welfare Terms for the Zebrafish CommunityImproving the Identification of Phenotypic Abnormalities and Sexual Dimorphism in Mice When Studying Rare Event Categorical Characteristics.Analysis of calibration methodologies for solvent effects in drug discovery studies using evanescent wave biosensors.Genome-wide in vivo screen identifies novel host regulators of metastatic colonization.IL-18 associated with lung lymphoid aggregates drives IFNγ production in severe COPD.Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Automated recording of home cage activity and temperature of individual rats housed in social groups: The Rodent Big Brother project.Evaluating and Optimizing Fish Health and Welfare During Experimental Procedures.A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.Addressing accuracy and precision issues in iTRAQ quantitation.The Experimental Design Assistant.Proteomic analysis reveals the role of synaptic vesicle cycling in sustaining the suprachiasmatic circadian clock.
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description
hulumtuese
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researcher
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հետազոտող
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name
Natasha A Karp
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Natasha A Karp
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Natasha A Karp
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Natasha A Karp
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Natasha Karp
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type
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Natasha A Karp
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Natasha A Karp
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Natasha A Karp
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Natasha A Karp
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Natasha Karp
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Natasha A Karp
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Natasha A Karp
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Natasha A Karp
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Natasha A Karp
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Natasha Karp
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P106
P21
P31
P496
0000-0002-8404-2907