about
Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosaReporting phenotypes in mouse models when considering body size as a potential confounderCLO: The cell line ontologyGateways to the FANTOM5 promoter level mammalian expression atlasThe International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping dataPhenStat: A Tool Kit for Standardized Analysis of High Throughput Phenotypic Data.Logical development of the cell ontology.Prevalence of sexual dimorphism in mammalian phenotypic traitsHematopoietic cell types: prototype for a revised cell ontologyCD8(+) T cells are not necessary for 1 alpha,25-dihydroxyvitamin D(3) to suppress experimental autoimmune encephalomyelitis in miceA promoter-level mammalian expression atlasAn atlas of active enhancers across human cell types and tissues.Ontology based molecular signatures for immune cell types via gene expression analysisAutism candidate genes via mouse phenomicsThe Cell Ontology 2016: enhanced content, modularization, and ontology interoperability.A mouse informatics platform for phenotypic and translational discovery.Epithelial and mucosal gamma delta T cells.Precision medicine: Look to the mice.Protection against colitis by CD100-dependent modulation of intraepithelial γδ T lymphocyte functionHigh-throughput discovery of novel developmental phenotypes.Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Transcribed enhancers lead waves of coordinated transcription in transitioning mammalian cells.A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.The vitamin D receptor is necessary for 1alpha,25-dihydroxyvitamin D(3) to suppress experimental autoimmune encephalomyelitis in mice.PDX-MI: Minimal Information for Patient-Derived Tumor Xenograft Models.Hypercalcemia produced by parathyroid hormone suppresses experimental autoimmune encephalomyelitis in female but not male mice.Identification of genetic elements in metabolism by high-throughput mouse phenotyping.Corrigendum: High-throughput discovery of novel developmental phenotypes.High-throughput mouse phenomics for characterizing mammalian gene function.Unexplored therapeutic opportunities in the human genome.The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservationPDX Finder: A Portal for Patient-Derived tumor Xenograft Model DiscoveryIdentification of genes required for eye development by high-throughput screening of mouse knockoutsPDX Finder: A portal for patient-derived tumor xenograft model discoveryUnexplored therapeutic opportunities in the human genomeSoft windowing application to improve analysis of high-throughput phenotyping dataKnow Thy PDX Model
P50
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P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Terrence F Meehan
@ast
Terrence F Meehan
@en
Terrence F Meehan
@es
Terrence F Meehan
@nl
Terrence F Meehan
@sl
type
label
Terrence F Meehan
@ast
Terrence F Meehan
@en
Terrence F Meehan
@es
Terrence F Meehan
@nl
Terrence F Meehan
@sl
altLabel
Terrence Meehan
@en
prefLabel
Terrence F Meehan
@ast
Terrence F Meehan
@en
Terrence F Meehan
@es
Terrence F Meehan
@nl
Terrence F Meehan
@sl
P106
P214
3153833207464332808
P2456
P31
P496
0000-0003-1980-3228