Pages that link to "Q28584453"
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The following pages link to Mouse Genome Database (MGD)-2017: community knowledge resource for the laboratory mouse (Q28584453):
Displaying 50 items.
- Harnessing public domain data to discover and validate therapeutic targets (Q30491667) (← links)
- Chromosome 1 Sequence Analysis of C57BL/6J-Chr1KM Mouse Strain. (Q33593047) (← links)
- GeMSTONE: orchestrated prioritization of human germline mutations in the cloud (Q36375736) (← links)
- The anatomy of phenotype ontologies: principles, properties and applications. (Q38378393) (← links)
- Implicating candidate genes at GWAS signals by leveraging topologically associating domains. (Q38430106) (← links)
- Gene expression profile data for mouse facial development (Q38601263) (← links)
- HDNetDB: A Molecular Interaction Database for Network-Oriented Investigations into Huntington's Disease. (Q38681978) (← links)
- modPhEA: model organism Phenotype Enrichment Analysis of eukaryotic gene sets (Q38699790) (← links)
- Gene2Function: An Integrated Online Resource for Gene Function Discovery (Q38701582) (← links)
- Naming CRISPR alleles: endonuclease-mediated mutation nomenclature across species (Q38739194) (← links)
- Ancient selection for derived alleles at a GDF5 enhancer influencing human growth and osteoarthritis risk (Q38931465) (← links)
- Large-Scale Identification of Common Trait and Disease Variants Affecting Gene Expression (Q40196315) (← links)
- Genome-wide association study identifies novel type II diabetes risk loci in Jordan subpopulations (Q41463700) (← links)
- Retinal pathology in the PPCD1 mouse (Q42370708) (← links)
- The integration site of the APP transgene in the J20 mouse model of Alzheimer's disease (Q42698634) (← links)
- Improving Metabolic Health Through Precision Dietetics in Mice (Q44877212) (← links)
- Xenbase: a genomic, epigenomic and transcriptomic model organism database. (Q46277313) (← links)
- Chemokine (C-C Motif) Receptor-Like 2 is not essential for lung injury, lung inflammation, or airway hyperresponsiveness induced by acute exposure to ozone (Q47114350) (← links)
- Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders (Q47138547) (← links)
- Single subject transcriptome analysis to identify functionally signed gene set or pathway activity (Q47161997) (← links)
- Mouse Phenome Database: an integrative database and analysis suite for curated empirical phenotype data from laboratory mice (Q47162966) (← links)
- Muscle molecular adaptations to endurance exercise training are conditioned by glycogen availability: a proteomics-based analysis in the McArdle mouse model (Q47176588) (← links)
- Methods for Using Small Non-Coding RNAs to Improve Recombinant Protein Expression in Mammalian Cells (Q47190209) (← links)
- Mouse Genome Database (MGD)-2018: knowledgebase for the laboratory mouse (Q47202657) (← links)
- Membrane Transporters for Bilirubin and Its Conjugates: A Systematic Review. (Q47272832) (← links)
- Integrative Bioinformatic Analysis of Transcriptomic Data Identifies Conserved Molecular Pathways Underlying Ionizing Radiation-Induced Bystander Effects (RIBE). (Q47302181) (← links)
- Construction of developmental lineage relationships in the mouse mammary gland by single-cell RNA profiling. (Q47321523) (← links)
- Knockdown of IARS2 suppressed growth of gastric cancer cells by regulating the phosphorylation of cell cycle-related proteins. (Q47602191) (← links)
- Exocyst Complex Member EXOC5 Is Required for Survival of Hair Cells and Spiral Ganglion Neurons and Maintenance of Hearing. (Q47657398) (← links)
- Defiant: (DMRs: easy, fast, identification and ANnoTation) identifies differentially Methylated regions from iron-deficient rat hippocampus. (Q48104108) (← links)
- Genetic sex determination assays in 53 mammalian species: Literature analysis and guidelines for reporting standardization. (Q48155476) (← links)
- Text-based phenotypic profiles incorporating biochemical phenotypes of inborn errors of metabolism improve phenomics-based diagnosis (Q48230175) (← links)
- Proteomic identification and characterization of hepatic glyoxalase 1 dysregulation in non-alcoholic fatty liver disease (Q49742817) (← links)
- Systematic Functional Characterization of Human 21st Chromosome Orthologs in Caenorhabditis elegans (Q49788245) (← links)
- Spontaneous Development of Cutaneous Squamous Cell Carcinoma in Mice with Cell-specific Deletion of Inhibitor of κB Kinase 2. (Q49958999) (← links)
- Evidence for convergent evolution of SINE-directed Staufen-mediated mRNA decay (Q50020101) (← links)
- FAIR principles and the IEDB: short-term improvements and a long-term vision of OBO-foundry mediated machine-actionable interoperability (Q50330852) (← links)
- Identification of errors in the IEDB using ontologies (Q50331679) (← links)
- Testis transcriptome alterations in zebrafish (Danio rerio) with reduced fertility due to developmental exposure to 17α-ethinyl estradiol (Q50419960) (← links)
- A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures (Q50422133) (← links)
- Sheep genome functional annotation reveals proximal regulatory elements contributed to the evolution of modern breeds (Q51418660) (← links)
- Genome-wide association for testis weight in the diversity outbred mouse population. (Q52310582) (← links)
- Aging Mouse Models Reveal Complex Tumor-Microenvironment Interactions in Cancer Progression. (Q52322881) (← links)
- A genomics approach reveals insights into the importance of gene losses for mammalian adaptations. (Q52343906) (← links)
- A survey of functional genomic variation in domesticated chickens. (Q52585144) (← links)
- A multitask clustering approach for single-cell RNA-seq analysis in Recessive Dystrophic Epidermolysis Bullosa. (Q52598818) (← links)
- An accurate and robust imputation method scImpute for single-cell RNA-seq data. (Q52665692) (← links)
- Delayed male germ cell sex-specification permits transition into embryonal carcinoma cells with features of primed pluripotency. (Q52689665) (← links)
- Different Neuronal Activity Patterns Induce Different Gene Expression Programs. (Q53072259) (← links)
- Weighted Burden Analysis of Exome-Sequenced Case-Control Sample Implicates Synaptic Genes in Schizophrenia Aetiology. (Q54120056) (← links)