Pages that link to "Q37661743"
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The following pages link to The Mouse Genome Database: integration of and access to knowledge about the laboratory mouse (Q37661743):
Displaying 50 items.
- PsyGeNET: a knowledge platform on psychiatric disorders and their genes (Q23793554) (← links)
- Capturing phenotypes for precision medicine (Q23815245) (← links)
- De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies (Q24563008) (← links)
- Orthology for comparative genomics in the mouse genome database (Q26801736) (← links)
- The BioGRID interaction database: 2015 update (Q28252221) (← links)
- Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia (Q28262977) (← links)
- An Integrated Data Driven Approach to Drug Repositioning Using Gene-Disease Associations (Q28552224) (← links)
- Mouse Genome Database (MGD)-2017: community knowledge resource for the laboratory mouse (Q28584453) (← links)
- Elf5 and Ets2 maintain the mouse extraembryonic ectoderm in a dosage dependent synergistic manner (Q28592029) (← links)
- Clinical interpretation of CNVs with cross-species phenotype data (Q28647107) (← links)
- DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes (Q28649649) (← links)
- OrthoDB v8: update of the hierarchical catalog of orthologs and the underlying free software (Q28650440) (← links)
- Conservation of pro-longevity genes among mammals. (Q30372988) (← links)
- Nonviral Reprogramming of Human Wharton's Jelly Cells Reveals Differences Between ATOH1 Homologues. (Q30382596) (← links)
- Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics (Q30389888) (← links)
- Transcriptional maturation of the mouse auditory forebrain. (Q30404856) (← links)
- Commentary on Shimoyama et al. (2012): three ontologies to define phenotype measurement data (Q30814239) (← links)
- Lean Big Data integration in systems biology and systems pharmacology (Q30841748) (← links)
- Methodology for the inference of gene function from phenotype data (Q30877319) (← links)
- Combining RNA and protein profiling data with network interactions identifies genes associated with spermatogenesis in mouse and human (Q30885504) (← links)
- Toll-like receptor signaling in vertebrates: testing the integration of protein, complex, and pathway data in the protein ontology framework. (Q30937032) (← links)
- DeAnnCNV: a tool for online detection and annotation of copy number variations from whole-exome sequencing data (Q30959267) (← links)
- Publisher’s Note:Abstraction for data integration:Fusing mammalian molecular, cellular and phenotype big datasets for better knowledge extraction (Q30976077) (← links)
- Mouse Genome Informatics (MGI): Resources for Mining Mouse Genetic, Genomic, and Biological Data in Support of Primary and Translational Research. (Q31147695) (← links)
- A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies (Q33430459) (← links)
- 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function (Q33612113) (← links)
- Representing kidney development using the gene ontology (Q33773781) (← links)
- Use of model organism and disease databases to support matchmaking for human disease gene discovery (Q33806132) (← links)
- PubServer: literature searches by homology (Q33860624) (← links)
- Cognition and hippocampal plasticity in the mouse is altered by monosomy of a genomic region implicated in Down syndrome (Q33895060) (← links)
- Genetic dissection of the ity3 locus identifies a role for ncf2 co-expression modules and suggests selp as a candidate gene underlying the ity3.2 locus. (Q34031597) (← links)
- Hybrid mice reveal parent-of-origin and Cis- and trans-regulatory effects in the retina (Q34395064) (← links)
- Systematic analysis of the phosphoproteome and kinase-substrate networks in the mouse testis (Q34442328) (← links)
- The Mouse Genome Database (MGD): facilitating mouse as a model for human biology and disease (Q34445051) (← links)
- Genenames.org: the HGNC resources in 2015 (Q34445762) (← links)
- Genome-wide Analysis of Body Proportion Classifies Height-Associated Variants by Mechanism of Action and Implicates Genes Important for Skeletal Development (Q34471319) (← links)
- Mouse genome database 2016. (Q34502040) (← links)
- Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome (Q34657870) (← links)
- Gene expression profiling studies in regenerating nerves in a mouse model for CMT1X: uninjured Cx32-knockout peripheral nerves display expression profile of injured wild type nerves (Q34670337) (← links)
- Mouse ENU Mutagenesis to Understand Immunity to Infection: Methods, Selected Examples, and Perspectives (Q34774733) (← links)
- Reconstructing genome-wide protein-protein interaction networks using multiple strategies with homologous mapping. (Q34989529) (← links)
- Chromatin decompaction by the nucleosomal binding protein HMGN5 impairs nuclear sturdiness. (Q35005815) (← links)
- Performance of case-control rare copy number variation annotation in classification of autism (Q35043091) (← links)
- PEAT: an intelligent and efficient paired-end sequencing adapter trimming algorithm (Q35092930) (← links)
- PTEN regulates natural killer cell trafficking in vivo (Q35128929) (← links)
- Diversity Outbred Mice Identify Population-Based Exposure Thresholds and Genetic Factors that Influence Benzene-Induced Genotoxicity. (Q35144644) (← links)
- Biochemical functional predictions for protein structures of unknown or uncertain function (Q35214509) (← links)
- Beyond protein expression, MOPED goes multi-omics (Q35254203) (← links)
- INFRAFRONTIER--providing mutant mouse resources as research tools for the international scientific community (Q35254294) (← links)
- EpilepsyGene: a genetic resource for genes and mutations related to epilepsy. (Q35254765) (← links)