Technology & Resource Development Scientist
Associate Research Scientist & Program Manager
NOD-scid IL2rgnull (NSG) and NOD-Rag1null IL2rgnull (NRG) mice support heightened levels of engraftment with human cells and tissues. These engrafted mice allow research on human disease processes without putting individuals at risk.
Researches genome informatics with a focus on gene ontology.
Senior Research Scientist
Bridging the digital biology divide, integrating computation with biomedical research.
Researches the genetics underlying behavior and identifies relationships among behavioral traits.
Senior Manager, Sequencing Technology
The Cre Portal contains curated data about all recombinase-containing transgenes and knock-ins developed in mice to provide a comprehensive resource delineating known recombinase activity patterns and allowing users to find relevant mouse resources for their studies.
Manager, IT Applications
Describes mouse models for ocular research available at The Jackson Laboratory and provides a list of known mouse mutations that affect vision.
The Gene Ontology (GO) project is a collaborative effort to address the need for consistent descriptions of gene products across databases.
Genetic Resource Science initiates and develops resource-generating research. Our team: identifies and implements innovative technologies for genetic research; makes and distributes new mouse models; and provides extensive genetic and phenotypic information on JAX mouse strains.
Bioinformatics Analyst II
Associate Director, Computational Sciences
The International Mouse Strain Resource offers users a combined catalog of worldwide mouse resources (live, cryopreserved, and embryonic stem cells), with direct access to repository sites holding those resources of interest.
Senior Research Scientist
Our specialized collection areas include: genetics, inbred mice, animal health and husbandry, development, embryology, complex traits, immunology, cancer, molecular biology, neuroscience and computational biology.
Senior Research Scientist
Uses advanced methods to research glaucoma and other neurodegenerative diseases.
Scientists around the world are working to generate a targeted knockout mutation for every gene in the mouse genome through the Knockout Mouse Project (KOMP) which is providing critical tools for understanding gene function and the genetic causes of human diseases.
Associate Research Scientist
Studies neural circuits in the brain and associated behavioral abnormalities.
International database resource for the laboratory mouse, providing integrated genetic, genomic, and biological data.
Mice harboring spontaneous mutations have long been a major source for animal models of human genetic disorders, particularly mendelian diseases. The Mouse Mutant Resource maintains over 700 established mutant strains.
This resource provides mouse models for facial, dental, eye, ear and skull development research, as well as mouse models of human craniofacial syndromes.
MouseMine is a powerful data warehouse providing comprehensive API (application programming interface) access to MGI data, as well as a forms-based user interface.
Investigating the genetic mechanisms of craniofacial development and developing new genetic tools and resources for the scientific community.
The Mutant Mouse Resource and Research Center (MMRRC) distributes and cryopreserves scientifically valuable, genetically engineered mouse strains and mouse ES cell lines with potential value for the genetics and biomedical research community.
Employs mouse models of human eye disease to study gene function and mechanisms underlying disease pathology.
We offer a growing number of mouse lines expressing proteins that activate, inhibit or detect neuronal activity.
The Parkinson’s Disease Mouse Model Resource characterizes and distributes new mouse models of Parkinsonism and Parkinson’s disease.
Serves as a centralized resource for mouse models and tools that have been validated for use in preclinical studies of peripheral neuropathy.
Dr. Reinholdt’s research focuses on comparative and functional mammalian genomics, reproductive development and stem cell biology.
Captures gene expression data and disseminates it to the research community.
Investigating the mechanisms of autoimmune disease to devise therapeutic approaches.
SeqFold is a tool for RNA secondary structure prediction from experimental data.
Investigates human immunological diseases and malignancy through the development and leveraging of novel humanized mouse models
Professor and Howard Hughes Medical Investigator
The SMSR maintains mice that are important tools for genetic analysis of complex diseases, including consomic strains.
Associate Professor, University of Pittsburgh School of Medicine; Director PITT Preclinical Phenotyping Core; Co-Head MODEL-AD Preclinical Testing Core
Senior Scientific Curator
The WORM Human OrthoLogy Explorer is a meta-tool that uses machine learning to predict novel least diverged orthologs (LDOs) by integrating ortholog predictions from 17 algorithms.
Studying the development and function of neural circuits and dysfunctions related to autism spectrum disorders.