Mice homozygous for the CAG-luc-eGFP L2G85 transgene are viable and fertile, with widespread expression of firefly luciferase and enhanced green fluorescence protein directed by the CAG promoter (human cytomegalovirus immediate early promoter enhancer with chicken beta-actin/r
This invention is from the Pritzker Neuropsychiatric Disorders Research Consortium, a collaborative research enterprise comprised of several leading academic institutions and based on a long-term relationship between the Pritzker family and scientists at the various institutio
Stanford researchers have built a sound powered, wireless medical implant. The implant contains a piezoelectric energy receiver, an integrated circuit chip, and a loop antenna.
Researchers at Stanford University have developed a newly patented method for reducing the physiological symptoms of opioid withdrawal by targeting a well-characterized receptor.
Stanford researchers have developed mutant Renilla luciferase proteins and reporter gene constructs which modify the physical characteristics of the Renilla luciferase protein for use in biological assays.
A team of Stanford scientists have developed a technique to rapidly convert adult somatic cells directly into functional neuronal cells without the intermediate step of generating iPS cells (induced pluripotent stem cells).
Researchers at Stanford have developed a non-invasive method, based on the identification of novel immune signatures in the blood, for diagnosing Crohn's disease (CD) or ulcerative colitis (UC) in patients with inflammatory bowel disease (IBD).
Stanford researchers at the Genome Technology Center have developed a simple, reliable, and accurate method for obtaining sequencing information for multiple sites within target nucleic acid.
Stanford researchers have derived human multipotent germline stem cells (hMGSCs) from a testis biopsy. The biopsied cells show multiple characteristics of pluripotency.
Stanford researchers at the Moore Lab have developed an algorithm for on-line, real time post processing of large amounts of neuronal data from high-density, multi-channel electrophysiological recordings to identify which neurons were firing (on-line spike recovery).
Researchers at Stanford have developed a technique to quantitatively measure protein structure and interactions in living cells by protein "footprinting"—monitoring the solvent accessibility of each residue under different environmental conditions.