Audio compression/frequency shifting
A cataract is a clouding of the lens inside the eye which leads to a decrease in vision. It is the most common cause of blindness worldwide and is conventionally treated with surgery. Visual loss o...
Autoimmune diseases arise from an abnormal immune response of the body against substances and tissues normally present in the body (autoimmunity). This may be restricted to certain organs (e.g. in ...
Lymphocyte cytosolic protein 2 (SH2 domain containing leukocyte protein of 76kDa), also known as LCP2 or SLP-76, is a gene that encodes a signal-transducing adaptor protein.
Neurostimulation is a therapeutic activation of part of the nervous system using microelectrodes. The electrodes are used to interface with excitable tissue in order to either restore sensation, su...
Neuregulin 1 or NRG1 is a protein that in humans is encoded by the NRG1 gene.[1][2] NRG1 is one of four proteins in the neuregulin family that act on the EGFR family of receptors. Neuregulin 1 is p...
Inner ear implants
Lession localizer
Near-infrared spectroscopy (NIRS) is a spectroscopic method that uses the near-infrared region of the electromagnetic spectrum (from about 800 nm to 2500 nm). Typical applications include pharmaceu...
Lesion localization device
External fixation is a surgical treatment used to stabilize bone and soft tissues at a distance from the operative or injury focus. They provide unobstructed access to the relevant skeletal and sof...
DNA sequencing is the process of determining the precise order of nucleotides within a DNA molecule. It includes any method or technology that is used to determine the order of the four bases—adeni...
Data filtering/padding
Gastrointestinal tract unraveling
Immunotherapeutic oligonucleotides/cytokines
Glaucoma is a term describing a group of ocular (eye) disorders that result in optic nerve damage, often associated with increased fluid pressure in the eye (intraocular pressure) (IOP).[1] The di...
Glaucoma is a term describing a group of ocular (eye) disorders that result in optic nerve damage, often associated with increased fluid pressure in the eye (intraocular pressure) (IOP).[1] The dis...
Congenital heart defect (CHD) or congenital heart anomaly[2] is a defect in the structure of the heart and great vessels that is present at birth. Many types of heart defects exist, most of which e...
Syntaxins are a family of membrane integrated Q-SNARE proteins participating in exocytosis. Syntaxins possess a single C-terminal transmembrane domain, a SNARE domain (known as H3), and an N-termi...
Polymorphisms associated with neuropsychiatric disorders
