{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=10940&ordering=name","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=10900&ordering=name","results":[{"accession":"UBERON:0000044","name":"dorsal root ganglion","definition":"['Sensory ganglia located on the dorsal spinal roots within the vertebral column. The spinal ganglion cells are pseudounipolar. The single primary branch bifurcates sending a peripheral process to carry sensory information from the periphery and a central branch which relays that information to the spinal cord or brain. (MSH) * ganglion found on the posterior root of each spinal nerve, composed of the unipolar nerve cell bodies of the sensory neurons of the nerve. (CSP).']","term_type":"cell line"},{"accession":"UBERON:0001137","name":"dorsum","definition":"['A major subdivision of an organism that is the entire part of the organism dorsal to a horizontal plane and bounded on one side by the same transverse plane. In vertebrares this includes the vertebral column..']","term_type":"cell line"},{"accession":"CLO:0002808","name":"DoTc2 4510 cell","definition":"[]","term_type":"cell line"},{"accession":"CL:0002489","name":"double negative thymocyte","definition":"['A thymocyte that lacks expression of CD4 and CD8.', 'These are precursors to mature T cells; normally, they do not circulate, but are found in the thymus and they have not undergone rearrangement of the alpha and beta T cell receptor genes.']","term_type":"cell line"},{"accession":"CL:0000809","name":"double-positive, alpha-beta thymocyte","definition":"['A thymocyte expressing the alpha-beta T cell receptor complex as well as both the CD4 and CD8 coreceptors.', 'Thymocytes of this stage are undergoing positive and negative selection.']","term_type":"cell line"},{"accession":"CL:0002428","name":"double-positive blast","definition":"['A double-positive thymocyte that is large (i.e. has a high forward scatter signal in flow cytometry) and is actively proliferating.']","term_type":"cell line"},{"accession":"EFO:0001064","name":"Down's syndrome","definition":"[\"A chromosomal dysgenesis syndrome resulting from a triplication or translocation of chromosome 21. Down syndrome occurs in approximately 1:700 live births. Abnormalities are variable from individual to individual and may include mental retardation, retarded growth, flat hypoplastic face with short nose, prominent epicanthic skin folds, small low-set ears with prominent antihelix, fissured and thickened tongue, laxness of joint ligaments, pelvic dysplasia, broad hands and feet, stubby fingers, transverse palmar crease, lenticular opacities and heart disease. Patients with Down syndrome have an estimated 10 to 30-fold increased risk for leukemia; most have symptoms of Alzheimer's disease by age 40. Also known as trisomy 21 syndrome. --2004\", 'A chromosome disorder associated either with an extra chromosome 21 or an effective trisomy for chromosome 21. Clinical manifestations include hypotonia, short stature, brachycephaly, upslanting palpebral fissures, epicanthus, Brushfield spots on the iris, protruding tongue, small ears, short, broad hands, fifth finger clinodactyly, Simian crease, and moderate to severe MENTAL RETARDATION. Cardiac and gastrointestinal malformations, a marked increase in the incidence of LEUKEMIA, and the early onset of ALZHEIMER DISEASE are also associated with this condition. Pathologic features include the development of NEUROFIBRILLARY TANGLES in neurons and the deposition of AMYLOID BETA-PROTEIN, similar to the pathology of ALZHEIMER DISEASE. (Menkes, Textbook of Child Neurology, 5th ed, p213)', 'A disorder caused by the presence of all or part of an extra 21st chromosome, characterized by structural abnormalities throughout the body. Often Down syndrome is associated with some impairment of cognitive ability and physical growth as well as facial appearance. (Adapted from Wikipedia)']","term_type":"cell line"},{"accession":"CLO:0002809","name":"DP-LL95 cell","definition":"[]","term_type":"cell line"},{"accession":"CLO:0002810","name":"DPS84 cell","definition":"[]","term_type":"cell line"},{"accession":"CLO:0002811","name":"DPSO 114/74 cell","definition":"[]","term_type":"cell line"},{"accession":"CLO:0002812","name":"DPW 5 cell","definition":"[]","term_type":"cell line"},{"accession":"CLO:0037254","name":"DPX2 cell","definition":"['DPX2 (aka DPX-2) is a HepG2-derived cell line stably integrated with a PXR (pregnane X receptor) expression vector plus a luciferase reporter, used to detect PXR activation/ CYP3A induction']","term_type":"cell line"},{"accession":"CLO:0002814","name":"DR4 MEF cell","definition":"['disease: feeder layer']","term_type":"cell line"},{"accession":"CLO:0002815","name":"D-R86 cell","definition":"[]","term_type":"cell line"},{"accession":"CLO:0002816","name":"DR89P cell","definition":"[]","term_type":"cell line"},{"accession":"CLO:0002813","name":"DR 9 cell","definition":"[]","term_type":"cell line"},{"accession":"CLO:0037217","name":"DRD cell","definition":"['DRD=BJ fibroblasts expressing hTERT, SV40 small T oncoprotein,  dominant negative p53, cyclin D1,  a mutant form of CDK4, along with the oncogene HRASV12']","term_type":"cell line"},{"accession":"CLO:0002817","name":"DREG200 cell","definition":"['disease: hybridoma']","term_type":"cell line"},{"accession":"CLO:0002818","name":"DREG56 cell","definition":"['disease: hybridoma']","term_type":"cell line"},{"accession":"EFO:0010180","name":"droplet-based cell isolation","definition":"['']","term_type":"Enrichment process"}]}