All terms in CLO
| Label | Id | Description |
|---|---|---|
| GM04761 cell | CLO_0019053 | [ CHROMOSOME POLYMORPHISM] |
| skeletal tissue | UBERON_0004755 | [Four classes of mineralized tissues are found in vertebrates: bone, cartilage, dentine, and enamel. We think of cartilage and bone as skeletal tissues and of enamel and dentine as dental tissues, but enamel and dentine arose evolutionarily together with bone as skeletal tissues in the dermal skeleton (exoskeleton) of early vertebrates. Scales and teeth of sharks are examples of dermal skeletal elements that are still composed of the three ancient components-enamel, dentine, and bone. Cartilage, on the other hand, provided the basis for the second vertebrate skeletal system, the endoskeleton (Smith and Hall, 1990; Hall, 1998a,b). some invertebrate skeletal tissues have surprisingly bone-like features. Examples include chondrocytes interconnected by cell processes in cephalopod cartilages (Cole and Hall, 2004a,b), and the calcium phosphate layer in the shells of brachiopods (Rodland et al., 2003). However, neither bone nor mineralized cartilage have been found in invertebrates. Editors notes: TODO - develops_from] |
| skeletogenic cell | CL_0007001 | [Needs logical definition. Should be capable_of skeletal system morphogenesis? or skeletal tissue development? needs to be added to GO. NOTES:a cell type of the early embryo (see also: mesenchymal cells) that will give rise to mineralized connective tissue. Scleroblasts can differentiate into osteoblasts (bone-forming cells), chondroblasts (cartilage-forming cells), odontoblasts (dentin-forming cells), ameloblasts (enamel-forming cells). The mesenchymal cells developing into osteoblasts and chondroblasts are derived from the mesoderm. Those developing into odontoblasts are neural crest cells. Those developing into ameloblasts are derived from the ectoderm. (http://www.copewithcytokines.de/cope.cgi?key=scleroblasts)] |
| Kasumi-1 cell | CLO_0007069 | [disease: acute myeloblastic leukemia] |
| GM11886 cell | CLO_0020047 | [ CEPH/UTAH PEDIGREE 1377] |
| KASUMI-1 cell | CLO_0007068 | [disease: leukemia, acute myeloid] |
| GM11885 cell | CLO_0020048 | [ CEPH/UTAH PEDIGREE 1377] |
| KARPAS-45 cell | CLO_0007067 | |
| ND08544 cell | CLO_0020049 | [ ASYMPTOMATIC AND GENETICALLY RELATED TO AN AFFECTED INDIVIDUAL] |
| KARPAS-422 cell | CLO_0007066 | |
| GM11878 cell | CLO_0020043 | [ CEPH/UTAH PEDIGREE 1347] |
| GM11877 cell | CLO_0020044 | [ CEPH/UTAH PEDIGREE 1347] |
| GM11884 cell | CLO_0020045 | [ CEPH/UTAH PEDIGREE 1377] |
| GM11883 cell | CLO_0020046 | [ CEPH/UTAH PEDIGREE 1347] |
| Kasumi-6 cell | CLO_0007072 | [disease: acute myeloid leukemia, subtype M2] |
| AG04555 cell | CLO_0034680 | [ GERONTOLOGY RESEARCH CENTER (GRC) CELL CULTURE COLLECTION BALTIMORE LONGITUDINAL STUDY ON AGING (BLSA)] |
| Kasumi-4 cell | CLO_0007071 | [disease: chronic myeloblastic leukemia] |
| AG04556 cell | CLO_0034681 | [ GERONTOLOGY RESEARCH CENTER (GRC) CELL CULTURE COLLECTION BALTIMORE LONGITUDINAL STUDY ON AGING (BLSA)] |
| Kasumi-3 cell | CLO_0007070 | [disease: acute myeloblastic leukemia] |
| AG04553 cell | CLO_0034682 | [ BALTIMORE LONGITUDINAL STUDY ON AGING (BLSA) GERONTOLOGY RESEARCH CENTER (GRC) CELL CULTURE COLLECTION] |