All terms in CLO
| Label | Id | Description |
|---|---|---|
| DAN-G cell | CLO_0002698 | |
| immortal human pancreas-derived cell line cell | CLO_0000551 | |
| pancreatic adenocarcinoma | DOID_4074 | |
| Ba/F3 cell line EpoR and JAK2V617F co-expression | CLO_0000037 | |
| DA03701 cell | CLO_0024000 | [ DIABETES MELLITUS FAMILY SAMPLE] |
| GM15463 cell | CLO_0026661 | [ DNA POLYMORPHISM DISCOVERY RESOURCE COLLECTION] |
| CHO cell line co-expression | CLO_0000038 | |
| CHO cell | CLO_0002421 | |
| GM15461 cell | CLO_0026660 | [ DNA POLYMORPHISM DISCOVERY RESOURCE COLLECTION] |
| adenohypophyseal placode | UBERON_0009122 | |
| non-neurogenic ectodermal placode | UBERON_0011814 | |
| cranial placode | UBERON_0002546 | |
| non-neural ectoderm | UBERON_0005497 | [Gene notes: One of the first genes to be expressed in nonneural ectoderm in amphioxus is BMP2/4 (Panopoulou et al. 1998). BMP2/4 homologues appear to have a very ancient role in distinguishing neural from nonneural ectoderm; in Drosophila as well as in amphioxus and vertebrates, BMP2/4 homologues are expressed in nonneural ectoderm and function in distinguishing neural from nonneural ectoderm (Francois & Bier, 1995 ; Sasai et al. 1995 ; Wilson & Hemmati-Brivanlou, 1995; Panopoulou et al. 1998). A change in level of BMP2/4 from very high in nonneural ectoderm to low in neural ectoderm appears to be a key factor in development of neural crest (Baker & Bronner-Fraser,1997a,1997b;Erickson&Reedy,1998;Marchantet al.1998 ;Selleck et al. 1998).] |
| CHO cell line co-expression of lactamase | CLO_0000039 | |
| DA03698 cell | CLO_0024009 | [ DIABETES MELLITUS FAMILY SAMPLE] |
| D-A92f cell | CLO_0002691 | |
| DA03692 cell | CLO_0024007 | [ DIABETES MELLITUS FAMILY SAMPLE] |
| D-A92a cell | CLO_0002690 | |
| DA06111 cell | CLO_0024008 | [ DIABETES MELLITUS FAMILY SAMPLE] |
| GM15452 cell | CLO_0026669 | [ CRICETULUS] |