Levic et al., 2015
- Animal model of Sar1b deficiency presents lipid absorption deficits similar to Anderson disease.
Journal of molecular medicine (Berlin, Germany)
93(2):165-176
Full text @ J. Mol. Med.
Marker Type | Symbol | Name |
---|---|---|
Gene | col2a1a | collagen, type II, alpha 1a |
Gene | cp | ceruloplasmin |
Gene | dlx2a | distal-less homeobox 2a |
Gene | fabp2 | fatty acid binding protein 2, intestinal |
Gene | foxa3 | forkhead box A3 |
Gene | neurod1 | neuronal differentiation 1 |
Gene | nkx2.2a | NK2 homeobox 2a |
Gene | pax6b | paired box 6b |
Gene | prox1a | prospero homeobox 1a |
Gene | prss1 | serine protease 1 |
Gene | sar1ab | secretion associated, Ras related GTPase 1Ab |
Gene | sar1b | secretion associated, Ras related GTPase 1B |
Gene | sox9a | SRY-box transcription factor 9a |