Phenotype
|
Conditions
|
Figures
|
bile canaliculus decreased length, abnormal
|
chemical treatment by environment: XAV939
|
Fig. 1,
Fig. 6
from So et al., 2017
|
bile canaliculus decreased length, abnormal
|
chemical treatment: tyrphostin AG 1478
|
Fig. 4
from Ningappa et al., 2015
|
bile canaliculus decreased length, abnormal
|
chemical treatment by environment: dimethyloxalylglycine
|
FIGURE 7
from Min et al., 2020
|
bile canaliculus increased amount, abnormal
|
chemical treatment by environment: dimethyloxalylglycine
|
FIGURE 7
from Min et al., 2020
|
bile canaliculus length, normal
|
chemical treatment by environment: olomoucine
|
Fig. 2
from Dimri et al., 2017
|
bile ductule branchiness, abnormal
|
chemical treatment by environment: olomoucine
|
Fig. 2
from Dimri et al., 2017
|
bile ductule decreased branchiness, abnormal
|
chemical treatment by environment: olomoucine
|
Fig. 4
from Dimri et al., 2017
|
bile ductule decreased branchiness, abnormal
|
chemical treatment by environment: cucurbitacin E
|
Fig. 4
from Dimri et al., 2017
|
bile ductule increased branchiness, abnormal
|
chemical treatment by environment: IPA-3
|
Fig. 4
from Dimri et al., 2017
|
bile ductule increased branchiness, abnormal
|
chemical treatment by environment: LimKi 3
|
Fig. 4 ,
Fig. 6
from Dimri et al., 2017
|
bile ductule actin filament disconnected, abnormal
|
chemical treatment by environment: XAV939
|
Fig. 1
from So et al., 2017
|
bile ductule cholangiocyte Ab5-pak labeling increased amount, abnormal
|
control
|
Fig. 3
from Dimri et al., 2017
|
bile ductule morphogenesis of a branching epithelium decreased occurrence, abnormal
|
chemical treatment by environment: cucurbitacin E
|
Fig. 4
from Dimri et al., 2017
|
bile ductule morphogenesis of a branching epithelium decreased occurrence, abnormal
|
chemical treatment by environment: olomoucine
|
Fig. 4
from Dimri et al., 2017
|
bile ductule morphogenesis of a branching epithelium increased occurrence, abnormal
|
chemical treatment by environment: IPA-3
|
Fig. 4
from Dimri et al., 2017
|
bile ductule morphogenesis of a branching epithelium increased occurrence, abnormal
|
chemical treatment by environment: LimKi 3
|
Fig. 4 ,
Fig. 6
from Dimri et al., 2017
|
caudal division of the internal carotid artery EGFP expression decreased amount, abnormal
|
chemical treatment: LY-411575
|
Fig. 2
from Rochon et al., 2015
|
cholangiocyte actin cytoskeleton organization process quality, abnormal
|
chemical treatment by environment: cucurbitacin E
|
Fig. 5
from Dimri et al., 2017
|
cholangiocyte actin cytoskeleton organization process quality, abnormal
|
chemical treatment by environment: LimKi 3
|
Fig. 5
from Dimri et al., 2017
|
cholangiocyte actin cytoskeleton organization process quality, abnormal
|
chemical treatment by environment: IPA-3
|
Fig. 5
from Dimri et al., 2017
|
cholangiocyte actin cytoskeleton organization process quality, abnormal
|
chemical treatment by environment: olomoucine
|
Fig. 5
from Dimri et al., 2017
|
cholangiocyte filopodium decreased length, abnormal
|
chemical treatment: tyrphostin AG 1478
|
Fig. 4
from Ningappa et al., 2015
|
cholangiocyte morphogenesis of a polarized epithelium process quality, normal
|
chemical treatment by environment: LimKi 3
|
Fig. 5
from Dimri et al., 2017
|
cholangiocyte morphogenesis of a polarized epithelium process quality, normal
|
chemical treatment by environment: olomoucine
|
Fig. 5
from Dimri et al., 2017
|
cranial vasculature artery EGFP expression absent, abnormal
|
chemical treatment: LY-411575
|
Fig. 2
from Rochon et al., 2015
|
dorsal aorta EGFP expression absent, abnormal
|
chemical treatment: LY-411575
|
Fig. 2
from Rochon et al., 2015
|
dorsal aorta EGFP expression decreased amount, abnormal
|
chemical treatment by environment: 17beta-estradiol
|
Fig. 4
from Carroll et al., 2014
|
dorsal aorta EGFP expression decreased amount, abnormal
|
chemical treatment by environment: genistein
|
Fig. 5
from Carroll et al., 2014
|
dorsal aorta EGFP expression decreased amount, abnormal
|
chemical treatment by environment: 17alpha-ethynylestradiol
|
Fig. 5
from Carroll et al., 2014
|
intrahepatic bile duct development disrupted, abnormal
|
chemical treatment: tyrphostin AG 1478
|
Fig. 4
from Ningappa et al., 2015
|
intrahepatic bile duct epithelial cell increased amount, abnormal
|
chemical treatment by environment: dimethyloxalylglycine
|
FIGURE 7
from Min et al., 2020
|
jaw flap has fewer parts of type breeding tubercle, abnormal
|
chemical treatment: DAPT
|
Fig. 8
from Fischer et al., 2014
|
jaw flap has fewer parts of type breeding tubercle, abnormal
|
chemical treatment: pharmaceutical
|
Fig. 8
from Fischer et al., 2014
|
jaw flap breeding tubercle decreased size, abnormal
|
chemical treatment: pharmaceutical
|
Fig. 8
from Fischer et al., 2014
|
jaw flap breeding tubercle decreased size, abnormal
|
chemical treatment: DAPT
|
Fig. 8
from Fischer et al., 2014
|
keratinocyte proliferation disrupted, abnormal
|
chemical treatment: DAPT
|
Fig. 8
from Fischer et al., 2014
|
liver has extra parts of type cholangiocyte, abnormal
|
chemical treatment by environment: IPA-3
|
Fig. 4
from Dimri et al., 2017
|
liver has extra parts of type cholangiocyte, abnormal
|
chemical treatment by environment: LimKi 3
|
Fig. 4
from Dimri et al., 2017
|
liver has normal numbers of parts of type cholangiocyte, normal
|
chemical treatment by environment: olomoucine
|
Fig. 2 ,
Fig. 4
from Dimri et al., 2017
|
liver has normal numbers of parts of type cholangiocyte, normal
|
chemical treatment by environment: cucurbitacin E
|
Fig. 4
from Dimri et al., 2017
|
liver volume, normal
|
chemical treatment by environment: olomoucine
|
Fig. 2
from Dimri et al., 2017
|
liver intrahepatic bile duct development decreased process quality, abnormal
|
chemical treatment by environment: olomoucine
|
Fig. 2
from Dimri et al., 2017
|
optic artery EGFP expression absent, abnormal
|
chemical treatment: LY-411575
|
Fig. 2
from Rochon et al., 2015
|
retina cell population proliferation increased occurrence, abnormal
|
chemical treatment by environment: ethanol, chemical treatment by environment: retinoic acid
|
Fig. 6
from Muralidharan et al., 2018
|
retina cell population proliferation increased occurrence, abnormal
|
chemical treatment by environment: ethanol
|
Fig. 6 ,
Fig. 7
from Muralidharan et al., 2018
|
retina cell population proliferation normal occurrence, ameliorated
|
chemical treatment by environment: ethanol, chemical treatment by environment: Wnt signalling activator
|
Fig. 7
from Muralidharan et al., 2018
|
retina cell population proliferation normal occurrence, ameliorated
|
chemical treatment by environment: ethanol, chemical treatment by environment: folic acid
|
Fig. 6
from Muralidharan et al., 2018
|
retina Notch signaling pathway decreased magnitude, abnormal
|
chemical treatment by environment: ethanol
|
Fig. 6 ,
Fig. 7
from Muralidharan et al., 2018
|
retina Notch signaling pathway normal occurrence, ameliorated
|
chemical treatment by environment: ethanol, chemical treatment by environment: retinoic acid
|
Fig. 6
from Muralidharan et al., 2018
|
retina Notch signaling pathway normal occurrence, ameliorated
|
chemical treatment by environment: ethanol, chemical treatment by environment: folic acid
|
Fig. 6
from Muralidharan et al., 2018
|
retina Notch signaling pathway normal occurrence, ameliorated
|
chemical treatment by environment: ethanol, chemical treatment by environment: Wnt signalling activator
|
Fig. 7
from Muralidharan et al., 2018
|
retinal outer nuclear layer zpr-1 labeling amount, ameliorated
|
chemical treatment by environment: ethanol, chemical treatment by environment: Wnt signalling activator
|
Fig. 7
from Muralidharan et al., 2018
|
retinal outer nuclear layer zpr-1 labeling decreased amount, abnormal
|
chemical treatment by environment: ethanol
|
Fig. 7
from Muralidharan et al., 2018
|
ventral wall of dorsal aorta has fewer parts of type hematopoietic multipotent progenitor cell, abnormal
|
chemical treatment by environment: calciol
|
Fig. 2
from Cortes et al., 2015
|
ventral wall of dorsal aorta has fewer parts of type hematopoietic multipotent progenitor cell, abnormal
|
chemical treatment by environment: Cyclopamine
|
Fig. 2
from Cortes et al., 2015
|
ventral wall of dorsal aorta has fewer parts of type hematopoietic stem cell, abnormal
|
chemical treatment by environment: calciol
|
Fig. 2
from Cortes et al., 2015
|
ventral wall of dorsal aorta has fewer parts of type hematopoietic stem cell, abnormal
|
chemical treatment by environment: Cyclopamine
|
Fig. 2
from Cortes et al., 2015
|
ventral wall of dorsal aorta lacks parts or has fewer parts of type hematopoietic stem cell, abnormal
|
chemical treatment by environment: Cyclopamine, chemical treatment by environment: calciol
|
Fig. 2
from Cortes et al., 2015
|
ventral wall of dorsal aorta lacks parts or has fewer parts of type hematopoietic multipotent progenitor cell, abnormal
|
chemical treatment by environment: Cyclopamine, chemical treatment by environment: calciol
|
Fig. 2
from Cortes et al., 2015
|