Human Disease model utilizes ck1Tg
No data available
RNA Expression
Protein Expression
Reporter Gene Expression
Expressed Gene | Structure | Conditions | Figures |
---|---|---|---|
EGFP | (all 7) | standard conditions | 10 figures from 7 publications |
EGFP | chemical treatment by environment: copper(2+) | Fig. 1 from Zhang et al., 2020 |
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- Lee, Y.R., Kim, S.H., Ben-Mahmoud, A., Kim, O.H., Choi, T.I., Lee, K.H., Ku, B., Eum, J., Kee, Y., Lee, S., Cha, J., Won, D., Lee, S.T., Choi, J.R., Lee, J.S., Kim, H.D., Kim, H.G., Bonkowsky, J.L., Kang, H.C., Kim, C.H. (2021) Eif2b3 mutants recapitulate phenotypes of Vanishing White Matter Disease and validate novel disease alleles in zebrafish. Human molecular genetics. 30(5):331-342
- Lu, S., Lyu, Z., Wang, Z., Kou, Y., Liu, C., Li, S., Hu, M., Zhu, H., Wang, W., Zhang, C., Kuan, Y.S., Liu, Y.W., Chen, J., Tian, J. (2021) Lipin 1 deficiency causes adult-onset myasthenia with motor neuron dysfunction in humans and neuromuscular junction defects in zebrafish. Theranostics. 11:2788-2805
- Ding, S., Gu, Y., Cai, Y., Cai, M., Yang, T., Bao, S., Shen, W., Ni, X., Chen, G., Xing, L. (2020) Integrative systems and functional analyses reveal a role of dopaminergic signaling in myelin pathogenesis. Journal of translational medicine. 18:109
- Zhang, T., Guan, P., Liu, W., Zhao, G., Fang, Y., Fu, H., Gui, J.F., Li, G., Liu, J.X. (2020) Copper Stress Induces Zebrafish Central Neural System Myelin Defects via WNT/NOTCH-hoxb5b Signaling and pou3f1/fam168a/fam168b DNA Methylation. Biochimica et biophysica acta. Gene regulatory mechanisms. 1863(10):194612
- Admati, I., Wasserman-Bartov, T., Tovin, A., Rozenblat, R., Blitz, E., Zada, D., Lerer-Goldshtein, T., Appelbaum, L. (2019) Neural alterations and hyperactivity of the hypothalamic-pituitary-thyroid axis in Oatp1c1-deficiency. Thyroid : official journal of the American Thyroid Association. 30(1):161-174
- Pant, D.C., Dorboz, I., Schlüter, A., Fourcade, S., Launay, N., Joya, J., Aguilera-Albesa, S., Yoldi, M.E., Casasnovas, C., Willis, M.J., Ruiz, M., Ville, D., Lesca, G., Siquier-Pernet, K., Desguerre, I., Yan, H., Wang, J., Burmeister, M., Brady, L., Tarnopolsky, M., Cornet, C., Rubbini, D., Terriente, J., James, K.N., Musaev, D., Zaki, M.S., Patterson, M.C., Lanpher, B.C., Klee, E.W., Pinto E Vairo, F., Wohler, E., Sobreira, N.L.M., Cohen, J.S., Maroofian, R., Galehdari, H., Mazaheri, N., Shariati, G., Colleaux, L., Rodriguez, D., Gleeson, J.G., Pujades, C., Fatemi, A., Boespflug-Tanguy, O., Pujol, A. (2019) Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leukodystrophy. The Journal of Clinical Investigation. 129(3):1240-1256
- Bhandari, S., Lee, J.N., Kim, Y.I., Nam, I.K., Kim, S.J., Kim, S.J., Kwak, S., Oh, G.S., Kim, H.J., Yoo, H.J., So, H.S., Choe, S.K., Park, R. (2016) The fatty acid chain elongase, Elovl1, is required for kidney and swim bladder development during zebrafish embryogenesis. Organogenesis. 12(2):78-93
- Zada, D., Tovin, A., Lerer-Goldshtein, T., Appelbaum, L. (2016) Pharmacological and BBB-targeted genetic therapies for thyroid hormone-dependent hypomyelination. Disease models & mechanisms. 9(11):1339-1348
- Kim, Y. I., Bhandari, S., Lee, J. N., Yoo, K. W., Kim, S. J., Oh, G. S., Kim, H. J., Cho, M., Kwak, J. Y., So, H. S., Park, R., Choe, S. K. (2014) Developmental roles of D-bifunctional protein-A zebrafish model of peroxisome dysfunction. Molecules and cells. 37(1):74-80
- Chung, A.Y., Kim, P.S., Kim, S., Kim, E., Kim, D., Jeong, I., Kim, H.K., Ryu, J.H., Kim, C.H., Choi, J., Seo, J.H., and Park, H.C. (2013) Generation of demyelination models by targeted ablation of oligodendrocytes in the zebrafish CNS. Molecules and cells. 36(1):82-7
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