ZFIN ID:
ZDB-ATB-150407-5
CITATIONS
(10 total)
Antibody Name:
Ab5-act
Antunes, A.T., Goos, Y.J., Pereboom, T.C., Hermkens, D., Wlodarski, M.W., Da Costa, L., MacInnes, A.W. (2015) Ribosomal Protein Mutations Result in Constitutive p53 Protein Degradation through Impairment of the AKT Pathway. PLoS Genetics. 11:e1005326
de Peralta, M.S., Mouguelar, V.S., Sdrigotti, M.A., Ishiy, F.A., Fanganiello, R.D., Passos-Bueno, M.R., Coux, G., Calcaterra, N.B. (2016) Cnbp ameliorates Treacher Collins Syndrome craniofacial anomalies through a pathway that involves redox-responsive genes. Cell Death & Disease. 7:e2397
Edens, B.M., Yan, J., Deng, H.X., Siddique, T., Ma, Y.C. (2017) A novel ALS-associated variant in
UBQLN4
regulates motor axon morphogenesis.. eLIFE. 6
Gioia, R., Tonelli, F., Ceppi, I., Biggiogera, M., Leikin, S., Fisher, S., Tenedini, E., Yorgan, T.A., Schinke, T., Tian, K., Schwartz, J.M., Forte, F., Wagener, R., Villani, S., Rossi, A., Forlino, A. (2017) The chaperone activity of 4PBA ameliorates the skeletal phenotype of Chihuahua, a zebrafish model for dominant osteogenesis imperfecta. Human Molecular Genetics. 26(15):2897-2911
Hao, K., Li, Y., Feng, J., Zhang, W., Zhang, Y., Ma, N., Zeng, Q., Pang, H., Wang, C., Xiao, L., He, X. (2015) Ozone promotes regeneration by regulating the inflammatory response in zebrafish. International Immunopharmacology. 28(1):369-75
Nakaya, N., Sultana, A., Tomarev, S.I. (2017) Impaired AMPA receptor trafficking by a double knockout of zebrafish olfactomedin1a/b. Journal of neurochemistry. 143(6):635-644
Piasecka, A., Brzuzan, P., Woźny, M., Ciesielski, S., Kaczmarczyk, D. (2015) Splice-acceptor site mutation in p53 gene of hu888 zebrafish line. Journal of applied genetics. 56(1):115-21
Schaeker, K., Bartsch, S., Patry, C., Cramer-Stoll, S., Hillebrands, J.L., Wieland, T., Kroll, J. (2015) The bipartite Rac1 guanine nucleotide exchange factor engulfment and cell motility 1/dedicator of cytokinesis 180 (Elmo1/Dock180) protects endothelial cells from apoptosis in blood vessel development. The Journal of biological chemistry. 290(10):6408-18
Yao, L., Chen, J., Wu, X., Jia, S., Meng, A. (2017) Zebrafish cdc6 hypomorphic mutation causes Meier-Gorlin syndrome-like phenotype. Human Molecular Genetics. 26(21):4168-4180
Additional Citations (1):
ZFIN Staff (2008) Antibody information from supplier. Manually curated data.