ZFIN Publication List

ZFIN ID: ZDB-ATB-140502-2

CITATIONS (21 total)

Antibody Name: Ab3-myc

Alhashem, Z., Feldner-Busztin, D., Revell, C., Alvarez-Garcillan Portillo, M., Camargo-Sosa, K., Richardson, J., Rocha, M., Gauert, A., Corbeaux, T., Milanetto, M., Argenton, F., Tiso, N., Kelsh, R., Prince, V.E., Bentley, K., Linker, C. (2022) Notch controls the cell cycle to define leader versus follower identities during collective cell migration. eLIFE. 11:

Bühler, A., Kustermann, M., Bummer, T., Rottbauer, W., Sandri, M., Just, S. (2016) Atrogin-1 Deficiency Leads to Myopathy and Heart Failure in Zebrafish. International Journal of Molecular Sciences. 17(2)

Chen, X., Liu, F., Chen, K., Wang, Y., Yin, A., Kang, X., Yang, S., Zhao, H., Dong, S., Li, Y., Chen, J., Wu, Y. (2022) TFG mutation induces haploinsufficiency and drives axonal Charcot-Marie-Tooth disease by causing neurite degeneration. CNS neuroscience & therapeutics. 28(12):2076-2089

Fasano, G., Muto, V., Radio, F.C., Venditti, M., Mosaddeghzadeh, N., Coppola, S., Paradisi, G., Zara, E., Bazgir, F., Ziegler, A., Chillemi, G., Bertuccini, L., Tinari, A., Vetro, A., Pantaleoni, F., Pizzi, S., Conti, L.A., Petrini, S., Bruselles, A., Prandi, I.G., Mancini, C., Chandramouli, B., Barth, M., Bris, C., Milani, D., Selicorni, A., Macchiaiolo, M., Gonfiantini, M.V., Bartuli, A., Mariani, R., Curry, C.J., Guerrini, R., Slavotinek, A., Iascone, M., Dallapiccola, B., Ahmadian, M.R., Lauri, A., Tartaglia, M. (2022) Dominant ARF3 variants disrupt Golgi integrity and cause a neurodevelopmental disorder recapitulated in zebrafish. Nature communications. 13:6841

Fischer, B., Metzger, M., Richardson, R., Knyphausen, P., Ramezani, T., Franzen, R., Schmelzer, E., Bloch, W., Carney, T.J., and Hammerschmidt, M. (2014) p53 and TAp63 promote keratinocyte proliferation and differentiation in breeding tubercles of the zebrafish. PLoS Genetics. 10(1):e1004048

He, M., Jiao, S., Zhang, R., Ye, D., Wang, H., Sun, Y. (2022) Translational control by maternal Nanog promotes oogenesis and early embryonic development. Development (Cambridge, England). 149(24):

Krueger, L.A., Morris, A.C. (2022) Generation of a zebrafish knock-in line expressing MYC-tagged Sox11a using CRISPR/Cas9 genome editing. Biochemical and Biophysical Research Communications. 608:8-13

Kustermann, M., Manta, L., Paone, C., Kustermann, J., Lausser, L., Wiesner, C., Eichinger, L., Clemen, C.S., Schröder, R., Kestler, H.A., Sandri, M., Rottbauer, W., Just, S. (2018) Loss of the novel Vcp (valosin containing protein) interactor Washc4 interferes with autophagy-mediated proteostasis in striated muscle and leads to myopathy in vivo. Autophagy. 14(11):1911-1927

LaFlamme, A., Young, K.E., Lang, I., Weiser, D.C. (2018) Alternative splicing of (ppp1r12a/mypt1) in zebrafish produces a novel myosin phosphatase targeting subunit. Gene. 675:15-26

Légaré, V.P., Rampal, C.J., Gurberg, T.J.N., Harji, Z.A., Allard-Chamard, X., Rodríguez, E.C., Armstrong, G.A.B. (2022) Development of an endogenously myc-tagged TARDBP (TDP-43) zebrafish model using the CRISPR/Cas9 system and homology directed repair. Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology. 261:110756

Marsden, A.N., Derry, S.W., Schneider, I., Scott, C.A., Westfall, T.A., Brastrom, L.K., Shea, M., Dawson, D.V., Slusarski, D.C. (2017) The Nkd EF-Hand Domain Modulates Divergent Wnt Signaling Outputs in Zebrafish. Developmental Biology. 434(1):63-73

Masselink, W., Masaki, M., Sieiro, D., Marcelle, C., Currie, P.D. (2017) Phosphorylation of Lbx1 controls lateral myoblast migration into the limb. Developmental Biology. 430:302-309

Pan, X., Sittaramane, V., Gurung, S., and Chandrasekhar, A. (2014) Structural and temporal requirements of Wnt/PCP protein Vangl2 function for convergence and extension movements and facial branchiomotor neuron migration in zebrafish. Mechanisms of Development. 131:1-14

Petel Légaré, V., Harji, Z.A., Rampal, C.J., Allard-Chamard, X., Rodríguez, E.C., Armstrong, G.A.B. (2019) Augmentation of spinal cord glutamatergic synaptic currents in zebrafish primary motoneurons expressing mutant human TARDBP (TDP-43). Scientific Reports. 9:9122

Scott, C.A., Marsden, A.N., Rebagliati, M.R., Zhang, Q., Chamling, X., Searby, C.C., Baye, L.M., Sheffield, V.C., Slusarski, D.C. (2017) Nuclear/cytoplasmic transport defects in BBS6 underlie congenital heart disease through perturbation of a chromatin remodeling protein. PLoS Genetics. 13:e1006936

Seese, S.E., Muheisen, S., Gath, N., Gross, J.M., Semina, E.V. (2022) Identification of HSPA8 as an interacting partner of MAB21L2 and an important factor in eye development. Developmental Dynamics : an official publication of the American Association of Anatomists. 252(4):510-526

Wen, L., Zhang, T., Wang, J., Jin, X., Rouf, M.A., Luo, D., Zhu, Y., Lei, D., Gregersen, H., Wang, Y., Wang, G. (2021) The blood flow-klf6a-tagln2 axis drives vessel pruning in zebrafish by regulating endothelial cell rearrangement and actin cytoskeleton dynamics. PLoS Genetics. 17:e1009690

Williams, M.L.K., Sawada, A., Budine, T., Yin, C., Gontarz, P., Solnica-Krezel, L. (2018) Gon4l regulates notochord boundary formation and cell polarity underlying axis extension by repressing adhesion genes. Nature communications. 9:1319

Xiong, Z., Lo, H.P., McMahon, K.A., Martel, N., Jones, A., Hill, M.M., Parton, R.G., Hall, T.E. (2021) In vivo proteomic mapping through GFP-directed proximity-dependent biotin labelling in zebrafish. eLIFE. 10:

Zhao, H., Di Mauro, G., Lungu-Mitea, S., Negrini, P., Guarino, A.M., Frigato, E., Braunbeck, T., Ma, H., Lamparter, T., Vallone, D., Bertolucci, C., Foulkes, N.S. (2018) Modulation of DNA Repair Systems in Blind Cavefish during Evolution in Constant Darkness. Current biology : CB. 28(20):3229-3243.e4

Additional Citations (1):

ZFIN Staff (2008) Antibody information from supplier. Manually curated data.