ZFIN Publication List

ZFIN ID: ZDB-ATB-121128-6

CITATIONS (13 total)

Antibody Name: Ab4-h2afx

Liu, S., Feng, Z., Su, M., Liu, C., Xi, Y., Chen, H., Luo, L., Tian, X., Zhao, F., Li, L. (2024) Tango6 regulates HSPC proliferation and definitive haematopoiesis via Ikzf1 and Cmyb in caudal haematopoietic tissue. Development (Cambridge, England). 152(1):

Xu, W., Liu, X., Li, J., Sun, C., Chen, L., Zhou, J., Li, K., Li, Q., Meng, A., Sun, Q. (2024) ULI-ssDRIP-seq revealed R-loop dynamics during vertebrate early embryogenesis. Cell insight. 3:100179100179

Chen, J., Ren, C., Yao, C., Baruscotti, M., Wang, Y., Zhao, L. (2023) Identification of the natural chalcone glycoside hydroxysafflor yellow A as a suppressor of P53 overactivation-associated hematopoietic defects. MedComm. 4:e352e352

Sun, K., Han, Y., Li, J., Yu, S., Huang, Y., Zhang, Y., Reilly, J., Tu, J., Gao, P., Jia, D., Chen, X., Hu, H., Ren, M., Li, P., Luo, J., Ren, X., Zhang, X., Shu, X., Liu, F., Liu, M., Tang, Z. (2023) The splicing factor DHX38 enables retinal development through safeguarding genome integrity. iScience. 26:108103108103

Zulueta-Coarasa, T., Fadul, J., Ahmed, M., Rosenblatt, J. (2022) Physical confinement promotes mesenchymal trans-differentiation of invading transformed cells in vivo. iScience. 25:105330

Chen, X., Huang, Y., Gao, P., Lv, Y., Jia, D., Sun, K., Han, Y., Hu, H., Tang, Z., Ren, X., Liu, M. (2021) Knockout of mafba Causes Inner-Ear Developmental Defects in Zebrafish via the Impairment of Proliferation and Differentiation of Ionocyte Progenitor Cells. Biomedicines. 9(11):

Li, X., Song, G., Zhao, Y., Ren, J., Li, Q., Cui, Z. (2021) Functions of SMC2 in the Development of Zebrafish Liver. Biomedicines. 9(9):

Jing, C.B., Fu, C., Prutsch, N., Wang, M., He, S., Look, A.T. (2020) Synthetic lethal targeting of TET2-mutant hematopoietic stem and progenitor cells (HSPCs) with TOP1-targeted drugs and PARP1 inhibitors. Leukemia. 34(11):2992-3006

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

Hsu, C.H., Lin, J.S., Lai, K.P., Li, J.W., Chan, T.F., You, M.S., Tse, W.K., Jiang, Y.J. (2015) A new mib allele with a chromosomal deletion covering foxc1a exhibits anterior somite specification defect.. Scientific Reports. 5:10673

Slaats, G.G., Saldivar, J.C., Bacal, J., Zeman, M.K., Kile, A.C., Hynes, A.M., Srivastava, S., Nazmutdinova, J., Ouden, K.D., Zagers, M.S., Foletto, V., Verhaar, M.C., Miles, C., Sayer, J.A., Cimprich, K.A., Giles, R.H. (2015) DNA replication stress underlies renal phenotypes in CEP290-associated Joubert syndrome. The Journal of Clinical Investigation. 125(9):3657-66

Zheng, X., Yang, S., Han, Y., Zhao, X., Zhao, L., Tian, T., Tong, J., Xu, P., Xiong, C., and Meng, A. (2012) Loss of zygotic NUP107 protein causes missing of pharyngeal skeleton and other tissue defects with impaired nuclear pore function in zebrafish embryos. The Journal of biological chemistry. 287(45):38254-38264

Additional Citations (1):

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