Generation of a ZEB2 deficient human iPSC line (KICRi002A-4)
Author:
Funder
Hjärnfonden
Uppsala Universitet
Vetenskapsradet
Publisher
Elsevier BV
Reference5 articles.
1. The crucial role of ZEB2: From development to epithelial-to-mesenchymal transition and cancer complexity;Fardi;J. Cell Physiol. 234(9):14783-14799,2019
2. Mowat-Wilson syndrome;Garavelli;Orphanet J. Rare Dis.,2007
3. Derivation of human iPS cell lines from monozygotic twins in defined and xeno free conditions;Uhlin;Stem Cell Res.,2017
4. Epifanova, E., Babaev, A., Newman, A.G., Tarabykin, V., 2019. Role of Zeb2/Sip1 in neuronal development. Brain Res.15:1705:24-31.
5. Schuster, J. ; Klar, J., Khalfallah, A., Laan, L., Hoeber, J., Fatima, A., Sequeira, V.M., Jin, Z., Korol, S.V., Huss, M., Nordgren, A., Anderlid, B.M., Gallant, C., Birnir, B., Dahl, N., 2022. ZEB2 haploinsufficient Mowat-Wilson syndrome induced pluripotent stem cells show disrupted GABAergic transcriptional regulation and function. Front Mol Neurosci. 24:15:988993.
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