Generation of a ST3GAL3 null mutant induced pluripotent stem cell (iPSC) line (UKWMPi002-A-3) by CRISPR/Cas9 genome editing
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,General Medicine
Reference5 articles.
1. Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder;Demontis;Nat. Genet.,2019
2. ST3GAL3 mutations impair the development of higher cognitive functions;Hu;Am. J. Hum. Genet.,2011
3. Indellicato, R., Domenighini, R., Malagolini, N., Cereda, A., Mamoli, D., Pezzani, L., Iascone, M., dall’Olio, F., & Trinchera, M. (2020). A novel nonsense and inactivating variant of ST3GAL3 in two infant siblings suffering severe epilepsy and expressing circulating CA19.9. Glycobiology, 30(2), 95-104.
4. Haploinsufficiency of the attention-deficit/hyperactivity disorder risk gene St3gal3 in mice causes alterations in cognition and expression of genes involved in myelination and sialylation;Rivero;Front. Genet.,2021
5. Sialic acids in the brain: gangliosides and polysialic acid in nervous system development, stability, disease, and regeneration;Schnaar;Physiol. Rev.,2014
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