SLC35A2 Deficiency Promotes an Epithelial-to-Mesenchymal Transition-like Phenotype in Madin–Darby Canine Kidney Cells

In mammalian cells, SLC35A2 delivers UDP–galactose for galactosylation reactions that take place predominantly in the Golgi lumen. Mutations in the corresponding gene cause a subtype of a congenital disorder of glycosylation (SLC35A2-CDG). Although more and more patients are diagnosed with SLC35A2-C...

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Detalles Bibliográficos
Autores principales: Kot, Magdalena, Mazurkiewicz, Ewa, Wiktor, Maciej, Wiertelak, Wojciech, Mazur, Antonina Joanna, Rahalevich, Andrei, Olczak, Mariusz, Maszczak-Seneczko, Dorota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9331475/
https://www.ncbi.nlm.nih.gov/pubmed/35892570
http://dx.doi.org/10.3390/cells11152273

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9331475/
https://www.ncbi.nlm.nih.gov/pubmed/35892570
http://dx.doi.org/10.3390/cells11152273

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