Generation of iPSC line NCHi012-A from a patient with Alagille syndrome and heterozygous pathogenic variant in the JAG1 gene

Alagille syndrome (ALGS) is an autosomal dominant disease affecting the liver, heart and other organs with high variability. About 95% of ALGS cases are associated with pathogenic variants in JAG1, encoding the Jagged1 ligand that binds to Notch receptors. The iPSC line NCHi012-A was derived from an...

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Detalles Bibliográficos
Autores principales: Cunningham, David, Stanberry, Isaac, Ye, Shiqiao, Alonzo, Matthew, Zhao, Ming-Tao, Garg, Vidu, Lilly, Brenda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10528323/
https://www.ncbi.nlm.nih.gov/pubmed/37549562
http://dx.doi.org/10.1016/j.scr.2023.103177

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10528323/
https://www.ncbi.nlm.nih.gov/pubmed/37549562
http://dx.doi.org/10.1016/j.scr.2023.103177

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