Establishment of an iPSC line from a NDD patient with a heterozygous mutation in the CTNNB1 gene-Reference-Cited by-同舟云学术

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Establishment of an iPSC line from a NDD patient with a heterozygous mutation in the CTNNB1 gene

Published:2024-09 Issue: Volume:79 Page:103487
ISSN:1873-5061
Container-title:Stem Cell Research
language:en
Short-container-title:Stem Cell Research

Author:

Ning Jiaying,Zhou Tiancheng,Luo Xianqiong,Ma Jian,Zhang Zhishuai,Gao Liwei,Zhu Yanling^ORCID

Publisher

Elsevier BV

Reference7 articles.

1. Excessive β-Catenin in Excitatory Neurons Results in Reduced Social and Increased Repetitive Behaviors and Altered Expression of Multiple Genes Linked to Human Autism;Alexander;Front. Synaptic Neurosci.,2020

2. Exon 3 mutations of CTNNB1 drive tumorigenesis: a review;Gao;Oncotarget,2017

3. A homozygous variant in INTS11 links mitosis and neurogenesis defects to a severe neurodevelopmental disorder;Kuang;Cell Rep.,2023

4. Optimized Approaches for Generation of Integration-free iPSCs from Human Urine-Derived Cells with Small Molecules and Autologous Feeder;Li;Stem Cell Rep.,2016

5. Neurodevelopmental disorders-the history and future of a diagnostic concept;Morris-Rosendahl;Dialogues Clin. Neurosci.,2020

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