Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,Genetics,Biochemistry
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1. Reply to: “Correspondence to bipolar disorder-iPSC derived neural progenitor cells exhibit dysregulation of store-operated Ca2+ entry and accelerated differentiation” by Yde Ohki and colleagues;Molecular Psychiatry;2024-07-31
2. Understanding copy number variations through their genes: a molecular view on 16p11.2 deletion and duplication syndromes;Frontiers in Pharmacology;2024-06-14
3. Dysregulation of mTOR signaling mediates common neurite and migration defects in both idiopathic and 16p11.2 deletion autism neural precursor cells;eLife;2024-03-25
4. Altered hippocampal neurogenesis in a mouse model of autism revealed by genetic polymorphisms and by atypical development of newborn neurons;Scientific Reports;2024-02-26
5. Distinct neurocognitive profiles and clinical phenotypes associated with copy number variation at the 22q11.2 locus;Autism Research;2023-11-23
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