Three lines of induced pluripotent stem cells derived from a 15q11.2-q13.1 duplication syndrome patient
Author:
Funder
AMED
MEXT KAKENHI
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,General Medicine
Reference4 articles.
1. Behavior of leucine-rich repeat-containing G-protein coupled receptor 5-expressing cells in the reprogramming process;Arioka;Stem Cell Res.,2017
2. Single-cell trajectory analysis of human homogenous neurons carrying a rare RELN variant;Arioka;Transl. Psychiatry,2018
3. Parental origin of interstitial duplications at 15q11.2-q13.3 in schizophrenia and neurodevelopmental disorders;Isles;PLoS Genet.,2016
4. Decreased exploratory activity in a mouse model of 15q duplication syndrome; implications for disturbance of serotonin signaling;Tamada;PLoS One,2010
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1. YETKİN YAŞLI ŞƏXSDƏ 15q11.2 XROMOSOM MİKRODUPLİKASİYASI SİNDROMUNUN DİAQNOSTİKASINA DAİR KLİNİK NÜMUNƏ;Azerbaijan Medical Journal;2024-03-28
2. Copy number variants (CNVs): a powerful tool for iPSC-based modelling of ASD;Molecular Autism;2020-06-01
3. Network Structure Analysis Identifying Key Genes of Autism and Its Mechanism;Computational and Mathematical Methods in Medicine;2020-03-23
4. A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System—A Close Look at Chromosome 15;International Journal of Molecular Sciences;2020-03-09
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