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

Recent cutting-edge human genetics technology has allowed us to identify copy number variations (CNVs) and has provided new insights for understanding causative mechanisms of human diseases. A growing number of studies show that CNVs could be associated with physiological mechanisms linked to evolut...

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Vydané v:	International journal of molecular sciences Ročník 21; číslo 5; s. 1860
Hlavní autori:	Casamassa, Alessia, Ferrari, Daniela, Gelati, Maurizio, Carella, Massimo, Vescovi, Angelo Luigi, Rosati, Jessica
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	Switzerland MDPI AG 09.03.2020 MDPI
Predmet:	Animals Brain Cellular Reprogramming - genetics Central Nervous System - physiology Chromosomes Chromosomes, Human, Pair 15 - genetics DNA Copy Number Variations - genetics Genetic Diseases, Inborn - genetics Genetic disorders Genomic Instability - genetics Humans Induced Pluripotent Stem Cells - physiology Mutation Review neurodevelopmental diseases 15q iPSCs Copy Number Variation (CNV) induced pluripotent stem cells (iPSCs) 15q mice neuropsychiatric diseases
ISSN:	1422-0067, 1661-6596, 1422-0067
On-line prístup:	Získať plný text
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