Molecular analyses of neurogenic defects in a human pluripotent stem cell model of fragile X syndrome. [electronic resource]
Producer: 20170529Description: 582-598 p. digitalISSN:- 1460-2156
- Animals
- Autism Spectrum Disorder -- genetics
- Cell Differentiation -- genetics
- Cell Movement -- genetics
- Cells, Cultured
- DNA Methylation -- genetics
- Fetus
- Fragile X Mental Retardation Protein -- genetics
- Fragile X Syndrome -- genetics
- Gene Expression Regulation -- genetics
- Gene Regulatory Networks
- Humans
- Male
- Mice
- Models, Biological
- Neurogenesis
- Pluripotent Stem Cells -- physiology
- Transfection
- Trinucleotide Repeats -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
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