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Induced pluripotent stem cell models of Zellweger spectrum disorder show impaired peroxisome assembly and cell type-specific lipid abnormalities.
- Published in:
- Stem Cell Research & Therapy, 2015, v. 6, n. 1, p. 1, doi. 10.1186/s13287-015-0149-3
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- Article
The gene expression profiles of induced pluripotent stem cells from individuals with childhood cerebral adrenoleukodystrophy are consistent with proposed mechanisms ofp athogenesis.
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- Stem Cell Research & Therapy, 2012, v. 3, n. 5, p. 130, doi. 10.1186/scrt130
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- Article
Derivation of induced pluripotent stem cells from orangutan skin fibroblasts.
- Published in:
- BMC Research Notes, 2015, p. 1, doi. 10.1186/s13104-015-1567-0
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- Article
Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.
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- Human Mutation, 2009, v. 30, n. 3, p. E467, doi. 10.1002/humu.20932
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- Article
A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population.
- Published in:
- BMC Medical Genetics, 2012, v. 13, n. 1, p. 72, doi. 10.1186/1471-2350-13-72
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- Article