Detalhe da pesquisa
1.
A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population.
BMC Med Genet
; 13: 72, 2012 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22894767
2.
Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.
Hum Mutat
; 30(3): E467-80, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19105186
3.
Derivation of induced pluripotent stem cells from orangutan skin fibroblasts.
BMC Res Notes
; 8: 577, 2015 Oct 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-26475477
4.
Induced pluripotent stem cell models of Zellweger spectrum disorder show impaired peroxisome assembly and cell type-specific lipid abnormalities.
Stem Cell Res Ther
; 6: 158, 2015 Aug 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-26319495
5.
The gene expression profiles of induced pluripotent stem cells from individuals with childhood cerebral adrenoleukodystrophy are consistent with proposed mechanisms of pathogenesis.
Stem Cell Res Ther
; 3(5): 39, 2012 Oct 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-23036268