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TranscriptomicsGenetic correction and analysis of induced pluripotent stem cells from a patient with gyrate atrophy
Gene-corrected patient-specific induced pluripotent stem (iPS) cells offer a novel approach to gene therapy. Yet it is unknown whether selective pressures during prolonged culture and multiple clonal events would introduce a mutational load incompatible with therapeutic use. Here we begin to assess ...
ORGANISM(S): Homo sapiens 
2011-03-01 | E-GEOD-26773 | biostudies-arrayexpress
UnknownClinical, biochemical and molecular analysis in a cohort of individuals with gyrate atrophy.
Not available
S-EPMC10476330 | biostudies-literature
UnknownVision on gyrate atrophy: why treat the eye?
Not available
S-EPMC10883273 | biostudies-literature
TranscriptomicsIdentification of osmotic stress-responsive genes dependent on HogA and AtfA in Aspergillus nidulans
Microarray analysis was used to identify the osmotic stress-responsive genes dependent on HogA and AtfA in the filamentous fungus Aspergillus nidulans. In order to identify such genes, we conducted the several types of experiment. One was a comparison between wild type with and without osmotic sho...
ORGANISM(S): Emericella nidulans 
2009-06-15 | E-GEOD-16566 | biostudies-arrayexpress
TranscriptomicsIdentification of the fludioxonil-responsive genes dependent on SskA, SrrA, HogA, and AtfA in Aspergillus nidulans
Microarray analysis was used to identify the fludioxonil-responsive genes dependent on SskA, SrrA, HogA, and AtfA in the filamentous fungus Aspergillus nidulans. In order to identify such genes, we conducted the several types of experiment. One was a comparison between wild type treated with fludio...
ORGANISM(S): Emericella nidulans 
2009-06-09 | E-GEOD-16509 | biostudies-arrayexpress
UnknownThe coincidence of two ultra-rare hereditary eye diseases: gyrate atrophy and Kjer optic atrophy - a surprising diagnosis based on next-generation sequencing.
Not available
S-EPMC8397824 | biostudies-literature
UnknownA neonate with ornithine aminotransferase deficiency; insights on the hyperammonemia-associated biochemical phenotype of gyrate atrophy.
Not available
S-EPMC9248225 | biostudies-literature
UnknownAutosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel C1QTNF5 Missense Variant.
Not available
S-EPMC7923301 | biostudies-literature
UnknownCRISPR correction of the Finnish ornithine delta-aminotransferase mutation restores metabolic homeostasis in iPSC from patients with gyrate atrophy.
Not available
S-EPMC9248217 | biostudies-literature
UnknownMild Phenotypes of Gyrate Atrophy in a Heterozygous Carrier with One Variant Allele of OAT.
Not available
S-EPMC11353755 | biostudies-literature
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