Sort   by:  
 Page size 
TranscriptomicsUbe3a-ATS characterization with strand-speicific microarray
This strand-specific array is performed to characterize expression features of Ube3a-ATS, including its imprinting status, its exon-intron structure, its transcriptional initiation and termination site as well as its polyadenylation status. The array contains reverse-complementary probes detecting t...
ORGANISM(S): Mus musculus 
2012-05-02 | E-GEOD-29254 | biostudies-arrayexpress
TranscriptomicsmicroRNA expression profiles from three arterial tortuosity syndrome (ATS) patients' skin fibroblasts with recessive SLC2A10 mutations [miRNA]
To screen for potential miRNA that may contribute to the pathomechanisms of ATS miRNA expression profiling using the Affymetrix GeneChip® miRNA 3.0 Array comparing the miRNA expression changes of skin fibroblasts of three ATS patients with those of three healthy individuals Comparison of miRNA expre...
ORGANISM(S): Homo sapiens 
2015-09-21 | E-GEOD-71172 | biostudies-arrayexpress
TranscriptomicsMicroarray expression data from three arterial tortuosity syndrome (ATS) patients' skin fibroblasts with recessive SLC2A10 mutations
To screen for candidate genes that may contribute to the pathogenesis of ATS Transcriptome-wide expression profiling using the Affymetrix Gene 1.0 ST platform comparing the gene expression patterns of skin fibroblasts of three ATS patients with those of three healthy individuals Comparison between t...
ORGANISM(S): Homo sapiens 
2015-09-21 | E-GEOD-70683 | biostudies-arrayexpress
ProteomicsITRAQ of HEK293T-cell protein 48 hours after transfection of phagocytophilic anaplastic effector protein Ats-1
ITRAQ of HEK293T-cell protein 48 hours after transfection of phagocytophilic anaplastic effector protein Ats-1
ORGANISM(S): Homo Sapiens 
2021-10-28 | PXD029412 |
TranscriptomicsThe Xq22.3 contiguous gene deletion syndrome (ATS-ID): from genotype to further delineation of the phenotype
Large Xq22.3 deletion in Czech family inherited from unaffaceted mother leading to manifestation of X-linked contiguous gene deletion syndrome known as Alport syndrome with intellectual disability (ATS-ID) or AMME complex (OMIM #300194)
ORGANISM(S): Homo sapiens 
2019-12-02 | E-MTAB-8324 | biostudies-arrayexpress
GenomicsThe Xq22.3 contiguous gene deletion syndrome (ATS-ID)
Alport syndrome with intellectual disability (ATS-ID), also known as AMME complex (OMIM #300194), is an X-linked contiguous gene deletion syndrome associated with an Xq22.3 locus mainly characterized by haematuria, renal failure, hearing loss/deafness, ID/mental retardation (MR), midface hypoplasia ...
EGAS00001005354 | EGA
TranscriptomicsUbe3a-ATS characterization with strand-speicific microarray
This strand-specific array is performed to characterize expression features of Ube3a-ATS, including its imprinting status, its exon-intron structure, its transcriptional initiation and termination site as well as its polyadenylation status. The array contains reverse-complementary probes detecting t...
ORGANISM(S): Mus musculus 
2012-05-03 | GSE29254 | GEO
TranscriptomicsMicroarray expression data from three arterial tortuosity syndrome (ATS) patients' skin fibroblasts with recessive SLC2A10 mutations
To screen for candidate genes that may contribute to the pathogenesis of ATS Transcriptome-wide expression profiling using the Affymetrix Gene 1.0 ST platform comparing the gene expression patterns of skin fibroblasts of three ATS patients with those of three healthy individuals
ORGANISM(S): Homo sapiens 
2015-09-21 | GSE70683 | GEO
GenomicsmicroRNA expression profiles from three arterial tortuosity syndrome (ATS) patients' skin fibroblasts with recessive SLC2A10 mutations [miRNA]
To screen for potential miRNA that may contribute to the pathomechanisms of ATS miRNA expression profiling using the Affymetrix GeneChip® miRNA 3.0 Array comparing the miRNA expression changes of skin fibroblasts of three ATS patients with those of three healthy individuals
ORGANISM(S): synthetic construct Homo sapiens 
2015-09-21 | GSE71172 | GEO
UnknownAnaplasma phagocytophilum Ats-1 enhances exosome secretion through Syntenin-1.
Not available
S-EPMC10523776 | biostudies-literature
Sort   by:  
 Page size