Genome-wide consequences of compromised NMD and their relavence for variable clinical phenotype of patients with UPF3B mutations - refine.bio

GSE27433

Homo sapiens

18 Downloadable Samples

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Affymetrix Human Exon 1.0 ST Array [transcript (gene) version (huex10st), Affymetrix Human Human Exon 1.0 ST Array (huex10st)

Submitter Supplied Information

Description

This SuperSeries is composed of the SubSeries listed below.

PubMed ID

Publication Title

Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability.

Total Samples

32

Submitter’s Institution

Authors

Nguyen LS, Jolly L, Shoubridge C, Chan WK, Huang L, Laumonnier F, Raynaud M, Hackett A, Field M, Rodriguez J, Srivastava AK, Lee Y, Long R, Addington AM, Rapoport JL, Suren S, Hahn CN, Gamble J, Wilkinson MF, Corbett MA, Gecz J

Source Repository

Gene Expression Omnibus (GEO)

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