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ProteomicsStress-induced NONO interactomes
Characterization of sulforaphane- and starvation-induced NONO interactomes in wild type andNEAT1 knockout MCF7 cells
ORGANISM(S): Homo sapiens (Human) 
2026-01-16 | PXD063223 | Pride
Nono Paraspeckles Hsp70 
GenomicsRNA binding properties of NONO and NONO-delta-ER in testis
RNA binding properties of NONO and NONO-delta-ER in testis
PRJNA1096719 | ENA
GenomicsNONO knockdown RNA-seq and neuroblastoma PARCLIP analysis of NONO
NONO knockdown RNA-seq and neuroblastoma PARCLIP analysis of NONO
PRJNA471190 | ENA
ProteomicsHuman triple negative breast cancer cell line MDA-MB-231 LC-MSMS
To detect the protein that interact with NONO and illustrate the important role and the biological mechanism it may involved of NONO in TNBC.
ORGANISM(S): Homo sapiens (Human) 
2025-05-06 | PXD051842 | Pride
Tbnc Nono 
GenomicsGene expression profile at single cell level of testicular cells from the adult NONO and NONO△ER mice testis
Gene expression profile at single cell level of testicular cells from the adult NONO and NONO△ER mice testis
PRJNA1097480 | ENA
GenomicsNONO gene expression profile in breast cancer cell
NONO gene expression profile in breast cancer cell
PRJNA483751 | ENA
ProteomicsRemodeling oncogenic transcriptomes by small molecules targeting NONO
A large swath of the human proteome is dedicated to mRNA homeostasis, but most RNA-binding proteins lack chemical probes. Here, we report the discovery through phenotypic screening of electrophilic small molecules that swiftly (within 4 h) and stereospecifically decrease transcripts encoding the and...
ORGANISM(S): Homo sapiens (Human) 
2024-01-26 | PXD039283 | Pride
Proteomics 22rv1 
GenomicsTranscriptomic analysis of CAFs with silencing of NONO
Transcriptomic analysis of CAFs with silencing of NONO
PRJNA1280127 | ENA
TranscriptomicsNONO mutations cause syndromic intellectual disability and inhibitory synaptic defects
Identifying causes of sporadic intellectual disability remains a considerable medical challenge. Here, we demonstrate that null mutations in the NONO gene, a member of the Drosophila Behavior Human Splicing (DBHS) protein family, are a novel cause of X-linked syndromic intellectual disability. Com...
ORGANISM(S): Homo sapiens 
2015-09-02 | E-MTAB-2894 | biostudies-arrayexpress
TranscriptomicsNONO mutations cause syndromic intellectual disability and inhibitory synaptic defects
Identifying causes of sporadic intellectual disability remains a considerable medical challenge. Here, we demonstrate that null mutations in the NONO gene, a member of the Drosophila Behavior Human Splicing (DBHS) protein family, are a novel cause of X-linked syndromic intellectual disability. Com...
ORGANISM(S): Mus musculus 
2015-09-02 | E-MTAB-2895 | biostudies-arrayexpress
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