Sort   by:  
 Page size 
UnknownA pilot study of risk-adapted radiotherapy and chemotherapy in patients with supratentorial PNET.
Not available
S-EPMC2718957 | biostudies-literature
UnknownA Premature Termination Codon Mutation in MYBPC3 Causes Hypertrophic Cardiomyopathy via Chronic Activation of Nonsense-Mediated Decay.
Not available
S-EPMC6443405 | biostudies-literature
TranscriptomicsTranscriptional super-enhancers connected to cell identity and disease
Super-enhancers are large clusters of transcriptional enhancers that drive expression of genes that control and define cell identity. Improved understanding of the roles super-enhancers play in biology would be afforded by knowing the constellation of factors that constitute these domains and by ide...
ORGANISM(S): Homo sapiens 
2013-10-23 | E-GEOD-51522 | biostudies-arrayexpress
TranscriptomicsDiminishment of NFIL3 by shRNA in HEK293 and BT549 cells
This SuperSeries is composed of the following subset Series: GSE31425: BT549 cells with control or NFIL3 shRNA treatment GSE31426: HEK293 cells with control or NFIL3 shRNA treatment Refer to individual Series
ORGANISM(S): Homo sapiens 
2012-09-02 | E-GEOD-31427 | biostudies-arrayexpress
TranscriptomicsBT549 cells with control or NFIL3 shRNA treatment
Transcriptional profiling with samples from BT549 cells that were infected with control or NFIL3 shRNA Two condition experiment: control (scr) shRNA (two replicates) and NFIL3 shRNA (two replicates)
ORGANISM(S): Homo sapiens 
2012-09-02 | E-GEOD-31425 | biostudies-arrayexpress
TranscriptomicsHEK293 cells with control or NFIL3 shRNA treatment
Transcriptional profiling with samples from HEK293 cells that were infected with control or NFIL3 shRNA Two condition experiment: control (scr) shRNA (six replicates) and NFIL3 shRNA (four replicates)
ORGANISM(S): Homo sapiens 
2012-09-02 | E-GEOD-31426 | biostudies-arrayexpress
UnknownBiallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder.
Not available
S-EPMC7447524 | biostudies-literature
UnknownThe landscape of reported VUS in multi-gene panel and genomic testing: Time for a change.
Not available
S-EPMC10825061 | biostudies-literature
UnknownDe Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Collosum, Axon, Cardiac, Ocular, and Genital Defects.
Not available
S-EPMC6817525 | biostudies-literature
UnknownProgressive cerebellar atrophy in a patient with complex II and III deficiency and a novel deleterious variant in SDHA: A Counseling Conundrum.
Not available
S-EPMC8222855 | biostudies-literature
Sort   by:  
 Page size