Résultats de la recherche

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(1 - 17 of 17)
Chromatin signatures and retrotransposon profiling in mouse embryos reveal regulation of LINE-1 by RNA
Samaritan myopathy, an ultimately benign congenital myopathy, is caused by a RYR1 mutation
Ikaros mediates gene silencing in T cells through Polycomb repressive complex 2
Genome-Wide Mapping of Collier In Vivo Binding Sites Highlights Its Hierarchical Position in Different Transcription Regulatory Networks
Essential role of microphthalmia transcription factor for DNA replication, mitosis and genomic stability in melanoma
The tumor suppressor Ikaros shapes the repertoire of notch target genes in T cells
Neuronal identity genes regulated by super-enhancers are preferentially down-regulated in the striatum of Huntington's disease mice
Sumoylation at chromatin governs coordinated repression of a transcriptional program essential for cell growth and proliferation
Cell-Type-Specific Gene Expression Profiling in Adult Mouse Brain Reveals Normal and Disease-State Signatures
Trim24-repressed VL30 retrotransposons regulate gene expression by producing noncoding RNA
An integrated diagnosis strategy for congenital myopathies
20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition
Next generation sequencing for molecular diagnosis of neuromuscular diseases
Reinstating plasticity and memory in a tauopathy mouse model with an acetyltransferase activator.
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement.
Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing

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