Résultats de la recherche

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Phosphorylation of the retinoic acid receptor RARgamma2 is crucial for the neuronal differentiation of mouse embryonic stem cells
Chromatin signatures and retrotransposon profiling in mouse embryos reveal regulation of LINE-1 by RNA
Transcription factor TEAD4 regulates expression of myogenin and the unfolded protein response genes during C2C12 cell differentiation
Samaritan myopathy, an ultimately benign congenital myopathy, is caused by a RYR1 mutation
Constitutive arsenite oxidase expression detected in arsenic-hypertolerant Pseudomonas xanthomarina S11
Genome Sequence of Halomonas sp. Strain A3H3, Isolated from Arsenic-Rich Marine Sediments
Genes involved in cell adhesion and signaling: a new repertoire of retinoic acid receptor target genes in mouse embryonic fibroblasts
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
The tumor suppressor Ikaros shapes the repertoire of notch target genes in T cells
Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophy
Trim24-repressed VL30 retrotransposons regulate gene expression by producing noncoding RNA
Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alstrom syndromes
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
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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