11 octobre 2020
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info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms21207491
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info:eu-repo/semantics/altIdentifier/pmid/33050604
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info:eu-repo/semantics/altIdentifier/eissn/1422-0067
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info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_F6A2CEF4CE242
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A. Lopes et al., « Emerging Roles of Single-Cell Multi-Omics in Studying Developmental Temporal Patterning. », Serveur académique Lausannois, ID : 10.3390/ijms21207491
The complexity of brain structure and function is rooted in the precise spatial and temporal regulation of selective developmental events. During neurogenesis, both vertebrates and invertebrates generate a wide variety of specialized cell types through the expansion and specification of a restricted set of neuronal progenitors. Temporal patterning of neural progenitors rests on fine regulation between cell-intrinsic and cell-extrinsic mechanisms. The rapid emergence of high-throughput single-cell technologies combined with elaborate computational analysis has started to provide us with unprecedented biological insights related to temporal patterning in the developing central nervous system (CNS). Here, we present an overview of recent advances in Drosophila and vertebrates, focusing both on cell-intrinsic mechanisms and environmental influences. We then describe the various multi-omics approaches that have strongly contributed to our current understanding and discuss perspectives on the various -omics approaches that hold great potential for the future of temporal patterning research.