The application of spatial transcriptomics to histological sections: A cutting-edge technique for medical diagnosis (notice n° 177752)

détails MARC
000 -LEADER
fixed length control field 02410cam a2200181 4500500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250112040737.0
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Language code of text/sound track or separate title fre
042 ## - AUTHENTICATION CODE
Authentication code dc
100 10 - MAIN ENTRY--PERSONAL NAME
Personal name Maitre, Marlène
Relator term author
245 00 - TITLE STATEMENT
Title The application of spatial transcriptomics to histological sections: A cutting-edge technique for medical diagnosis
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Date of publication, distribution, etc. 2024.<br/>
500 ## - GENERAL NOTE
General note 81
520 ## - SUMMARY, ETC.
Summary, etc. Spatial omics have been evolving rapidly in recent years and due to the richness of the data they provide, they appear to offer opportunities for understanding biological phenomena and improving healthcare. Spatial omics enable the analysis of genomic, transcriptional, proteomic, and metabolic content at very high resolution. Beyond identifying molecular cell subpopulations, these approaches also provide information about the spatial location of the identified subpopulations within tissue, their proximity to each other, and their relationship with the extracellular matrix, blood vessels, and other tissue components. Spatial transcriptomics (ST) is an emerging research field that combines high-throughput genetic analysis with the spatial localization of cells within tissues. Unlike traditional sequencing methods, ST offers a more comprehensive understanding of the molecular and cellular organization of tissues. Our review explores various ST profiling strategies, including laser microdissection, which isolates specific cells from tissue for in-depth omics analyses. We then present various fluorescence in situ hybridization (FISH) techniques used in ST. Some state-of-the-art techniques allow simultaneous visualization of numerous targeted transcripts and proteins with 3D subcellular resolution. ST techniques based on higher-resolution sequencing are also described in the final section. Future challenges for ST include improving the spatial resolution of NGS-based methods and gaining an in-depth understanding of cellular networks and tissue interactions. The rapid evolution of these technologies offers exciting opportunities to better understand complex biological mechanisms in the spatial context of tissues.
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Daubon, Thomas
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Martins, Frédéric
Relator term author
786 0# - DATA SOURCE ENTRY
Note Innovations & Thérapeutiques en Oncologie | Volume 10 | 2 | 2024-04-17 | p. 93-103 | 2431-3203
856 41 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://shs.cairn.info/journal-innovations-therapeutiques-en-oncologie-2024-2-page-93?lang=en">https://shs.cairn.info/journal-innovations-therapeutiques-en-oncologie-2024-2-page-93?lang=en</a>

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