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  EASI-FISH for thick tissue defines lateral hypothalamus spatio-molecular organization.

Wang, Y., Eddison, M., Fleishman, G., Weigert, M., Xu, S., Wang, T., et al. (2021). EASI-FISH for thick tissue defines lateral hypothalamus spatio-molecular organization. Cell, 184(26), 6361-6377. doi:10.1016/j.cell.2021.11.024.

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Wang, Yuhan, Autor
Eddison, Mark, Autor
Fleishman, Greg, Autor
Weigert, Martin1, Autor           
Xu, Shengjin, Autor
Wang, Tim, Autor
Rokicki, Konrad, Autor
Goina, Cristian, Autor
Henry, Fredrick E, Autor
Lemire, Andrew L, Autor
Schmidt, Uwe1, Autor           
Yang, Hui, Autor
Svoboda, Karel, Autor
Myers, Eugene W1, Autor           
Saalfeld, Stephan1, Autor           
Korff, Wyatt, Autor
Sternson, Scott M, Autor
Tillberg, Paul W, Autor
Affiliations:
1Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society, ou_2340692              

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 Zusammenfassung: Determining the spatial organization and morphological characteristics of molecularly defined cell types is a major bottleneck for characterizing the architecture underpinning brain function. We developed Expansion-Assisted Iterative Fluorescence In Situ Hybridization (EASI-FISH) to survey gene expression in brain tissue, as well as a turnkey computational pipeline to rapidly process large EASI-FISH image datasets. EASI-FISH was optimized for thick brain sections (300 μm) to facilitate reconstruction of spatio-molecular domains that generalize across brains. Using the EASI-FISH pipeline, we investigated the spatial distribution of dozens of molecularly defined cell types in the lateral hypothalamic area (LHA), a brain region with poorly defined anatomical organization. Mapping cell types in the LHA revealed nine spatially and molecularly defined subregions. EASI-FISH also facilitates iterative reanalysis of scRNA-seq datasets to determine marker-genes that further dissociated spatial and morphological heterogeneity. The EASI-FISH pipeline democratizes mapping molecularly defined cell types, enabling discoveries about brain organization.

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 Datum: 2021-12-22
 Publikationsstatus: Erschienen
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 Ort, Verlag, Ausgabe: -
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 Identifikatoren: DOI: 10.1016/j.cell.2021.11.024
Anderer: cbg-8242
PMID: 34875226
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Titel: Cell
  Andere : Cell
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 184 (26) Artikelnummer: - Start- / Endseite: 6361 - 6377 Identifikator: -