Evidence map›Paper›PMID 39745639›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Probing Cell-Type Specificity of Mutant Phenotype at Transcriptomic Level Using Mosaic Analysis with Double Markers (MADM).

Giselle Cheung, Florian M Pauler, Simon Hippenmeyer

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Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Giselle Cheung *Institute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Florian M Pauler *Institute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Simon HippenmeyerInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria. simon.hippenmeyer@ist.ac.at.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mosaic Analysis with Double Markers (MADM) represents a mouse genetic approach coupling differential fluorescent labeling to genetic manipulations in dividing cells and their lineages. MADM uniquely enables the generation and visualization of individual control or homozygous mutant cells in a heterozygous genetic environment. Among its diverse applications, MADM has been used to dissect cell-autonomous gene functions important for cortical development and neural development in general. The high cellular resolution offered by MADM also permits the analysis of transcriptomic changes of individual cells upon genetic manipulations. In this chapter, we describe an experimental protocol combining the generation and isolation of MADM-labeled cells with downstream single-cell RNA-sequencing technologies to probe cell-type specific phenotypes due to genetic mutations at single-cell resolution.

Indexed as

MutationPhenotypeSingle-Cell AnalysisTranscriptomeAnimalsGene Expression ProfilingGenetic MarkersMiceMosaicismGenetic MarkersCell-type diversityCell-type identityDevelopmentGenetic mosaicsLineageMosaic Analysis with Double Markers (MADM)Single-cell RNA sequencing

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.