Mosaic analysis with a repressible cell marker (MARCM) for Drosophila neural development.

By Tzumin Lee, Liqun Luo. Trends in Neurosciences, 2001

1,005 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/3cd61783a889bc72a4bbb004347e4d5db3208d2e

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Cellular and Molecular Neuroscience

1. Wayne Pereanu
2. Volker Hartenstein
3. A. Younossi‐Hartenstein
4. Diana Shy
5. Shana R. Spindler
6. S. Fung
7. H. Reichert
8. Abilasha Kumar

In Molecular Biology

1. Wayne Pereanu
2. Jin Jiang
3. S. Zipursky
4. T. Newsome
5. C. Tsui
6. Yi Chen
7. Volker Hartenstein
8. Barry J. Dickson

In Plant Science

1. Volker Hartenstein
2. T. Newsome
3. Barry J. Dickson
4. B. Åsling
5. Wayne Pereanu

Citations in the corpus

• The TEAD/TEF family of transcription factor Scalloped mediates Hippo signaling in organ size control. (2008, methodology): “The MARCM system was used to express transgenes in mitotic clones (Lee and Luo, 2001).”
• Invasive and indigenous microbiota impact intestinal stem cell activity through multiple pathways in Drosophila. (2009, background): “We further tested the effect of reducing JAK–STAT signaling by generating mosaic animals with clones that are mutant for the STAT92E transcription factor (Lee and Luo 2001; Krezmien et al. 2007).”
• Neural Lineages of the Drosophila Brain: A Three-Dimensional Digital Atlas of the Pattern of Lineage Location and Projection at the Late Larval Stage (2006, methodology): “We also used the MARCM technique to generate labeled clones (Lee and Luo, 2001).”
• Development‐based compartmentalization of the Drosophila central brain (2010, methodology): “For MARCM experiments (Lee and Luo, 2001), embryos of the appropriate genotype were collected on standard cornmeal/yeast/agar medium supplemented with live yeast over a 4-hour time window and raised at 25 C for 21–25 hours before heat-shock treatment.”
• Analysis of Drosophila photoreceptor axon guidance in eye-specific mosaics. (2000, methodology): “Where these cells need not be eliminated, but merely excluded from analysis, Lee and Luo (1999) have developed an elegant method, the MARCM system, to positively rather than negatively label mutant cells.”
• Patterns of growth, axonal extension and axonal arborization of neuronal lineages in the developing Drosophila brain. (2009, methodology): “For MARCM experiments (Lee and Luo, 2001), embryos of the appropriate genotype were collected on standard cornmeal/yeast/agar medium supplemented with live yeast over a 4 hour time window and raised at 25°C for 21 to 25 hours before heat-shock treatment.”
• Cell-type Specific Labeling of Synapses in vivo through Synaptic Tagging with Recombination (STaR) (2014, background): “The synaptic markers can be readily integrated into genetic schemes, such as RNA interference and mosaic analysis with a repressible cell marker (MARCM), to study the molecular mechanisms underlying synaptic specificity (Dietzl et al., 2007; Lee and Luo, 2001; Ni et al., 2009).”