SILAC mouse for quantitative proteomics uncovers kindlin-3 as an essential factor for red blood cell function.

By M. Krüger, M. Moser, S. Ussar, I. Thievessen, Christian A. Luber, Francesca Forner, S. Schmidt, Sara Zanivan, R. Fässler, Matthias Mann. Cell, 2008

730 citations recorded by the source corpus.

Subfields: Physiology, Spectroscopy

View Paper: https://www.semanticscholar.org/paper/21eb24ddfad6db566f7aea19b6d9bace21ed4331

How researchers see this paper

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

In Physiology

1. J. Tschopp

In Spectroscopy

1. Jüergen Cox
2. Matthias Mann
3. John R. Yates III
4. C. Ruse
5. A. Nakorchevsky
6. Christian A. Luber
7. Matthias Selbach
8. M. Krüger

Citations in the corpus

• Acquisition of the contractile phenotype by murine arterial smooth muscle cells depends on the Mir143/145 gene cluster. (2009, methodology): “Our experimental system was based on quantitative, mass spectrometry–based (MS-based) proteomics using reference mice that were completely labeled with a (13)C6-lysine–substituted version of lysine (“SILAC mice”) (15), combined with microarraybased transcriptional profiling.”
• Quantitative proteomics reveals subset-specific viral recognition in dendritic cells. (2010, methodology): “We showed recently that the SILAC approach can also be used to label entire mice (Krüger et al., 2008).”
• Proteomics by mass spectrometry: approaches, advances, and applications. (2009, methodology): “Recently, SILAC has been applied to labeling of primary cells (184) and mice (185).”