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Bardet–Biedl syndrome: Is it only cilia dysfunction?
- Published in:
- FEBS Letters, 2015, v. 589, n. 22, p. 3479, doi. 10.1016/j.febslet.2015.07.031
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- Article
The Bardet–Biedl syndrome-related protein CCDC28B modulates mTORC2 function and interacts with SIN1 to control cilia length independently of the mTOR complex.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4031, doi. 10.1093/hmg/ddt253
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- Article
Characterization of CCDC28B reveals its role in ciliogenesis and provides insight to understand its modifier effect on Bardet-Biedl syndrome.
- Published in:
- Human Genetics, 2013, v. 132, n. 1, p. 91, doi. 10.1007/s00439-012-1228-5
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- Article
Generation and characterization of Ccdc28b mutant mice links the Bardet-Biedl associated gene with mild social behavioral phenotypes.
- Published in:
- PLoS Genetics, 2022, v. 18, n. 6, p. 1, doi. 10.1371/journal.pgen.1009896
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- Article
Optimization of transgenesis conditions for the generation of CXCL2-luciferase reporter mice line.
- Published in:
- Electronic Journal of Biotechnology, 2013, v. 16, n. 6, p. 1, doi. 10.2225/vol16-issue6-fulltext-3
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- Article