Signaling from Within: Endocytic Trafficking of the Robo Receptor Is Required for Midline Axon Repulsion
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Vyšlo v časopise:
Signaling from Within: Endocytic Trafficking of the Robo Receptor Is Required for Midline Axon Repulsion. PLoS Genet 11(9): e32767. doi:10.1371/journal.pgen.1005441
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prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pgen.1005441
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Zdroje
1. Chance RK, Bashaw GJ. Slit-dependent endocytic trafficking of the Robo receptor is required for Son of Sevenless recruitment and midline axon repulsion. PLoS Genet. 2015; 11(9): e1005371.
2. Piper M, Salih S, Weinl C, Holt C, Harris W (2005) Endocytosis-dependent desensitization and protein synthesis-dependent resensitization in retinal growth cone adaptation. Nat Neurosci 8: 179–186. 15643427
3. Yang L, Bashaw GJ (2006) Son of sevenless directly links the Robo receptor to rac activation to control axon repulsion at the midline. Neuron 52: 595–607. 17114045
4. Piper M, Anderson R, Dwivedy A, Weinl C, van Horck F, et al. (2006) Signaling mechanisms underlying Slit2-induced collapse of Xenopus retinal growth cones. Neuron 49: 215–228. 16423696
5. Jen JC, Chan W-M, Bosley TM, Wan J, Carr JR, et al. (2004) Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis. Science 304: 1509–1513. 15105459
6. Anitha A, Nakamura K, Yamada K, Suda S, Thanseem I, et al. (2008) Genetic analyses of roundabout (ROBO) axon guidance receptors in autism. Am J Med Genet B Neuropsychiatr Genet 147B: 1019–1027. doi: 10.1002/ajmg.b.30697 18270976
7. Potkin SG, Turner JA, Guffanti G, Lakatos A, Fallon JH, et al. (2009) A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. Schizophr Bull 35: 96–108. doi: 10.1093/schbul/sbn155 19023125
8. Hannula-Jouppi K, Kaminen-Ahola N, Taipale M, Eklund R, Nopola-Hemmi J, et al. (2005) The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia. PLoS Genet 1: e50. 16254601
Štítky
Genetika Reprodukčná medicínaČlánok vyšiel v časopise
PLOS Genetics
2015 Číslo 9
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