Species-Dependent Post-Transcriptional Regulation of NOS1 by FMRP in the Developing Cerebral Cortex

Fragile X syndrome (FXS), the leading monogenic cause of intellectual disability and autism, results from loss of function of the RNA-binding protein FMRP. Here we show that FMRP regulates the translation of neuronal nitric oxide synthase 1 (NOS1) in the developing human neocortex. Whereas NOS1 mRNA...

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Bibliografiset tiedot
Päätekijät: Kwan, Kenneth Y., Lam, Mandy M. S., Johnson, Matthew B., Dube, Umber, Shim, Sungbo, Rašin, Mladen-Roko, Sousa, André M. M., Fertuzinhos, Sofia, Chen, Jie-Guang, Arellano, Jon I., Chan, Daniel W., Pletikos, Mihovil, Vasung, Lana, Rowitch, David H., Huang, Eric J., Schwartz, Michael L., Willemsen, Rob, Oostra, Ben A., Rakic, Pasko, Heffer, Marija, Kostović, Ivica, Judaš, Milos, Šestan, Nenad
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2012
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3351852/
https://ncbi.nlm.nih.gov/pubmed/22579290
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2012.02.060
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