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Apparent bias toward long gene misregulation in MeCP2 syndromes disappears after controlling for baseline variations

Recent studies have suggested that genes longer than 100 kb are more likely to be misregulated in neurological diseases associated with synaptic dysfunction, such as autism and Rett syndrome. These length-dependent transcriptional changes are modest in MeCP2-mutant samples, but, given the low sensit...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Nat Commun
Päätekijät: Raman, Ayush T., Pohodich, Amy E., Wan, Ying-Wooi, Yalamanchili, Hari Krishna, Lowry, William E., Zoghbi, Huda Y., Liu, Zhandong
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Nature Publishing Group UK 2018
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6089998/
https://ncbi.nlm.nih.gov/pubmed/30104565
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-018-05627-1
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