15q11.2–13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain

Copy number variations (CNVs) within human 15q11.2–13.3 show reduced penetrance and variable expressivity in a range of neurologic disorders. Therefore, characterizing 15q11.2–13.3 chromatin structure is important for understanding the regulation of this locus during normal neuronal development. Del...

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Hlavní autoři: Yasui, Dag H., Scoles, Haley A., Horike, Shin-ichi, Meguro-Horike, Makiko, Dunaway, Keith W., Schroeder, Diane I., LaSalle, Janine M.
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2011
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3196884/
https://ncbi.nlm.nih.gov/pubmed/21840925
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr357
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