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A Prevalence of Imprinted Genes within the Total Transcriptomes of Human Tissues and Cells

Genomic imprinting is an epigenetic phenomenon that causes a differential expression of paternally and maternally inherited alleles of a subset of genes (the so-called imprinted genes). Imprinted genes are distributed throughout the genome and it is predicted that about 1% of the human genes may be...

Täydet tiedot

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Bibliografiset tiedot
Päätekijä: Anisimov, Sergey V.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Hindawi Publishing Corporation 2012
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3446743/
https://ncbi.nlm.nih.gov/pubmed/22997578
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2012/793506
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