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RPSA, a candidate gene for isolated congenital asplenia, is required for pre-rRNA processing and spleen formation in Xenopus

A growing number of tissue-specific inherited disorders are associated with impaired ribosome production, despite the universal requirement for ribosome function. Recently, mutations in RPSA, a protein component of the small ribosomal subunit, were discovered to underlie approximately half of all is...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Development
Päätekijät: Griffin, John N., Sondalle, Samuel B., Robson, Andrew, Mis, Emily K., Griffin, Gerald, Kulkarni, Saurabh S., Deniz, Engin, Baserga, Susan J., Khokha, Mustafa K.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: The Company of Biologists Ltd 2018
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6215398/
https://ncbi.nlm.nih.gov/pubmed/30337486
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dev.166181
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