Minor spliceosome and disease-Reference-Cited by-同舟云学术

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Minor spliceosome and disease

Published:2018-07 Issue: Volume:79 Page:103-112
ISSN:1084-9521
Container-title:Seminars in Cell & Developmental Biology
language:en
Short-container-title:Seminars in Cell & Developmental Biology

Author:

Verma Bhupendra,Akinyi Maureen V.,Norppa Antto J.,Frilander Mikko J.

Funder

Academy of Finland

Sigrid Jusélius Foundation

Integrative Life Science doctoral program

Publisher

Elsevier BV

Subject

Cell Biology,Developmental Biology

Reference76 articles.

1. Are splicing mutations the most frequent cause of hereditary disease?;Lopez-Bigas;FEBS Lett.,2005

2. Using positional distribution to identify splicing elements and predict pre-mRNA processing defects in human genes;Lim;Proc. Natl. Acad. Sci. U. S. A.,2011

3. RNA splicing is a primary link between genetic variation and disease;Li;Science,2016

4. Synonymous mutations frequently act as driver mutations in human cancers;Supek;Cell,2014

5. Splicing in disease: disruption of the splicing code and the decoding machinery;Wang;Nat. Rev. Genet.,2007

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