High-throughput analysis revealed mutations’ diverging effects on SMN1 exon 7 splicing-Reference-Cited by-同舟云学术

High-throughput analysis revealed mutations’ diverging effects on SMN1 exon 7 splicing

Published:2019-06-19 Issue:10 Volume:16 Page:1364-1376
ISSN:1547-6286
Container-title:RNA Biology
language:en
Short-container-title:RNA Biology

Author:

Souček Přemysl¹²^ORCID,Réblová Kamila¹^ORCID,Kramárek Michal²,Radová Lenka¹,Grymová Tereza²^ORCID,Hujová Pavla²,Kováčová Tatiana¹,Lexa Matej³^ORCID,Grodecká Lucie²^ORCID,Freiberger Tomáš¹²⁴^ORCID

Affiliation:

1. Medical Genomics RG, Central European Institute of Technology, Masaryk University, Brno, Czech Republic

2. Molecular Genetics Laboratory, Centre for Cardiovascular Surgery and Transplantation, Brno, Czech Republic

3. Faculty of Informatics, Masaryk University, Brno, Czech Republic

4. Faculty of Medicine, Masaryk University, Brno, Czech Republic

Funder

Grantová Agentura České Republiky

Ministerstvo Zdravotnictví Ceské Republiky

Ministerstvo Školství, Mládeže a Tělovýchovy

Publisher

Informa UK Limited

Subject

Cell Biology,Molecular Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/15476286.2019.1630796

Reference70 articles.

1. Splicing regulation: From a parts list of regulatory elements to an integrated splicing code

2. Global identification of hnRNP A1 binding sites for SSO-based splicing modulation

3. iCLIP reveals the function of hnRNP particles in splicing at individual nucleotide resolution

4. The human splicing factors ASF/SF2 and SC35 possess distinct, functionally significant RNA binding specificities.

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