Exploring Splicing-Switching Molecules For Seckel Syndrome Therapy-Reference-Cited by-同舟云学术

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Exploring Splicing-Switching Molecules For Seckel Syndrome Therapy

Published:2017-01 Issue:1 Volume:1863 Page:15-20
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Scalet Daniela,Balestra Dario,Rohban Sara,Bovolenta Matteo,Perrone Daniela,Bernardi Francesco,Campaner Stefano,Pinotti Mirko

Funder

Telethon-Italy

University of Ferrara

Italian Association for Cancer Research

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference39 articles.

1. Central nervous system anomalies in Seckel syndrome: report of a new family and review of the literature;Shanske;Am. J. Med. Genet.,1997

2. A splicing mutation affecting expression of ataxia-telangiectasia and Rad3-related protein (ATR) results in Seckel syndrome;O'Driscoll;Nat. Genet.,2003

3. The DNA damage response: putting checkpoints in perspective;Zhou;Nature,2000

4. DNA-PK, ATM and ATR as sensors of DNA damage: variations on a theme?;Durocher;Curr. Opin. Cell Biol.,2001

5. ATM and ATR: networking cellular responses to DNA damage;Shiloh;Curr. Opin. Genet. Dev.,2001

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1. Counteracting the Common Shwachman–Diamond Syndrome-Causing SBDS c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing;International Journal of Molecular Sciences;2023-02-16

2. Targeted Therapeutics for Rare Disorders;Reference Module in Biomedical Sciences;2022

3. OTC intron 4 variations mediate pathogenic splicing patterns caused by the c.386G>A mutation in humans and spfash mice, and govern susceptibility to RNA-based therapies;Molecular Medicine;2021-12

4. U5 snRNA Interactions With Exons Ensure Splicing Precision;Frontiers in Genetics;2021-07-02

5. U5 snRNA interactions with exons ensure splicing precision;2021-03-08

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