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Literature DB >> 16340982

Nonsense mutations: running the red light.

Claire Ainsworth.

Abstract

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Year: 2005 PMID： 16340982 DOI： 10.1038/438726a

Source DB: PubMed Journal: Nature ISSN： 0028-0836 Impact factor: 49.962

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7 in total

1. A mouse model for nonsense mutation bypass therapy shows a dramatic multiday response to geneticin.

Authors: Chunmei Yang; Jinong Feng; Wenjia Song; Jicheng Wang; Becky Tsai; Yunwu Zhang; William A Scaringe; Kathleen A Hill; Paris Margaritis; Katherine A High; Steve S Sommer
Journal: Proc Natl Acad Sci U S A Date: 2007-09-19 Impact factor: 11.205

Review 2. Small molecules as therapeutic agents for inborn errors of metabolism.

Authors: Leslie Matalonga; Laura Gort; Antonia Ribes
Journal: J Inherit Metab Dis Date: 2016-12-13 Impact factor: 4.982

3. Effect of Readthrough Treatment in Fibroblasts of Patients Affected by Lysosomal Diseases Caused by Premature Termination Codons.

Authors: Leslie Matalonga; Ángela Arias; Frederic Tort; Xènia Ferrer-Cortés; Judit Garcia-Villoria; Maria Josep Coll; Laura Gort; Antonia Ribes
Journal: Neurotherapeutics Date: 2015-10 Impact factor: 7.620

4. Nonsense-mediated mRNA decay affects nonsense transcript levels and governs response of cystic fibrosis patients to gentamicin.

Authors: Liat Linde; Stephanie Boelz; Malka Nissim-Rafinia; Yifat S Oren; Michael Wilschanski; Yasmin Yaacov; Dov Virgilis; Gabriele Neu-Yilik; Andreas E Kulozik; Eitan Kerem; Batsheva Kerem
Journal: J Clin Invest Date: 2007-02-08 Impact factor: 14.808

Nonsense mutations: running the red light.

1. A mouse model for nonsense mutation bypass therapy shows a dramatic multiday response to geneticin.

Review 2. Small molecules as therapeutic agents for inborn errors of metabolism.

3. Effect of Readthrough Treatment in Fibroblasts of Patients Affected by Lysosomal Diseases Caused by Premature Termination Codons.

4. Nonsense-mediated mRNA decay affects nonsense transcript levels and governs response of cystic fibrosis patients to gentamicin.

5. Large-scale evidence for conservation of NMD candidature across mammals.

6. Restoration of W1282X CFTR activity by enhanced expression.

7. Functions of the nonsense-mediated mRNA decay pathway in Drosophila development.