Specific correction of a splice defect in brain by nutritional supplementation-Reference-Cited by-同舟云学术

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Specific correction of a splice defect in brain by nutritional supplementation

Published:2011-08-05 Issue:21 Volume:20 Page:4093-4101
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Shetty R. S.,Gallagher C. S.,Chen Y.-T.,Hims M. M.,Mull J.,Leyne M.,Pickel J.,Kwok D.,Slaugenhaupt S. A.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/20/21/4093/1543418/ddr333.pdf

Reference46 articles.

1. Alternative Splicing: New Insights from Global Analyses

2. Genome-Wide Survey of Human Alternative Pre-mRNA Splicing with Exon Junction Microarrays

3. A genomic view of alternative splicing

4. Listening to silence and understanding nonsense: exonic mutations that affect splicing

5. Pre-mRNA splicing and human disease

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1. Reduction of retinal ganglion cell death in mouse models of familial dysautonomia using AAV-mediated gene therapy and splicing modulators;Scientific Reports;2023-10-30

2. Reduction of retinal ganglion cell death in mouse models of familial dysautonomia using AAV-mediated gene therapy and splicing modulators;2023-05-24

3. Development of an oral treatment that rescues gait ataxia and retinal degeneration in a phenotypic mouse model of familial dysautonomia;The American Journal of Human Genetics;2023-03

4. Development of a novel oral treatment that rescues gait ataxia and retinal degeneration in a phenotypic mouse model of familial dysautonomia;2022-11-04

5. Selective retinal ganglion cell loss and optic neuropathy in a humanized mouse model of familial dysautonomia;Human Molecular Genetics;2021-12-15

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