A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing-Reference-Cited by-同舟云学术

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A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing

Published:2011-10-28 Issue:3 Volume:21 Page:577-585
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Soldà Giulia,Robusto Michela,Primignani Paola,Castorina Pierangela,Benzoni Elena,Cesarani Antonio,Ambrosetti Umberto,Asselta Rosanna,Duga Stefano

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/21/3/577/17257866/ddr493.pdf

Reference36 articles.

1. Gene silencing by microRNAs: contributions of translational repression and mRNA decay;Huntzinger;Nat. Rev. Genet.,2011

2. MicroRNAs: target recognition and regulatory functions;Bartel;Cell,2009

3. The widespread regulation of microRNA biogenesis, function and decay;Krol;Nat. Rev. Genet.,2010

4. Tissue-dependent paired expression of miRNAs;Ro;Nucleic Acids Res.,2007

5. The regulatory activity of microRNA* species has substantial influence on microRNA and 3′ UTR evolution;Okamura;Nat. Struct. Mol. Biol.,2008

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2. Targeted genome editing restores auditory function in adult mice with progressive hearing loss caused by a human microRNA mutation;Science Translational Medicine;2024-07-10

3. A cell type–specific approach to elucidate the role of miR-96 in inner ear hair cells;Frontiers in Audiology and Otology;2024-05-09

4. Pathological mechanisms and candidate therapeutic approaches in the hearing loss of mice carrying humanMIR96mutations;2024-02-21

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