Lost in Translation: Defects in Transfer RNA Modifications and Neurological Disorders-Reference-Cited by-同舟云学术

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Lost in Translation: Defects in Transfer RNA Modifications and Neurological Disorders

Published:2017-05-09 Issue: Volume:10 Page:
ISSN:1662-5099
Container-title:Frontiers in Molecular Neuroscience
language:
Short-container-title:Front. Mol. Neurosci.

Author:

Bednářová Andrea,Hanna Marley,Durham Isabella,VanCleave Tara,England Alexis,Chaudhuri Anathbandhu,Krishnan Natraj

Funder

Akademie Věd České Republiky

Mississippi State University

Publisher

Frontiers Media SA

Subject

Cellular and Molecular Neuroscience,Molecular Biology

Reference91 articles.

1. Mutations in NSUN2 cause autosomal-recessive intellectual disability;Abbasi-Moheb;Am. J. Hum. Genet.,2012

2. Wobble position modified nucleosides evolved to select transfer RNA codon recognition: a modified-wobble hypothesis;Agris;Biochimie,1991

3. Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus;Alazami;J. Med. Genet.,2013

4. Rapid tRNA decay can result from lack of nonessential modifications;Alexandrov;Mol. Cell,2006

5. The essential Gcd10p-Gcd14p nuclear complex is required for 1-methyladenosine modification and maturation of initiator methionyl-tRNA;Anderson;Genes Dev.,1998

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