Alport syndrome caused by a COL4A5 deletion and exonization of an adjacent AluY-Reference-Cited by-同舟云学术

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Alport syndrome caused by a COL4A5 deletion and exonization of an adjacent AluY

Published:2014-05-28 Issue:5 Volume:2 Page:451-453
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Nozu Kandai¹,Iijima Kazumoto¹,Ohtsuka Yasufumi²,Fu Xue Jun¹,Kaito Hiroshi¹,Nakanishi Koichi³,Vorechovsky Igor⁴

Affiliation:

1. Department of Pediatrics Kobe University Graduate School of Medicine Kobe Japan

2. Department of Pediatrics Faculty of Medicine Saga University Saga Japan

3. Department of Pediatrics Wakayama Medical University Wakayama Japan

4. Faculty of Medicine University of Southampton Southampton U.K

Funder

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.89

Reference11 articles.

1. Ab initio prediction of mutation-induced cryptic splice-site activation and exon skipping

2. Alu-SINE Exonization: En Route to Protein-Coding Function

3. The Birth of an Alternatively Spliced Exon: 3' Splice-Site Selection in Alu Exons

4. Alu sequences in the coding regions of mRNA: a source of protein variability

5. Disease-causing mutations improving the branch site and polypyrimidine tract: Pseudoexon activation of LINE-2 and antisenseAlulacking the poly(T)-tail

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1. Dynamic Variations of 3′UTR Length Reprogram the mRNA Regulatory Landscape;Biomedicines;2021-10-28

2. Alu RNA and their roles in human disease states;RNA Biology;2021-10-21

3. Altered DNA repair creates novel Alu/Alu repeat‐mediated deletions;Human Mutation;2021-03-19

4. Transposable element-derived sequences in vertebrate development;Mobile DNA;2021-01-06

5. Identifying NAHR mechanism between two distinct Alu elements through breakpoint junction mapping by NGS;Meta Gene;2020-06

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