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Fernando Cardona holds a PhD in Molecular Biology from the University of Valencia. He has published 18 articles indexed in JCR and 10 indexed in Scopus, as well as a textbook and other teaching materials. He has participated in more than 35 international congresses. In addition, he has an intense editorial activity, having reviewed more than 140 articles indexed in JCR journals and acting as an editor for 40. He conducts his research activity at the Molecular Genetics Unit of the Institute of Biomedicine of Valencia (CSIC) and teaches at the Department of Biotechnology of the Polytechnic University of Valencia.
Fernando's work focuses on studying various mutations identified in patients with neurodegenerative diseases. The effects of single nucleotide polymorphisms (SNPs) in transcription regulatory regions, such as promoters and UTRs, are investigated in some cases. In other instances, splicing alterations are examined using the exon trapping technique. Regarding nonsense mutations, the study involves investigating the inhibition of the NMD pathway in cellular models to assess its impact on protein levels. In addition, an in-silico analysis can be performed to assess the impact of missense mutations on protein structure and function.
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论文共 33 篇作者统计合作学者相似作者
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Neurology Geneticsno. 4 (2023): e200079-e200079
Brain sciencesno. 6 (2023): 899-899
Neurology. Geneticsno. 4 (2023): e200079-e200079
medrxiv(2022)
medRxiv (Cold Spring Harbor Laboratory) (2022)
Proceedings INNODOCT/20. International Conference on Innovation, Documentation and Education (2020)
Proceedings INNODOCT/20. International Conference on Innovation, Documentation and Education (2020)
Proceedings INNODOCT/19. International Conference on Innovation, Documentation and Education (2019)
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