The N-terminal 209-aa domain of high molecular- weight 4.1R isoforms abrogates 4.1R targeting to the nucleus

An extensive repertoire of protein 4.1R isoforms is predominantly generated by alternative pre-mRNA splicing and differential usage of two translation initiation sites. The usage of the most upstream ATG (ATG-1) generates isoforms containing N-terminal extensions of up to 209 aa compared with those...

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Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	Luque, Carlos M., Lallena, María-José, Pérez-Ferreiro, Carmen M., de Isidro, Yolanda, De Cárcer, Guillermo, Alonso, Miguel A., Correas, Isabel
Formato:	Artigo
Idioma:	Inglês
Publicado em:	National Academy of Sciences 1999
Assuntos:	Biological Sciences
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC24749/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10611314/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.96.26.14925
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