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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Hlavní autoři: Luque, Carlos M., Lallena, María-José, Pérez-Ferreiro, Carmen M., de Isidro, Yolanda, De Cárcer, Guillermo, Alonso, Miguel A., Correas, Isabel
Médium: Artigo
Jazyk:Inglês
Vydáno: The National Academy of Sciences 1999
Témata:
Biological Sciences
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC24749/
https://ncbi.nlm.nih.gov/pubmed/10611314
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