Human Calmodulin Methyltransferase: Expression, Activity on Calmodulin, and Hsp90 Dependence

Deletion of the first exon of calmodulin-lysine N-methyltransferase (CaM KMT, previously C2orf34) has been reported in two multigene deletion syndromes, but additional studies on the gene have not been reported. Here we show that in the cells from 2p21 deletion patients the loss of CaM KMT expressio...

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Detalles Bibliográficos
Autores principales: Magen, Sophia, Magnani, Roberta, Haziza, Sitvanit, Hershkovitz, Eli, Houtz, Robert, Cambi, Franca, Parvari, Ruti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527508/
https://www.ncbi.nlm.nih.gov/pubmed/23285036
http://dx.doi.org/10.1371/journal.pone.0052425

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527508/
https://www.ncbi.nlm.nih.gov/pubmed/23285036
http://dx.doi.org/10.1371/journal.pone.0052425

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