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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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| Hoofdauteurs: | , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Public Library of Science
2012
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3527508/ https://ncbi.nlm.nih.gov/pubmed/23285036 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0052425 |
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