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CAMKMT gene

Known as: CaM KMT, CALMODULIN LYSINE N-METHYLTRANSFERASE, C2ORF34 
National Institutes of Health

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1 relation
Calmodulin 1

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Exploring Genetic Biomarkers in a Sample of Depressed Patients in the UAE
This study focuses on exploring the expression of genes associated with depressive and anxiety disorders (AD) among depressed… 
2017
2017
Novel deletion alleles of a C. elegans gene Y48E1C.1, named as tm5468, tm5625 and tm5626
Description: We report tm5468, tm5625 and tm5626 as novel deletion alleles of the gene Y48E1C.1 that is the only ortholog of… 
2012
2012
PERGELARAN BAYANGAN WAYANG KULIT PURWA DALAM KAJIAN BAHASA RUPA GERAK (Lakon Parta Krama Gaya Yogyakarta)
Abstrak : Efek gerak dari wayang kulit bayangan kelir merupakan bagian yang menentukan dari suatu pertunjukan hasil kreasi para… 
2009
2009
Deletion of C2orf34, PREPL and SLC3A1 causes atypical hypotonia–cystinuria syndrome
Hypotonia–cystinuria syndrome (HCS) and 2p21 deletion syndrome are two recessive contiguous gene deletion syndromes associated… 
2008
2008
Deletion of C2orf34, PREPL and SLC3A1 causes atypical hypotonia–cystinuria syndrome
Background: Hypotonia–cystinuria syndrome (HCS) and 2p21 deletion syndrome are two recessive contiguous gene deletion syndromes… 
1996
1996
Calmodulin N-Methyltransferase
The present study was undertaken to determine kinetic and inhibition parameters and the mechanism of S-adenosyl-L-methionine… 
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