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CAMKMT gene

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

Papers overview

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2018
2018
Abstract The interplay between transcription factors and epigenetic writers like the DNA methyltransferases (DNMTs), and the role… Expand
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2018
2018
PurposePREPL deficiency causes neonatal hypotonia, ptosis, neonatal feeding difficulties, childhood obesity, xerostomia, and… Expand
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2016
2016
Our previous genome-wide association study in sheep revealed that OAR3-84073899.1 (SNP31) in intron 8 of the CAMKMT gene was… Expand
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Highly Cited
2013
Highly Cited
2013
Background Growth and meat production traits are significant economic traits in sheep. The aim of the study is to identify… Expand
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2013
2013
Homozygous contiguous gene deletion syndromes are rare. On 2p21, however, several overlapping homozygous gene deletion syndromes… Expand
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Highly Cited
2010
Highly Cited
2010
Calmodulin (CaM) is a key mediator of calcium-dependent signalling and is subject to regulatory post-translational modifications… Expand
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2009
2009
Hypotonia–cystinuria syndrome (HCS) and 2p21 deletion syndrome are two recessive contiguous gene deletion syndromes associated… Expand
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2008
2008
Background: Hypotonia–cystinuria syndrome (HCS) and 2p21 deletion syndrome are two recessive contiguous gene deletion syndromes… Expand
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2008
2008
BackgroundMany mammalian genes are organized as bidirectional (head-to-head) gene pairs with the two genes separated only by less… Expand
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1996
1996
The present study was undertaken to determine kinetic and inhibition parameters and the mechanism of S-adenosyl-L-methionine… Expand
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