#Kdm2a demethylates #H3K36me2 to mediate fast-to-slow-twitch #myofiber transition and reshape #SkeletalMuscle metabolic flexibility under #metabolic stress conditions
#Kdm2a demethylates #H3K36me2 to mediate fast-to-slow-twitch #myofiber transition and reshape #SkeletalMuscle metabolic flexibility under #metabolic stress conditions
#Epigenetics #KDM2A #GermCells #Polycomb
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High-resolution insights without cell sorting; epigenometech.com
#Epigenetics #KDM2A #GermCells #Polycomb
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High-resolution insights without cell sorting; epigenometech.com
www.nature.com/articles/s42...
www.nature.com/articles/s42...
#KDM2A loss in #skeletal #muscle confers flexible protection against #metabolic stress
#KDM2A loss in #skeletal #muscle confers flexible protection against #metabolic stress
📄De novo variants in KDM2A cause a syndromic neurodevelopmental disorder
📄De novo variants in KDM2A cause a syndromic neurodevelopmental disorder
A Nature Metabolism article supports Kdm2a as a viable target against metabolic stress
#Epigenetics #Metabolism #Stress
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High-res insight without cell sorting; epigenome.us
A Nature Metabolism article supports Kdm2a as a viable target against metabolic stress
#Epigenetics #Metabolism #Stress
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High-res insight without cell sorting; epigenome.us
KDM2A loss in skeletal muscle shifts fuel use from glucose to lipids in mice under HFD by increasing the proportion of mitochondria-rich slow-twitch myofibers, which protects mice against metabolic stress.
rdcu.be/d7GbF
KDM2A loss in skeletal muscle shifts fuel use from glucose to lipids in mice under HFD by increasing the proportion of mitochondria-rich slow-twitch myofibers, which protects mice against metabolic stress.
rdcu.be/d7GbF
www.cell.com/developmenta...
www.cell.com/developmenta...
Structure and mechanism of inhibition of lysine demethylase 2A (KDM2A) by compound 183c.
Read more here: buff.ly/7caT1d5
#SBGrid #StayConnected
Structure and mechanism of inhibition of lysine demethylase 2A (KDM2A) by compound 183c.
Read more here: buff.ly/7caT1d5
#SBGrid #StayConnected
De novo KDM2A variants cause a syndromic neurodevelopmental disorder. Functional assays and methylation data support this novel gene–disease association.
#RareDisease #NDD #EpiSignature
www.cell.com/ajhg/fulltex...
De novo KDM2A variants cause a syndromic neurodevelopmental disorder. Functional assays and methylation data support this novel gene–disease association.
#RareDisease #NDD #EpiSignature
www.cell.com/ajhg/fulltex...
www.nature.com/articles/s41...
www.nature.com/articles/s41...
#Drosophila
#Drosophila
#Drosophila
#Drosophila