CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
Por um escritor misterioso
Last updated 24 dezembro 2024
PDF) Loss of CBP acetyltransferase activity by PHD finger mutations in Rubinstein-Taybi syndrome
Publications
Schematic illustration of HSF1-HSF2 heterotrimerization as a mechanism
Stress pathways in neurodevelopmental disorders
PDF) Author Correction: CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
Static posture. a, Experimental setup (a1) ; Representative
The TAP tag–based Hsp70/Hsp110 interaction network. The main figure
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
Ultra-Rare Syndromes: The Example of Rubinstein-Taybi Syndrome. - Abstract - Europe PMC
Microdeletions and mutations of CREBBP (CBP) gene can cause
Gene expression changes in the transition from neural progenitors to
Rubinstein-Taybi Syndrome 2 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
CBP/EP300-dependent acetylation and stabilization of HSF2 are compromised in Rubinstein-Taybi syndrome
LacZ expression as a reporter of the HSF2 expression pro®le. ( A and B
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
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