CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
Por um escritor misterioso
Descrição
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
PDF) Loss of CBP acetyltransferase activity by PHD finger mutations in Rubinstein-Taybi syndrome
CBP/EP300-dependent acetylation and stabilization of HSF2 are compromised in Rubinstein-Taybi syndrome
Publications
Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract - Europe PMC
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
CBP/EP300-dependent acetylation and stabilization of HSF2 are compromised in Rubinstein-Taybi syndrome
Abnormal structure of the HSF2-de®cient adult brain. Brain transverse
CK2a 0 heterozygosity ameliorates biochemical and neurobiological
Immunofluorescence characterization of cortical markers in
de
por adulto (o preço varia de acordo com o tamanho do grupo)
