CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
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CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
Variations in brain defects result from cellular mosaicism in the activation of heat shock signalling
Immunofluorescence characterization of cortical markers in
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
Ubiquitination of HSF2 is enhanced by heat stress. (A) HEK293 cells
In vitro characterization of AIRAP promoter-HSF complexes in
Rubinstein-Taybi Syndrome 2 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Exploratory data analysis. a Table showing RSTS patients selected for
Microdeletions and mutations of CREBBP (CBP) gene can cause
Gene expression changes in the transition from neural progenitors to
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
The HDAC Inhibitor, TSA, Rescues the Decreased Cortical Precursor
Immunofluorescence and morphological characterization of iPSC-derived
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