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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

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_9f7e7aecc3a8463b9a5732585bfbb110

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Patients carrying autosomal dominant mutations in the histone/lysine acetyl transferases CBP or EP300 develop a neurodevelopmental disorder: Rubinstein-Taybi syndrome (RSTS). The biological pathways underlying these neurodevelopmental defects remain elusive. Here, we unravel the contribution of a stress-responsive pathway to RSTS. We characterize t...

Alternative Titles

Full title

CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_9f7e7aecc3a8463b9a5732585bfbb110

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_9f7e7aecc3a8463b9a5732585bfbb110

Other Identifiers

ISSN

2041-1723

E-ISSN

2041-1723

DOI

10.1038/s41467-022-34476-2