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A de novo variant in the human HIST1H4J gene causes a syndrome analogous to the HIST1H4C-associated neurodevelopmental disorder

scientific article published on 05 December 2019

ABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9

scientific article published on 01 October 2019

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

scientific article published on 10 December 2021

Large-scale chromatin de-compaction induced by low light is not accompanied by nucleosomal displacement ⬇️

artículo científico publicado el 1 de diciembre de 2010

Notch and Bmp signaling pathways act coordinately during the formation of the proepicardium

artículo científico publicado en 2020

Shedding Light on Large-Scale Chromatin Reorganization in Arabidopsis thaliana ⬇️

artículo científico publicado el 22 de abril de 2012

Stable S/MAR-based episomal vectors are regulated at the chromatin level ⬇️

artículo científico publicado el 16 de noviembre de 2010

Zebrafish prrx1a mutants have normal hearts

scientific article published on 23 September 2020

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