Cargando…
Breaking enhancers to gain insights into developmental defects
Despite ground-breaking genetic studies that have identified thousands of risk variants for developmental diseases, how these variants lead to molecular and cellular phenotypes remains a gap in knowledge. Many of these variants are non-coding and occur at enhancers, which orchestrate key regulatory...
Autores principales: | Armendariz, Daniel A, Sundarrajan, Anjana, Hon, Gary C |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374278/ https://www.ncbi.nlm.nih.gov/pubmed/37497775 http://dx.doi.org/10.7554/eLife.88187 |
Ejemplares similares
-
CHD-associated enhancers shape human cardiomyocyte lineage commitment
por: Armendariz, Daniel A, et al.
Publicado: (2023) -
Mechanistic Insights From Single-Molecule Studies of Repair of Double Strand Breaks
por: Kong, Muwen, et al.
Publicado: (2021) -
Cerebellar nuclei excitatory neurons regulate developmental scaling of presynaptic Purkinje cell number and organ growth
por: Willett, Ryan T, et al.
Publicado: (2019) -
Developmental biology
por: Browder, Leon W.
Publicado: (1991) -
FGF10 and Lipofibroblasts in Lung Homeostasis and Disease: Insights Gained From the Adipocytes
por: Lv, Yu-Qing, et al.
Publicado: (2021)