Cargando…
Recurrent Chromosome 16p13.1 Duplications Are a Risk Factor for Aortic Dissections
Chromosomal deletions or reciprocal duplications of the 16p13.1 region have been implicated in a variety of neuropsychiatric disorders such as autism, schizophrenia, epilepsies, and attention-deficit hyperactivity disorder (ADHD). In this study, we investigated the association of recurrent genomic c...
Autores principales: | Kuang, Shao-Qing, Guo, Dong-Chuan, Prakash, Siddharth K., McDonald, Merry-Lynn N., Johnson, Ralph J., Wang, Min, Regalado, Ellen S., Russell, Ludivine, Cao, Jiu-Mei, Kwartler, Callie, Fraivillig, Kurt, Coselli, Joseph S., Safi, Hazim J., Estrera, Anthony L., Leal, Suzanne M., LeMaire, Scott A., Belmont, John W., Milewicz, Dianna M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3116911/ https://www.ncbi.nlm.nih.gov/pubmed/21698135 http://dx.doi.org/10.1371/journal.pgen.1002118 |
Ejemplares similares
-
4573 Characterization of vascular disease in an Acta2 mutant mouse model
por: Kaw, Anita, et al.
Publicado: (2020) -
Cholesterol-Induced Phenotypic Modulation of Smooth Muscle Cells to Macrophage/Fibroblast–like Cells Is Driven by an Unfolded Protein Response
por: Chattopadhyay, Abhijnan, et al.
Publicado: (2020) -
Recurrent Rare Genomic Copy Number Variants and Bicuspid Aortic Valve Are Enriched in Early Onset Thoracic Aortic Aneurysms and Dissections
por: Prakash, Siddharth, et al.
Publicado: (2016) -
Heritable aortic root aneurysms
por: Ouzounian, Maral, et al.
Publicado: (2023) -
Smooth muscle α-actin missense variant promotes atherosclerosis through modulation of intracellular cholesterol in smooth muscle cells
por: Kaw, Kaveeta, et al.
Publicado: (2023)