Cargando…
Hyaluronidase 2 Deficiency Causes Increased Mesenchymal Cells, Congenital Heart Defects, and Heart Failure
BACKGROUND—: Hyaluronan (HA) is required for endothelial-to-mesenchymal transition and normal heart development in the mouse. Heart abnormalities in hyaluronidase 2 (HYAL2)–deficient (Hyal2(−)(/−)) mice and humans suggested removal of HA is also important for normal heart development. We have perfor...
Autores principales: | Chowdhury, Biswajit, Xiang, Bo, Liu, Michelle, Hemming, Richard, Dolinsky, Vernon W., Triggs-Raine, Barbara |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331876/ https://www.ncbi.nlm.nih.gov/pubmed/28196902 http://dx.doi.org/10.1161/CIRCGENETICS.116.001598 |
Ejemplares similares
Ejemplares similares
-
Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice
por: Muggenthaler, Martina M. A., et al.
Publicado: (2017) -
Mutation of EMG1 causing Bowen–Conradi syndrome results in reduced cell proliferation rates concomitant with G2/M arrest and 18S rRNA processing delay
por: Armistead, Joy, et al.
Publicado: (2014) -
Preeclampsia and Fetal Congenital Heart Defects
por: Ferreira, Bárbara D., et al.
Publicado: (2022) -
Surgery for Congenital Heart Defects
por: Singleton, Matthew J.
Publicado: (2008) -
Folate Deficiency and Folic Acid Supplementation: The Prevention of Neural-Tube Defects and Congenital Heart Defects
por: Czeizel, Andrew E., et al.
Publicado: (2013)