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LYRM1, a Gene that Promotes Proliferation and Inhibits Apoptosis during Heart Development

Congenital heart disease (CHD) is the most common type of birth defect, but its underlying molecular mechanisms remain unidentified. Previous studies determined that Homo sapiens LYR motif containing 1 (LYRM1) is a novel nucleoprotein expressed at the highest level in adipose tissue and in high leve...

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Detalles Bibliográficos
Autores principales: Zhu, Chun, Liu, Yao-Qiu, Chen, Fu-Kun, Hu, De-Liang, Yu, Zhang-Bin, Qian, Ling-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259564/
https://www.ncbi.nlm.nih.gov/pubmed/20938407
http://dx.doi.org/10.3390/molecules15106974