Associated Papers
Association Between Clonal Hematopoiesis and Left Ventricular Reverse Remodeling in Nonischemic Dilated Cardiomyopathy.
Inoue S et al.
Jacc. Basic to Translational Science, 2024
39297129 (PubMed )
Supplement: mmc1.pdf
A novel BAG5 variant impairs the ER stress response pathway, causing dilated cardiomyopathy and arrhythmia.
Wongong R et al.
Scientific Reports, 2024
Compound Heterozygous Truncating Variants in the BAG5 Gene As a Cause of Early-Onset Dilated Cardiomyopathy.
Inoue S et al.
Circulation. Genomic and Precision Medicine, 2023
Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies.
Lipov A et al.
Nature Cardiovascular Research, 2023
38666070 (PubMed )
Supplement: 44161_2023_346_MOESM1_ESM.pdf
Refractory Ventricular Arrhythmias in a Patient With Dilated Cardiomyopathy Caused by a Nonsense Mutation in BAG5.
Hakui H et al.
Circulation Journal : Official Journal of the Japanese Circulation Society, 2022
Loss-of-function mutations in the co-chaperone protein BAG5 cause dilated cardiomyopathy requiring heart transplantation.
Hakui H et al.
Science Translational Medicine, 2022
Role of BAG5 in Protein Quality Control: Double-Edged Sword?
Gupta MK et al.
Frontiers in Aging, 2022
Identification of candidates for driver oncogenes in scirrhous-type gastric cancer cell lines.
Sai E et al.
Cancer Science, 2019
31222839 (PubMed )
Supplement: CAS-110-2643-s002.xlsx › Table_S1
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