Cargando…
Extracellular Vesicles Contribute to the Metabolism of Transthyretin Amyloid in Hereditary Transthyretin Amyloidosis
Hereditary (variant) transthyretin amyloidosis (ATTRv amyloidosis), which is caused by variants in the transthyretin (TTR) gene, leads to TTR amyloid deposits in multiple organs and various symptoms such as limb ataxia, muscle weakness, and cardiac failure. Interaction between amyloid proteins and e...
Autores principales: | Yamaguchi, Hiroki, Kawahara, Hironori, Kodera, Noriyuki, Kumaki, Ayanori, Tada, Yasutake, Tang, Zixin, Sakai, Kenji, Ono, Kenjiro, Yamada, Masahito, Hanayama, Rikinari |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8983912/ https://www.ncbi.nlm.nih.gov/pubmed/35402512 http://dx.doi.org/10.3389/fmolb.2022.839917 |
Ejemplares similares
-
Hereditary transthyretine amyloidosis in Slovenia
por: Zidar, Janez
Publicado: (2015) -
Hereditary transthyretin amyloidosis overview
por: Manganelli, Fiore, et al.
Publicado: (2020) -
Frequency of hereditary transthyretin amyloidosis among elderly patients with transthyretin cardiomyopathy
por: Maestro‐Benedicto, Alba, et al.
Publicado: (2022) -
Screening for hereditary transthyretin amyloidosis in Bulgaria
por: Nakov, Radislav, et al.
Publicado: (2021) -
Hereditary transthyretin amyloid cardiomyopathy
por: Zheng, Yiliang, et al.
Publicado: (2023)