Cargando…
Analysis of the complete lambda light chain germline usage in patients with AL amyloidosis and dominant heart or kidney involvement
Light chain amyloidosis is one of the most common forms of systemic amyloidosis. The disease is caused by the misfolding and aggregation of immunoglobulin light chains to insoluble fibrils. These fibrils can deposit in different tissues and organs such as heart and kidney and cause organ impairments...
Autores principales: | Berghaus, Natalie, Schreiner, Sarah, Granzow, Martin, Müller-Tidow, Carsten, Hegenbart, Ute, Schönland, Stefan O., Huhn, Stefanie |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880859/ https://www.ncbi.nlm.nih.gov/pubmed/35213605 http://dx.doi.org/10.1371/journal.pone.0264407 |
Ejemplares similares
-
Seroconversion Rates After the Second COVID-19 Vaccination in Patients With Systemic Light Chain (AL) amyloidosis
por: Liebers, Nora, et al.
Publicado: (2022) -
Cryo-EM structure of a light chain-derived amyloid fibril from a patient with systemic AL amyloidosis
por: Radamaker, Lynn, et al.
Publicado: (2019) -
Concurrent light chain amyloidosis and proximal tubulopathy: Insights into different aggregation behavior—A case report
por: Feurstein, Simone, et al.
Publicado: (2022) -
Seeded fibrils of the germline variant of human λ-III immunoglobulin light chain FOR005 have a similar core as patient fibrils with reduced stability
por: Pradhan, Tejaswini, et al.
Publicado: (2021) -
Role of mutations and post-translational modifications in systemic AL amyloidosis studied by cryo-EM
por: Radamaker, Lynn, et al.
Publicado: (2021)