The role of gelsolin domain 3 in familial amyloidosis (Finnish type)
In the disease familial amyloidosis, Finnish type (FAF), also known as AGel amyloidosis (AGel), the mechanism by which point mutations in the calcium-regulated actin-severing protein gelsolin lead to furin cleavage is not understood in the intact protein. Here, we provide a structural and biochemica...
Hlavní autoři: | Zorgati, H, Larsson, M, Ren, W, Sim, A, Gettemans, J, Grimes, J, Li, W, Robinson, R |
---|---|
Médium: | Journal article |
Jazyk: | English |
Vydáno: |
National Academy of Sciences
2019
|
Podobné jednotky
-
Corneal lattice dystrophy type II – familial amyloid neuropathy type IV (gelsolin amyloidosis)
Autor: Evandro Penteado Villar Felix, a další
Vydáno: (2008-12-01) -
Hearing problems in patients with hereditary gelsolin amyloidosis
Autor: Tuuli Mustonen, a další
Vydáno: (2021-10-01) -
Subtle neuropsychiatric and neurocognitive changes in hereditary gelsolin amyloidosis (AGel amyloidosis)
Autor: Mari Kantanen, a další
Vydáno: (2014-07-01) -
Finnish gelsolin amyloidosis causes significant disease burden but does not affect survival: FIN-GAR phase II study
Autor: Eeva-Kaisa Schmidt, a další
Vydáno: (2020-01-01) -
The First Argentinian Family with Familial Amyloidosis of the Finnish Type
Autor: Francisco Lucero Saá, a další
Vydáno: (2017-08-01)