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Protein β2-microglobulin (β2-m) is the causative agent of dialysis-related amyloidosis (DRA), a prev...
Aggregation of initially stably structured proteins is involved in more than 20 human amyloid diseas...
Systemic amyloidosis is a fatal disease caused by misfolding of native globular proteins, which then...
A major component of ex vivo amyloid plaques of patients with dialysis-related amyloidosis (DRA) is ...
(Article begins on next page) The Harvard community has made this article openly available. Please s...
We use molecular dynamics simulations of a full atomistic Gō model to explore the impact of selected...
The D76N variant of human β2-microglobulin (β2m) is the causative agent of a hereditary amyloid dise...
Beta-2 microglobulin (β2m) is a protein responsible for a pathologic condition, known as dialys...
Article first published online: 2 SEP 2008This mini-review focuses on the processes and consequences...
Transiently populated oligomers are commonly formed in the early stages of amyloid assembly. Determi...
Beta-2 microglobulin (β2m) is a protein responsible for a pathologic condition, known as dialysis-re...
Amyloidoses are clinical disorders caused by deposition of insoluble fibrils, derived from misfoldin...
Systemic amyloidosis is a fatal disease caused by misfolding of native globular proteins, which then...
<div><p>A major component of <i>ex vivo</i> amyloid plaques of patients with dialysis-related amyloi...
Systemic amyloidosis is a fatal disease caused by misfolding of native globular proteins, which then...
Protein β2-microglobulin (β2-m) is the causative agent of dialysis-related amyloidosis (DRA), a prev...
Aggregation of initially stably structured proteins is involved in more than 20 human amyloid diseas...
Systemic amyloidosis is a fatal disease caused by misfolding of native globular proteins, which then...
A major component of ex vivo amyloid plaques of patients with dialysis-related amyloidosis (DRA) is ...
(Article begins on next page) The Harvard community has made this article openly available. Please s...
We use molecular dynamics simulations of a full atomistic Gō model to explore the impact of selected...
The D76N variant of human β2-microglobulin (β2m) is the causative agent of a hereditary amyloid dise...
Beta-2 microglobulin (β2m) is a protein responsible for a pathologic condition, known as dialys...
Article first published online: 2 SEP 2008This mini-review focuses on the processes and consequences...
Transiently populated oligomers are commonly formed in the early stages of amyloid assembly. Determi...
Beta-2 microglobulin (β2m) is a protein responsible for a pathologic condition, known as dialysis-re...
Amyloidoses are clinical disorders caused by deposition of insoluble fibrils, derived from misfoldin...
Systemic amyloidosis is a fatal disease caused by misfolding of native globular proteins, which then...
<div><p>A major component of <i>ex vivo</i> amyloid plaques of patients with dialysis-related amyloi...
Systemic amyloidosis is a fatal disease caused by misfolding of native globular proteins, which then...
Protein β2-microglobulin (β2-m) is the causative agent of dialysis-related amyloidosis (DRA), a prev...
Aggregation of initially stably structured proteins is involved in more than 20 human amyloid diseas...
Systemic amyloidosis is a fatal disease caused by misfolding of native globular proteins, which then...