Mechanisms of disease: monoclonal immunoglobulin deposition. Amyloidosis, light chain deposition disease, and light and heavy chain deposition disease.
about
Localized AL amyloidosis: a suicidal neoplasm?Amyloid fibrils derived from the apolipoprotein A1 Leu174Ser variant contain elements of ordered helical structurePrimary cerebral low-grade B-cell lymphoma, monoclonal immunoglobulin deposition disease, cerebral light chain deposition disease and "aggregoma": an update on classification and diagnosis.In vitro aggregation behavior of a non-amyloidogenic λ light chain dimer deriving from U266 multiple myeloma cells.Formation of amyloid fibers by monomeric light chain variable domains.A role for destabilizing amino acid replacements in light-chain amyloidosisRecombinant immunoglobulin variable domains generated from synthetic genes provide a system for in vitro characterization of light-chain amyloid proteins.Natural history and outcome of light chain deposition disease.The effect of membranes on the in vitro fibrillation of an amyloidogenic light-chain variable-domain SMA.Amyloid Arthropathy of the Hip Joint Associated with Multiple Myeloma: A Case Report.Effect of methionine oxidation on the structural properties, conformational stability, and aggregation of immunoglobulin light chain LEN.Systemic amyloidoses.Inhibition by small-molecule ligands of formation of amyloid fibrils of an immunoglobulin light chain variable domain.The Kinetic Stability of a Full-Length Antibody Light Chain Dimer Determines whether Endoproteolysis Can Release Amyloidogenic Variable DomainsAggregates, crystals, gels, and amyloids: intracellular and extracellular phenotypes at the crossroads of immunoglobulin physicochemical property and cell physiology.Serum Free Light Chain Assay and κ/λ Ratio: Performance in Patients With Monoclonal Gammopathy-High False Negative Rate for κ/λ RatioBiochemical and aggregation analysis of Bence Jones proteins from different light chain diseases.A father and his son with systemic AL amyloidosis.Incomplete Refolding of Antibody Light Chains to Non-Native, Protease-Sensitive Conformations Leads to Aggregation: A Mechanism of Amyloidogenesis in Patients?Structure and energetic basis of overrepresented λ light chain in systemic light chain amyloidosis patients.
P2860
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P2860
Mechanisms of disease: monoclonal immunoglobulin deposition. Amyloidosis, light chain deposition disease, and light and heavy chain deposition disease.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Mechanisms of disease: monoclo ...... eavy chain deposition disease.
@ast
Mechanisms of disease: monoclo ...... eavy chain deposition disease.
@en
type
label
Mechanisms of disease: monoclo ...... eavy chain deposition disease.
@ast
Mechanisms of disease: monoclo ...... eavy chain deposition disease.
@en
prefLabel
Mechanisms of disease: monoclo ...... eavy chain deposition disease.
@ast
Mechanisms of disease: monoclo ...... eavy chain deposition disease.
@en
P1476
Mechanisms of disease: monoclo ...... eavy chain deposition disease.
@en
P2093
P304
P577
1992-04-01T00:00:00Z