Results 211 to 220 of about 14,209 (224)
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Immunoglobulin Light Chain and Systemic Light-Chain Amyloidosis

2007
Light-chain amyloidosis (AL) is characterized by the clonal expansion of plasma B cells that secrete large amounts of monoclonal immunoglobulin light chains. The free light chains circulate in serum and form amyloid fibrils on vital organs such as the kidney, heart, and liver causing organ failure and eventually death.
Richard W. McLaughlin   +5 more
openaire   +2 more sources

Stem cell transplantation for immunoglobulin light chain amyloidosis

Current Problems in Cancer, 2017
Systemic chemotherapy aimed at eradicating transformed plasma cells is the mainstay of treatment for immunoglobulin light chain amyloidosis (AL). Autologous stem cell transplantation (SCT) is a highly effective treatment for AL and can lead to long term survival in excess of 10 years in patients who achieve complete remission.
Taimur Sher, Morie A. Gertz
openaire   +3 more sources

Immunohistochemical study of immunoglobulin light chain amyloidosis with antibodies to the immunoglobulin light chain variable region

Pathology International, 2006
To detect immunoglobulin (Ig) light chain amyloidosis (AL amyloidosis) in formalin‐fixed, paraffin‐embedded tissue sections by immunohistochemistry, polyclonal antibodies were generated against synthetic peptides corresponding to amino acids 1–19 of the Ig λ light chain V λ VI subgroup (anti‐V λ VI (1–19)) and the Ig κ light chain Vκ I subgroup (anti ...
Dan Cui   +4 more
openaire   +3 more sources

The Challenge of Systemic Immunoglobulin Light-Chain Amyloidosis (AL)

2012
The cardiac involvement and associated mortality that occur in systemic AL amyloidosis remain among the most challenging aspects of the systemic amyloid-related diseases. Monoclonal immunoglobulin light chains produced by a clone of plasma cells are usually the cause of symptoms and organ dysfunction via both poorly understood toxic effects of ...
PALLADINI, GIOVANNI, Comenzo, Raymond L.
openaire   +4 more sources

Antibody‐based immunotherapy for treatment of immunoglobulin light‐chain amyloidosis

British Journal of Haematology, 2020
SummaryImmunoglobulin light‐chain (AL) amyloidosis is a clonal plasma cell disorder characterised by production and deposition of misfolded monoclonal light chains in vital organs with potential to cause irreversible organ damage. The treatment of AL amyloidosis has evolved along the lines of multiple myeloma (MM) owing to clonal plasma cells being at ...
Ricardo D. Parrondo   +2 more
openaire   +3 more sources

Diagnosis and Therapy of Immunoglobulin Light Chain Amyloidosis (AL Amyloidosis)

2012
Amyloidosis is a group of disorders that have in common the deposition of protein fibrils composed of protofibrils that have a crystallographic β(beta)-pleated sheet structure. Disease results from these proteinaceous deposits in one or more organ systems [1].
Morie A. Gertz, Robert A. Kyle
openaire   +2 more sources

Flow cytometry in immunoglobulin light chain amyloidosis: Short review

Leukemia Research, 2015
Flow cytometry (FCM) has found its application in clinical diagnosis and evaluation of monoclonal gammopathies (MG). Although, research has been mainly focused on multiple myeloma (MM), nowadays FCM becomes to be potential tool in the field of AL amyloidosis.
Elena Kryukova   +6 more
openaire   +3 more sources

Amyloidosis Related to a λ IV Immunoglobulin Light Chain Protein

Scandinavian Journal of Immunology, 1989
Amyloid subunit proteins related to the λ IV subgroup of immunoglobulin light chains have not been previously reported. We have determined the amino acid sequence of an AL amyloid protein BAK and shown that it has the structure typical of λ IV light chain proteins.
Merrill D. Benson   +3 more
openaire   +3 more sources

Immunoglobulin Light Chain Amyloidosis

2018
Taxiarchis Kourelis, Morie A. Gertz
openaire   +1 more source

Glycosylation of Immunoglobulin Light Chains is Associated with Amyloidosis

Clinical Lymphoma Myeloma and Leukemia, 2017
David R. Barnidge   +6 more
openaire   +2 more sources

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