Results 111 to 120 of about 235,597 (396)
Immunoglobulin light chain amyloidosis: 2018 Update on diagnosis, prognosis, and treatment
American journal of hematology/oncology, 2018 Immunoglobulin light chain amyloidosis is a clonal, nonproliferative plasma cell disorder in which fragments of immunoglobulin light or heavy chain are deposited in tissues.
M. Gertz
semanticscholar +1 more source
Long-term cultures of murine fetal liver retain very early B lymphoid phenotype. [PDF]
, 1984 Long-term cultures of murine fetal liver have been successfully established using a modification of our in vitro bone marrow culture system (14, 15).
Denis, KA +3 more
core
Advanced Science, EarlyView.Draper is evolutionarily conserved across most insect species. Loss of Draper inhibits autophagy activation, delaying middle silk gland degradation in the silkworm during metamorphosis. Draper interacts with autophagy ‐ related protein 3 (ATG3) to orchestrate autophagosome formation—a process essential for silk gland degradation during the larval‐pupal
Shiyu Zou +9 more
wiley +1 more source
Involution of the mouse mammary gland is associated with an immune cascade and an acute-phase response, involving LBP, CD14 and STAT3 [PDF]
, 2004 INTRODUCTION: Involution of the mammary gland is a complex process of controlled apoptosis and tissue remodelling. The aim of the project was to identify genes that are specifically involved in this process.
Bell, A.K. +9 more
core
BLOC1S1 Attenuates B. Melitensis 16M LPS‐Triggered Autophagy by Spatial Confinement of TDP‐43
Advanced Science, EarlyView.This study explores how B. melitensis 16M LPS and BLOC1S1 regulate autophagy in goat spermatogonial stem cells. The 16M LPS is activating AMPK‐dependent autophagy, increasing LC3B‐II/I ratios and lysosomal genes, while Escherichia coli LPS shows no effect.
Shicheng Wan +13 more
wiley +1 more source
Immunoglobulin heavy chain gene rearrangements in patients with Gaucher disease [PDF]
Journal of Medical Biochemistry, 2018 Background: Several studies support the evidence of increased incidence of hematological complications in Gaucher disease including monoclonal and polyclonal gammopathies and blood malignancies, especially multiple myeloma.
Rodić Predrag +8 more
doaj
Acquired cutis laxa associated with light and heavy chain deposition disease
Indian Dermatology Online Journal, 2018 Acquired cutis laxa (ACL) is a rare connective tissue disorder characterized by pendulous and coarsely wrinkled skin. There have been few cases of its association to monoclonal immunoglobulin deposition disease (MIDD), which constitutes the light chain ...
Reena A Majithia +3 more
doaj +1 more source
VH-RELATED IDIOTOPES DETECTED BY SITE-DIRECTED MUTAGENESIS [PDF]
, 1992 The function of the CD4 cell surface protein as coreceptor on T helper lymphocytes and as receptor for HIV makes this glycoprotein a prime target for an immune intervention with mAb.
Cheng, Y. H. +4 more
core +1 more source
Franklin's disease: immunoglobulin heavy chain disease.
Stem cell investigation, 2015 A 64-year-old male presented with persistent fatigue, weakness and abdominal discomfort. He was found to have pancytopenia and hepatosplenomegaly. His bone marrow examination was mildly hypocellular with trilineage hematopoiesis. Serum protein electrophoresis revealed broad beta protein area but no gamma monoclonal spike (A).
John C. Nelson +4 more
openaire +3 more sources
Advanced Science, EarlyView.Quaternary ammonium salts are used to control the spacing between GO layers, enabling in situ growth of ZIF‐8. The resulting ZIF‐8‐GO membrane exhibits nearly complete rejection of n‐docosane in n‐hexane, solvent permeance of 16.4 ± 0.8 L m−2 h−1 bar−1, and enriches alkanes and aromatics with a molecular weight cut‐off of 310 g mol−1 in shale oil ...
Hang Wang +6 more
wiley +1 more source