Results 131 to 140 of about 4,786,755 (237)
This study identifies Igκ expression in cardiomyocytes, with predominant localization at ICDs. Cardiomyocyte‐specific Igκ knockout induces cardiac dysfunction and ICDs structural disorganization. Mechanistically, Igκ stabilizes plectin to facilitate desmin‒actin network assembly and anchor desmin to DSP, which is critical for maintaining ICDs ...
Zhu Zhu +12 more
wiley +1 more source
Gradually Enlarging Nodular Pulmonary Amyloidosis Associated With Sjögren's Syndrome
A woman with Sjögren's syndrome presented with progressively enlarging pulmonary nodules showing calcification and cystic changes, mimicking metastatic malignancy. Histological examination confirmed AL λ‐type nodular pulmonary amyloidosis. Recognition of this radiological pattern is important to avoid misdiagnosis and unnecessary invasive interventions.
Noboru Morikawa +2 more
wiley +1 more source
Predicting Structural Consequences of Antibody Light Chain N-Glycosylation in AL Amyloidosis
Background/Objectives: Antibody light chains form amyloid fibrils that lead to progressive tissue damage in amyloid light chain (AL) amyloidosis. The properties of each patient’s unique light chain appear to determine its propensity to form amyloid.
Gareth J. Morgan +4 more
doaj +1 more source
Pulmonary amyloidosis presents with diverse radiological manifestations ranging from nodular lesions to diffuse interstitial abnormalities. Conventional forceps TBLB may serve different clinical roles according to disease presentation: distinguishing localized nodular amyloidosis from malignancy and providing an initial diagnostic clue to systemic ...
Masaki Tanaka +9 more
wiley +1 more source
Importance of tissue diagnosis in pulmonary amyloidosis, a rare albeit treatable cause of interstitial lung disease. ABSTRACT Pulmonary amyloidosis is a rare manifestation of amyloid deposition which can present as a rare albeit treatable cause of interstitial lung disease.
Kai Wen Hwang +3 more
wiley +1 more source
Hepatic amyloidosis with light chain deposition disease. A rare association.
Monoclonal immunoglobulin deposition diseases are due to pathological protein deposition in various tissues and organs. Protein deposits may be found in a single tissue or systemically and the organs most frequently involved are kidney, heart, peripheral
De Paoli A +7 more
core +1 more source
The identification of the glymphatic system (GS) and meningeal lymphatic vessels (mLVs) challenges the century‐old “immune‐privileged” dogma of the central nervous system (CNS), establishing a critical mechanistic link between impaired waste clearance (Aβ/tau) and the pathogenesis of Alzheimer's disease (AD).
Bingbing Song +10 more
wiley +1 more source
Systemic light-chain amyloidosis presenting with rapid progressive heart failure
Systemic amyloid light-chain (AL) amyloidosis is caused by deposition of immunoglobulin light-chain proteins. AL amyloidosis is a rapidly progressive disease that affects multiple organs. Cardiac involvement is frequent (50%) and the median survival is 5
SÜNBÜL, MURAT +2 more
core +1 more source
In this 28‐patient retrospective cohort, rituximab‐based regimens for IgM‐related neuropathy yielded significant, sustained functional and neurological improvements over a 2‐year follow‐up. Furthermore, reductions in serum IgM levels correlated with improved Inflammatory Neuropathy Cause and Treatment disability scores, highlighting the long‐term ...
Maria Gavriatopoulou +15 more
wiley +1 more source
Integrated Engineering of CAR‐T Cells for Solid Tumours
Solid tumours pose multifactorial barriers including antigen heterogeneity, immunosuppressive microenvironment, and poor T‐cell trafficking, limiting CAR‐T efficacy compared to hematologic malignancies. Integrated engineering strategies are essential, combining logic‐gated receptors for precision, metabolic‐epigenetic reprogramming for resilience, and ...
Chao Yang +5 more
wiley +1 more source

