A case of pancreatic cancer including osteoclast-like gaiant cells.
Hirotaka Iwase +4 more
openalex +2 more sources
Sphingomyelinase and ceramide inhibit formation of F‐actin ring in and bone resorption by rabbit mature osteoclasts [PDF]
Hiroyuki Takeda +5 more
openalex +1 more source
Nanozymes for Non‐Neoplastic Diseases: Catalytic Therapy Redefined
Non‐neoplastic diseases pose a significant health burden. Nanozymes, enzyme‐like nanomaterials, offer promising strategies for regulating oxidative stress and inflammation. This review explores their development, structure–function relationships, and therapeutic potential, with a focus on precision medicine through targeted delivery and multimodal ...
Ling Mei +8 more
wiley +1 more source
Effects of Occlusal Hypofunction on Osteoclastogenesis Induced by Periodontal Ligament Cells. [PDF]
Takahashi T, Iizuka T.
europepmc +1 more source
Lipopolysaccharide (LPS) Stimulates the Production of Tumor Necrosis Factor (TNF)‐α and Expression of Inducible Nitric Oxide Synthase (iNOS) by Osteoclasts (OCL) in Murine Bone Marrow Cell Culture [PDF]
Ichiro Kikkawa +5 more
openalex +1 more source
Artificial Intelligence for Bone: Theory, Methods, and Applications
Advances in artificial intelligence (AI) offer the potential to improve bone research. The current review explores the contributions of AI to pathological study, biomarker discovery, drug design, and clinical diagnosis and prognosis of bone diseases. We envision that AI‐driven methodologies will enable identifying novel targets for drugs discovery. The
Dongfeng Yuan +3 more
wiley +1 more source
Macropinocytosis fuels osteoclast differentiation in bone-related diseases. [PDF]
Gu M +7 more
europepmc +1 more source
Cathepsin B and L activities in isolated osteoclasts
Barry R. Rifkin +5 more
openalex +1 more source
Osteoclasts from Human Giant Cell Tumors of Bone Lack Estrogen Receptors [PDF]
Fiona Collier
openalex +1 more source
ABSTRACT Chondrocalcinosis (CCAL), also known as calcium pyrophosphate dihydrate deposition disease (CPPDD), is a frequent multifactorial condition in the elderly, but there are two rare autosomal dominant Mendelian forms, CCAL1 (OMIM %600668) and CCAL2. Only three families with molecularly proven CCAL1 have been reported.
Anna‐Christina Pansa +4 more
wiley +1 more source

