Results 161 to 170 of about 598,872 (375)
Non‐Porous Hydrogel Scaffolds for Locoregional Chemotherapy: A One‐Pot Synthesis Approach
This hydrogel scaffold with tunable mechanical, water retention, degradation, and drug release properties is obtained by polymerizing the hydrophilic OEGMEMA monomer in the presence of PLGA and DOX under concentrated conditions. Its non‐porous structure provides diffusion‐based drug release, while extended drug release is possible by incorporating PLGA.
Sadik Kaga, Gizem Fatma Erguner
wiley +1 more source
Smart Surface Engineering in Microcarriers: Toward Applications in Cancer Therapy
A microcarrier with dual surface modification integrates two distinct pH‐sensitive nanoreservoirs, enabling precise, site‐specific drug delivery and potential extracellular matrix degradation. This dual functionalization strategy ensures the separation of therapeutic functions, effectively preventing cross‐process interference and aiming synergistic ...
Fatemeh Rajabasadi+9 more
wiley +1 more source
Benign Uterine Corpus Mixed Epithelial and Mesenchymal Neoplasm [PDF]
openalex +1 more source
A Rare Case of Synchronous Primary Uterine Cervical Minimal Deviation Adenocarcinoma and low-grade appendiceal mucinous neoplasm [PDF]
Junmiao Xiang, Zhuhua Cai, Sisi Yu
openalex +1 more source
Uterine Perivascular Epithelioid Cell Tumour Presenting as a Cervical Mass [PDF]
Perivascular Epithelioid Cell Tumour (PEComa) also known as myelomelanocytic tumours are uncommon, recently described mesenchymal tumours that include angiomyolipoma, clear cell sugar tumour of the lung, lymphangioleiomyoma and tumours composed ...
Azad, Najamul Sahar+3 more
core +1 more source
ABSTRACT Familial adenomatous polyposis (FAP) is a well‐characterized hereditary colorectal cancer syndrome driven by germline mutations in the APC gene. KRAS mutations, although more common in sporadic colorectal and endometrial cancers, are rarely seen concurrently in patients with FAP.
Tongchuan Yin+4 more
wiley +1 more source
Novel Findings in Pediatric and Adolescent Patients With Cancer and a Germline SMARCA4 Variant
ABSTRACT Introduction SMARCA4 is a known susceptibility gene for malignant rhabdoid tumors (MRT) in children and small cell carcinoma of the ovary hypercalcemic type (SCCOHT) in young females and women. Recently, a novel association between germline SMARCA4 variants and predisposition to neuroblastoma was proposed.
Nienke van Engelen+12 more
wiley +1 more source